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Employment (1)

INSTITUT NATIONAL MONGI BEN HAMIDA DE NEUROLOGIE: TUNIS, TUNIS, TN

2000 to present | ASSOCIATE PROFESSOR (MOLECULAR NEUROBIOLOGY AND NEUROPATHOLOGY)
Employment
Source: Self-asserted source
RIM AMOURI

Education and qualifications (5)

Université Pierre et Marie Curie: PARIS, PARIS, FR

Master's degree in Neurosciences
Education
Source: Self-asserted source
RIM AMOURI

Université de Tunis El Manar Faculté des Sciences de Tunis: Tunis, TN

PhD
Education
Source: Self-asserted source
RIM AMOURI

Sorbonne Université Campus Pierre et Marie Curie: Paris, Île-de-France, FR

Master's degree in Celullar and Molecular Neurophysiology
Education
Source: Self-asserted source
RIM AMOURI

Université de Paris: PARIS, FR

2020 | Certification in Bioinformatic for Medical genetic
Education
Source: Self-asserted source
RIM AMOURI

Université de Bourgogne: Dijon, Bourgogne, FR

2019 | Master's degree in Genomic and Personalized medicine
Education
Source: Self-asserted source
RIM AMOURI

Professional activities (4)

Mediterranean Society of Myology : Italy, IT

Member of the Executive Board
Membership
Source: Self-asserted source
RIM AMOURI

Gaetano Conte Academy: ROMA, IT

Honorary member
Membership
Source: Self-asserted source
RIM AMOURI

Association Tunisienne pour le Developpement des Neurosciences: Tunis, TN

General secretary
Membership
Source: Self-asserted source
RIM AMOURI

Sanofi SA: Paris, Île-de-France, FR

2004 | Aventis Medical Research Price
Distinction
Source: Self-asserted source
RIM AMOURI

Works (50 of 58)

Items per page:
Page 1 of 2

Discriminative expression of CD39 and CD73 in Cerebrospinal fluid of patients with Multiple Sclerosis and Neuro-Behçet's disease

Cytokine
2020 | Journal article
DOI: 10.1016/j.cyto.2020.155054
EID:

2-s2.0-85080977858

Part of ISSN: 10960023 10434666
Contributors: Bahrini, K.; Belghith, M.; Maghrebi, O.; Bekir, J.; Kchaou, M.; Jeridi, C.; Amouri, R.; Hentati, F.; Belal, S.; Ben Sassi, S. et al.
Source: Self-asserted source
RIM AMOURI via Scopus - Elsevier

Bi-allelic variants in RNF170 are associated with hereditary spastic paraplegia

Nature Communications
2019 | Journal article
DOI: 10.1038/s41467-019-12620-9
EID:

2-s2.0-85073656623

Part of ISSN: 20411723
Contributors: Wagner, M.; Osborn, D.P.S.; Gehweiler, I.; Nagel, M.; Ulmer, U.; Bakhtiari, S.; Amouri, R.; Boostani, R.; Hentati, F.; Hockley, M.M. et al.
Source: Self-asserted source
RIM AMOURI via Scopus - Elsevier

SLC25A46 Mutations Associated with Autosomal Recessive Cerebellar Ataxia in North African Families

Neurodegenerative Diseases
2017 | Journal article
DOI: 10.1159/000464445
EID:

2-s2.0-85020237066

Part of ISSN: 16602862 16602854
Contributors: Hammer, M.B.; Ding, J.; Mochel, F.; Eleuch-Fayache, G.; Charles, P.; Coutelier, M.; Gibbs, J.R.; Arepalli, S.K.; Chong, S.B.; Hernandez, D.G. et al.
Source: Self-asserted source
RIM AMOURI via Scopus - Elsevier

Defects in the CAPN1 Gene Result in Alterations in Cerebellar Development and Cerebellar Ataxia in Mice and Humans

Cell Reports
2016 | Journal article
DOI: 10.1016/j.celrep.2016.05.044
EID:

2-s2.0-85008225485

Part of ISSN: 22111247
Contributors: Wang, Y.; Hersheson, J.; Lopez, D.; Hammer, M.; Liu, Y.; Lee, K.-H.; Pinto, V.; Seinfeld, J.; Wiethoff, S.; Sun, J. et al.
Source: Self-asserted source
RIM AMOURI via Scopus - Elsevier

