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Items: 32


Clinical aspects, neuroimaging, and electroencephalography of 35 cases of hemiconvulsion-hemiplegia syndrome.

Albakaye M, Belaïdi H, Lahjouji F, Errguig L, Kuate C, Maiga Y, Diallo SH, Kissani N, Ouazzani R.

Epilepsy Behav. 2018 Mar;80:184-190. doi: 10.1016/j.yebeh.2017.12.018. Epub 2018 Feb 3.


Loss of Function of GALNT2 Lowers High-Density Lipoproteins in Humans, Nonhuman Primates, and Rodents.

Khetarpal SA, Schjoldager KT, Christoffersen C, Raghavan A, Edmondson AC, Reutter HM, Ahmed B, Ouazzani R, Peloso GM, Vitali C, Zhao W, Somasundara AV, Millar JS, Park Y, Fernando G, Livanov V, Choi S, Noé E, Patel P, Ho SP; Myocardial Infarction Exome Sequencing Study, Kirchgessner TG, Wandall HH, Hansen L, Bennett EP, Vakhrushev SY, Saleheen D, Kathiresan S, Brown CD, Abou Jamra R, LeGuern E, Clausen H, Rader DJ.

Cell Metab. 2016 Aug 9;24(2):234-45. doi: 10.1016/j.cmet.2016.07.012.


Mutations in CAPN1 Cause Autosomal-Recessive Hereditary Spastic Paraplegia.

Gan-Or Z, Bouslam N, Birouk N, Lissouba A, Chambers DB, Vérièpe J, Androschuk A, Laurent SB, Rochefort D, Spiegelman D, Dionne-Laporte A, Szuto A, Liao M, Figlewicz DA, Bouhouche A, Benomar A, Yahyaoui M, Ouazzani R, Yoon G, Dupré N, Suchowersky O, Bolduc FV, Parker JA, Dion PA, Drapeau P, Rouleau GA, Ouled Amar Bencheikh B.

Am J Hum Genet. 2016 Jun 2;98(6):1271. doi: 10.1016/j.ajhg.2016.05.009. Epub 2016 Jun 2. No abstract available.


Mutations in CAPN1 Cause Autosomal-Recessive Hereditary Spastic Paraplegia.

Gan-Or Z, Bouslam N, Birouk N, Lissouba A, Chambers DB, Vérièpe J, Androschuk A, Laurent SB, Rochefort D, Spiegelman D, Dionne-Laporte A, Szuto A, Liao M, Figlewicz DA, Bouhouche A, Benomar A, Yahyaoui M, Ouazzani R, Yoon G, Dupré N, Suchowersky O, Bolduc FV, Parker JA, Dion PA, Drapeau P, Rouleau GA, Ouled Amar Bencheikh B.

Am J Hum Genet. 2016 May 5;98(5):1038-1046. doi: 10.1016/j.ajhg.2016.04.002. Erratum in: Am J Hum Genet. 2016 Jun 2;98 (6):1271.


Cerebral Hemispheric Lateralization Associated with Hippocampal Sclerosis May Affect Interictal Cardiovascular Autonomic Functions in Temporal Lobe Epilepsy.

Ghchime R, Benjelloun H, Kiai H, Belaidi H, Lahjouji F, Ouazzani R.

Epilepsy Res Treat. 2016;2016:7417540. doi: 10.1155/2016/7417540. Epub 2016 Feb 24.


A homozygous loss-of-function variant in MYH11 in a case with megacystis-microcolon-intestinal hypoperistalsis syndrome.

Gauthier J, Ouled Amar Bencheikh B, Hamdan FF, Harrison SM, Baker LA, Couture F, Thiffault I, Ouazzani R, Samuels ME, Mitchell GA, Rouleau GA, Michaud JL, Soucy JF.

Eur J Hum Genet. 2015 Sep;23(9):1266-8. doi: 10.1038/ejhg.2014.256. Epub 2014 Nov 19.


Role of the phosphoinositide phosphatase FIG4 gene in familial epilepsy with polymicrogyria.

Baulac S, Lenk GM, Dufresnois B, Ouled Amar Bencheikh B, Couarch P, Renard J, Larson PA, Ferguson CJ, Noé E, Poirier K, Hubans C, Ferreira S, Guerrini R, Ouazzani R, El Hachimi KH, Meisler MH, Leguern E.

Neurology. 2014 Mar 25;82(12):1068-75. doi: 10.1212/WNL.0000000000000241. Epub 2014 Mar 5.


