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Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|January 17, 2012

[Acute consciousness disorders]J Mounach, Y Sekkach, A Satté, et al.

Revue Neurologique|October 20, 2009

[Cerebral venous thrombosis and acute polyradiculoneuritis revealing systemic lupus erythematosus]N Ahbeddou, A Benomar, K Rasmouni, et al.

Revue Neurologique|March 12, 2010

[Cortical blindness secondary to carbon monoxide poisoning]J Mounach, A Zerhouni, A Satté, et al.

Revue Neurologique|November 17, 2005

[A report of 9 cases of neurosarcoidosis]A Karouache, J Mounach, N Aziz, et al.

Annals of Neurology|April 1, 1994

Autosomal-dominant cerebellar ataxia with retinal degeneration (ADCA type II) is genetically different from ADCA type IA Benomar, E Le Guern, A Dürr, et al.

Revue Neurologique|February 24, 2004

[Sneddon's syndrome: 4 cases and a review of the literature]A Abouzahir, A Bourazza, R Rafik, et al.

Nature Genetics|May 1, 1995

The gene for autosomal dominant cerebellar ataxia with pigmentary macular dystrophy maps to chromosome 3p12-p21.1A Benomar, L Krols, G Stevanin, et al.

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Search research articles

Showing results (11-20 of 17) with videos related to

Sort By:

Pageof 2

You have reached the last page of results.This site can display upto 17 results.

Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|January 17, 2012

[Acute consciousness disorders]J Mounach, Y Sekkach, A Satté, et al.

Revue Neurologique|October 20, 2009

[Cerebral venous thrombosis and acute polyradiculoneuritis revealing systemic lupus erythematosus]N Ahbeddou, A Benomar, K Rasmouni, et al.

Revue Neurologique|March 12, 2010

[Cortical blindness secondary to carbon monoxide poisoning]J Mounach, A Zerhouni, A Satté, et al.

Revue Neurologique|November 17, 2005

[A report of 9 cases of neurosarcoidosis]A Karouache, J Mounach, N Aziz, et al.

Annals of Neurology|April 1, 1994

Autosomal-dominant cerebellar ataxia with retinal degeneration (ADCA type II) is genetically different from ADCA type IA Benomar, E Le Guern, A Dürr, et al.

Revue Neurologique|February 24, 2004

[Sneddon's syndrome: 4 cases and a review of the literature]A Abouzahir, A Bourazza, R Rafik, et al.

Nature Genetics|May 1, 1995

The gene for autosomal dominant cerebellar ataxia with pigmentary macular dystrophy maps to chromosome 3p12-p21.1A Benomar, L Krols, G Stevanin, et al.

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