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health.ucsd.edu › news › releases › Pages › scientists-disc...Scientists Discover New Genetic Forms of Neurodegeneration
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... Mashhad Medical Genetic Counseling Center, Iran; Naima Bouslam, Ahmed Bouhouche and Ali Benomar, University Mohammed C Souissi, ...
Biomining : Workshop on Biological and Genomics Data Mining
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Biomining : Workshop on Biological and Genomics Data Mining
Le calendrier des compétitions pour l'année dévoilé | Radio...
radioalgerie.dz
Vendredi 12 et samedi 13 : Festival National de Jeunes BM « Ahmed Bouhouche » Ain-Defla. Aout : Samedi 01 et dimanche 02 : Championnat ...
Gene Mutation Shown to Cause Form of Hereditary Spastic Paraplegia in...
neurosciencenews.com
... Dan Spiegelman, Alexandre Dionne-Laporte, Anna Szuto, Meijiang Liao, Denise A. Figlewicz, Ahmed Bouhouche, Ali Benomar, Mohamed ...
Network Profiles
LinkedIn: Ahmed Bouhouche | LinkedIn
تُعدّ LinkedIn أكبر شبكة أعمال تجارية في العالم تساعد محترفين مثل Ahmed Bouhouche على اكتشاف زملاء يعملون في الشركات المعلنة عن وظائف، خبراء في المجال، أو ...
Interests
agris.fao.org › agris-search › searchExome Sequencing Links Corticospinal Motor agris - FAO
agris.fao.org
Exome Sequencing Links Corticospinal Motor Neuron Disease to Common Neurodegenerative Disorders [2014]. Novarino, Gaia Ahmed Bouhouche Ahmet ...
www.sciencedaily.com › releases › Gene mutations shown to cause form of HSP: Discovery will ...
www.sciencedaily.com
... Dan Spiegelman, Alexandre Dionne-Laporte, Anna Szuto, Meijiang Liao, Denise A. Figlewicz, Ahmed Bouhouche, Ali Benomar, Mohamed ...
Étude comparative entre des patients présentant une ataxie avec...
www.em-consulte.com
Naima Bouslam, Fatima Imounan, Ali Benomar, Ahmed Bouhouche, Mohamed Yahyaoui. a Laboratoire de neurogenetique Specilaites, Rabat, Maroc.
www.cell.com › AJHG › abstractA Locus for an Axonal Form of Autosomal Recessive Charcot ...
www.cell.com
A Locus for an Axonal Form of Autosomal Recessive Charcot-Marie-Tooth Disease Maps to Chromosome 1q21.2-q Ahmed Bouhouche.
Business Profiles
Researchgate: Ahmed Bouhouche
Rabat, Morocco
Ahmed Bouhouche, En amc - Algérie | Viadeo
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Chef de service achats/gds, en amc depuis Voir le profil professionnel de Ahmed Bouhouche. Viadeo aide les professionnels comme Ahmed Bouhouche ...
Books & Literature
Ahmed Bouhouche | XanEdu Customization Platform
www.academicpub.com
Author: Ahmed Bouhouche. Results. A novel locus for autosomal recessive spastic ataxia on chromosome 17p Springer Science+Business Media ...
books.google.com › booksNeuroscience in Africa - Page 5 - Google Books Result
books.google.de
... With Parkinson's Disease Combining Microarray and Gene Panel Ahmed Bouhouche, Christelle Tesson, Wafaa Regragui, Mounia Rahmani, Valérie Drouet, ...
Etude des mutants neurologiques minibrain [exposant] 3 et no-bridge...
books.google.de
Ahmed Bouhouche pages. 0 Reviewshttp://books.google.com/books/ about/Etude_des_mutants_neurologiques_minibrai.html?id=k67MMgEACAAJ.
Related Documents
CiteSeerX — RESEARCH ARTICLE Open Access
citeseerx.ist.psu.edu
by Ahmed Bouhouche , Ali Benomar , Leila Errguig , Lamiae Lachhab , Naima Bouslam , Jehanne Aasfara , Sanaa Sefiani , Layachi Chabraoui , Elmostafa El ...
