Revue de la littérature récente sur les neuropathies héréditaires = Review of the recent literature on hereditary neuropathiesBIROUK, N.Revue neurologique (Paris). 2014, Vol 170, Num 12, pp 846-849, issn 0035-3787, 4 p.Conference Paper

Neuropathie amyloïde liée à une protéine non identifiée = Amyloid neuropathy resulting from an unknown proteinYOUNSI, R; BIROUK, N; KISSAN, N et al.La Revue de médecine interne (Paris). 2009, Vol 30, Num 3, pp 277-278, issn 0248-8663, 2 p.Article

High incidence of SMN1 gene deletion in Moroccan adult-onset spinal muscular atrophy patientsBOUHOUCHE, A; BENOMAR, A; BIROUK, N et al.Journal of neurology. 2003, Vol 250, Num 10, pp 1209-1213, issn 0340-5354, 5 p.Article

Méningite carcinomateuse révélant un cancer digestif : deux observations avec revue de la littérature = Carcinomatous meningitis as the first manifestation of digestive tract cancer. Two case reports with a review of the literatureBIROUK, N; ZEMRAG, S; BENOMAR, A et al.La Semaine des hôpitaux de Paris. 1993, Vol 69, Num 18, pp 541-544, issn 0037-1777Article

Polyradiculonévrite aiguë de type Guillain-Barré révélant un lupus érythémateux aigu disséminé: Étude de deux cas et revue de la littérature = Acute Guillain-Barré-like polyradiculoneuritis revealing acute systemic lupus erythematosus: two case studies and review of the literatureAÏT BENHADDOU, E; BIROUK, N; EL ALAOUI-FARIS, M et al.Revue neurologique (Paris). 2003, Vol 159, Num 3, pp 300-306, issn 0035-3787, 7 p.Article

A locus for an axonal form of autosomal recessive charcot-marie-tooth disease maps to chromosome 1q21.2-q21.3BOUHOUCHE, A; BENOMAR, A; BRICE, A et al.American journal of human genetics. 1999, Vol 65, Num 3, pp 722-727, issn 0002-9297Article

Syndrome de la colonne vertébrale rigide ou Rigid Spine Syndrome : A propos de deux cas = Rigid Spine Syndrome. Two case-reportsNIAMANE, R; BIROUK, N; BENOMAR, A et al.Revue du rhumatisme (Ed. française). 1999, Vol 66, Num 6, pp 400-403, issn 1169-8330Article

Patients homozygous for the 17p11.2 duplication in Charcot-Marie-Tooth type 1A diseaseLEGUERN, E; GOUIDER, R; MABIN, D et al.Annals of neurology. 1997, Vol 41, Num 1, pp 104-108, issn 0364-5134Article

Méningomyélite et polyradiculonévrite aiguës révélant un lupus érythémateux disséminé = Acute meningomyelitis and polyradiculoneuritis disclosing systemic lupus erythematosusMOUTI, O; HARMOUCH, H; EL ALAOUI FARIS, M et al.Revue neurologique (Paris). 2002, Vol 158, Num 1, pp 81-83, issn 0035-3787Article

The first de novo mutation of the connexin 32 gene associated with X linked Charcot-Marie-Tooth diseaseMEGGOUH, F; BENOMAR, A; LEGUERN, E et al.Journal of medical genetics. 1998, Vol 35, Num 3, pp 251-252, issn 0022-2593Article

X-linked Charcot-Marie-Tooth disease with connexin 32 mutations : Clinical and electrophysiologic studyBIROUK, N; LEGUERN, E; BRICE, A et al.Neurology. 1998, Vol 50, Num 4, pp 1074-1082, issn 0028-3878Article

Neuropathies motrices pures post-radiques : 6 cas = Pure motor weakness after radiation therapy : 6 casesLALU, T; MERCIER, B; BIROUK, N et al.Revue neurologique (Paris). 1998, Vol 154, Num 1, pp 40-44, issn 0035-3787Article

SMN gene analysis of the spinal form of Charcot-Marie-Tooth diseaseHANASH, A; LEGUERN, E; BIROUK, N et al.Journal of medical genetics. 1997, Vol 34, Num 6, pp 507-508, issn 0022-2593Article

La maladie de Charcot-Marie-Tooth = The Charcot-Marie-Tooth diseaseLEGUERN, E; BIROUK, N; GUILBOT, A et al.Annales de l'Institut Pasteur. Actualités. 1996, Vol 7, Num 3, pp 179-185, issn 0924-4204Article

Pseudo-aïnhum et neuropathie axonale = Pseudoainhum and peripheral neuropathyAKALLAL, N; BELGNAOUI, F. Z; BENAMEUR, H et al.Annales de dermatologie et de vénéréologie. 2006, Vol 133, Num 10, pp 791-794, issn 0151-9638, 4 p.Article

Charcot-Marie-Tooth disease type 1A with 17p11.2 duplication: Clinical and electrophysiological phenotype study and factors influencing disease severity in 119 casesBIROUK, N; GOUIDER, R; LE GUERN, E et al.Brain. 1997, Vol 120, pp 813-823, issn 0006-8950, 5Article

Recurrent polyradiculoneuropathy with the 17P11.2 deletionLE FORESTIER, N; LEGUERN, E; COULLIN, P et al.Muscle & nerve. 1997, Vol 20, Num 9, pp 1184-1186, issn 0148-639XArticle

Maladie de Charcot-Marie-Tooth : L'électromyogramme reste utile au diagnostic et à la classification = Charcot-Marie-Tooth disease : electromyography is still useful in diagnosis and classificationBIROUK, N; MAISONOBE, T; LE FORESTIER, N et al.Revue neurologique (Paris). 1997, Vol 153, Num 12, pp 727-736, issn 0035-3787Article

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 1ALOPES, J; LEGUERN, E; GOUIDER, R et al.American journal of human genetics. 1996, Vol 58, Num 6, pp 1223-1230, issn 0002-9297Article

Syndrome de Fahr et dysparathyroïdie : 3 observations = Fahr's disease and dysparathyroidism.Three case reportsEL MAGHRAOUI, A; BIROUK, N; ZAIM, A et al.La Presse médicale (1983). 1995, Vol 24, Num 28, pp 1301-1304, issn 0755-4982Conference Paper