Amouri R - Search Results

1

Phenotypic features and genetic findings in sacsin-related autosomal recessive ataxia in Tunisia.

El Euch-Fayache G, Lalani I, Amouri R, Turki I, Ouahchi K, Hung WY, Belal S, Siddique T, Hentati F. El Euch-Fayache G, et al. Among authors: amouri r. Arch Neurol. 2003 Jul;60(7):982-8. doi: 10.1001/archneur.60.7.982. Arch Neurol. 2003. PMID: 12873855

2

Linkage to chromosome 13q11-12 of an autosomal recessive cerebellar ataxia in a Tunisian family.

Mrissa N, Belal S, Hamida CB, Amouri R, Turki I, Mrissa R, Hamida MB, Hentati F. Mrissa N, et al. Among authors: amouri r. Neurology. 2000 Apr 11;54(7):1408-14. doi: 10.1212/wnl.54.7.1408. Neurology. 2000. PMID: 10751248 Clinical Trial.

3

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

Driss A, Amouri R, Ben Hamida C, Souilem S, Gouider-Khouja N, Ben Hamida M, Hentati F. Driss A, et al. Among authors: amouri r. Neuromuscul Disord. 2000 Jun;10(4-5):240-6. doi: 10.1016/s0960-8966(00)00099-7. Neuromuscul Disord. 2000. PMID: 10838249

4

Giant axonal neuropathy locus refinement to a < 590 kb critical interval.

Cavalier L, BenHamida C, Amouri R, Belal S, Bomont P, Lagarde N, Gressin L, Callen D, Demir E, Topaloglu H, Landrieu P, Ioos C, Hamida MB, Koenig M, Hentati F. Cavalier L, et al. Among authors: amouri r. Eur J Hum Genet. 2000 Jul;8(7):527-34. doi: 10.1038/sj.ejhg.5200476. Eur J Hum Genet. 2000. PMID: 10909853

5

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

Barhoumi C, Amouri R, Ben Hamida C, Ben Hamida M, Machghoul S, Gueddiche M, Hentati F. Barhoumi C, et al. Among authors: amouri r. Neuromuscul Disord. 2001 Jan;11(1):27-34. doi: 10.1016/s0960-8966(00)00162-0. Neuromuscul Disord. 2001. PMID: 11166163

6

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

Driss A, Noguchi S, Amouri R, Kefi M, Sasaki T, Sugie K, Souilem S, Hayashi YK, Shimizu N, Minoshima S, Kudoh J, Hentati F, Nishino I. Driss A, et al. Among authors: amouri r. Neurology. 2003 Apr 22;60(8):1341-4. doi: 10.1212/01.wnl.0000065886.82930.c5. Neurology. 2003. PMID: 12707439

7

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

Gouider-Khouja N, Larnaout A, Amouri R, Sfar S, Belal S, Ben Hamida C, Ben Hamida M, Hattori N, Mizuno Y, Hentati F. Gouider-Khouja N, et al. Among authors: amouri r. Parkinsonism Relat Disord. 2003 Jun;9(5):247-51. doi: 10.1016/s1353-8020(03)00016-6. Parkinsonism Relat Disord. 2003. PMID: 12781588

8

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

Ammar N, Nelis E, Merlini L, Barisić N, Amouri R, Ceuterick C, Martin JJ, Timmerman V, Hentati F, De Jonghe P. Ammar N, et al. Among authors: amouri r. Neuromuscul Disord. 2003 Nov;13(9):720-8. doi: 10.1016/s0960-8966(03)00093-2. Neuromuscul Disord. 2003. PMID: 14561495

9

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

Kefi M, Amouri R, Driss A, Ben Hamida C, Ben Hamida M, Kunkel LM, Hentati F. Kefi M, et al. Among authors: amouri r. Neuromuscul Disord. 2003 Dec;13(10):779-87. doi: 10.1016/s0960-8966(03)00136-6. Neuromuscul Disord. 2003. PMID: 14678800

10

Aprataxin gene mutations in Tunisian families.

Amouri R, Moreira MC, Zouari M, El Euch G, Barhoumi C, Kefi M, Belal S, Koenig M, Hentati F. Amouri R, et al. Neurology. 2004 Sep 14;63(5):928-9. doi: 10.1212/01.wnl.0000137044.06573.46. Neurology. 2004. PMID: 15365154

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