Literature DB >> 5364870

[Some progeroid cases and their diagnostic classification].

H R Wiedemann.   

Abstract

Mesh：

Year:  1969        PMID： 5364870

Source DB:  PubMed          Journal:  Z Kinderheilkd        ISSN： 0044-2917


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  6 in total

1.  Glycosaminoglycan-free small proteoglycan core protein is secreted by fibroblasts from a patient with a syndrome resembling progeroid.

Authors:  H Kresse; S Rosthøj; E Quentin; J Hollmann; J Glössl; S Okada; T Tønnesen
Journal:  Am J Hum Genet       Date:  1987-09       Impact factor: 11.025

2.  An unidentified neonatal progeroid syndrome: follow-up report.

Authors:  H R Wiedemann
Journal:  Eur J Pediatr       Date:  1979-01-18       Impact factor: 3.183

3.  De Barsy syndrome--an autosomal recessive, progeroid syndrome.

Authors:  J Kunze; F Majewski; P Montgomery; A Hockey; I Karkut; T Riebel
Journal:  Eur J Pediatr       Date:  1985-11       Impact factor: 3.183

4.  Progeria: a cell culture study and clinical report of familial incidence.

Authors:  T Rautenstrauch; F Snigula
Journal:  Eur J Pediatr       Date:  1977-01-26       Impact factor: 3.183

Review 5.  The neonatal pseudo-hydrocephalic progeroid syndrome (Wiedemann-Rautenstrauch). Report of a new patient and review of the literature.

Authors:  C Rudin; L Thommen; C Fliegel; B Steinmann; U Bühler
Journal:  Eur J Pediatr       Date:  1988-05       Impact factor: 3.183

6.  Biochemical, morphological and immunological findings in a patient with a cutis laxa-associated inborn disorder (De Barsy syndrome).

Authors:  B F Pontz; F Zepp; H Stöss
Journal:  Eur J Pediatr       Date:  1986-10       Impact factor: 3.183
  6 in total

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