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Aminoacidopathies and organic acidurias in Tunisia: a retrospective survey over 23 years.
Hadj-Taieb S, Nasrallah F, Hammami MB, Elasmi M, Sanhaji H, Moncef F, Kaabachi N. Hadj-Taieb S, et al. Among authors: kaabachi n. Tunis Med. 2012 Mar;90(3):258-61. Tunis Med. 2012. PMID: 22481200
Clinical and pathological study of three Tunisian siblings with L-2-hydroxyglutaric aciduria.
Larnaout A, Hentati F, Belal S, Ben Hamida C, Kaabachi N, Ben Hamida M. Larnaout A, et al. Among authors: kaabachi n. Acta Neuropathol. 1994;88(4):367-70. doi: 10.1007/BF00310381. Acta Neuropathol. 1994. PMID: 7839830
Familial encephalopathy and L-2-hydroxyglutaric aciduria.
Kaabachi N, Larnaout A, Rabier D, Jakobs C, Belal S, Hentati F, Parvey P, Bardet J, Ben Hamida M, Mebazaa A, et al. Kaabachi N, et al. J Inherit Metab Dis. 1993;16(5):893. doi: 10.1007/BF00714285. J Inherit Metab Dis. 1993. PMID: 8295407 No abstract available.
[Argininosuccinic aciduria. Apropos of the 1st Tunisian case in a newborn].
Chabchoub A, M'kadmi T, Marrakchi Z, Khiari D, Kaabachi N, Ayachi R, Mebazzaa R, Khrouf N. Chabchoub A, et al. Among authors: kaabachi n. Tunis Med. 1995 Oct;73(10):411-4. Tunis Med. 1995. PMID: 9506166 French. No abstract available.
Methylmalonic acidaemia with bilateral globus pallidus involvement: a neuropathological study.
Larnaout A, Mongalgi MA, Kaabachi N, Khiari D, Debbabi A, Mebazza A, Ben Hamida M, Hentati F. Larnaout A, et al. Among authors: kaabachi n. J Inherit Metab Dis. 1998 Aug;21(6):639-44. doi: 10.1023/a:1005428432730. J Inherit Metab Dis. 1998. PMID: 9762599
Juvenile form of dihydropteridine reductase deficiency in 2 Tunisian patients.
Larnaout A, Belal S, Miladi N, Kaabachi N, Mebazza A, Dhondt JL, Hentati F. Larnaout A, et al. Among authors: kaabachi n. Neuropediatrics. 1998 Dec;29(6):322-3. doi: 10.1055/s-2007-973586. Neuropediatrics. 1998. PMID: 10029353
[Distribution of cardiovascular risk factors in a Tunisian cohort of 6901 coronary patients].
Jemaa R, Kafsi MN, Kallel A, Mechmeche R, Zaouali RM, Haouala H, Elasmi M, Gueddiche M, Slimane L, Belhani A, Kaabachi N, Mebazaa A. Jemaa R, et al. Among authors: kaabachi n. Arch Mal Coeur Vaiss. 2004 Jan;97(1):20-4. Arch Mal Coeur Vaiss. 2004. PMID: 15002706 French.
Vitamin D deficiency in Tunisia.
Meddeb N, Sahli H, Chahed M, Abdelmoula J, Feki M, Salah H, Frini S, Kaabachi N, Belkahia Ch, Mbazaa R, Zouari B, Sellami S. Meddeb N, et al. Among authors: kaabachi n. Osteoporos Int. 2005 Feb;16(2):180-3. doi: 10.1007/s00198-004-1658-6. Epub 2004 Jun 10. Osteoporos Int. 2005. PMID: 15197539
Clinical and mutational investigations of tyrosinemia type II in Northern Tunisia: identification and structural characterization of two novel TAT mutations.
Charfeddine C, Monastiri K, Mokni M, Laadjimi A, Kaabachi N, Perin O, Nilges M, Kassar S, Keirallah M, Guediche MN, Kamoun MR, Tebib N, Ben Dridi MF, Boubaker S, Ben Osman A, Abdelhak S. Charfeddine C, et al. Among authors: kaabachi n. Mol Genet Metab. 2006 Jun;88(2):184-91. doi: 10.1016/j.ymgme.2006.02.006. Epub 2006 Mar 30. Mol Genet Metab. 2006. PMID: 16574453
[Homocysteinemia and coronary artery disease: a case-control study in a Tunisian population].
Souissi M, Feki M, Mourali S, Enneifer M, Omar S, Sanhaji H, Mechmeche R, Mebazaa A, Kaabachi N. Souissi M, et al. Among authors: kaabachi n. Arch Mal Coeur Vaiss. 2006 Sep;99(9):781-5. Arch Mal Coeur Vaiss. 2006. PMID: 17067095 French.
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