A novel locus for autosomal recessive spastic ataxia on chromosome...
www.proquest.com
Naima Bouslam · Ahmed Bouhouche · Ali Benomar · Sylvain Hanein · Stephan Klebe · ... Naima Bouslam and Ahmed Bouhouche are co-first authors.
papers.ssrn.com › ...Genetic and Phenotypic Characterisation of Autosomal ...
papers.ssrn.com
Frantz Fanon Hospital. Ahmed Bouhouche. Mohammed V University of Rabat ... Frantz Fanon Hospital. Algeria. Ahmed Bouhouche ...
An autosomal recessive leucoencephalopathy with ischemic stroke,...
www.scienceopen.com
Authors: Ahmed Bouhouche, Ali Benomar,, Leila Errguig,, Lamiae Lachhab, Naima Bouslam, Jehanne Aasfara, Sanaa Sefiani,, Layachi ...
Scientific Publications
An autosomal recessive leucoencephalopathy with ischemic stroke,...
bmcmedgenet.biomedcentral.com
Single-gene disorders related to ischemic stroke seem to be an important cause of stroke in young patients without known risk factors. To identify new genes...
Clinical and genetic data of Huntington disease in Moroccan patients
www.ncbi.nlm.nih.gov
Ahmed Bouhouche,1,2 Wafaa Regragui,1,2 Hind Lamghari,3 Khadija Khaldi,4 Nazha Birouk,5 Safaa Lytim,2 Soufiane Bellamine,6 Yamna Kriouile,7 Naima ...
Publications
Calaméo - Ahmed Bouhouche
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Publications from Ahmed Bouhouche on Calaméo. Leading publishing platform for digital magazines, interactive publications and online catalogs.
www.pubfacts.com › author › Ahmed+BouhouchePublications Authored by Ahmed Bouhouche | PubFacts
www.pubfacts.com
Publications by authors named "Ahmed Bouhouche". Are you Ahmed Bouhouche? Register this Author. 24Publications. 867Reads. 19Profile Views ...
A novel locus for autosomal recessive spastic ataxia on chromosome...
link.springer.com
Autosomal recessive spastic ataxias are a heterogeneous group of neurodegenerative diseases usually characterized by the early onset of cerebellar and pyra
Ahmed Bouhouche's Research | CureHunter
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Send password reminder... Ahmed Bouhouche Selected Research. Ahmed Bouhouche Research Topics. Disease. 1, Hereditary Spastic Paraplegia
Video & Audio
www.youtube.com › watch250m hais minimes champions national d'Algérie à stade ...
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▶ 0:37250m hais minimes champions national d'Algérie à stade bateau cassé Ahmed bouhouche recred d'Algéri ...
Reports & Statements
www.nature.com › european journal of human genetics › short reportAutosomal recessive mutilating sensory neuropathy with ...
www.nature.com
Autosomal recessive mutilating sensory neuropathy with spastic paraplegia maps to chromosome 5p15.31– Ahmed Bouhouche ,; Ali ...
spatax.wordpress.com › KIF1C mutations in two families with hereditary spatax
spatax.wordpress.com
Authors. Talya Dor, Yuval Cinnamon, Laure Raymond, Avraham Shaag, Naima Bouslam, Ahmed Bouhouche, Marion Gaussen, Vincent Meyer, ...
DBWorld Message
research.cs.wisc.edu
... India Olivier Alata, University of St-Etienne, France Ahmed Bouhouche, CHR- FMP Rabat, Morocco Brigitte Vannier, University of Poitiers, France Lynda Zaoui, ...
Autosomal recessive mutilating sensory neuropathy with spastic...
www.nature.com
Autosomal recessive ulcero-mutilating neuropathy with spastic paraplegia is a very rare disease since only few cases were described up to date. We report in...
Miscellaneous
Ahmed Bouhouche | LinkedIn
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View Ahmed Bouhouche's professional profile on LinkedIn. LinkedIn is the world's largest business network, helping professionals like Ahmed Bouhouche ...
A Locus for an Axonal Form of Autosomal Recessive Charcot-Marie-Tooth...
www.infona.pl
Ahmed Bouhouche. Laboratoire de Neurogénétique et Laboratoire de Neurophysiologie, Service de Neurologie, Hôpital des…
hal.sorbonne-universite.fr › hal Mutation Analysis of Consanguineous Moroccan Patients with ...
hal.sorbonne-universite.fr
Ahmed Bouhouche, Christelle Tesson, Wafaa Regragui, Mounia Rahmani, Valérie Drouet, et al.. Mutation Analysis of Consanguineous Moroccan Patients with ...
