Ataxia-ocular motor apraxia syndrome: an investigation of cellular radiosensitivity of patients and their families (Q24514997)

1 July 2017

Ataxia-ocular motor apraxia syndrome: an investigation of cellular radiosensitivity of patients and their families (English)

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1 July 2017

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Hannan MA

1

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1 July 2017

Sigut D

series ordinal

2

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1 July 2017

Waghray M

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3

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1 July 2017

Gascon GG

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4

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1 July 2017

language of work or name

English

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publication date

1 December 1994

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Journal of Medical Genetics

1 July 2017

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1 July 2017

31

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1 July 2017

12

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1 July 2017

953-956

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Ataxia-ocular motor apraxia: a syndrome mimicking ataxia-telangiectasia

1 July 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016697

Ataxia-telangiectasia: an inherited disorder of ionizing-radiation sensitivity in man. Progress in the elucidation of the underlying biochemical defect

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016697

Cancer in ataxia-telangiectasia patients: analysis of factors leading to radiation--induced and spontaneous tumors

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016697

Variant forms of ataxia telangiectasia

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016697

Damage-resistant DNA synthesis in eukaryotes

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016697

Fusion of cultured multiple-sclerosis brain cells with indicator cells: presence of nucleocapsids and virions and isolation of parainfluenza-type virus

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016697

Mortality and cancer incidence in 263 patients with ataxia-telangiectasia

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016697

Neurological disease in xeroderma pigmentosum. Documentation of a late onset type of the juvenile onset form.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016697

Cytogenetic investigations in three cell types of a Saudi family with ataxia telangiectasia

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016697

Adrenal cortical-anterior pituitary relationships during embryonic life.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016697

Variant of ataxia-telangiectasia with low-level radiosensitivity

29 November 2018

1 reference

12 December 2020

Ataxia-Telangiectasia: A Multisystem Hereditary Disease with Immunodeficiency, Impaired Organ Maturation, X-Ray Hypersensitivity, and a High Incidence of Neoplasia

1 reference

12 December 2020

Pattern of degenerative ataxias in the eastern province of Saudi Arabia

1 reference

12 December 2020

Ataxia-without-telangiectasia in two sisters with rearrangements of chromosomes 7 and 14

1 reference

12 December 2020

Spontaneous cytogenetic abnormalities in lymphocytes from thirteen patients with ataxia telangiectasia

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12 December 2020

Incidence of cancer in 161 families affected by ataxia-telangiectasia

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12 December 2020

Identifiers

DOI

10.1136/JMG.31.12.953

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1 July 2017

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