Literature DB >> 2325106

Wiedemann-Rautenstrauch syndrome.

H V Toriello1.   

Abstract

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Year:  1990        PMID： 2325106      PMCID： PMC1017029          DOI： 10.1136/jmg.27.4.256

Source DB:  PubMed          Journal:  J Med Genet        ISSN： 0022-2593            Impact factor:   6.318


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  6 in total

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

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

2.  The Wiedemann-Rautenstrauch or neonatal progeroid syndrome. Neuropathological study of a case.

Authors:  J J Martin; C M Ceuterick; J G Leroy; E A Devos; J G Roelens
Journal:  Neuropediatrics       Date:  1984-02       Impact factor: 1.947

3.  A new neonatal progeroid syndrome.

Authors:  F Snigula; T Rautenstrauch
Journal:  Eur J Pediatr       Date:  1981-07       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

5.  The Wiedemann-Rautenstrauch or neonatal progeroid syndrome. Report of a patient with consanguineous parents.

Authors:  E A Devos; J G Leroy; J P Frijns; H Van den Berghe
Journal:  Eur J Pediatr       Date:  1981-07       Impact factor: 3.183

Review 6.  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 in total
  6 in total

1.  Wiedemann-Rautenstrauch syndrome prenatal diagnosis.

Authors:  C H Becerra; G A Contreras-García; L A Perez Vera; L A Díaz-Martínez; M A Beltran Avendaño; H A Salazar Martínez
Journal:  J Perinatol       Date:  2014-12       Impact factor: 2.521

Review 2.  Two sibs with Wiedemann-Rautenstrauch syndrome: possibilities of prenatal diagnosis by ultrasound.

Authors:  G Castiñeyra; M Panal; H Lopez Presas; E Goldschmidt; J M Sánchez
Journal:  J Med Genet       Date:  1992-06       Impact factor: 6.318

Review 3.  Clinical and Molecular Delineation of Cutis Laxa Syndromes: Paradigms for Homeostasis.

Authors:  Aude Beyens; Lore Pottie; Patrick Sips; Bert Callewaert
Journal:  Adv Exp Med Biol       Date:  2021       Impact factor: 2.622

4.  LMNA is mutated in Hutchinson-Gilford progeria (MIM 176670) but not in Wiedemann-Rautenstrauch progeroid syndrome (MIM 264090).

Authors:  Henian Cao; Robert A Hegele
Journal:  J Hum Genet       Date:  2003-04-03       Impact factor: 3.172

5.  A case of systemic aplasia cutis congenita: a newly recognized syndrome?

Authors:  Tokio Sugiura; Masanori Kouwaki; Shusuke Kiyosawa; Yoshie Sasada; Matsuyoshi Maeda; Kenji Goto; Norihisa Koyama
Journal:  Eur J Pediatr       Date:  2007-05-23       Impact factor: 3.183

6.  Extensive form of aplasia cutis congenita: a new syndrome?

Authors:  M S Park; S H Hahn; C H Hong; J S Kim; H S Kim
Journal:  J Med Genet       Date:  1998-07       Impact factor: 6.318
  6 in total

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