DNM3 and genetic modifiers of age of onset in LRRK2 Gly2019Ser parkinsonism: a genome-wide linkage and association study

The Lancet Neurology
2016 | Journal article
DOI: 10.1016/S1474-4422(16)30203-4
EID:

2-s2.0-84993940059

Part of ISSN: 14744465 14744422
Contributors: Trinh, J.; Gustavsson, E.K.; Vilariño-Güell, C.; Bortnick, S.; Latourelle, J.; McKenzie, M.B.; Tu, C.S.; Nosova, E.; Khinda, J.; Milnerwood, A. et al.
Source: Self-asserted source
RIM AMOURI via Scopus - Elsevier

Motor phenotype of LRRK2-associated Parkinson's disease: A tunisian longitudinal study

Movement Disorders
2015 | Journal article
DOI: 10.1002/mds.26097
EID:

2-s2.0-84922260502

Part of ISSN: 15318257 08853185
Contributors: Nabli, F.; Ben Sassi, S.; Amouri, R.; Duda, J.E.; Farrer, M.J.; Hentati, F.
Source: Self-asserted source
RIM AMOURI via Scopus - Elsevier

A comparative study of Parkinson's disease and leucine-rich repeat kinase 2 p.G2019S parkinsonism

Neurobiology of Aging
2014 | Journal article
DOI: 10.1016/j.neurobiolaging.2013.11.015
EID:

2-s2.0-84893770183

Part of ISSN: 01974580 15581497
Contributors: Trinh, J.; Amouri, R.; Duda, J.E.; Morley, J.F.; Read, M.; Donald, A.; Vilariño-Güell, C.; Thompson, C.; Szu Tu, C.; Gustavsson, E.K. et al.
Source: Self-asserted source
RIM AMOURI via Scopus - Elsevier

Clinical features and molecular genetics of two Tunisian families with abetalipoproteinemia

Journal of Clinical Neuroscience
2014 | Journal article
DOI: 10.1016/j.jocn.2013.04.016
EID:

2-s2.0-84892605665

Part of ISSN: 09675868 15322653
Contributors: Hammer, M.B.; El Euch-Fayache, G.; Nehdi, H.; Feki, M.; Maamouri-Hicheri, W.; Hentati, F.; Amouri, R.
Source: Self-asserted source
RIM AMOURI via Scopus - Elsevier

Molecular, clinical and peripheral neuropathy study of Tunisian patients with ataxia with vitamin E deficiency

Brain
2014 | Journal article
DOI: 10.1093/brain/awt339
EID:

2-s2.0-84893842653

Part of ISSN: 14602156 00068950
Contributors: Euch-Fayache, G.E.; Bouhlal, Y.; Amouri, R.; Feki, M.; Hentati, F.
Source: Self-asserted source
RIM AMOURI via Scopus - Elsevier

Exome sequencing: An efficient diagnostic tool for complex neurodegenerative disorders

European Journal of Neurology
2013 | Journal article
DOI: 10.1111/j.1468-1331.2012.03883.x
EID:

2-s2.0-84873991913

Part of ISSN: 13515101 14681331
Contributors: Hammer, M.B.; Eleuch-Fayache, G.; Gibbs, J.R.; Arepalli, S.K.; Chong, S.B.; Sassi, C.; Bouhlal, Y.; Hentati, F.; Amouri, R.; Singleton, A.B.
Source: Self-asserted source
RIM AMOURI via Scopus - Elsevier

Giant axonal neuropathy

Handbook of Clinical Neurology
2013 | Book chapter
DOI: 10.1016/B978-0-444-52902-2.00052-7
EID:

2-s2.0-84881498492

Part of ISSN: 00729752
Contributors: Hentati, F.; Hentati, E.; Amouri, R.
Source: Self-asserted source
RIM AMOURI via Scopus - Elsevier

Mutations in GBA2 cause autosomal-recessive cerebellar ataxia with spasticity

American Journal of Human Genetics
2013 | Journal article
DOI: 10.1016/j.ajhg.2012.12.012
EID:

