Azzouz H - Search Results

1

Severe respiratory complex III defect prevents liver adaptation to prolonged fasting.

Kremer LS, L'hermitte-Stead C, Lesimple P, Gilleron M, Filaut S, Jardel C, Haack TB, Strom TM, Meitinger T, Azzouz H, Tebib N, Ogier de Baulny H, Touati G, Prokisch H, Lombès A. Kremer LS, et al. Among authors: azzouz h. J Hepatol. 2016 Aug;65(2):377-85. doi: 10.1016/j.jhep.2016.04.017. Epub 2016 May 2. J Hepatol. 2016. PMID: 27151179 Free PMC article.

2

[Richner-Hanhart syndrome].

Zribi H, Souissi A, Azzouz H, Tebib N, Mokni M. Zribi H, et al. Among authors: azzouz h. Presse Med. 2016 Feb;45(2):264-5. doi: 10.1016/j.lpm.2015.03.016. Epub 2016 Feb 12. Presse Med. 2016. PMID: 26880079 French. No abstract available.

3

Phenotypic continuum of type 2 Gaucher's disease: an intermediate phenotype between perinatal-lethal and classic type 2 Gaucher's disease.

Ben Turkia H, Tebib N, Azzouz H, Abdelmoula MS, Ben Chehida A, Caillaud C, Ben Dridi MF. Ben Turkia H, et al. Among authors: azzouz h. J Perinatol. 2009 Feb;29(2):170-2. doi: 10.1038/jp.2008.179. J Perinatol. 2009. PMID: 19177047

4

[Enzyme replacement therapy for Gaucher paediatric disease: the only Tunisian experience].

Ben Turkia H, Azzouz H, Tebib N, Abdelmoula MS, Ben Chehida A, Hlel Y, Caillaud C, Sahli H, Ben Dridi MF. Ben Turkia H, et al. Among authors: azzouz h. Tunis Med. 2009 May;87(5):344-8. Tunis Med. 2009. PMID: 19927767 French.

5

[A novel mutation in PEX 26 gene in Zellweger syndrome: a case report].

Ben Turkia H, Yangui M, Azzouz H, Ben Chehida A, Ben Abelaziz R, Abdelmoula MS, Nasrallah F, Kaabachi N, Wanders R, Tebib N, Ben Dridi MF. Ben Turkia H, et al. Among authors: azzouz h. Tunis Med. 2011 Mar;89(3):288-91. Tunis Med. 2011. PMID: 21387236 French.

6

A novel 22bp deletion in a Tunisian phenylketonuria family.

Khemir S, Siala H, Azzouz H, Tebib N, Dhondt JL, Messaoud T, Abdelhak S, Ben Dridi MF, Kaabachi N. Khemir S, et al. Among authors: azzouz h. Pathol Biol (Paris). 2012 Dec;60(6):e87-9. doi: 10.1016/j.patbio.2012.03.007. Epub 2012 May 7. Pathol Biol (Paris). 2012. PMID: 22572109

7

First report of a molecular prenatal diagnosis in a tunisian family with lysinuric protein intolerance.

Esseghir N, Bouchlaka CS, Fredj SH, Chehida AB, Azzouz H, Fontaine M, Tebib N, Dridi MF, Briand G, Messaoud T, Elgaaied AB, Kaabachi N. Esseghir N, et al. Among authors: azzouz h. JIMD Rep. 2011;1:37-8. doi: 10.1007/8904_2011_13. Epub 2011 Jun 22. JIMD Rep. 2011. PMID: 23430825 Free PMC article.

8

Congenital hyperinsulinism: review of 12 Tunisian cases.

Ben Turkia H, Brahim K, Azzouz H, Tebib N, Abdelmoula MS, Ben Chehida A, Fekih M, Sayed S, Kaabar N, Francoise Ben Dridi M. Ben Turkia H, et al. Among authors: azzouz h. Tunis Med. 2011 Apr;89(4):369-73. Tunis Med. 2011. PMID: 21484688

9

A novel homozygous missense mutation in the insulin receptor gene results in an atypical presentation of Rabson-Mendenhall syndrome.

Ben Abdelaziz R, Ben Chehida A, Azzouz H, Boudabbous H, Lascols O, Ben Turkia H, Tebib N. Ben Abdelaziz R, et al. Among authors: azzouz h. Eur J Med Genet. 2016 Jan;59(1):16-9. doi: 10.1016/j.ejmg.2015.11.015. Epub 2015 Dec 9. Eur J Med Genet. 2016. PMID: 26691667

10

Glycogen storage disease type I in Tunisia: an epidemiological analysis.

Ben Chehida A, Tebib N, Cherif W, Ben Turkia H, Abdelmoula S, Azzouz H, Ben Dridi MF. Ben Chehida A, et al. Among authors: azzouz h. J Inherit Metab Dis. 2008 Dec;31 Suppl 2:S199-204. doi: 10.1007/s10545-008-0707-2. Epub 2008 Aug 5. J Inherit Metab Dis. 2008. PMID: 18679824

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