Genetic Aspects of Amyloidosis (Q37130426)

18 August 2017

1 reference

title

Genetic aspects of amyloidosis (English)

1 reference

18 August 2017

Genetic Aspects of Amyloidosis (English)

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

7 December 2022

author name string

D. R. Jacobson

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1839349

7 December 2022

J. N. Buxbaum

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1839349

7 December 2022

language of work or name

English

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=1839349

7 December 2022

publication date

1 January 1991

1 reference

full work available at URL

18 August 2017

http://link.springer.com/content/pdf/10.1007/978-1-4684-5958-6_2.pdf

file format

Portable Document Format

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

Advances in human genetics

7 December 2022

published in

1 reference

18 August 2017

20

1 reference

18 August 2017

69-123, 309-11

1 reference

The human cystatin C gene (CST3), mutated in hereditary cystatin C amyloid angiopathy, is located on chromosome 20.

18 August 2017

1

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

Familial renal amyloidosis. Case reports, literature review and classification

7 December 2022

2

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

Familial periodic disease with renal damage

7 December 2022

4

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

A peculiar form of peripheral neuropathy; familiar atypical generalized amyloidosis with special involvement of the peripheral nerves

7 December 2022

7

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

Treatment by pacemaker in familial amyloid polyneuropathy

7 December 2022

9

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

Polyneuritic amyloidosis in a Japanese family

7 December 2022

10

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

AMYLOIDOSIS IN RHEUMATOID ARTHRITIS INVESTIGATED BY MEANS OF RECTAL BIOPSY.

7 December 2022

11

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

Plasma dopamine beta-hydroxylase: rapid diagnostic test for recurrent hereditary polyserositis

7 December 2022

15

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

The place of human gamma-trace (cystatin C) amongst the cysteine proteinase inhibitors

7 December 2022

16

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

Hereditary amyloidosis--disease entity and clinical model

7 December 2022

17

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

Generalized amyloid in a family of Swedish origin. A study of 426 family members in seven generations of a new kinship with neuropathy, nephropathy, and central nervous system involvement

7 December 2022

18

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

Prealbumin and retinol binding protein serum concentrations in the Indiana type hereditary amyloidosis

7 December 2022

19

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

Identification of carriers of a variant plasma prealbumin (transthyretin) associated with familial amyloidotic polyneuropathy type I.

7 December 2022

20

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

Hereditary amyloidosis: description of a new American kindred with late onset cardiomyopathy. Appalachian amyloid

7 December 2022

22

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

DNA methylation and the frequency of CpG in animal DNA.

7 December 2022

25

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

Structure of prealbumin: secondary, tertiary and quaternary interactions determined by Fourier refinement at 1.8 A

7 December 2022

27

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

Amyloidosis as the sole manifestation of familial Mediterranean fever (FMF). Further evidence of its genetic nature

7 December 2022

28

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

Periodic fever: occurrence in five generations

7 December 2022

29

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

Human cystatin, a new protein inhibitor of cysteine proteinases

7 December 2022

30

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

Senile cardiac amyloidosis

7 December 2022

31

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

Aberrant immunoglobulin synthesis in light chain amyloidosis. Free light chain and light chain fragment production by human bone marrow cells in short-term tissue culture

7 December 2022

33

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

Type I familial amyloid polyneuropathy in a Chinese family

7 December 2022

35

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

The transthyretin cDNA sequence is normal in transthyretin-derived senile systemic amyloidosis

7 December 2022

36

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

Amyloid fibril in hereditary cerebral hemorrhage with amyloidosis (HCHWA) is related to the gastroentero-pancreatic neuroendocrine protein, gamma trace

7 December 2022

37

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

The mutational spectrum of single base-pair substitutions causing human genetic disease: patterns and predictions

7 December 2022

38

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

The CpG dinucleotide and human genetic disease

7 December 2022

39

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

Frequency and distribution of senile cardiovascular amyloid. A clinicopathologic correlation

7 December 2022

40

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

Amyloid fibril protein related to prealbumin in familial amyloidotic polyneuropathy

7 December 2022

41

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

A liver-specific DNA-binding protein recognizes multiple nucleotide sites in regulatory regions of transthyretin, alpha 1-antitrypsin, albumin, and simian virus 40 genes

7 December 2022

42

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

Transcriptional control of the mouse prealbumin (transthyretin) gene: both promoter sequences and a distinct enhancer are cell specific

7 December 2022

43

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

Pathology and Histochemistry of Amyloidosis in Old Age

7 December 2022

45

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

Beta amyloid gene duplication in Alzheimer's disease and karyotypically normal Down syndrome.