2-s2.0-84873733145

Part of ISSN: 00029297 15376605
Contributors: Hammer, M.B.; Eleuch-Fayache, G.; Schottlaender, L.V.; Nehdi, H.; Gibbs, J.R.; Arepalli, S.K.; Chong, S.B.; Hernandez, D.G.; Sailer, A.; Liu, G. et al.
Source: Self-asserted source
RIM AMOURI via Scopus - Elsevier

A phase i trial of adeno-associated virus serotype 1-γ-sarcoglycan gene therapy for limb girdle muscular dystrophy type 2C

Brain
2012 | Journal article
DOI: 10.1093/brain/awr342
EID:

2-s2.0-84857206862

Part of ISSN: 14602156 00068950
Contributors: Herson, S.; Hentati, F.; Rigolet, A.; Behin, A.; Romero, N.B.; Leturcq, F.; Laforêt, P.; Maisonobe, T.; Amouri, R.; Haddad, H. et al.
Source: Self-asserted source
RIM AMOURI via Scopus - Elsevier

Ataxia with vitamin E deficiency and abetalipoproteinemia

Handbook of Clinical Neurology
2012 | Book chapter
DOI: 10.1016/B978-0-444-51892-7.00018-8
EID:

2-s2.0-79961147537

Part of ISSN: 00729752
Contributors: Hentati, F.; El-euch, G.; Bouhlal, Y.; Amouri, R.
Source: Self-asserted source
RIM AMOURI via Scopus - Elsevier

Clinical and molecular findings of ataxia with oculomotor apraxia type 2 (AOA2) in 5 Tunisian families

Diagnostic Molecular Pathology
2012 | Journal article
DOI: 10.1097/PDM.0b013e318257ad9a
EID:

2-s2.0-84870238319

Part of ISSN: 10529551 15334066
Contributors: Hammer, M.B.; El Euch-Fayache, G.; Nehdi, H.; Saidi, D.; Nasri, A.; Nabli, F.; Bouhlal, Y.; Maamouri-Hicheri, W.; Hentati, F.; Amouri, R.
Source: Self-asserted source
RIM AMOURI via Scopus - Elsevier

Cognitive dysfunction in Tunisian LRRK2 associated Parkinson's disease

Parkinsonism and Related Disorders
2012 | Journal article
DOI: 10.1016/j.parkreldis.2011.10.009
EID:

2-s2.0-84857440387

Part of ISSN: 13538020 18735126
Contributors: Ben Sassi, S.; Nabli, F.; Hentati, E.; Nahdi, H.; Trabelsi, M.; Ben Ayed, H.; Amouri, R.; Duda, J.E.; Farrer, M.J.; Hentati, F.
Source: Self-asserted source
RIM AMOURI via Scopus - Elsevier

A novel mitochondrial tRNA<sup>Ile</sup> point mutation associated with chronic progressive external ophthalmoplegia and hyperCKemia

Journal of the Neurological Sciences
2011 | Journal article
DOI: 10.1016/j.jns.2010.08.065
EID:

2-s2.0-78650492862

Part of ISSN: 0022510X
Contributors: Souilem, S.; Chebel, S.; Mancuso, M.; Petrozzi, L.; Siciliano, G.; Frihayed, M.; Hentati, F.; Amouri, R.
Source: Self-asserted source
RIM AMOURI via Scopus - Elsevier

Autosomal recessive spastic ataxia of Charlevoix-Saguenay: An overview

Parkinsonism and Related Disorders
2011 | Journal article
DOI: 10.1016/j.parkreldis.2011.03.005
EID:

2-s2.0-79959348337

Part of ISSN: 13538020 18735126
Contributors: Bouhlal, Y.; Amouri, R.; El Euch-Fayeche, G.; Hentati, F.
Source: Self-asserted source
RIM AMOURI via Scopus - Elsevier

Molecular diagnosis of known recessive ataxias by homozygosity mapping with SNP arrays

Journal of Neurology
2011 | Journal article
DOI: 10.1007/s00415-010-5682-5
EID:

2-s2.0-78751642158

Part of ISSN: 03405354 14321459
Contributors: H'mida-Ben Brahim, D.; M'Zahem, A.; Assoum, M.; Bouhlal, Y.; Fattori, F.; Anheim, M.; Ali-Pacha, L.; Ferrat, F.; Chaouch, M.; Lagier-Tourenne, C. et al.
Source: Self-asserted source
RIM AMOURI via Scopus - Elsevier

