Aissa K - Search Results

1

[Autoimmune polyglandular syndrome type I].

Matoussi N, Aissa K, Fitouri Z, Makni S, Ben Becher S. Matoussi N, et al. Among authors: aissa k. Tunis Med. 2008 May;86(5):519-20. Tunis Med. 2008. PMID: 19469319 French. No abstract available.

2

[Hyperlipidaemia associated to inaugurated diabetic ketoacidosis].

Matoussi N, Aissa K, Fitouri Z, Cheour M, Ben Becher S. Matoussi N, et al. Among authors: aissa k. Tunis Med. 2006 Oct;84(10):658-9. Tunis Med. 2006. PMID: 17193862 French.

3

[Central diabetes insipidus: diagnostic difficulties].

Matoussi N, Aissa K, Fitouri Z, Hajji M, Makni S, Bellagha I, Ben Becher S. Matoussi N, et al. Among authors: aissa k. Ann Endocrinol (Paris). 2008 Jun;69(3):231-9. doi: 10.1016/j.ando.2007.11.003. Epub 2008 May 19. Ann Endocrinol (Paris). 2008. PMID: 18486932 French.

4

Klippel Trenaunay syndrome in association with Sturge Weber syndrome about one case.

Sfaihi L, Aissa K, Fourati H, Kamoun F, Mnif Z, Kamoun T, Hachicha M. Sfaihi L, et al. Among authors: aissa k. Tunis Med. 2014 Feb;92(2):173-4. Tunis Med. 2014. PMID: 24938246 Free article. No abstract available.

5

[Primary hypertriglyceridemia type IV : early presentation of a severe case].

Bouaziz Abed A, Maaloul I, Mustapha R, Chiha M, Aissa K. Bouaziz Abed A, et al. Among authors: aissa k. Tunis Med. 2013 Nov;91(11):683. Tunis Med. 2013. PMID: 24343502 Free article. French. No abstract available.

6

[Congenital hepatic fibrosis in children. Report of 9 cases and review of the literature].

Mazigh MS, Aloui N, Fetni I, Boukthir S, Aissa K, Sellami N, Bellagha I, Bousnina S, Barsaoui S. Mazigh MS, et al. Among authors: aissa k. Tunis Med. 2006 Mar;84(3):182-8. Tunis Med. 2006. PMID: 16755960 Review. French.

7

[Upper gastrointestinal endoscopy in neonates--experience of pediatric gastroenterology unit].

Mazigh M'rad S, Boukthir S, Aissa K, Fetni I, Barsaoui S. Mazigh M'rad S, et al. Among authors: aissa k. Tunis Med. 2006 Oct;84(10):607-10. Tunis Med. 2006. PMID: 17193850 French.

8

Hemolytic anemia and progressive neurologic impairment: think about triosephosphate isomerase deficiency.

Aissa K, Kamoun F, Sfaihi L, Ghedira ES, Aloulou H, Kamoun T, Pissard S, Hachicha M. Aissa K, et al. Fetal Pediatr Pathol. 2014 Aug;33(4):234-8. doi: 10.3109/15513815.2014.915365. Epub 2014 May 19. Fetal Pediatr Pathol. 2014. PMID: 24840153

9

Van Wyk-Grumbach syndrome: A rare cause of precocious puberty.

Hachicha M, Maaloul I, Aissa K, Kamoun T, Aloulou H. Hachicha M, et al. Among authors: aissa k. Presse Med. 2018 May;47(5):483-486. doi: 10.1016/j.lpm.2018.02.012. Epub 2018 Mar 17. Presse Med. 2018. PMID: 29555166 No abstract available.

10

[Cholelithiasis associated with portal cavernoma in children: 2 case reports].

Chabchoub I, Maalej B, Turki H, Aloulou H, Aissa K, Ben Mansour L, Kamoun T, Hachicha M. Chabchoub I, et al. Among authors: aissa k. Arch Pediatr. 2010 May;17(5):507-10. doi: 10.1016/j.arcped.2010.01.023. Epub 2010 Mar 19. Arch Pediatr. 2010. PMID: 20303244 French.

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