7 December 2022

46

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

Amyloidosis in the rheumatic diseases

7 December 2022

47

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

Immunocytochemical demonstration of prealbumin in the vitreous in heredofamilial amyloidosis

7 December 2022

49

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

Polymorphism of human plasma thyroxine binding prealbumin.

7 December 2022

51

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

Primary structure of an amyloid prealbumin and its plasma precursor in a heredofamilial polyneuropathy of Swedish origin

7 December 2022

52

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

Characterization of a transthyretin (prealbumin) variant associated with familial amyloidotic polyneuropathy type II (Indiana/Swiss).

7 December 2022

53

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

Highly refractile myocardial echoes in familial amyloidosis with polyneuropathy. A correlative echocardiographic and histopathological study

7 December 2022

56

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

Cardiac arrhythmias in familial amyloid polyneuropathy during anaesthesia.

7 December 2022

57

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

Immunoglobulin heavy-chain-associated amyloidosis

7 December 2022

59

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

Erosive arthritis in hereditary amyloidosis

7 December 2022

60

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

Internal mammary arteriovenous fistula

7 December 2022

61

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

Negative cooperativity in the binding of thyroxine to human serum prealbumin. Preparation of tritium-labeled 8-anilino-1-naphthalenesulfonic acid

7 December 2022

62

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

The amyloidosis of juvenile rheumatoid arthritis--comparative studies in Polish and American children. I. Levels of serum SAA protein

7 December 2022

64

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

Familial primary amyloidosis with severe amyloid heart disease

7 December 2022

67

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

Molecular analysis of a variant type of familial amyloidotic polyneuropathy showing cerebellar ataxia and pyramidal tract signs

7 December 2022

70

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

Amyloid beta-protein gene duplication is not common in Alzheimer's disease: analysis by polymorphic restriction fragments.

7 December 2022

71

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

Multiple endocrine neoplasia type 2a associated with cutaneous lichen amyloidosis

7 December 2022

74

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

Autosomal dominant familial Mediterranean fever-like syndrome with amyloidosis

7 December 2022

77

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

Amyloid fibrils in hereditary cerebral hemorrhage with amyloidosis of Icelandic type is a variant of gamma-trace basic protein (cystatin C)

7 December 2022

78

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

Amyloid deposits and amyloidosis. The beta-fibrilloses (first of two parts).

7 December 2022

79

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

Amyloidosis of the nervous system

7 December 2022

80

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

Alzheimer's disease: Initial report of the purification and characterization of a novel cerebrovascular amyloid protein

7 December 2022

81

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

Characterization and chromosomal localization of a cDNA encoding brain amyloid of Alzheimer's disease

7 December 2022

83

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

Prealbumin. A major constituent of vitreous amyloid

7 December 2022

85

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

Systemic senile amyloidosis. Identification of a new prealbumin (transthyretin) variant in cardiac tissue: immunologic and biochemical similarity to one form of familial amyloidotic polyneuropathy

7 December 2022

86

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

Are sodium bicarbonate and potassium bicarbonate fully dissociated under physiological conditions?

7 December 2022

88

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

Abnormal metabolism of gamma-trace alkaline microprotein. The basic defect in hereditary cerebral hemorrhage with amyloidosis

7 December 2022

89

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

Hereditary cerebral haemorrhage with amyloidosis

7 December 2022

90

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

Amyloid protein in familial amyloidosis (Finnish type) is homologous to gelsolin, an actin-binding protein

7 December 2022

92

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

Peripheral nerve pathological findings in familial amyloid polyneuropathy: a correlative study of proximal sciatic nerve and sural nerve lesions

7 December 2022

94

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

Lack of association of a restriction fragment length polymorphism for serum amyloid P gene with reactive amyloidosis

7 December 2022

95

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

Evaluation of systemic amyloidosis by scintigraphy with 123I-labeled serum amyloid P component

7 December 2022

96

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

Familial Mediterranean fever

7 December 2022

98

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

Transthyretin: a choroid plexus-specific transport protein in human brain. The 1986 S. Weir Mitchell award

7 December 2022

99

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

Hot spot mutations in adenosine deaminase deficiency

7 December 2022

102

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

Homozygosity for the transthyretin-met30-gene in two Swedish sibs with familial amyloidotic polyneuropathy

7 December 2022

104

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

Molecular genetics of amyloid neuropathy in Europe

7 December 2022

106

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

Echocardiographic assessment of the evolution of amyloid heart disease: a study with familial amyloid polyneuropathy

7 December 2022

107

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

Early identification of amyloid heart disease by technetium-99m-pyrophosphate scintigraphy: a study with familial amyloid polyneuropathy

7 December 2022

108

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

Hereditary generalized amyloidosis with polyneuropathy. Clinicopathological study of 65 Japanese patients

7 December 2022

109

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

Restriction fragment analysis confirms the position 33 mutation in transthyretin from an Israeli patient (SKO) with familial amyloidotic polyneuropathy

7 December 2022

113

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

Transthyretin immunoreactivity in human and porcine liver, choroid plexus, and pancreatic islets

7 December 2022

116

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

Hereditary cystatin C (gamma-trace) amyloid angiopathy of the CNS causing cerebral hemorrhage.