Spinal muscular atrophy due to double gene conversion event

International Journal of Neuroscience
2011 | Journal article
DOI: 10.3109/00207454.2010.529209
EID:

2-s2.0-78651064220

Part of ISSN: 00207454 15635279
Contributors: Maamouri, W.; Hammer, M.B.; Bouhlel, Y.; Souilem, S.; Khmiri, N.; Nehdi, H.; Hentati, F.; Amouri, R.
Source: Self-asserted source
RIM AMOURI via Scopus - Elsevier

A comparative study of LRRK2, PINK1 and genetically undefined familial Parkinson's disease

Journal of Neurology, Neurosurgery and Psychiatry
2010 | Journal article
DOI: 10.1136/jnnp.2009.185231
EID:

2-s2.0-77950613042

Part of ISSN: 00223050 1468330X
Contributors: Nishioka, K.; Kefi, M.; Jasinska-Myga, B.; Wider, C.; Vilariño-Güell, C.; Ross, O.A.; Heckman, M.G.; Middleton, L.T.; Ishihara-Paul, L.; Gibson, R.A. et al.
Source: Self-asserted source
RIM AMOURI via Scopus - Elsevier

A novel heteroplasmic tRNASer(UCN) mtDNA point mutation associated with progressive ophthalmoplegia and dysphagia

Diagnostic Molecular Pathology
2010 | Journal article
DOI: 10.1097/PDM.0b013e3181b00f02
EID:

2-s2.0-77749334755

Part of ISSN: 10529551
Contributors: Souilem, S.; Kefi, M.; Mancuso, M.; Nesti, C.; Hentati, F.; Amouri, R.
Source: Self-asserted source
RIM AMOURI via Scopus - Elsevier

Axonal neuropathy revealing pleural lymphoma as a long-term outcome of therapeutic pneumothorax,Neuropathie axonale révélant un lymphome pleural primitif sur séquelles de collapsothérapie

Revue de Medecine Interne
2010 | Journal article
DOI: 10.1016/j.revmed.2009.08.010
EID:

2-s2.0-77955412416

Part of ISSN: 02488663 17683122
Contributors: Fajraoui, N.; Ben Hamida, K.; Hadj Kacem, A.; Amouri, R.; Ben Ghars, K.; Khiari, I.; Charfi, M.R.
Source: Self-asserted source
RIM AMOURI via Scopus - Elsevier

Comprehensive sequencing of the LRRK2 gene in patients with familial Parkinson's disease from North Africa

Movement Disorders
2010 | Journal article
DOI: 10.1002/mds.23283
EID:

2-s2.0-78649372272

Part of ISSN: 08853185 15318257
Contributors: Jasinska-Myga, B.; Kachergus, J.; Vilariño-Güell, C.; Wider, C.; Soto-Ortolaza, A.I.; Kefi, M.; Middleton, L.T.; Ishihara-Paul, L.; Gibson, R.A.; Amouri, R. et al.
Source: Self-asserted source
RIM AMOURI via Scopus - Elsevier

A novel SACS gene mutation in a Tunisian family

Journal of Molecular Neuroscience
2009 | Journal article
DOI: 10.1007/s12031-009-9212-9
EID:

2-s2.0-73849102633

Part of ISSN: 08958696
Contributors: Bouhlal, Y.; El Euch-Fayeche, G.; Hentati, F.; Amouri, R.
Source: Self-asserted source
RIM AMOURI via Scopus - Elsevier

Allelic ROBO3 heterogeneity in Tunisian patients with horizontal gaze palsy with progressive scoliosis

Journal of Molecular Neuroscience
2009 | Journal article
DOI: 10.1007/s12031-009-9217-4
EID:

2-s2.0-73849119309

Part of ISSN: 08958696
Contributors: Amouri, R.; Nehdi, H.; Bouhlal, Y.; Kefi, M.; Larnaout, A.; Hentati, F.
Source: Self-asserted source
RIM AMOURI via Scopus - Elsevier

ATP13A2 variability in Parkinson disease

Human Mutation
2009 | Journal article
DOI: 10.1002/humu.20877
EID:

2-s2.0-61649086420

Part of ISSN: 10597794
Contributors: Vilariño-Güell, C.; Soto, A.I.; Lincoln, S.J.; Yahmed, S.B.; Kefi, M.; Heckman, M.G.; Hulihan, M.M.; Chai, H.; Diehl, N.N.; Amouri, R. et al.
Source: Self-asserted source
RIM AMOURI via Scopus - Elsevier

Autosomal recessive ataxia caused by three distinct gene defects in a single consanguineous family.

