Literature DB >> 6013082

Norrie's disease. A congenital progressive oculo-acoustico-cerebral degeneration.

M Warburg.   

Abstract

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Year:  1966        PMID： 6013082

Source DB:  PubMed          Journal:  Acta Ophthalmol (Copenh)        ISSN： 0001-639X


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  30 in total

1.  The ocular pathology of Norrie disease in a fetus of 11 weeks' gestational age.

Authors:  M A Parsons; D Curtis; C E Blank; H N Hughes; A C McCartney
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  1992       Impact factor: 3.117

2.  Genes for synapsin I, a neuronal phosphoprotein, map to conserved regions of human and murine X chromosomes.

Authors:  T L Yang-Feng; L J DeGennaro; U Francke
Journal:  Proc Natl Acad Sci U S A       Date:  1986-11       Impact factor: 11.205

3.  Familial cases of Norrie disease detected by copy number analysis.

Authors:  Eisuke Arai; Takuro Fujimaki; Ai Yanagawa; Keiko Fujiki; Toshiyuki Yokoyama; Akihisa Okumura; Toshiaki Shimizu; Akira Murakami
Journal:  Jpn J Ophthalmol       Date:  2014-07-15       Impact factor: 2.447

4.  Retinopathy of prematurity in infants of birth weight > 2000 g after haemorrhagic shock at birth.

Authors:  C Jandeck; U Kellner; H Kössel; M Bartsch; H T Versmold; M H Foerster
Journal:  Br J Ophthalmol       Date:  1996-08       Impact factor: 4.638

5.  Norrie's disease in an Asian family.

Authors:  D G Harendra de Silva; D B de Silva
Journal:  Br J Ophthalmol       Date:  1988-01       Impact factor: 4.638

6.  Deletion of MAOA and MAOB in a male patient causes severe developmental delay, intermittent hypotonia and stereotypical hand movements.

Authors:  Annabel Whibley; Jill Urquhart; Jonathan Dore; Lionel Willatt; Georgina Parkin; Lorraine Gaunt; Graeme Black; Dian Donnai; F Lucy Raymond
Journal:  Eur J Hum Genet       Date:  2010-05-19       Impact factor: 4.246

7.  Whole exome sequence analysis of Peters anomaly.

Authors:  Eric Weh; Linda M Reis; Hannah C Happ; Alex V Levin; Patricia G Wheeler; Karen L David; Erin Carney; Brad Angle; Natalie Hauser; Elena V Semina
Journal:  Hum Genet       Date:  2014-09-03       Impact factor: 4.132

8.  [Congenital toxoplasmosis with atypical detachment and necrosis of the retina, persistence of the primary vitreous body, additional abnormalities and extensive intraocular ectopic hematopoiesis].

Authors:  B Gloor; R Haller
Journal:  Albrecht Von Graefes Arch Klin Exp Ophthalmol       Date:  1968

9.  Genetic linkage studies in a Negro kindred with Norrie's disease.

Authors:  W E Nance; S Hara; A Hansen; J Elliott; M Lewis; B Chown
Journal:  Am J Hum Genet       Date:  1969-09       Impact factor: 11.025

10.  Congenital retinal fold as a sign of dominant exudative vitreoretinopathy.

Authors:  C E van Nouhuys
Journal:  Albrecht Von Graefes Arch Klin Exp Ophthalmol       Date:  1981
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