Kammoun T - Search Results

1

A Tunisian patient with Pearson syndrome harboring the 4.977kb common deletion associated to two novel large-scale mitochondrial deletions.

Ayed IB, Chamkha I, Mkaouar-Rebai E, Kammoun T, Mezghani N, Chabchoub I, Aloulou H, Hachicha M, Fakhfakh F. Ayed IB, et al. Among authors: kammoun t. Biochem Biophys Res Commun. 2011 Jul 29;411(2):381-6. doi: 10.1016/j.bbrc.2011.06.154. Epub 2011 Jun 29. Biochem Biophys Res Commun. 2011. PMID: 21741369

2

[Delayed growth due to growth hormone deficiency (study of 16 cases)].

Hachicha M, Kammoun T, Kolsi S, Mahfoudh A, Jardak N, Aloulou H, Bouaziz N, Triki A. Hachicha M, et al. Among authors: kammoun t. Tunis Med. 2002 Jun;80(6):317-23. Tunis Med. 2002. PMID: 12534042 French.

3

[Cowden's disease: a new paediatric observation].

Hachicha M, Kammoun T, Chabchoub I, Bahloul S, Turki H, Drira M, Zahaf A, Triki A. Hachicha M, et al. Among authors: kammoun t. Arch Pediatr. 2006 May;13(5):459-62. doi: 10.1016/j.arcped.2005.11.025. Epub 2006 Mar 29. Arch Pediatr. 2006. PMID: 16564682 French.

4

[Hepatopulmonary syndrome and portal hypertension].

Kammoun T, Ben Abdallah R, Chabchoub I, Bahloul S, Aloulou H, Mahfoudh A, Hachicha M. Kammoun T, et al. Tunis Med. 2007 Feb;85(2):170-3. Tunis Med. 2007. PMID: 17665669 French.

5

[Aplasia cutis congenita of the scalp (5 observations)].

Aloulou H, Chaari W, Khanfir S, Zroud N, Kammoun TH, Abdelmoula M, Hachicha M. Aloulou H, et al. Among authors: kammoun th. Arch Pediatr. 2008 Apr;15(4):382-7. doi: 10.1016/j.arcped.2007.12.011. Epub 2008 Mar 10. Arch Pediatr. 2008. PMID: 18329865 French.

6

[Moyamoya and Down syndrome: about 2 cases].

Sfaihi Ben Mansour L, Ayedi A, Chaari W, Aloulou H, Kammoun T, Mnif Z, Mahfoudh A, Triki C, Hachicha M. Sfaihi Ben Mansour L, et al. Among authors: kammoun t. Arch Pediatr. 2008 Jul;15(7):1197-200. doi: 10.1016/j.arcped.2008.04.005. Epub 2008 May 27. Arch Pediatr. 2008. PMID: 18508248 French.

7

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

8

[Factor VII deficiency revealed by intracranial hemorrhage].

Sfaihi Ben Mansour L, Thabet A, Aloulou H, Turki H, Chabchoub I, Mhiri F, Mnif Z, Ben Ali H, Kammoun T, Hachicha M. Sfaihi Ben Mansour L, et al. Among authors: kammoun t. Arch Pediatr. 2009 Jul;16(7):1024-7. doi: 10.1016/j.arcped.2009.03.009. Epub 2009 May 5. Arch Pediatr. 2009. PMID: 19409767 French.

9

[Pulmonary invasive aspergillosis with thyroid and bony locations].

Ben Mansour L, Mahfoudh A, Djemel N, Aloulou H, Kammoun T, Keskes H, Ghorbel M, Hachicha M. Ben Mansour L, et al. Among authors: kammoun t. Tunis Med. 2008 Jul;86(7):720-2. Tunis Med. 2008. PMID: 19472744 French. No abstract available.

10

Descriptive analyses of Turner syndrome: 49 cases in Tunisia.

Elleuch M, Mnif Feki M, Kammoun M, Charfi N, Rekik N, Bouraoui A, Kammoun T, Belguith N, Kammoun H, Sfar MT, Hachicha M, Abid M. Elleuch M, et al. Among authors: kammoun t, kammoun m, kammoun h. Ann Endocrinol (Paris). 2010 Mar;71(2):111-6. doi: 10.1016/j.ando.2009.12.013. Epub 2010 Feb 12. Ann Endocrinol (Paris). 2010. PMID: 20153455

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