(Q41294147)

29 September 2017

title

Childhood neuromuscular disorders: a decade's experience in Saudi Arabia (English)

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29 September 2017

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Salih MA

1

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29 September 2017

Mahdi AH

2

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29 September 2017

al-Jarallah AA

3

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29 September 2017

al Jarallah AS

4

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29 September 2017

al-Saadi M

5

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29 September 2017

Hafeez MA

6

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29 September 2017

Aziz SA

7

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29 September 2017

publication date

1 December 1996

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Annals of Tropical Paediatrics

29 September 2017

published in

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29 September 2017

volume

16

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29 September 2017

issue

4

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29 September 2017

page(s)

271-280

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Population frequencies of inherited neuromuscular diseases—A world survey

29 September 2017

cites work

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https://api.crossref.org/works/10.1080%2F02724936.1996.11747838

Severe childhood muscular dystrophy affecting both sexes and frequent in Tunisia

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F02724936.1996.11747838

Presence of normal dystrophin in Tunisian severe childhood autosomal recessive muscular dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F02724936.1996.11747838

Deficiency of the 50K dystrophin-associated glycoprotein in severe childhood autosomal recessive muscular dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F02724936.1996.11747838

Congenital muscular dystrophy with abnormal radiographic myelin pattern

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F02724936.1996.11747838

Diagnostic criteria for Walker-Warburg syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F02724936.1996.11747838

Occidental type cerebromuscular dystrophy: a report of eleven cases

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F02724936.1996.11747838

A community survey of neurological disorders in Saudi Arabia: the Thugbah study

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F02724936.1996.11747838

Linkage analysis of families with severe childhood autosomal recessive muscular dystrophy in Morocco indicates genetic homogeneity of the disease in north Africa

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F02724936.1996.11747838

Muscular dystrophy in Saskatchewan Hutterites.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F02724936.1996.11747838

Childhood muscular dystrophy: an African review

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F02724936.1996.11747838

Dystrophin: the protein product of the Duchenne muscular dystrophy locus

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F02724936.1996.11747838

Survey of Duchenne type and congenital type of muscular dystrophy in Shimane, Japan

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F02724936.1996.11747838

Molecular studies of spinal muscular atrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F02724936.1996.11747838

Neurological disorders in Nigerian Africans: a community-based study

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F02724936.1996.11747838

Epidemiology of tropical nutritional neuropathy in Nigerians

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F02724936.1996.11747838

Severe childhood autosomal recessive muscular dystrophy with the deficiency of the 50 kDa dystrophin-associated glycoprotein maps to chromosome 13q12

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F02724936.1996.11747838

Epidemiology of neuromuscular disorders in the under-20 population in Bologna province, Italy

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F02724936.1996.11747838

10.1080/02724936.1996.11747838

21 January 2018

Identifiers

DOI

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29 September 2017

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