Turki I - 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: turki i. Arch Neurol. 2003 Jul;60(7):982-8. doi: 10.1001/archneur.60.7.982. Arch Neurol. 2003. PMID: 12873855

2

Electrophysiology and nerve biopsy: comparative study in Friedreich's ataxia and Friedreich's ataxia phenotype with vitamin E deficiency.

Zouari M, Feki M, Ben Hamida C, Larnaout A, Turki I, Belal S, Mebazaa A, Ben Hamida M, Hentati F. Zouari M, et al. Among authors: turki i. Neuromuscul Disord. 1998 Aug;8(6):416-25. doi: 10.1016/s0960-8966(98)00051-0. Neuromuscul Disord. 1998. PMID: 9713861

3

[Hemifacial spasm and its treatment with botulinum toxin].

Gouider-Khouja N, Turki I, Ben Hamida M, Hentati F. Gouider-Khouja N, et al. Among authors: turki i. Tunis Med. 1999 Jan;77(1):41-4. Tunis Med. 1999. PMID: 10333697 Clinical Trial. French. No abstract available.

4

[Treatment of cervical dystonia with botulinum toxin].

Gouider-Khouja N, Turki I, Ben Hamida M, Hentati F. Gouider-Khouja N, et al. Among authors: turki i. Tunis Med. 1999 Feb;77(2):101-4. Tunis Med. 1999. PMID: 10333707 French. No abstract available.

5

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: turki i. Neurology. 2000 Apr 11;54(7):1408-14. doi: 10.1212/wnl.54.7.1408. Neurology. 2000. PMID: 10751248 Clinical Trial.

6

Effect of vitamin E supplementation in patients with ataxia with vitamin E deficiency.

Gabsi S, Gouider-Khouja N, Belal S, Fki M, Kefi M, Turki I, Ben Hamida M, Kayden H, Mebazaa R, Hentati F. Gabsi S, et al. Among authors: turki i. Eur J Neurol. 2001 Sep;8(5):477-81. doi: 10.1046/j.1468-1331.2001.00273.x. Eur J Neurol. 2001. PMID: 11554913 Clinical Trial.

7

[Acute polyradiculoneuropathy. Guillain-Barre syndrome].

Turki I, Djaïet S, Boukhris S, Hentati F. Turki I, et al. Tunis Med. 2003 Oct;81(10):781-7. Tunis Med. 2003. PMID: 17722794 French.

8

Duchenne muscular dystrophy in Tunisia: a clinical and morphological study of 77 cases.

Ben Hamida M, Miladi N, Turki I, Zaiem H. Ben Hamida M, et al. Among authors: turki i. J Neurol Sci. 1992 Jan;107(1):60-4. doi: 10.1016/0022-510x(92)90209-4. J Neurol Sci. 1992. PMID: 1578235

9

3-Phosphoglycerate dehydrogenase deficiency: description of two new cases in Tunisia and review of the literature.

Kraoua I, Wiame E, Kraoua L, Nasrallah F, Benrhouma H, Rouissi A, Turki I, Chaabouni H, Briand G, Kaabachi N, Van Schaftingen E, Gouider-Khouja N. Kraoua I, et al. Among authors: turki i. Neuropediatrics. 2013 Oct;44(5):281-5. doi: 10.1055/s-0033-1338133. Epub 2013 Apr 6. Neuropediatrics. 2013. PMID: 23564319 Review.

10

Lesch Nyhan syndrome: a novel complex mutation in a Tunisian child.

Rebai I, Kraoua I, Benrhouma H, Rouissi A, Turki I, Ceballos-Picot I, Gouider-Khouja N. Rebai I, et al. Among authors: turki i. Brain Dev. 2014 Nov;36(10):921-3. doi: 10.1016/j.braindev.2014.01.006. Epub 2014 Feb 3. Brain Dev. 2014. PMID: 24503445

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