Bilateral brachial plexus injury following acute carbon monoxide poisoning.

Rahmani M, Belaidi H, Benabdeljlil M, Bouchhab W, El Jazouli N, El Brini A, Aidi S, Ouazzani RM, El Alaoui Faris M.

BMC Pharmacol Toxicol. 2013 Dec 7;14:61. doi: 10.1186/2050-6511-14-61.


Peri-ictal water drinking and other ictal vegetative symptoms: Localizing and lateralizing the epileptogenic zone in temporal lobe epilepsy? Two case reports and review of the literature.

Errguig L, Lahjouji F, Belaidi H, Jiddane M, Elkhamlichi A, Dakka T, Ouazzani R.

Rev Neurol (Paris). 2013 Nov;169(11):903-10. doi: 10.1016/j.neurol.2013.06.005. Epub 2013 Oct 15. Review.


[Congenital insensitivity to pain: clinical and neurophysiological study in three sisters of a Moroccan family].

Kissani N, Krrati H, Alarcon G, Belaaidi H, Ouazzani R.

Arch Pediatr. 2013 Nov;20(11):1219-24. doi: 10.1016/j.arcped.2013.08.015. Epub 2013 Oct 2. French.


Carboxypeptidase A6 gene (CPA6) mutations in a recessive familial form of febrile seizures and temporal lobe epilepsy and in sporadic temporal lobe epilepsy.

Salzmann A, Guipponi M, Lyons PJ, Fricker LD, Sapio M, Lambercy C, Buresi C, Ouled Amar Bencheikh B, Lahjouji F, Ouazzani R, Crespel A, Chaigne D, Malafosse A.

Hum Mutat. 2012 Jan;33(1):124-35. doi: 10.1002/humu.21613. Epub 2011 Oct 31.


A locus for bilateral occipital polymicrogyria maps to chromosome 6q16-q22.

Ben Cheikh BO, Baulac S, Lahjouji F, Bouhouche A, Couarch P, Khalili N, Regragui W, Lehericy S, Ruberg M, Benomar A, Heath S, Chkili T, Yahyaoui M, Jiddane M, Ouazzani R, LeGuern E.

Neurogenetics. 2009 Feb;10(1):35-42. doi: 10.1007/s10048-008-0143-3. Epub 2008 Aug 29.


A novel GDAP1 mutation P78L responsible for CMT4A disease in three Moroccan families.

Bouhouche A, Birouk N, Benomar A, Ouazzani R, Chkili T, Yahyaoui M.

Can J Neurol Sci. 2007 Nov;34(4):421-6.


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

Rahmani M, Birouk N, Amarti A, Loukili Idrissi A, Marnissi F, Belaidi H, El Alaoui Faris M, Benchekroun S, Ouazzani R.

Rev Neurol (Paris). 2007 Apr;163(4):462-70. French.


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

Bouhouche A, Birouk N, Azzedine H, Benomar A, Durosier G, Ente D, Muriel MP, Ruberg M, Slassi I, Yahyaoui M, Dubourg O, Ouazzani R, LeGuern E.

Brain. 2007 Apr;130(Pt 4):1062-75. Epub 2007 Mar 8.


Drug resistance and hippocampal damage after delayed treatment of pilocarpine-induced epilepsy in the rat.

Chakir A, Fabene PF, Ouazzani R, Bentivoglio M.

Brain Res Bull. 2006 Dec 11;71(1-3):127-38. Epub 2006 Sep 12.


Autosomal recessive mutilating sensory neuropathy with spastic paraplegia maps to chromosome 5p15.31-14.1.

Bouhouche A, Benomar A, Bouslam N, Ouazzani R, Chkili T, Yahyaoui M.

Eur J Hum Genet. 2006 Feb;14(2):249-52.


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

Bouhouche A, Benomar A, Birouk N, Bouslam N, Ouazzani R, Yahyaoui M, Chkili T.

J Neurol. 2003 Oct;250(10):1209-13.


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

Birouk N, Azzedine H, Dubourg O, Muriel MP, Benomar A, Hamadouche T, Maisonobe T, Ouazzani R, Brice A, Yahyaoui M, Chkili T, Le Guern E.

Arch Neurol. 2003 Apr;60(4):598-604.


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

Aït Benhaddou E, Birouk N, El Alaoui-Faris M, Mzalek-Tazi Z, Aïdi S, Belaïdi H, Kably B, Ouazzani R, Chkili T.

