N. Birouk

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Charcot-Marie-Tooth disease type 1A with 17p11.2 duplication. Clinical and electrophysiological phenotype study and factors influencing disease severity in 119 cases.

Y. Agid, A. Brice, N. Birouk, 1997, Brain : a journal of neurology.

Recombination hot spot in a 3.2-kb region of the Charcot-Marie-Tooth type 1A repeat sequences: new tools for molecular diagnosis of hereditary neuropathy with liability to pressure palsies and of Charcot-Marie-Tooth type 1A. French CMT Collaborative Research Group.

Y. Agid, A. Brice, N. Birouk, 1996, American journal of human genetics.

Autosomal-recessive forms of demyelinating Charcot-Marie-Tooth disease

M. Ruberg, A. Brice, N. Birouk, 2007, NeuroMolecular Medicine.

Mutations in MTMR13, a new pseudophosphatase homologue of MTMR2 and Sbf1, in two families with an autosomal recessive demyelinating form of Charcot-Marie-Tooth disease associated with early-onset glaucoma.

R. Ravazzolo, A. Brice, N. Birouk, 2003, American journal of human genetics.

A Novel GDAP1 Mutation P78L Responsible for CMT4A Disease in Three Moroccan Families

N. Birouk, A. Bouhouche, A. Benomar, 2007, Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques.

Clinical, electrophysiological and molecular genetic characteristics of 93 patients with X-linked Charcot-Marie-Tooth disease.

A. Brice, N. Birouk, R. Gouider, 2001, Brain : a journal of neurology.

The frequency of 17p11.2 duplication and Connexin 32 mutations in 282 Charcot-Marie-Tooth families in relation to the mode of inheritance and motor nerve conduction velocity

A. Brice, N. Birouk, R. Gouider, 2001, Neuromuscular Disorders.

High frequency of mutations in codon 98 of the peripheral myelin protein P0 gene in 20 French CMT1 patients.

Y. Agid, A. Brice, N. Birouk, 1996 .

Spectrum of clinical and electrophysiologic features in HNPP patients with the 17p11.2 deletion

A. Brice, N. Birouk, R. Gouider, 1999, Neurology.

Patients homozygous for the 17p 11.2 duplication in charcot‐marie‐tooth type 1A Disease

A. Brice, N. Birouk, R. Gouider, 1997, Annals of neurology.

Recurrent polyradiculoneuropathy with the 17p11.2 deletion

A. Brice, N. Birouk, T. Maisonobe, 1997, Muscle & nerve.

A locus for an axonal form of autosomal recessive Charcot-Marie-Tooth disease maps to chromosome 1q21.2-q21.3.

A. Brice, N. Birouk, D. Grid, 1999, American journal of human genetics.

Autosomal recessive axonal Charcot-Marie-Tooth disease (ARCMT2): phenotype-genotype correlations in 13 Moroccan families.

M. Ruberg, N. Birouk, O. Dubourg, 2006, Brain : a journal of neurology.

Phenotypical features of a Moroccan family with autosomal recessive Charcot-Marie-Tooth disease associated with the S194X mutation in the GDAP1 gene.

A. Brice, N. Birouk, E. Le Guern, 2003, Archives of neurology.

The first de novo mutation of the connexin 32 gene associated with X linked Charcot-Marie-Tooth disease.

A. Brice, N. Birouk, S. Tardieu, 1998, Journal of medical genetics.

[Multifocal motor neuropathies with conduction blocks. 39 cases].

V. Meininger, N. Baumann, N. Birouk, 1997, Revue neurologique.

High incidence of SMN1 gene deletion in Moroccan adult-onset spinal muscular atrophy patients

N. Birouk, N. Bouslam, A. Bouhouche, 2003, Journal of Neurology.

Neuropathies motrices multifocales avec blocs de conduction: 39 cas

V. Meininger, N. Baumann, N. Birouk, 1997 .

[Thrombosis of the upper longitudinal sinus and syphilitic cranial osteitis].

