Kammoun F - Search Results

1

Moyamoya Angiopathy: An Underdiagnosed Cause of Ischemic Stroke in a Tunisian Pediatric Cohort.

Bouchaala W, Laroussi S, Mzid Y, Maaloul I, Jallouli O, Zouari S, Ben Nsir S, Mnif Z, Kammoun F, Triki C. Bouchaala W, et al. Among authors: kammoun f. Pediatr Neurol. 2024 Jan;150:3-9. doi: 10.1016/j.pediatrneurol.2023.09.017. Epub 2023 Oct 5. Pediatr Neurol. 2024. PMID: 37925769

2

[Viral hepatitis C in chronic hemodialyzed patients in southern Tunisia. Prevalence and risk factors].

Hachicha J, Hammami A, Masmoudi H, Ben Hmida M, Karray H, Kharrat M, Kammoun F, Jarraya A. Hachicha J, et al. Among authors: kammoun f. Ann Med Interne (Paris). 1995;146(5):295-8. Ann Med Interne (Paris). 1995. PMID: 8526312 French.

3

Genetic screening of two Tunisian families with generalized epilepsy with febrile seizures plus.

Fendri-Kriaa N, Kammoun F, Rebai A, Kolsi D, Hadj Salem I, Fakhfakh F, Triki C. Fendri-Kriaa N, et al. Among authors: kammoun f. Eur J Neurol. 2009 Jun;16(6):697-704. doi: 10.1111/j.1468-1331.2009.02570.x. Epub 2009 Feb 19. Eur J Neurol. 2009. PMID: 19236456

4

Two new mutations in the MT-TW gene leading to the disruption of the secondary structure of the tRNA(Trp) in patients with Leigh syndrome.

Mkaouar-Rebai E, Chamkha I, Kammoun F, Kammoun T, Aloulou H, Hachicha M, Triki C, Fakhfakh F. Mkaouar-Rebai E, et al. Among authors: kammoun t, kammoun f. Mol Genet Metab. 2009 Jul;97(3):179-84. doi: 10.1016/j.ymgme.2009.03.003. Epub 2009 Mar 16. Mol Genet Metab. 2009. PMID: 19349200

5

A de novo mutation in the adenosine triphosphatase (ATPase) 8 gene in a patient with mitochondrial disorder.

Mkaouar-Rebai E, Kammoun F, Chamkha I, Kammoun N, Hsairi I, Triki C, Fakhfakh F. Mkaouar-Rebai E, et al. Among authors: kammoun n, kammoun f. J Child Neurol. 2010 Jun;25(6):770-5. doi: 10.1177/0883073809344351. Epub 2010 Mar 4. J Child Neurol. 2010. PMID: 20207608

6

The first genome-wide scan in a tunisian family with generalized epilepsy with febrile seizure plus (GEFS+).

Fendri-Kriaa N, Louhichi N, Mkaouar-Rebai E, Chabchoub G, Kammoun F, Salem IH, Rebai A, Triki C, Fakhfakh F. Fendri-Kriaa N, et al. Among authors: kammoun f. J Child Neurol. 2010 Nov;25(11):1362-8. doi: 10.1177/0883073810365739. Epub 2010 Apr 9. J Child Neurol. 2010. PMID: 20382841

7

Molecular-clinical correlation in a family with a novel heteroplasmic Leigh syndrome missense mutation in the mitochondrial cytochrome c oxidase III gene.

Mkaouar-Rebai E, Ellouze E, Chamkha I, Kammoun F, Triki C, Fakhfakh F. Mkaouar-Rebai E, et al. Among authors: kammoun f. J Child Neurol. 2011 Jan;26(1):12-20. doi: 10.1177/0883073810371227. Epub 2010 Jun 4. J Child Neurol. 2011. PMID: 20525945

8

New mutation c.374C>T and a putative disease-associated haplotype within SCN1B gene in Tunisian families with febrile seizures.

Fendri-Kriaa N, Kammoun F, Salem IH, Kifagi C, Mkaouar-Rebai E, Hsairi I, Rebai A, Triki C, Fakhfakh F. Fendri-Kriaa N, et al. Among authors: kammoun f. Eur J Neurol. 2011 May;18(5):695-702. doi: 10.1111/j.1468-1331.2010.03216.x. Epub 2010 Oct 6. Eur J Neurol. 2011. PMID: 21040232

9

How MRI can contribute to the diagnosis of acute demyelinating encephalomyelitis in children.

Daoud E, Chabchoub I, Neji H, Toumi N, Abdallah RB, Aloulou H, Kammoun F, Mahfoudh A, Hachicha M, Mnif J, Mahfoudh KB, Mnif Z. Daoud E, et al. Among authors: kammoun f. Neurosciences (Riyadh). 2011 Apr;16(2):137-45. Neurosciences (Riyadh). 2011. PMID: 21427663

10

A putative disease-associated haplotype within the SCN1A gene in Dravet syndrome.

Fendri-Kriaa N, Boujilbene S, Kammoun F, Mkaouar-Rebai E, Ben Mahmoud A, Hsairi I, Rebai A, Triki C, Fakhfakh F. Fendri-Kriaa N, et al. Among authors: kammoun f. Biochem Biophys Res Commun. 2011 May 20;408(4):654-7. doi: 10.1016/j.bbrc.2011.04.079. Epub 2011 Apr 21. Biochem Biophys Res Commun. 2011. PMID: 21531204

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