Optic Atrophy and Visual Loss in Craniometaphyseal Dysplasia-Reference-Cited by-同舟云学术

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Optic Atrophy and Visual Loss in Craniometaphyseal Dysplasia

Published:1981-11 Issue:5 Volume:92 Page:696-701
ISSN:0002-9394
Container-title:American Journal of Ophthalmology
language:en
Short-container-title:American Journal of Ophthalmology

Author:

Puliafito Carmen A.,Wray Shirley H.,Murray Joseph E.,Boger William P.

Publisher

Elsevier BV

Subject

Ophthalmology

Reference13 articles.

1. Bone Dysplasias. An Atlas of Constitutional Disorders of Skeletal Development;Spranger,1974

2. Genetic craniotubular bone dysplasias and hyperostoses. A critical analysis;Gorlin;Birth Defects,1969

3. Craniometaphyseal dysplasia (Pyle's disease). Autosomal dominant inheritance in a large kindred;Rimoin;Birth Defects,1969

4. Familial metaphyseal dysplasia?;Spranger;Lancet,1970

5. A case of unusual bone development;Pyle;J. Bone Joint Surg.,1931

Cited by 22 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Cochlear Implantation in Craniometaphyseal Dysplasia;Otology & Neurotology;2020-03

2. A Rare Cause of Recurrent Stroke in a Visually Impaired 10-year-old Girl;The Indian Journal of Pediatrics;2016-09-09

3. Optic Atrophy in Children;Pediatric Neuro-Ophthalmology;2016

4. Visual and otologic manifestation of Camurati–Engelmann's disease: a case report;Radiology Case Reports;2015-12

5. Induced Pluripotent Stem Cell Reprogramming by Integration-Free Sendai Virus Vectors from Peripheral Blood of Patients with Craniometaphyseal Dysplasia;Cellular Reprogramming;2013-12

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