FIND

researchers

DISCOVER

relevant articles

PROMOTE

your research

now for free

Farid Meggouh

Research Profile

Disorders

Charcot-Marie-Tooth Disease

Physiology

Geographic Areas

Morocco

Concepts & Ideas

Chemicals & Drugs

Phenomena

Blotting, Southern

Anatomy

Axons

Procedures

Co-author Network

Publications

TOP 3
Marian A J Weterman; Fred van Ruissen; Marit de Wissel; Lou Bordewijk; Johnny P A Samijn; W-Ludo van der Pol; Farid Meggouh; Frank Baas
Copy number variation upstream of PMP22 in Charcot-Marie-Tooth disease.
H M E Bienfait; Frank Baas; J H T M Koelman; Rob J De Haan; B G M van Engelen; A A W M Gabreëls-Festen; Bram Ongerboer de Visser; Farid Meggouh; Marian A J Weterman; Peter De Jonghe; Vincent Timmerman; Marianne De Visser
Phenotype of Charcot-Marie-Tooth disease Type 2.
Farid Meggouh; H M E Bienfait; Marian A J Weterman; Marianne De Visser; Frank Baas
Charcot-Marie-Tooth disease due to a de novo mutation of the RAB7 gene.

Register for free to view:

Visualized networks:

See your personal network in
sophisticated graphical views

GeoTargeted Searches:

Locate experts around the world
and connect with global collaborators

Research Profiles:

See the research activity
of experts around the globe

Geonetwork of Farid Meggouh (preview)

Cities where this author has publications
Cities where co-authors of this author have publications

Flash Player Required

All Publications

2010: Marian A J Weterman; Fred van Ruissen; Marit de Wissel; Lou Bordewijk; Johnny P A Samijn; W-Ludo van der Pol; Farid Meggouh; Frank Baas
Copy number variation upstream of PMP22 in Charcot-Marie-Tooth disease.
European journal of human genetics : EJHG 2010;18(4):421-8.
2007: H M E Bienfait; Frank Baas; J H T M Koelman; Rob J De Haan; B G M van Engelen; A A W M Gabreëls-Festen; Bram Ongerboer de Visser; Farid Meggouh; Marian A J Weterman; Peter De Jonghe; Vincent Timmerman; Marianne De Visser
Phenotype of Charcot-Marie-Tooth disease Type 2.
Neurology 2007;68(20):1658-67.
2006: Farid Meggouh; H M E Bienfait; Marian A J Weterman; Marianne De Visser; Frank Baas
Charcot-Marie-Tooth disease due to a de novo mutation of the RAB7 gene.
Neurology 2006;67(8):1476-8.
2005: Farid Meggouh; Marianne De Visser; W F M Arts; Rene I F M De Coo; Ivo van Schaik; Frank Baas
Early onset neuropathy in a compound form of Charcot-Marie-Tooth disease.
Annals of neurology 2005;57(4):589-91.
2002: Abdelilah Laraqui; Nawal Bennouar; Farid Meggouh; Abdellatif Allami; Nizar El Kadiri; Fatima Benkouka; Houssine Azeddoug; N el Haitem; Ali Benomar; Seddik Fellat; Mohamed Benomar
[Homocysteine, lipoprotein (a): risk factors for coronary heart disease].
Annales de biologie clinique 2002;60(5):549-57.
2002: Ali Benomar; Mohamed Yahyaoui; Farid Meggouh; Ahmed Bouhouche; Mohammed Boutchich; Naima Bouslam; Abdelhaq Zaim; Michèle Schmitt; Halima Belaidi; Reda Ouazzani; Taïeb Chkili; Michel Koenig
Clinical comparison between AVED patients with 744 del A mutation and Friedreich ataxia with GAA expansion in 15 Moroccan families.
Journal of the neurological sciences 2002;198(1-2):25-9.
1999: Ahmed Bouhouche; Ali Benomar; Nazha Birouk; A Mularoni; Farid Meggouh; JP Tassin; Djamel Grid; Antoon Vandenberghe; Mohamed Yahyaoui; Taïeb Chkili; Alexis Brice; Eric LeGuern
A locus for an axonal form of autosomal recessive Charcot-Marie-Tooth disease maps to chromosome 1q21.2-q21.3.
American journal of human genetics 1999;65(3):722-7.
1998: Farid Meggouh; Ali Benomar; H Rouger; Sandrine Tardieu; Nazha Birouk; JP Tassin; C Barhoumi; Mohamed Yahyaoui; Taïeb Chkili; Alexis Brice; Eric LeGuern
The first de novo mutation of the connexin 32 gene associated with X linked Charcot-Marie-Tooth disease.
Journal of medical genetics 1998;35(3):251-2.