Malika Chaouch

Malika Chaouch

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Malika Chaouch

Malika Chaouch

Publications by authors named "Malika Chaouch"

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Greater improvement in LRRK2 G2019S patients undergoing Subthalamic Nucleus Deep Brain Stimulation compared to non-mutation carriers.

BMC Neurosci 2016 Feb 1;17. Epub 2016 Feb 1.

Laboratory of Behavioral and Cognitive Neuroscience, FSB, University of Science and Technology Houari Boumediene, El Alia, Bab Ezzouar, BP 32, 16111, Algiers, Algeria.

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http://dx.doi.org/10.1186/s12868-016-0240-4DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4736184PMC
February 2016

Refining the phenotype associated with CASC5 mutation.

Neurogenetics 2016 Jan 1;17(1):71-8. Epub 2015 Dec 1.

INSERM UMR 1163, Laboratory of Molecular and Pathophysiological Bases of Cognitive Disorders, Imagine Institute, Necker-Enfants Malades Hospital, Paris Descartes-Sorbonne Paris Cité University, 75015, Paris, France.

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http://dx.doi.org/10.1007/s10048-015-0468-7DOI Listing
January 2016

Familial epilepsy in Algeria: Clinical features and inheritance profiles.

Seizure 2015 Sep 3;31:12-8. Epub 2015 Jul 3.

Department of Genetic Medicine and Development, University of Geneva Medical School, Geneva, Switzerland; Department of Genetic Medicine and Laboratory, University Hospitals of Geneva, Geneva, Switzerland; Institute of Genetics and Genomics in Geneva (iGE3), Geneva, Switzerland.

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https://linkinghub.elsevier.com/retrieve/pii/S10591311150016
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http://dx.doi.org/10.1016/j.seizure.2015.06.015DOI Listing
September 2015

Galanin pathogenic mutations in temporal lobe epilepsy.

Hum Mol Genet 2015 Jun 17;24(11):3082-91. Epub 2015 Feb 17.

Department of Genetic Medicine and Development, University of Geneva Medical School and University Hospitals of Geneva, Geneva, Switzerland Institute of Genetics and Genomics in Geneva (iGE3), Geneva, Switzerland.

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http://dx.doi.org/10.1093/hmg/ddv060DOI Listing
June 2015

Molecular and clinical study of a cohort of 110 Algerian patients with autosomal recessive ataxia.

BMC Med Genet 2015 Jun 12;16:36. Epub 2015 Jun 12.

Laboratoire de Biologie Cellulaire et Moléculaire, Faculté des Sciences Biologiques, USTHB, Alger, Algeria.

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http://dx.doi.org/10.1186/s12881-015-0180-3DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4630839PMC
June 2015

Consanguinity and epilepsy in Oran, Algeria: A case-control study.

Epilepsy Res 2015 Mar 8;111:10-7. Epub 2015 Jan 8.

Department of Neurologie, Benaknoun University Hospital, Algiers 16000, Algeria.

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http://dx.doi.org/10.1016/j.eplepsyres.2014.12.014DOI Listing
March 2015

Mutation in TTI2 reveals a role for triple T complex in human brain development.

Hum Mutat 2013 Nov 10;34(11):1472-6. Epub 2013 Sep 10.

INSERM U781, Université Paris Descartes, Sorbonne Paris Cité, Institut IMAGINE, Hôpital Necker-Enfants Malades, Paris, France.

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http://dx.doi.org/10.1002/humu.22399DOI Listing
November 2013

Compound heterozygous ASPM mutations associated with microcephaly and simplified cortical gyration in a consanguineous Algerian family.

Eur J Med Genet 2009 Jul-Aug;52(4):180-4. Epub 2009 Mar 28.

Department of Neurology, Etablissement hospitalier spécialisé de Benaknoun, and Department of Biochemistry, Centre Hospitalo-Universitaire Mustapha Bacha, Algiers, Algeria.

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https://linkinghub.elsevier.com/retrieve/pii/S17697212090003
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http://dx.doi.org/10.1016/j.ejmg.2009.03.013DOI Listing
November 2009