Saad A - Search Results

1

[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: saad a. 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.

2

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: saad a. 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

3

Reduction of palmoplantar keratoderma Buschke-Fischer-Brauer locus to only 0.967 Mb.

Mamaï O, Boussofara L, Adala L, Amara A, Ben Charfeddine I, Ghariani N, Sriha B, Denguezli M, Mili A, Belazreg T, Saad A, Gribaa M. Mamaï O, et al. Among authors: saad a. J Dermatol Sci. 2012 Sep;67(3):210-2. doi: 10.1016/j.jdermsci.2012.06.011. Epub 2012 Jul 6. J Dermatol Sci. 2012. PMID: 22789686 No abstract available.

4

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: saad a. Placenta. 2008 May;29(5):454-60. doi: 10.1016/j.placenta.2008.01.001. Epub 2008 Mar 17. Placenta. 2008. PMID: 18342934

5

Identification of the translocation t(15;17) in acute myeloid leukemia (AML) initially classified as FAB M1: case report and review of the literature.

Braham Jmili N, Omri H, Senana Sendi H, Fekih S, Hizem S, Sriha B, Khelif A, Saad A, Kortas M. Braham Jmili N, et al. Among authors: saad a. Clin Lab. 2006;52(3-4):125-30. Clin Lab. 2006. PMID: 16584058 Review.

6

[Haematological characteristics, FAB and WHO classification of 153 cases of myeloid acute leukaemia in Tunisia].

Braham-Jmili N, Sendi-Senana H, Labiadh S, Ben Abdelali R, Ben Abdelaziz A, Khelif A, Saad A, Kortas M. Braham-Jmili N, et al. Among authors: saad a. Ann Biol Clin (Paris). 2006 Sep-Oct;64(5):457-65. Ann Biol Clin (Paris). 2006. PMID: 17040877 Free article. French.

7

Molecular cytogenetic aberrations in Tunisian patients with multiple myeloma identified by cIg-FISH in fixed bone marrow cells.

Gmidène A, Avet-Loiseau H, Sennana H, Ben Abdallah I, Khlif A, Meddeb B, Elloumi M, Saad A. Gmidène A, et al. Among authors: saad a. Cytogenet Genome Res. 2012;136(1):44-9. doi: 10.1159/000334878. Epub 2011 Dec 22. Cytogenet Genome Res. 2012. PMID: 22188899

8

Meiotic segregation and sperm DNA fragmentation in Tunisian men with dysplasia of the fibrous sheath (DFS) associated with head abnormalities.

Ghedir H, Mehri A, Mehdi M, Brahem S, Saad A, Ibala-Romdhane S. Ghedir H, et al. Among authors: saad a. J Assist Reprod Genet. 2014 Sep;31(9):1167-74. doi: 10.1007/s10815-014-0290-4. Epub 2014 Jul 8. J Assist Reprod Genet. 2014. PMID: 25001634 Free PMC article.

9

NOBOX is a strong autosomal candidate gene in Tunisian patients with primary ovarian insufficiency.

Bouali N, Francou B, Bouligand J, Lakhal B, Malek I, Kammoun M, Warszawski J, Mougou S, Saad A, Guiochon-Mantel A. Bouali N, et al. Among authors: saad a. Clin Genet. 2016 May;89(5):608-13. doi: 10.1111/cge.12750. Epub 2016 Mar 4. Clin Genet. 2016. PMID: 26848058

10

[Place of pelvic ultrasonography using transabdominal technique in the investigation of premature ovarian failure].

Braham R, Hidar S, Chaieb M, Trimeche S, Zaouali M, Lakhal B, Saâd A, Ach K, Chaieb L, Elghezal H. Braham R, et al. Among authors: saad a. Ann Endocrinol (Paris). 2010 Sep;71(4):286-90. doi: 10.1016/j.ando.2010.03.008. Epub 2010 Jun 2. Ann Endocrinol (Paris). 2010. PMID: 20627259 French.

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