Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

96 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Publication Date timeline is not available.
Page 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.
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
[Atypical presentation of Wegener disease in childhood].
Ben Turkia H, Amdouni N, Azzouz H, Tebib N, Abdelmoula MS, El Mazni F, Hamzaoui A, Ben Dridi MF. Ben Turkia H, et al. Among authors: azzouz h. J Mal Vasc. 2008 Dec;33(4-5):242-6. doi: 10.1016/j.jmv.2008.09.007. Epub 2008 Nov 20. J Mal Vasc. 2008. PMID: 19022597 French.
Homogénéité mutationnelle de la glycogénose de type Ia en Tunisie.
Cherif W, Rhouma FB, Chehida AB, Azzouz H, Monastiri K, Amri F, Chemli J, Kaabachi N, Abdelhak S, Tebib N, Dridi MF. Cherif W, et al. Among authors: azzouz h. Pathol Biol (Paris). 2011 Aug;59(4):e93-6. doi: 10.1016/j.patbio.2009.05.004. Epub 2009 Nov 5. Pathol Biol (Paris). 2011. PMID: 19896294
Incidence of mucopolysaccharidoses in Tunisia.
Ben Turkia H, Tebib N, Azzouz H, Abdelmoula MS, Ben Chehida A, Chemli J, Monastiri K, Chaabouni M, Sanhagi H, Zouari B, Kaabachi N, Ben Dridi MF. Ben Turkia H, et al. Among authors: azzouz h. Tunis Med. 2009 Nov;87(11):782-5. Tunis Med. 2009. PMID: 20209839 Free article.
[Phenotype and mutational spectrum in Tunisian pediatric gaucher disease].
Ben Turkia H, Riahi I, Azzouz H, Ladab S, Cherif W, Ben Chehida A, Abdelmoula MS, Caillaud C, Chemli J, Abdelhak S, Tebib N, Ben Dridi MF. Ben Turkia H, et al. Among authors: azzouz h. Tunis Med. 2010 Mar;88(3):158-62. Tunis Med. 2010. PMID: 20415187 Free article. French.
[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 Free article. French.
96 results