A locus for bilateral occipital polymicrogyria maps to chromosome...
read.qxmd.com
Bouchra Ouled Amar Ben Cheikh, Stéphanie Baulac, Fatiha Lahjouji, Ahmed Bouhouche, Philippe Couarch, Naima Khalili, Wafae Regragui, Stéphane Lehericy ...
n.neurology.org › content › 1_SupplementCombination of Positional Cloning and New Generation ...
n.neurology.org
... Emeline Mundwiller, Mohammed Al Balwi, Amir Boukhris, Ahmed Bouhouche, Elodie Martin, Salah Elmalik, Abdulrahman Alswaid, Fanny ...
read.qxmd.com › keywordPapers with the keyword Hereditary spastic paraparesis (Page ...
read.qxmd.com
Talya Dor, Yuval Cinnamon, Laure Raymond, Avraham Shaag, Naima Bouslam, Ahmed Bouhouche, Marion Gaussen, Vincent Meyer, Alexandra Durr, Alexis ...
Clinical and Genetic Study of Friedreich’s Ataxia and Ataxia with...
www.jourlib.org
Fatima Imounan, Naima Bouslam, El Hachmia Aitbenhaddou, Wafa Regragui, Ahmed Bouhouche, Ali Benomar, Mohammed Yahyaoui. Keywords: Friedreich's ...
www.ajol.info › index.php › ahs › article › viewClinical and genetic data of Huntington disease in Moroccan ...
www.ajol.info
Ahmed Bouhouche, Wafaa Regragui, Hind Lamghari, Khadjia Khaldi, Nazha Birouk, Safaa Lytim, Soufiane Bellamine, Yamna Kriouile, Naima Bouslam, ...
www.altmetric.com › detailsDeep Brain Stimulation in Moroccan Patients With Altmetric
www.altmetric.com
... Abdelmjid Moussaoui, Afifa Semlali, Saadia Aidi, El Hachmia Ait Benhaddou, Ali Benomar, Ahmed Bouhouche, Mohamed Yahyaoui, Abdeslam El Khamlichi, ...
Autosomal recessive axonal Charcot–Marie–Tooth disease (ARCMT2):...
academic.oup.com
Abstract. Charcot–Marie–Tooth disease is a genetically heterogeneous group of hereditary motor and sensory neuropathies. Three loci for the axonal autosomal re
Committee
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Committee, Cours Maghrébins de la Maladie de Pakinson et Autres Mouvements Anormaux, designed by Web Events & APP.
www.hal.inserm.fr › APHP › hal AP-HP - A novel locus for autosomal recessive spastic ataxia ...
www.hal.inserm.fr
Naima Bouslam, Ahmed Bouhouche, Ali Benomar, Sylvain Hanein, Stephan Klebe, et al.. A novel locus for autosomal recessive spastic ataxia on chromosome ...
Combination of Positional Cloning and New Generation Sequencing...
www.neurology.org
... Amir Boukhris,; Ahmed Bouhouche,; Elodie Martin,; Salah Elmalik,; Abdulrahman Alswaid,; Fanny Mochel,; Filippo Santorelli,; Ali Benomar, ...
Evidence for prehistoric origins of the G2019S mutation in the North...
journals.plos.org
Ahmed Bouhouche. Roles Conceptualization, Funding acquisition, Investigation, Methodology, Project administration, Resources, Supervision, ...
PhDTree: academic genealogy & family tree
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phdtree is the most comprehensive online database & wiki on academic genealogy & academic family tree for every disciplines.
Journées de Printemps de Neurologie - Fès 2017
smneurologie.org
Ahmed Bouhouche (Rabat) Troubles somatoformes en neurologie. Wafaa El Fakir (Rabat). 15H00-16H30, Médecine interne : Les vascularites du système ...
Farid Meggouh
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... mutation and Friedreich ataxia with GAA expansion in 15 Moroccan families · Ali Benomar, Mohammed Yahyaoui, Farid Meggouh, Ahmed Bouhouche, more.
GDAP1
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Genomes and Genes, Research Topics, Publications, Research Grants, Species, Scientific Experts about GDAP1
www.wegatherapp.com › ahmed-bouhoucheahmed.bouhouche's Profile - WeGather
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Theresa May will make a third attempt to get her EU withdrawal deal through Parliament in the next week. She told MPs that if her deal fails again to get their ...
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