Gribaa M - Search Results

1

Clinical, biological, radiological, and genetic study of LPAC syndrome in Tunisian patients.

Halleb Y, Ben Jazia E, Akkari I, Zaghouani H, Hmila F, Ghrissi R, Saad A, Gribaa M. Halleb Y, et al. Among authors: gribaa m. Arab J Gastroenterol. 2022 Aug;23(3):210-217. doi: 10.1016/j.ajg.2022.06.002. Epub 2022 Jul 31. Arab J Gastroenterol. 2022. PMID: 35922258

2

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

3

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

4

[Prognostic impact of karyotype in de novo acute myeloid leukemia: study of 139 cases].

Sennana Sendi H, Elghezal H, Temmi H, Gribaa M, Laatiri A, Ben Abid H, Ben Abdeladhime A, Elloumi M, Hafsia A, Saad A. Sennana Sendi H, et al. Among authors: gribaa m. Tunis Med. 2002 Sep;80(9):531-5. Tunis Med. 2002. PMID: 12632766 French.

5

Placental mesenchymal dysplasia with beckwith-wiedemann syndrome fetus in the context of biparental and androgenic cell lines.

H'mida D, Gribaa M, Yacoubi T, Chaieb A, Adala L, Elghezal H, Saad A. H'mida D, et al. Among authors: gribaa m. Placenta. 2008 May;29(5):454-60. doi: 10.1016/j.placenta.2008.01.001. Epub 2008 Mar 17. Placenta. 2008. PMID: 18342934

6

An autosomal dominant hypophosphatemic rickets phenotype in a Tunisian family caused by a new FGF23 missense mutation.

Gribaa M, Younes M, Bouyacoub Y, Korbaa W, Ben Charfeddine I, Touzi M, Adala L, Mamay O, Bergaoui N, Saad A. Gribaa M, et al. J Bone Miner Metab. 2010;28(1):111-5. doi: 10.1007/s00774-009-0111-5. Epub 2009 Aug 5. J Bone Miner Metab. 2010. PMID: 19655082

7

[Clinical and genetic characteristics of Buschke-Fischer-Brauer's disease in a Tunisian family].

El Amri I, Mamai O, Ghariani N, Denguezli M, Sriha B, Adala L, Saad A, Gribaa M, Nouira R. El Amri I, et al. Among authors: gribaa m. Ann Dermatol Venereol. 2010 Apr;137(4):269-75. doi: 10.1016/j.annder.2010.02.002. Epub 2010 Mar 4. Ann Dermatol Venereol. 2010. PMID: 20417359 French.

8

A case of a Tunisian Rett patient with a novel double-mutation of the MECP2 gene.

Fendri-Kriaa N, Hsairi I, Kifagi C, Ellouze E, Mkaouar-Rebai E, Triki C, Fakhfakh F; Tunisian network on mental retardation study. Fendri-Kriaa N, et al. Biochem Biophys Res Commun. 2011 Jun 3;409(2):270-4. doi: 10.1016/j.bbrc.2011.04.140. Epub 2011 May 7. Biochem Biophys Res Commun. 2011. PMID: 21575601

9

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

10

A c.3216_3217delGA mutation in AGL gene in Tunisian patients with a glycogen storage disease type III: evidence of a founder effect.

Mili A, Ben Charfeddine I, Amara A, Mamaï O, Adala L, Ben Lazreg T, Bouguila J, Saad A, Limem K, Gribaa M. Mili A, et al. Among authors: gribaa m. Clin Genet. 2012 Dec;82(6):534-9. doi: 10.1111/j.1399-0004.2011.01806.x. Epub 2011 Nov 23. Clin Genet. 2012. PMID: 22035446

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