Journal of neurogenetics
2008 | Journal article
DOI: 10.1080/01677060802025233
EID:

2-s2.0-58149102217

Part of ISSN: 15635260
Contributors: Bouhlal, Y.; Zouari, M.; Kefi, M.; Ben Hamida, C.; Hentati, F.; Amouri, R.
Source: Self-asserted source
RIM AMOURI via Scopus - Elsevier

L-2-Hydroxyglutaric aciduria: Clinical and molecular study in three Tunisian families. Identification of a new mutation and inter-familial phenotype variability

Journal of Inherited Metabolic Disease
2008 | Journal article
DOI: 10.1007/s10545-008-0934-6
EID:

2-s2.0-84859896380

Part of ISSN: 15732665 01418955
Contributors: Larnaout, A.; Amouri, R.; Kefi, M.; Hentati, F.
Source: Self-asserted source
RIM AMOURI via Scopus - Elsevier

LRRK2 Gly2019Ser penetrance in Arab-Berber patients from Tunisia: a case-control genetic study

The Lancet Neurology
2008 | Journal article
DOI: 10.1016/S1474-4422(08)70116-9
EID:

2-s2.0-48849092336

Part of ISSN: 14744422
Contributors: Hulihan, M.M.; Ishihara-Paul, L.; Kachergus, J.; Warren, L.; Amouri, R.; Elango, R.; Prinjha, R.K.; Upmanyu, R.; Kefi, M.; Zouari, M. et al.
Source: Self-asserted source
RIM AMOURI via Scopus - Elsevier

PINK1 mutations and parkinsonism

Neurology
2008 | Journal article
DOI: 10.1212/01.wnl.0000323812.40708.1f
EID:

2-s2.0-54049123048

Part of ISSN: 1526632X 00283878
Contributors: Ishihara-Paul, L.; Hulihan, M.M.; Kachergus, J.; Upmanyu, R.; Warren, L.; Amouri, R.; Elango, R.; Prinjha, R.K.; Soto, A.; Kefi, M. et al.
Source: Self-asserted source
RIM AMOURI via Scopus - Elsevier

Variable cardiac in involvement in Tunisian siblings harboring FKRP gene mutations

Neuropediatrics
2008 | Journal article
DOI: 10.1055/s-2008-1081465
EID:

2-s2.0-50649107669

Part of ISSN: 0174304X
Contributors: Kefi, M.; Amouri, R.; Chabrak, S.; Mechmeche, R.; Hentati, F.
Source: Self-asserted source
RIM AMOURI via Scopus - Elsevier

Osteoma of the calvaria in L-2-hydroxyglutaric aciduria.

Journal of inherited metabolic disease
2007 | Journal article
DOI: 10.1007/s10545-007-0576-0
EID:

2-s2.0-38449104994

Part of ISSN: 15732665
Contributors: Larnaout, A.; Amouri, R.; Neji, S.; Zouari, M.; Kaabachi, N.; Hentati, F.
Source: Self-asserted source
RIM AMOURI via Scopus - Elsevier

Screening for Lrrk2 G2019S and clinical comparison of Tunisian and North American Caucasian Parkinson's disease families

Movement Disorders
2007 | Journal article
DOI: 10.1002/mds.21180
EID:

2-s2.0-33847751421

Part of ISSN: 08853185 15318257
Contributors: Ishihara, L.; Gibson, R.A.; Warren, L.; Amouri, R.; Lyons, K.; Wielinski, C.; Hunter, C.; Swartz, J.E.; Elango, R.; Akkari, P.A. et al.
Source: Self-asserted source
RIM AMOURI via Scopus - Elsevier

