Literature DB >> 13998843

Norie's disease (atrofia bulborum hereditaria).

M WARBURG.   

Abstract

Entities:  

Keywords:  BLINDNESS; DEAFNESS; GENETICS, HUMAN; MENTAL DEFICIENCY; RETINA

Mesh：

Year:  1963        PMID： 13998843     DOI： 10.1111/j.1755-3768.1963.tb03533.x

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


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  10 in total

1.  Linkage analysis of Norrie disease with X-chromosomal ornithine aminotransferase.

Authors:  J B Bateman
Journal:  Trans Am Ophthalmol Soc       Date:  1992

2.  Persistent Fetal Vasculature and Severe Protein C Deficiency.

Authors:  A G L Douglas; H Rafferty; P Hodgkins; A Nagra; N C Foulds; M Morgan; I K Temple
Journal:  Mol Syndromol       Date:  2010-04-23

3.  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

4.  Vascular defects and sensorineural deafness in a mouse model of Norrie disease.

Authors:  Heidi L Rehm; Duan-Sun Zhang; M Christian Brown; Barbara Burgess; Chris Halpin; Wolfgang Berger; Cynthia C Morton; David P Corey; Zheng-Yi Chen
Journal:  J Neurosci       Date:  2002-06-01       Impact factor: 6.167

5.  Norrie's disease: a prospective study of development.

Authors:  H M Goodyear; P M Sonksen; H McConachie
Journal:  Arch Dis Child       Date:  1989-11       Impact factor: 3.791

6.  Ocular manifestations of Chinese patients with copy number variants in the NDP gene.

Authors:  Li Huang; Linyan Zhang; Xiaoyu Li; Jinglin Lu; Limei Sun; Limei Chen; Xiaoyan Ding; Zhan Li
Journal:  Mol Vis       Date:  2022-03-25       Impact factor: 2.711

7.  Hydrocephalus, agyria, pseudoencephalocele, retinal dysplasia, and anterior chamber anomalies.

Authors:  R M Winter; A Garner
Journal:  J Med Genet       Date:  1981-08       Impact factor: 6.318

Review 8.  Neurodegenerative disorders associated with diabetes mellitus.

Authors:  Michael Ristow
Journal:  J Mol Med (Berl)       Date:  2004-06-03       Impact factor: 4.599

Review 9.  Molecular genetics of retinitis pigmentosa.

Authors:  D B Farber; J R Heckenlively; R S Sparkes; J B Bateman
Journal:  West J Med       Date:  1991-10

10.  Endolymphatic Hydrop Phenotype in Familial Norrie Disease Caused by Large Fragment Deletion of NDP.

Authors:  Yuerong Gong; Zhang Liu; Xiaolin Zhang; Shuang Shen; Qijun Xu; Hongchun Zhao; Jing Shang; Weiguo Li; Yanfei Wang; Jun Chen; Xiuzhen Liu; Qing Yin Zheng
Journal:  Front Aging Neurosci       Date:  2022-04-18       Impact factor: 5.750
  10 in total

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