Literature DB >> 3088278

Walker-Warburg syndrome (Warburg syndrome, HARD +/- E syndrome).

D Donnai, P A Farndon.   

Abstract

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Mesh：

Year:  1986        PMID： 3088278      PMCID： PMC1049627          DOI： 10.1136/jmg.23.3.200

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


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  8 in total

Review 1.  Clinicopathological conference: an adolescent girl with severe mental impairment and mucopolysacchariduria.

Authors:  M D Haust; B A Gordon; R Hong; J H Choi; L O Langer; J Spranger; J M Opitz
Journal:  Am J Med Genet       Date:  1985-09

2.  Cerebro-ocular dysgenesis (Walker-Warburg syndrome): neuropathologic and etiologic analysis.

Authors:  R S Williams; C N Swisher; M Jennings; M Ambler; V S Caviness
Journal:  Neurology       Date:  1984-12       Impact factor: 9.910

3.  Hydrocephalus, agyria, retinal dysplasia, encephalocele (HARD +/- E) syndrome: an autosomal recessive condition.

Authors:  R A Pagon; J W Chandler; W R Collie; S K Clarren; J Moon; S A Minkin; J G Hall
Journal:  Birth Defects Orig Artic Ser       Date:  1978

4.  A familial syndrome of central nervous system and ocular malformations.

Authors:  J Chemke; B Czernobilsky; G Mundel; Y R Barishak
Journal:  Clin Genet       Date:  1975-01       Impact factor: 4.438

5.  Warburg syndrome.

Authors:  R A Levine; D L Gray; N Gould; E Pergament; M L Stillerman
Journal:  Ophthalmology       Date:  1983-12       Impact factor: 12.079

Review 6.  The heterogeneity of microphthalmia in the mentally retarded.

Authors:  M Warburg
Journal:  Birth Defects Orig Artic Ser       Date:  1971-03

7.  Autosomal recessive eye and brain anomalies: Warburg syndrome.

Authors:  R A Pagon; S K Clarren; D F Milam; A E Hendrickson
Journal:  J Pediatr       Date:  1983-04       Impact factor: 4.406

8.  Congenital muscular dystrophy and cerebral dysgenesis in a Dutch family.

Authors:  J B Krijgsman; P G Barth; F C Stam; J L Slooff; H H Jaspar
Journal:  Neuropadiatrie       Date:  1980-05
  8 in total
  3 in total

1.  Dominantly inherited unilateral retinal dysplasia.

Authors:  I C Lloyd; A Colley; A B Tullo; R Bonshek
Journal:  Br J Ophthalmol       Date:  1993-06       Impact factor: 4.638

2.  Ocular malformations and lissencephaly.

Authors:  M Warburg
Journal:  Eur J Pediatr       Date:  1987-09       Impact factor: 3.183

Review 3.  Congenital hydrocephalus: nosology and guidelines for clinical approach and genetic counselling.

Authors:  C Schrander-Stumpel; J P Fryns
Journal:  Eur J Pediatr       Date:  1998-05       Impact factor: 3.183
  3 in total

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