7 December 2022

117

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

The relation of atrial natriuretic factor to isolated atrial amyloid

7 December 2022

118

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

A seroepidemiologic survey of the prevalence of herpes simplex virus type 2 infection in the United States

7 December 2022

119

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

A variant prealbumin-related low molecular weight amyloid fibril protein in familial amyloid polyneuropathy of Japanese origin

7 December 2022

123

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

Localization of immunoreactive transthyretin (prealbumin) and of transthyretin mRNA in fetal and adult rat brain.

7 December 2022

125

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

Impaired left ventricular diastolic filling in patients with familial amyloid polyneuropathy: a pulsed Doppler echocardiographic study

7 December 2022

127

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

Localization of human SAA gene(s) to chromosome 11 and detection of DNA polymorphisms

7 December 2022

130

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

Human serum amyloid A. Three hepatic mRNAs and the corresponding proteins in one person

7 December 2022

131

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

Amyloidogenesis in Organ-Limited Cutaneous Amyloidosis: An Antigenic Identity Between Epidermal Keratin and Skin Amyloid

7 December 2022

132

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

Left ventricular systolic and diastolic time intervals in familial amyloid polyneuropathy

7 December 2022

133

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

7 December 2022

Systemic amyloidosis

134

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

7 December 2022

Cardiac amyloidosis

135

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

Degradation of serum amyloid A protein by surface-associated enzymes of human blood monocytes

7 December 2022

137

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

The Amino Acid Sequence of a Major Nonimmunoglobulin Component of Some Amyloid Fibrils

7 December 2022

139

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

Mutation of the Alzheimer's disease amyloid gene in hereditary cerebral hemorrhage, Dutch type.

7 December 2022

140

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

Pathology of the senescent heart: anatomic observations on 237 autopsy studies of patients 90 to 105 years old

7 December 2022

141

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

Transthyretin is synthesized in the mammalian eye

7 December 2022

144

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

A linked genetic marker for multiple endocrine neoplasia type 2A on chromosome 10

7 December 2022

145

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

C5a-inhibitor deficiency in peritoneal fluids from patients with familial Mediterranean fever

7 December 2022

146

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

Finnish hereditary amyloidosis. Amino acid sequence homology between the amyloid fibril protein and human plasma gelsoline

7 December 2022

148

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

Cloning and sequence analysis of cDNA for human prealbumin

7 December 2022

153

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

Familial renal amyloidosis: case reports and genetic studies

7 December 2022

154

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

Molecular biology of Alzheimer's disease

7 December 2022

156

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

Acute-phase response of mRNAs for serum amyloid P component, C-reactive protein and prealbumin (transthyretin) in mouse liver

7 December 2022

158

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

Beta-amyloid gene dosage in Alzheimer's disease

7 December 2022

159

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

Ten year mortality and causes of death in patients with rheumatoid arthritis

7 December 2022

160

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

Revised analysis of amino acid replacement in a prealbumin variant (SKO-III) associated with familial amyloidotic polyneuropathy of Jewish origin

7 December 2022

161

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

Diagnostic radioimmunoassay for familial amyloidotic polyneuropathy before clinical onset

7 December 2022

162

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

Abnormal transthyretin in asymptomatic relatives in familial amyloidotic polyneuropathy.

7 December 2022

163

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

Hereditary amyloidosis: detection of variant prealbumin genes by restriction enzyme analysis of amplified genomic DNA sequences

7 December 2022

164

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

Variant apolipoprotein AI as a major constituent of a human hereditary amyloid

7 December 2022

165

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

Direct sequencing of the gene for Maryland/German familial amyloidotic polyneuropathy type II and genotyping by allele-specific enzymatic amplification

7 December 2022

166

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

Autonomic neuropathy in familial amyloidotic polyneuropathy. A clinical study based on heart rate variability

7 December 2022

168

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

NINE CASES OF HEREDITARY AND NON-HEREDITARY PERIODIC DISEASES.

