Gribaa M - Search Results

1

Sanjad-Sakati syndrome in a Tunisian child.

Kerkeni E, Sakka R, Sfar S, Bouaziz S, Ghedira N, Ben Ameur K, Ben Hmida H, Chioukh FZ, Ghédira ES, Gribaa M, Monastiri K. Kerkeni E, et al. Among authors: gribaa m. Arch Pediatr. 2015 Sep;22(9):951-5. doi: 10.1016/j.arcped.2015.06.003. Epub 2015 Jul 29. Arch Pediatr. 2015. PMID: 26231322

2

Molecular characterization of piebaldism in a Tunisian family.

Kerkeni E, Boubaker S, Sfar S, Bizid M, Besbes H, Bouaziz S, Ghedira N, Amara A, Manoubi W, Gribaa M, Monastiri K. Kerkeni E, et al. Among authors: gribaa m. Pathol Biol (Paris). 2015 Jun;63(3):113-6. doi: 10.1016/j.patbio.2015.03.004. Epub 2015 Apr 21. Pathol Biol (Paris). 2015. PMID: 25910686

3

Cytogenetic analysis in 139 Tunisian patients with de novo acute myeloid leukemia.

Sendi HS, Elghezal H, Temmi H, Hichri H, Gribaa M, Elomri H, Meddeb B, Ben Othmane T, Elloumi M, Saad A. Sendi HS, et al. Among authors: gribaa m. Ann Genet. 2002 Jan-Mar;45(1):29-32. doi: 10.1016/s0003-3995(02)01098-5. Ann Genet. 2002. PMID: 11934387

4

Cytogenetic survey of 117 Tunisian patients with de novo myelodysplastic syndrome.

Sendi HS, Hichri H, Elghezal H, Gribaa M, Laatiri A, Elloumi M, Ben Lakhal R, Saad A. Sendi HS, et al. Among authors: gribaa m. Ann Genet. 2002 Jul-Sep;45(3):131-5. doi: 10.1016/s0003-3995(02)01123-1. Ann Genet. 2002. PMID: 12381443

5

[Hereditary sensory and autonomic neuropathy type IV: a report on two cases].

Achouri E, Gribaa M, Bouguila J, Haddad S, Souayeh N, Saad A, Essoussi AS. Achouri E, et al. Among authors: gribaa m. Arch Pediatr. 2011 Apr;18(4):390-3. doi: 10.1016/j.arcped.2010.12.024. Arch Pediatr. 2011. PMID: 21397470 French.

6

Correlation of SMN2, NAIP, p44, H4F5 and Occludin genes copy number with spinal muscular atrophy phenotype in Tunisian patients.

Amara A, Adala L, Ben Charfeddine I, Mamaï O, Mili A, Lazreg TB, H'mida D, Amri F, Salem N, Boughammura L, Saad A, Gribaa M. Amara A, et al. Among authors: gribaa m. Eur J Paediatr Neurol. 2012 Mar;16(2):167-74. doi: 10.1016/j.ejpn.2011.07.007. Epub 2011 Aug 6. Eur J Paediatr Neurol. 2012. PMID: 21821450

7

Molecular and biochemical characterization of Tunisian patients with glycogen storage disease type III.

Mili A, Ben Charfeddine I, Mamaï O, Abdelhak S, Adala L, Amara A, Pagliarani S, Lucchiarri S, Ayadi A, Tebib N, Harbi A, Bouguila J, H'Mida D, Saad A, Limem K, Comi GP, Gribaa M. Mili A, et al. Among authors: gribaa m. J Hum Genet. 2012 Mar;57(3):170-5. doi: 10.1038/jhg.2011.122. Epub 2011 Nov 17. J Hum Genet. 2012. PMID: 22089644

8

Two novel CYP11B1 mutations in congenital adrenal hyperplasia due to steroid 11β hydroxylase deficiency in a Tunisian family.

Ben Charfeddine I, Riepe FG, Kahloul N, Kulle AE, Adala L, Mamaï O, Amara A, Mili A, Amri F, Saad A, Holterhus PM, Gribaa M. Ben Charfeddine I, et al. Among authors: gribaa m. Gen Comp Endocrinol. 2012 Feb 1;175(3):514-8. doi: 10.1016/j.ygcen.2011.12.017. Epub 2011 Dec 22. Gen Comp Endocrinol. 2012. PMID: 22210247

9

Steroid 21-hydroxylase gene mutational spectrum in 50 Tunisian patients: characterization of three novel polymorphisms.

Ben Charfeddine I, Riepe FG, Clauser E, Ayedi A, Makni S, Sfar MT, Sboui H, Kahloul N, Ben Hamouda H, Chouchane S, Trimech S, Zouari N, M'Rabet S, Amri F, Saad A, Holterhus PM, Gribaa M. Ben Charfeddine I, et al. Among authors: m rabet s, gribaa m. Gene. 2012 Oct 1;507(1):20-6. doi: 10.1016/j.gene.2012.07.027. Epub 2012 Jul 25. Gene. 2012. PMID: 22841790

10

Modulation at age of onset in tunisian huntington disease patients: implication of new modifier genes.

Hmida-Ben Brahim D, Chourabi M, Ben Amor S, Harrabi I, Trabelsi S, Haddaji-Mastouri M, Gribaa M, Sassi S, Gahbiche FE, Lamouchi T, Mougou-Zereli S, Ben Ammou S, Saad A. Hmida-Ben Brahim D, et al. Among authors: gribaa m. Genet Res Int. 2014;2014:210418. doi: 10.1155/2014/210418. Epub 2014 Sep 1. Genet Res Int. 2014. PMID: 25254119 Free PMC article.

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