N. Birouk, M. Jiddane, M. el Alaoui Faris, 1992, Revue neurologique.

Spine deformities in Charcot-Marie-Tooth 4C caused by SH3TC2 gene mutations

M. Ruberg, A. Brice, N. Birouk, 2006, Neurology.

Neuropathies motrices pures post-radiques: 6 cas.

N. Birouk, T. Maisonobe, P. Bouche, 1998 .

[Pure motor neuropathy after radiation therapy: 6 cases].

N. Birouk, T. Maisonobe, N. le Forestier, 1998, Revue neurologique.

Genetic, cytogenetic and physical refinement of the autosomal recessive CMT linked to 5q31–q33: exclusion of candidate genes including EGR1

A. Brice, N. Birouk, T. Maisonobe, 1999, European Journal of Human Genetics.

X-linked Charcot-Marie-Tooth disease with connexin 32 mutations

Y. Agid, A. Brice, N. Birouk, 1998, Neurology.

Mutations in CAPN1 Cause Autosomal-Recessive Hereditary Spastic Paraplegia.

O. Suchowersky, G. Rouleau, P. Drapeau, 2016, American journal of human genetics.

[Acute Guillain-Barré-like polyradiculoneuritis revealing acute systemic lupus erythematosus: two case studies and review of the literature].

B. Kably, N. Birouk, S. Aïdi, 2003, Revue neurologique.

[Fahr syndrome and dysparathyroidism. 3 cases].

N. Birouk, A. El Maghraoui, M. Yahyaoui, 1995, Presse medicale.

Hereditary therrnosensitive neuropathy

N. Birouk, R. Gouider, T. Maisonobe, 1997, Neurology.

SMN gene analysis of the spinal form of Charcot-Marie-Tooth disease.

J. Melki, A. Brice, J. Pouget, 1997, Journal of medical genetics.

Middle Cerebral Artery Occlusion Due to Hydatid Cysts of Myocardial and Intraventricular Cavity Cardiac Origin: Two Cases

M. Vidailhet, N. Birouk, A. Benomar, 1994, Stroke.

The effectiveness of the median nerve neurodynamic mobilisation techniques in women with mild or moderate bilateral carpal tunnel syndrome: A single-blind clinical randomised trial

B. Kably, N. Birouk, A. Marfak, 2022, The South African journal of physiotherapy.

Early diagnosis of congenital muscular pathologies using next-generation sequencing: experiences from a tertiary center in Morocco

N. Birouk, J. Lyahyai, A. Sefiani, 2023, Egyptian Journal of Medical Human Genetics.

Charcot‐Marie‐Tooth disease with intermediate motor nerve conduction velocities: Characterization of 14 C×32 mutations in 35 families

Y. Agid, A. Brice, N. Birouk, 1997, Human mutation.

Phenotypic and genetic study of a family with hereditary sensory neuropathy and prominent weakness

A. Brice, N. Birouk, P. Bouche, 2000, Muscle & nerve.

Juvenile-onset permanent weakness in muscle phosphofructokinase deficiency

E. Malfatti, N. Romero, J. Hogrel, 2012, Journal of the Neurological Sciences.

Mutations in CAPN1 Cause Autosomal-Recessive Hereditary Spastic Paraplegia.

O. Suchowersky, G. Rouleau, P. Drapeau, 2016, American journal of human genetics.

[Acute meningomyelitis and polyradiculoneuritis disclosing systemic lupus erythematosus].

N. Birouk, M. Jiddane, W. Maazouzi, 2002, Revue neurologique.

[T-cell lymphoma revealed by a mononeuritis multiplex: case report and review of literature].

N. Birouk, R. Ouazzani, A. Amarti, 2007, Revue neurologique (Paris).

Clinical and genetic data of Huntington disease in Moroccan patients.

N. Birouk, N. Bouslam, A. Bouhouche, 2016, African health sciences.

Charcot‐Marie‐Tooth disease with intermediate motor nerve conduction velocities: Characterization of 14 C×32 mutations in 35 families

Y. Agid, A. Brice, N. Birouk, 1997, Human mutation.