7 December 2022

169

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

A new prealbumin variant in familial amyloid cardiomyopathy of Danish origin

7 December 2022

171

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

Immunofluorescence and histochemical studies of localized cutaneous amyloidosis

7 December 2022

172

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

Heart valve involvement in familial amyloidosis with polyneuropathy

7 December 2022

173

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

Senile cardiac amyloidosis with myocardial dysfunction. Diagnosis by endomyocardial biopsy and immunohistochemistry.

7 December 2022

174

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

The secreted form of the Alzheimer's amyloid precursor protein with the Kunitz domain is protease nexin-II.

7 December 2022

175

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

Familial Mediterranean fever in Turkey. A report of twenty cases

7 December 2022

177

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

Amino acid sequence of amyloid-related apoprotein (apoSAA1) from human high-density lipoprotein

7 December 2022

179

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

X-linked cutaneous amyloidosis: further clinical and pathological observations

7 December 2022

180

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

Mapping of the gene encoding the beta-amyloid precursor protein and its relationship to the Down syndrome region of chromosome 21

7 December 2022

181

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

Gene dosage of the amyloid beta precursor protein in Alzheimer's disease

7 December 2022

183

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

Senile cardiac amyloidosis

7 December 2022

184

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

The pathology of senile cardiac amyloidosis

7 December 2022

185

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

The characterization of soluble amyloid prepared in water

7 December 2022

186

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

Primary structure of an amyloid prealbumin variant in familial polyneuropathy of Jewish origin

7 December 2022

188

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

Periodic peritonitis; heredity and pathology: report of seventy-two cases

7 December 2022

192

1 reference

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Amyloid A4 protein and its precursor in Down's syndrome and Alzheimer's disease.

7 December 2022

195

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

Genetic analysis of familial amyloidotic polyneuropathy, an autosomal dominant disease

7 December 2022

197

1 reference

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Restless legs syndrome and nocturnal myoclonus: initial clinical manifestation of familial amyloid polyneuropathy

7 December 2022

199

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

Restriction fragment length polymorphism analysis of mutated transthyretin in vitreous amyloidosis

7 December 2022

200

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

Amyloid fibril protein in familial amyloidotic polyneuropathy, Portuguese type. Definition of molecular abnormality in transthyretin (prealbumin).

7 December 2022

202

1 reference

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Biochemical marker in familial amyloidotic polyneuropathy, Portuguese type. Family studies on the transthyretin (prealbumin)-methionine-30 variant

7 December 2022

203

1 reference

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Genetic expression of a transthyretin mutation in typical and late-onset Portuguese families with familial amyloidotic polyneuropathy

7 December 2022

204

1 reference

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Cardiac amyloidosis: report of a patient heterozygous for the transthyretin isoleucine 122 variant

7 December 2022

207

1 reference

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Diagnosis of familial amyloidotic polyneuropathy by recombinant DNA techniques.

7 December 2022

209

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

Structure of the chromosomal gene for human serum prealbumin

7 December 2022

210

1 reference

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Familial amyloid polyneuropathy: report of an autopsy case with neuropathy, vitreous opacities and polycystic kidney

7 December 2022

211

1 reference

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Absence of Linkage of Chromosome 21q21 Markers to Familial Alzheimer's Disease

7 December 2022

212

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

Familial Mediterranean Fever in Armenians. Analysis of 100 cases.

7 December 2022

213

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

Deciphering Alzheimer's disease: the amyloid precursor protein yields new clues

7 December 2022

214

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

Assignment of multiple endocrine neoplasia type 2A to chromosome 10 by linkage

7 December 2022

218

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

Evidence that beta-amyloid protein in Alzheimer's disease is not derived by normal processing

7 December 2022

219

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

A new mutation causing familial amyloidotic polyneuropathy

7 December 2022

220

1 reference

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The prealbumin nature of the amyloid protein in familial amyloid polyneuropathy (FAP)-swedish variety

7 December 2022

222

1 reference

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Lowered prealbumin levels in patients with familial amyloid polyneuropathy (FAP) and their non-affected but at risk relatives.

7 December 2022

223

1 reference

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The Complete Amino-Acid Sequence of Non-Immunolobulin Amyloid Fibril Protein AS in Rheumatoid Arthritis

7 December 2022

226

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

Characterization of amyloid fibril proteins from medullary carcinoma of the thyroid

7 December 2022

228

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

Senile cardiac amyloid is related to prealbumin

7 December 2022

229

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

Type and distribution of pulmonary parenchymal and vascular amyloid. Correlation with cardiac amyloid

7 December 2022

230

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

Clinical significance of histopathologic patterns of cardiac amyloidosis

7 December 2022

231

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

Familial Mediterranean fever. A survey of 470 cases and review of the literature

7 December 2022

234

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

Absence of duplication of chromosome 21 genes in familial and sporadic Alzheimer's disease

7 December 2022

236

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

The genetic defect causing familial Alzheimer's disease maps on chromosome 21.

