The Hutchinson-Gilford progeria syndrome. Report of 4 cases and review of the literature (Q39914175)

15 September 2017

title

The Hutchinson-Gilford progeria syndrome. Report of 4 cases and review of the literature (English)

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15 September 2017

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DeBusk FL

1

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15 September 2017

publication date

1 April 1972

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The Journal of Pediatrics

15 September 2017

language of work or name

English

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published in

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15 September 2017

volume

80

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15 September 2017

issue

4

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15 September 2017

page(s)

697-724

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publication type of scholarly work

15 September 2017

review article

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On a Condition of Mixed Premature and Immature Development

cites work

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https://api.crossref.org/works/10.1016%2FS0022-3476%2872%2980229-4

A case of progeronanism (progeria of Gilford)

7 January 2021

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Progeria (Hutchinson-Gilford syndrome). Report of a case and review of the literature

7 January 2021

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The rate of growth in progeria, with a report of two cases

7 January 2021

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Progeria: report of a case with post-mortem findings

7 January 2021

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Progeria, a pathologic study

7 January 2021

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Report of a patient with typical progeria, including data from urinary hormone studies

7 January 2021

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Progeria and atherosclerosis

7 January 2021

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7 January 2021

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Amino-aciduria and hypermetabolism in progeria

7 January 2021

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Progeria; report of a case

7 January 2021

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Cardiovascular manifestations in progeria. Report of clinical and pathologic findings in a patient with severe arteriosclerotic heart disease and aortic stenosis

7 January 2021

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7 January 2021

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PROGERIA: AUDIOLOGIC ASPECTS. FINAL REPORT OF A CASE.

7 January 2021

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Progressive osteolysis in progeria

7 January 2021

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Growth and Growth Hormone: I. changes in Serum Level of Growth Hormone Following Hypoglycemia in 134 children with Growth Rctardation

7 January 2021

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Lifespan of cultured cells in progeria

7 January 2021

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Progeria: Case Report with Long-term Studies of Serum Lipids

7 January 2021

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Sleep characteristics and endocrine response in progeria

7 January 2021

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NOTE ON A CASE OF PREMATURE SENILITY (PROGERIA).

7 January 2021

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Progeria with nanism and congenital cataracts in a five year old child

7 January 2021

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A syndrome resembling progeria: A review of two cases

7 January 2021

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Zur Differentialdiagnose und ocularen Symptomatologie der Cutis marmorata teleangiectatica congenita und der Progerie

7 January 2021

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Progeria. Case description

7 January 2021

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The early formation of irregular secondary dentine in progeria

7 January 2021

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Mandibulofacial dysmorphia with ocular abnormalities

7 January 2021

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Hallermann-Streiff syndrome, a dyscephaly with congenital cataracts and hypotrichosis

7 January 2021

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DYSCEPHALIA MANDIBULO-OCULO-FACIALIS. (HALLERMANN-STREIFF SYNDROME).

7 January 2021

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Dwarfism with retinal atrophy and deafness

7 January 2021

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Dwarfism with Retinal Atrophy and Deafness

7 January 2021

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https://api.crossref.org/works/10.1016%2FS0022-3476%2872%2980229-4

Multiple congenital abnormalities with diaphyseal dysplasia (Camurati—Engelmann's syndrome)

7 January 2021

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A possible case of delayed mutation in man

7 January 2021

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Delayed mutation in man; a critical observation on the work of Ch. Auerbachs (1956)

7 January 2021

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Parental age and mutation

7 January 2021

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7 January 2021

https://api.crossref.org/works/10.1016%2FS0022-3476%2872%2980229-4

inferred from DOI database lookup

7 January 2021

based on heuristic

Dermatohistopathology of various types of scleroderma

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2872%2980229-4

Pathologic observations concerning the cutaneous lesion of progressive systemic sclerosis: an electron microscopic histochemical and immunohistochemical study

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2872%2980229-4

Pathologic findings in progeria: myocardial fibrosis and lipofuscin pigment

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2872%2980229-4

10.1016/S0022-3476(72)80229-4

7 January 2021

Identifiers

DOI

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15 September 2017

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