Kammoun T - Search Results

1

[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.

2

[Upper gastrointestinal hemorrhages in children: 166 cases].

Chaabouni M, Kammoun T, Mahfoudh A, Medhioub B, Njeh M, Karray A, Hachicha M, Salah Krichen M, Triki A. Chaabouni M, et al. Among authors: kammoun t. Tunis Med. 1999 Apr;77(4):197-204. Tunis Med. 1999. PMID: 10392019 French. No abstract available.

3

[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.

4

[The cortico-resistent idiopathic nephrotic syndrome of child. Study of 14 observations].

Hachicha M, Kammoun T, Mahfoudh A, Aloulou H, Sfaihi L, Hammami Y, Zaghden N, Hachicha J, Triki A. Hachicha M, et al. Among authors: kammoun t. Tunis Med. 2005 Apr;83(4):187-93. Tunis Med. 2005. PMID: 15966661 French.

5

[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.

6

[Vasculitis with renal involvement and antineutrophil cytoplasmic antibodies (ANCA) in a child receiving benzylthiouracil].

Hachicha M, Kammoun T, Ben Romdhane W, Ben Abdallah R, Mahfoudh A, Kammoun K, Hachicha J, Triki A. Hachicha M, et al. Among authors: kammoun t, kammoun k. Nephrol Ther. 2007 Jul;3(4):147-51. doi: 10.1016/j.nephro.2007.04.001. Epub 2007 May 23. Nephrol Ther. 2007. PMID: 17658441 French.

7

[Epidemiological, etiological and evolutionary aspects of children cirrhosis in a developing country: experience of the pediatric department of SFAX University hospital, Tunisia].

Chaabouni M, Bahloul S, Ben Romdhane W, Ben Saleh M, Ben Halima N, Chouchene C, Ben Hmad A, Zroud N, Kammoun T, Karray A. Chaabouni M, et al. Among authors: kammoun t. Tunis Med. 2007 Sep;85(9):738-43. Tunis Med. 2007. PMID: 18254302 French.

8

[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.

9

[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.

10

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

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