M. Kéfi - Concepedia

Author

M. Kéfi

National Institute of Neurology Mongi-Ben Hamida

Also Known As

M El kefi, M Kefi, M Kéfi, M. Kefi, M. Kéfi, Maelle El Kefi

Publications

470

Citations

H-Index

Concepts

All Affiliations

National Institute of Neurology Mongi-Ben Hamida National Center of Neurology and Psychiatry Institut National de Santé Publique

About

M. Kéfi is an author at National Institute of Neurology Mongi-Ben Hamida specializing in medicine, pathology, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	5	5	165
2	Molecular Genetics	3	3	99
3	Biology	1	1	45
4	Immunology	1	1	43
5	Neurology	1	1	45

M. Kéfi

Publications

464

Citations

H-Index

Page 1

	Year	Citations
Effect of vitamin E supplementation in patients with ataxia with vitamin E deficiency S. Gabsi, N. Gouider‐Khouja, Samir Belal, European Journal of Neurology	2001	144
<i>PINK1</i> mutations and parkinsonism L. Ishihara-Paul, Mary Hulihan, Jennifer M. Kachergus, Neurology	2008	62
A comparative study of LRRK2, PINK1 and genetically undefined familial Parkinson's disease Kenya Nishioka, M. Kéfi, Barbara Jasińska‐Myga, Journal of Neurology Neurosurgery & Psychiatry	2009	51
Aprataxin gene mutations in Tunisian families Rim Amouri, Maria-Ceù Moreira, M. Zouari, Neurology BiologyMendelian DisorderGenetic DisorderAcceptor Splice SiteGenetics	2004	45
Phenotype and sarcoglycan expression in Tunisian LGMD 2C patients sharing the same del521-T mutation M. Kéfi, Rim Amouri, Adel Driss, Neuromuscular Disorders Mendelian DisorderAutoimmune DiseaseSarcoglycan ExpressionMedicineGenetic Disorder	2003	43
Allelic heterogeneity of GNE gene mutation in two Tunisian families with autosomal recessive inclusion body myopathy Rim Amouri, Adel Driss, K. Murayama, Neuromuscular Disorders Allelic VariantMendelian DisorderGenetic DisorderMedicineGenetics	2005	37
Fukutin-related protein gene mutated in the original kindred limb-girdle MD 2I Adel Driss, S. Noguchi, Rim Amouri, Neurology	2003	30
Variable Cardiac Involvement in Tunisian Siblings Harboring FKRP Gene Mutations M. Kéfi, Rim Amouri, Sonia Chabrak, Neuropediatrics CardiomyopathyHeart FailureCardiovascular DiseaseVariable Cardiac InvolvementMedicine	2008	23
Genetic heterogeneity within a consanguineous family involving the LGMD 2D and the LGMD 2C genes Khaled Fendri, M. Kéfi, Fayçal Hentati, Neuromuscular Disorders Mendelian DisorderGenetic DisorderMedicineGeneticsPathology	2006	17
<scp>l</scp>‐2‐Hydroxyglutaric aciduria: Clinical and molecular study in three Tunisian families. Identification of a new mutation and inter‐familial phenotype variability A. Larnaout, Rim Amouri, M. Kéfi, Journal of Inherited Metabolic Disease	2008	12

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