Kammoun F[au] - Search Results

Year	Number of Results
1993	1
1995	1
2004	2
2009	2
2010	6
2011	4
2012	1
2013	1
2015	2
2016	1
2017	1
2019	1
2020	1
2021	4
2022	1
2023	3

1

Central diabetes insipidus revealing a hypophysitis induced by SARS-CoV-2 vaccine.

Ach T, Kammoun F, Fekih HE, Slama NBH, Kahloun S, Fredj FB, Laouani C, Ach K. Ach T, et al. Among authors: kammoun f. Therapie. 2023 Jul-Aug;78(4):453-455. doi: 10.1016/j.therap.2022.09.007. Epub 2022 Oct 6. Therapie. 2023. PMID: 36280400 Free PMC article. No abstract available.

2

A new case with the recurrent PURA p.(Phe233del) pathogenic variant: Expansion of the phenotype and review of the literature.

Ben Issa A, Ben Ayed I, Jallouli O, Souissi A, Bouchaalla W, Ben Said M, Mallouli S, Masmoudi S, Charfi Triki C, Hadj Kacem H, Kammoun F. Ben Issa A, et al. Among authors: kammoun f. Int J Dev Neurosci. 2023 Jun;83(4):383-395. doi: 10.1002/jdn.10266. Epub 2023 May 19. Int J Dev Neurosci. 2023. PMID: 37204304 Review.

3

SRD5A3-CDG: 3D structure modeling, clinical spectrum, and computer-based dysmorphic facial recognition.

Ben Ayed I, Ouarda W, Frikha F, Kammoun F, Souissi A, Ben Said M, Bouzid A, Elloumi I, Hamdani TM, Gharbi N, Baklouti N, Guirat M, Mejdoub F, Kharrat N, Boujelbene I, Abdelhedi F, Belguith N, Keskes L, Gibriel AA, Kamoun H, Triki C, Alimi AM, Masmoudi S. Ben Ayed I, et al. Among authors: kammoun f. Am J Med Genet A. 2021 Apr;185(4):1081-1090. doi: 10.1002/ajmg.a.62065. Epub 2021 Jan 6. Am J Med Genet A. 2021. PMID: 33403770

4

Mitochondrial DNA triplication and punctual mutations in patients with mitochondrial neuromuscular disorders.

Mkaouar-Rebai E, Felhi R, Tabebi M, Alila-Fersi O, Chamkha I, Maalej M, Ammar M, Kammoun F, Keskes L, Hachicha M, Fakhfakh F. Mkaouar-Rebai E, et al. Among authors: kammoun f. Biochem Biophys Res Commun. 2016 Apr 29;473(2):578-85. doi: 10.1016/j.bbrc.2016.03.126. Epub 2016 Mar 28. Biochem Biophys Res Commun. 2016. PMID: 27033601

5

A Very Rare Cerebral Complication of Chemotherapy in a Young Girl: A Difficult Diagnosis.

Kridis WB, Khanfir A, Kammoun F, Mahfoudh KB, Triki C, Frikha M. Kridis WB, et al. Among authors: kammoun f. Curr Drug Saf. 2015;10(3):257-60. doi: 10.2174/1574886310666150518112823. Curr Drug Saf. 2015. PMID: 25981579

6

A first description of ataxia with vitamin E deficiency associated with MT-TG gene mutation.

Maalej M, Kammoun F, Kharrat M, Bouchaala W, Ammar M, Mkaouar-Rebai E, Triki C, Fakhfakh F. Maalej M, et al. Among authors: kammoun f. Acta Neurol Belg. 2021 Dec;121(6):1733-1740. doi: 10.1007/s13760-020-01490-4. Epub 2020 Sep 26. Acta Neurol Belg. 2021. PMID: 32979145

7

Molecular confirmation of founder mutation c.-167A>G in Tunisian patients with PMLD disease.

Kammoun Jellouli N, Salem IH, Ellouz E, Louhichi N, tlili A, Kammoun F, Triki C, Fakhfakh F; Tunisian Network on Mental Retardation Study. Kammoun Jellouli N, et al. Among authors: kammoun f. Gene. 2013 Jan 25;513(2):233-8. doi: 10.1016/j.gene.2012.10.070. Epub 2012 Nov 7. Gene. 2013. PMID: 23142375

8

[Multiple cerebral cavernomatosis in a 1-year-old child].

Chabbchoub Ben Abdallah R, Kammoun F, Ayedi M, Trabelsi L, Ben Salah M, Ben Hlima N, Mahfoudh A. Chabbchoub Ben Abdallah R, et al. Among authors: kammoun f. Arch Pediatr. 2010 Aug;17(8):1156-8. doi: 10.1016/j.arcped.2010.05.002. Epub 2010 Jun 9. Arch Pediatr. 2010. PMID: 20542671 French.

9

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

10

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

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