Optical Coherence Tomography in an Infant with Walker-Warburg Syndrome.

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Bilateral total retinal detachment at birth: a case report of Walker-Warburg syndrome.Case Report of Proliferative Peripheral Retinopathy in Two Familial Lissencephaly Infants with Miller-Dieker Syndrome

P2860

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P2860

Optical Coherence Tomography in an Infant with Walker-Warburg Syndrome.

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http://www.wikidata.org/entity/Q42406942

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2015 nî lūn-bûn

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2015年の論文

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2015年論文

@yue

2015年論文

@zh-hant

2015年論文

@zh-hk

2015年論文

@zh-mo

2015年論文

@zh-tw

2015年论文

@wuu

2015年论文

@zh

2015年论文

@zh-cn

name

Optical Coherence Tomography in an Infant with Walker-Warburg Syndrome.

@en

Optical Coherence Tomography in an Infant with Walker-Warburg Syndrome.

@nl

type

Item

label

Optical Coherence Tomography in an Infant with Walker-Warburg Syndrome.

@en

Optical Coherence Tomography in an Infant with Walker-Warburg Syndrome.

@nl

prefLabel

Optical Coherence Tomography in an Infant with Walker-Warburg Syndrome.

@en

Optical Coherence Tomography in an Infant with Walker-Warburg Syndrome.

@nl

P1476

Optical Coherence Tomography in an Infant with Walker-Warburg Syndrome.

@en

P2093

Hiroko Watanabe

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Kazuhiro Shimizu

http://www.w3.org/2001/XMLSchema#string

Makiko Miyamoto

http://www.w3.org/2001/XMLSchema#string

Mari Ueki

http://www.w3.org/2001/XMLSchema#string

Michiko Miki

http://www.w3.org/2001/XMLSchema#string

Natsuko Mano

http://www.w3.org/2001/XMLSchema#string

Tatsuma Mitsutsuji

http://www.w3.org/2001/XMLSchema#string

Tsunehiko Ikeda

http://www.w3.org/2001/XMLSchema#string

Yamato Yoshikawa

http://www.w3.org/2001/XMLSchema#string

P2860

POMT2 mutations cause alpha-dystroglycan hypoglycosylation and Walker-Warburg syndrome

Walker-Warburg syndrome.

Walker-Warburg syndrome: congenital neurodysplasia and bilateral retinal folds.

A comparison of macular structure imaged by optical coherence tomography in preterm and full-term children.

Optimizing hand-held spectral domain optical coherence tomography imaging for neonates, infants, and children.

Mutations of the POMT1 gene found in patients with Walker-Warburg syndrome lead to a defect of protein O-mannosylation.

Fukuyama-type congenital muscular dystrophy (FCMD) and alpha-dystroglycanopathy.

Subfoveal fluid in healthy full-term newborns observed by handheld spectral-domain optical coherence tomography

Walker Warburg syndrome associated with microphthalmos and megalophthalmos: A rare combination

Clinicopathological study on eyes from cases of Fukuyama type congenital muscular dystrophy.

P304

210-215

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scholarly article

case report

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10.1159/000435771

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P433

http://www.w3.org/2001/XMLSchema#string

P478

http://www.w3.org/2001/XMLSchema#string

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Masashi Mimura

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2015-05-01T00:00:00Z

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280999213

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26265907

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P932

4519600

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Optical Coherence Tomography in an Infant with Walker-Warburg Syndrome.

about

P2860

P2860

Optical Coherence Tomography in an Infant with Walker-Warburg Syndrome.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P5875

P698

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P5875

P698

P932