A case of cerebello-oculo-renal syndrome with situs inversus totalis: a new phenotype. (Q48110302)

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1 January 2020

title

A case of cerebello-oculo-renal syndrome with situs inversus totalis: a new phenotype (English)

1 reference

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1 January 2020

1 reference

1

1 reference

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1 January 2020

Atilla Ersen

2

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1 January 2020

author name string

Ferhan Karademir

3

1 reference

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1 January 2020

Selami Suleymanoglu

4

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1 January 2020

Halit Ozkaya

5

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1 January 2020

Ismail Gocmen

6

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1 January 2020

publication date

1 February 2007

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Journal of Child Neurology

1 January 2020

published in

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1 January 2020

volume

22

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1 January 2020

issue

2

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1 January 2020

page(s)

204-207

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Joubert syndrome: a review

1 January 2020

cites work

1 reference

https://api.crossref.org/works/10.1177%2F0883073807300303

Renal dysplasia, situs inversus totalis, and multisystem fibrosis: a new syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073807300303

"Joubert syndrome" revisited: key ocular motor signs with magnetic resonance imaging correlation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073807300303

Molar tooth sign in Joubert syndrome: clinical, radiologic, and pathologic significance

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073807300303

Follow-up in children with Joubert syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073807300303

Familial agenesis of the cerebellar vermis. A syndrome of episodic hyperpnea, abnormal eye movements, ataxia, and retardation

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073807300303

Cerebro-oculo-hepato-renal syndrome (Arima' syndrome): a distinct clinicopathological entity.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073807300303