Boussetta K - Search Results

1

Perianal presentation of Langerhans cell histiocytosis in children.

Tinsa F, Brini I, Kharfi M, Mrad K, Boussetta K, Bousnina S. Tinsa F, et al. Among authors: boussetta k. Gastroenterol Clin Biol. 2010 Jan;34(1):95-7. doi: 10.1016/j.gcb.2009.06.016. Epub 2009 Oct 27. Gastroenterol Clin Biol. 2010. PMID: 19864102 Free article.

2

[Bilateral stenosing ureteritis in Henoch-Schnlein purpura].

Maherzi A, Kaabar N, Boussetta K, Salem M, Hammou A, Chaouachi B, Bousnina S. Maherzi A, et al. Among authors: boussetta k. Arch Pediatr. 1997 Jan;4(1):36-9. doi: 10.1016/s0929-693x(97)84305-9. Arch Pediatr. 1997. PMID: 9091100 French.

3

[Apropos of a mediastinal teratoma invading the lung].

Boussetta K, Jaziri F, Bousnina D, Aloui N, Maherzi A, Kilani T, Kammoun Sellami N, Bousnina S. Boussetta K, et al. Arch Pediatr. 2001 Dec;8(12):1344-7. doi: 10.1016/s0929-693x(01)00657-1. Arch Pediatr. 2001. PMID: 11811031 French.

4

[Community-acquired pneumonia due to Panton-Valentine producing Staphylococcus aureus: first description in Tunisia].

Saïdani M, Mesrati I, Benzarti A, Boussetta K, Bousnina S, Hamdoun M, Ben Redjeb S. Saïdani M, et al. Among authors: boussetta k. Tunis Med. 2008 Oct;86(10):924-7. Tunis Med. 2008. PMID: 19472814 French.

5

Monosomy 10q26-qter and trisomy 11q13-qter as a result of de novo unbalanced translocation.

Tinsa F, Chebbi Y, Meddeb M, Bousnina D, Boussetta K, Bousnina S. Tinsa F, et al. Among authors: boussetta k. J Appl Genet. 2009;50(3):289-91. doi: 10.1007/BF03195685. J Appl Genet. 2009. PMID: 19638686

6

Nodular regenerative hyperplasia of the liver, celiac disease and Sjogren's syndrome in a child.

Tinsa F, Brini I, El May A, Bousnina D, Boussetta K, Bousnina S. Tinsa F, et al. Among authors: boussetta k. Gastroenterol Clin Biol. 2010 Jan;34(1):40-2. doi: 10.1016/j.gcb.2009.07.035. Epub 2009 Sep 17. Gastroenterol Clin Biol. 2010. PMID: 19765928 Free article. No abstract available.

7

[Recessive autosomic polycystic kidney in a Tunisian family: correlation between genotype and phenotype?].

Tinsa F, Yahyaoui S, Brini I, Michel-Calemard L, Boussetta K, Bousnina S. Tinsa F, et al. Among authors: boussetta k. Tunis Med. 2010 Jan;88(1):68-9. Tunis Med. 2010. PMID: 20415225 French. No abstract available.

8

[Laryngotracheobronchial foreign body in children: predictive factors of respiratory sequelae].

Tinsa F, Yahyaoui S, Jallouli M, Bousnina D, Slim I, Zouari B, Boussetta K, Bousnina S. Tinsa F, et al. Among authors: boussetta k. Tunis Med. 2010 May;88(5):330-4. Tunis Med. 2010. PMID: 20517829 French.

9

A novel large deletion in CCM1 gene in a Tunisian family.

Tinsa F, Bel Hadj I, Riant F, Ben Romdhane M, Brini I, Tournier-Lasserve E, Louati H, Abdelhak S, Hamouda S, Boussetta K. Tinsa F, et al. Among authors: boussetta k. Rev Neurol (Paris). 2019 Mar;175(3):194-197. doi: 10.1016/j.neurol.2018.04.013. Epub 2018 Oct 9. Rev Neurol (Paris). 2019. PMID: 30314744

10

Unusual feature of neonatal hypernatremic dehydration due to microvillus inclusion disease: a case report.

Khalsi F, Boukhris MR, Brini I, Hugot JP, Berrebi PD, Boussetta K. Khalsi F, et al. Among authors: boussetta k. Pan Afr Med J. 2018 Jun 11;30:109. doi: 10.11604/pamj.2018.30.109.12330. eCollection 2018. Pan Afr Med J. 2018. PMID: 30364420 Free PMC article. French.

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