Rev Neurol (Paris). 2003 Mar;159(3):300-6. French.


Haplotype study of West European and North African Unverricht-Lundborg chromosomes: evidence for a few founder mutations.

Moulard B, Genton P, Grid D, Jeanpierre M, Ouazzani R, Mrabet A, Morris M, LeGuern E, Dravet C, Mauguière F, Utermann B, Baldy-Moulinier M, Belaidi H, Bertran F, Biraben A, Ali Chérif A, Chkili T, Crespel A, Darcel F, Dulac O, Geny C, Humbert-Claude V, Kassiotis P, Buresi C, Malafosse A.

Hum Genet. 2002 Sep;111(3):255-62. Epub 2002 Jul 23.


Clinical comparison between AVED patients with 744 del A mutation and Friedreich ataxia with GAA expansion in 15 Moroccan families.

Benomar A, Yahyaoui M, Meggouh F, Bouhouche A, Boutchich M, Bouslam N, Zaim A, Schmitt M, Belaidi H, Ouazzani R, Chkili T, Koenig M.

J Neurol Sci. 2002 Jun 15;198(1-2):25-9.


[Late discovery of Lafora disease: a family study].

Messouak O, Yahyaoui M, Benabdeljalil M, Benomar A, Ouazzani R, Amarti A, Saidi A, Chkili T.

Rev Neurol (Paris). 2002 Jan;158(1):74-6. French.


[Flat angioma and idiopathic facial neuralgia. Association or coincidence?].

Kissani N, Belaidi H, Ouazzani R, Chkili T.

Ann Dermatol Venereol. 2001 Dec;128(12):1350-1. French. No abstract available.


[Epileptic seizures and epilepsy in subacute sclerosing panencephalitis (report of 30 cases].

Kissani N, Ouazzani R, Belaidi H, Ouahabi H, Chkili T.

Neurophysiol Clin. 2001 Dec;31(6):398-405. French.


Vitamin E deficiency ataxia associated with adenoma.

Benomar A, Yahyaoui M, Marzouki N, Birouk N, Bouslam N, Belaidi H, Amarti A, Ouazzani R, Chkili T.

J Neurol Sci. 1999 Jan 1;162(1):97-101.


A PCR amplification method reveals instability of the dodecamer repeat in progressive myoclonus epilepsy (EPM1) and no correlation between the size of the repeat and age at onset.

Lalioti MD, Scott HS, Genton P, Grid D, Ouazzani R, M'Rabet A, Ibrahim S, Gouider R, Dravet C, Chkili T, Bottani A, Buresi C, Malafosse A, Antonarakis SE.

Am J Hum Genet. 1998 Apr;62(4):842-7.


Allelic heterogeneity of Mediterranean myoclonus and the cystatin B gene.

Labauge P, Ouazzani R, M'Rabet A, Grid D, Genton P, Dravet C, Chkili T, Beck C, Buresi C, Baldy-Moulinier M, Malafosse A.

Ann Neurol. 1997 May;41(5):686-9.


Identification of mutations in cystatin B, the gene responsible for the Unverricht-Lundborg type of progressive myoclonus epilepsy (EPM1).

Lalioti MD, Mirotsou M, Buresi C, Peitsch MC, Rossier C, Ouazzani R, Baldy-Moulinier M, Bottani A, Malafosse A, Antonarakis SE.

Am J Hum Genet. 1997 Feb;60(2):342-51.


[Isaacs syndrome: clinical remission after methylprednisolone bolus].

Elalaoui-Faris M, Ouahabi H, Slassi I, Medejel A, Ouazzani R, Saidi A, Miri A, Alaoui I, Chkili T.

Rev Neurol (Paris). 1993;149(6-7):426-7. French. No abstract available.


[Neurologic manifestations in Wilson's disease. Clinical, biological, x-ray computed tomographic and developmental study of 11 cases].

Alzemmouri K, el Alaoui Faris M, Yahyaoui M, el Khalidy A, Hamdouch N, Belaidi H, Ouazzani R, Medejel A, Chkili T.

Maroc Med. 1985 Dec;7(4):790-5. French. No abstract available.


[Neuropsychiatric forms of tuberculous meningoencephalitis].

el Alaoui Faris M, Belaidi H, Al Zemmouri K, Yahyaoui M, el Khalidy AF, Ouazzani R, Medejel A, Chkili T.

Maroc Med. 1985 Jun;7(2):580-96. French. No abstract available.


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