7 December 2022

237

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

Genetic linkage studies suggest that Alzheimer's disease is not a single homogeneous disorder.

7 December 2022

238

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

Identification and characterization of a human transthyretin variant

7 December 2022

239

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

Multiple endocrine neoplasia type 2

7 December 2022

240

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

The amyloid beta protein gene is not duplicated in brains from patients with Alzheimer's disease

7 December 2022

241

1 reference

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Amyloid beta protein gene: cDNA, mRNA distribution, and genetic linkage near the Alzheimer locus.

7 December 2022

242

1 reference

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The genetic defect in familial Alzheimer's disease is not tightly linked to the amyloid beta-protein gene.

7 December 2022

243

1 reference

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Identification of amyloid prealbumin variant in familial amyloidotic polyneuropathy (Japanese type)

7 December 2022

244

1 reference

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Primary cardiac amyloidosis

7 December 2022

246

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

Observations on the brains of non-demented old people

7 December 2022

247

1 reference

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Expression of the genes for transthyretin, cystatin C and beta A4 amyloid precursor protein in sheep choroid plexus during development

7 December 2022

249

1 reference

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A novel variant of transthyretin (Tyr114 to Cys) deduced from the nucleotide sequences of gene fragments from familial amyloidotic polyneuropathy in Japanese sibling cases

7 December 2022

250

1 reference

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Two novel variants of transthyretin identified in Japanese cases with familial amyloidotic polyneuropathy: transthyretin (Glu42 to Gly) and transthyretin (Ser50 to Arg)

7 December 2022

251

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

Inherited predisposition to generalized amyloidosis. Clinical and pathological study of a family with neuropathy, nephropathy, and peptic ulcer

7 December 2022

252

1 reference

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Amyloid beta protein precursor gene and hereditary cerebral hemorrhage with amyloidosis (Dutch)

7 December 2022

253

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

Hereditary cerebral hemorrhage with amyloidosis in patients of Dutch origin is related to Alzheimer disease

7 December 2022

254

1 reference

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Protease nexin-II, a potent antichymotrypsin, shows identity to amyloid beta-protein precursor

7 December 2022

256

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

Familial primary cutaneous amyloidosis. Clinical, genetic, and immunofluorescent studies

7 December 2022

257

1 reference

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Brain amyloid and Alzheimer disease

7 December 2022

258

1 reference

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Apolipoprotein A-I variants. Naturally occurring substitutions of proline residues affect plasma concentration of apolipoprotein A-I.

7 December 2022

259

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Structural comparisons between mouse and human prealbumin

7 December 2022

260

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Localization of the human prealbumin gene to chromosome 18.

7 December 2022

261

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Biochemical and molecular genetic characterization of a new variant prealbumin associated with hereditary amyloidosis

7 December 2022

262

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Identification of a new hereditary amyloidosis prealbumin variant, Tyr-77, and detection of the gene by DNA analysis

7 December 2022

263

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Familial cerebral amyloid angiopathy presenting as recurrent cerebral haemorrhage.

7 December 2022

264

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Senile Cardiac Amyloidosis: Evidence of Two Different Amyloid Substances in the Ageing Heart

7 December 2022

266

1 reference

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Fibril in senile systemic amyloidosis is derived from normal transthyretin

7 December 2022

269

1 reference

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Neuritic plaques and cerebrovascular amyloid in Alzheimer disease are antigenically related

7 December 2022

272

1 reference

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A genetic marker for systemic amyloidosis in juvenile arthritis

7 December 2022

274

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Amyloid in the Aged Heart: Frequency and Clinical Significance

7 December 2022

275

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"Sporadic" prealbumin-related amyloid polyneuropathy: report of two cases

7 December 2022

277

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Absence of the cystatin C amyloid in the cerebral amyloid angiopathy, senile plaque, and extra-CNS amyloid deposits of aged Japanese.

7 December 2022

278

1 reference

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Distinct positive and negative elements control the limited hepatocyte and choroid plexus expression of transthyretin in transgenic mice

7 December 2022

279

1 reference

https://api.crossref.org/works/10.1007/978-1-4684-5958-6_2

Haplotype analysis of familial amyloidotic polyneuropathy

7 December 2022

280

1 reference

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A controlled trial of colchicine in preventing attacks of familial mediterranean fever

7 December 2022

283

1 reference

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7 December 2022

Identifiers

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=1839349

7 December 2022

1 reference