Clinical features of Parkinson disease patients with homozygous leucine-rich repeat kinase 2 G2019S mutations

Archives of Neurology
2006 | Journal article
DOI: 10.1001/archneur.63.9.1250
EID:

2-s2.0-33748621731

Part of ISSN: 00039942 15383687
Contributors: Ishihara, L.; Warren, L.; Gibson, R.; Amouri, R.; Lesage, S.; Dürr, A.; Tazir, M.; Wszolek, Z.K.; Uitti, R.J.; Nichols, W.C. et al.
Source: Self-asserted source
RIM AMOURI via Scopus - Elsevier

Clinicogenetic study of mutations in LRRK2 exon 41 in Parkinsons's disease patients from 18 countries

Movement Disorders
2006 | Journal article
DOI: 10.1002/mds.20886
EID:

2-s2.0-33645130652

Part of ISSN: 08853185 15318257
Contributors: Tomiyama, H.; Li, Y.; Funayama, M.; Hasegawa, K.; Yoshino, H.; Kubo, S.-I.; Sato, K.; Hattori, T.; Lu, C.-S.; Inzelberg, R. et al.
Source: Self-asserted source
RIM AMOURI via Scopus - Elsevier

Genetic heterogeneity within a consanguineous family involving the LGMD 2D and the LGMD 2C genes

Neuromuscular Disorders
2006 | Journal article
DOI: 10.1016/j.nmd.2006.02.007
EID:

2-s2.0-33646192015

Part of ISSN: 09608966
Contributors: Fendri, K.; Kefi, M.; Hentati, F.; Amouri, R.
Source: Self-asserted source
RIM AMOURI via Scopus - Elsevier

Allelic heterogeneity of GNE gene mutation in two Tunisian families with autosomal recessive inclusion body myopathy

Neuromuscular Disorders
2005 | Journal article
DOI: 10.1016/j.nmd.2005.01.012
EID:

2-s2.0-17044385422

Part of ISSN: 09608966
Contributors: Amouri, R.; Driss, A.; Murayama, K.; Kefi, M.; Nishino, I.; Hentati, F.
Source: Self-asserted source
RIM AMOURI via Scopus - Elsevier

Distinct phenotypes within autosomal recessive ataxias not linked to already known loci

Acta Myologica
2005 | Journal article
EID:

2-s2.0-33644506479

Part of ISSN: 11282460
Contributors: Bouhlal, Y.; El Euch-Fayeche, G.; Amouri, R.; Hentati, F.
Source: Self-asserted source
RIM AMOURI via Scopus - Elsevier

Aprataxin gene mutations in Tunisian families

Neurology
2004 | Journal article
DOI: 10.1212/01.WNL.0000137044.06573.46
EID:

2-s2.0-4644369308

Part of ISSN: 00283878
Contributors: Amouri, R.; Moreira, M.-C.; Zouari, M.; El Euch, G.; Barhoumi, C.; Kefi, M.; Belal, S.; Koenig, M.; Hentati, F.
Source: Self-asserted source
RIM AMOURI via Scopus - Elsevier

Autosomal recessive parkinsonism linked to parkin gene in a Tunisian family. Clinical, genetic and pathological study

Parkinsonism and Related Disorders
2003 | Journal article
DOI: 10.1016/S1353-8020(03)00016-6
EID:

2-s2.0-0038699003

Part of ISSN: 13538020
Contributors: Gouider-Khouja, N.; Larnaout, A.; Amouri, R.; Sfar, S.; Belal, S.; Ben Hamida, C.; Ben Hamida, M.; Hattori, N.; Mizuno, Y.; Hentati, F.
Source: Self-asserted source
RIM AMOURI via Scopus - Elsevier

Familial Ataxia with Isolated Vitamin E Deficiency (AVED)

Genetics of Movement Disorders
2003 | Book chapter
Part of DOI: 10.1016/B978-012566652-7/50021-6
EID:

2-s2.0-84902414803
Contributors: Hentati, F.; Gabsi-Gherairi, S.; Amouri, R.; Belal, S.; Feki, M.
Source: Self-asserted source
RIM AMOURI via Scopus - Elsevier

Fukutin-related protein gene mutated in the original kindred limb-girdle MD 2I

Neurology
2003 | Journal article
DOI: 10.1212/01.WNL.0000065886.82930.C5
EID:

2-s2.0-0037461326

Part of ISSN: 00283878
Contributors: Driss, A.; Noguchi, S.; Amouri, R.; Kefi, M.; Sasaki, T.; Sugie, K.; Souilem, S.; Hayashi, Y.K.; Shimizu, N.; Minoshima, S. et al.
Source: Self-asserted source
RIM AMOURI via Scopus - Elsevier

Identification of novel GDAP1 mutations causing autosomal recessive Charcot-Marie-Tooth disease

Neuromuscular Disorders
2003 | Journal article
DOI: 10.1016/S0960-8966(03)00093-2
EID:

2-s2.0-0141956367

Part of ISSN: 09608966
Contributors: Ammar, N.; Nelis, E.; Merlini, L.; Barišić, N.; Amouri, R.; Ceuterick, C.; Martin, J.-J.; Timmerman, V.; Hentati, F.; De Jonghe, P.
Source: Self-asserted source
RIM AMOURI via Scopus - Elsevier

Phenotype and sarcoglycan expression in Tunisian LGMD 2C patients sharing the same del521-T mutation

Neuromuscular Disorders
2003 | Journal article
DOI: 10.1016/S0960-8966(03)00136-6
EID:

2-s2.0-0346849960

Part of ISSN: 09608966
Contributors: Kefi, M.; Amouri, R.; Driss, A.; Hamida, C.B.; Hamida, M.B.; Kunkel, L.M.; Hentati, F.
Source: Self-asserted source
RIM AMOURI via Scopus - Elsevier

Association of a gliotoxic activity with active multiple sclerosis in US patients.

Cellular and molecular biology (Noisy-le-Grand, France)
2002 | Journal article
EID:

2-s2.0-0036510919

Part of ISSN: 01455680
Contributors: Pierig, R.; Belliveau, J.; Amouri, R.; Ménard, A.; Rieger, F.
Source: Self-asserted source
RIM AMOURI via Scopus - Elsevier

Genotype phenotype relation analysis in autosomal recessive Charcot-Marie-Tooth disease in Tunisia

Acta Myologica
2001 | Journal article
EID:

2-s2.0-0034895945

Part of ISSN: 11282460
Contributors: Hentati, F.; Ben Othmane, K.; Barhoumi, C.; Amouri, R.; Ben Hamida, Ch.; Ben Hamida, M.
Source: Self-asserted source
RIM AMOURI via Scopus - Elsevier

Linkage of a new locus for autosomal recessive axonal form of Charcot-Marie-Tooth disease to chromosome 8q21.3

Neuromuscular Disorders
2001 | Journal article
DOI: 10.1016/S0960-8966(00)00162-0
EID:

2-s2.0-0035144845

Part of ISSN: 09608966
Contributors: Barhoumi, C.; Amouri, R.; Ben Hamida, C.; Ben Hamida, M.; Machghoul, S.; Gueddiche, M.; Hentati, F.
Source: Self-asserted source
RIM AMOURI via Scopus - Elsevier

A new locus for autosomal recessive limb-girdle muscular dystrophy in a large consanguineous Tunisian family maps to chromosome 19q13.3

Neuromuscular Disorders
2000 | Journal article
DOI: 10.1016/S0960-8966(00)00099-7
EID:

2-s2.0-0034214277

Part of ISSN: 09608966
Contributors: Driss, A.; Amouri, R.; Ben Hamida, C.; Souilem, S.; Gouider-Khouja, N.; Ben Hamida, M.; Hentati, F.
Source: Self-asserted source
RIM AMOURI via Scopus - Elsevier

Giant axonal neuropathy locus refinement to a &lt; 590 kb critical interval

European Journal of Human Genetics
2000 | Journal article
DOI: 10.1038/sj.ejhg.5200476
EID:

2-s2.0-17944390744

Part of ISSN: 10184813
Contributors: Cavalier, L.; BenHamida, C.; Amouri, R.; Belal, S.; Bomont, P.; Lagarde, N.; Gressin, L.; Callen, D.; Demir, E.; Topaloglu, H. et al.
Source: Self-asserted source
RIM AMOURI via Scopus - Elsevier
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