Fakhfakh F - Search Results

1

An interethnic variability and a functional prediction of DNA repair gene polymorphisms: the example of XRCC3 (p.Thr241>Met) and XPD (p.Lys751>Gln) in a healthy Tunisian population.

Ben Salah G, Fendri-Kriaa N, Kamoun H, Kallabi F, Mkaouar-Rebai E, Fourati A, Ayadi H, Fakhfakh F. Ben Salah G, et al. Among authors: fakhfakh f. Mol Biol Rep. 2012 Oct;39(10):9639-47. doi: 10.1007/s11033-012-1829-z. Epub 2012 Jun 28. Mol Biol Rep. 2012. PMID: 22740138

2

Alpha heavy chain disease alpha mRNA contain nucleotide sequences of unknown origins.

Fakhfakh F, Dellagi K, Ayadi H, Bouguerra A, Fourati R, Ben Ayed F, Brouet JC, Tsapis A. Fakhfakh F, et al. Eur J Immunol. 1992 Nov;22(11):3037-40. doi: 10.1002/eji.1830221141. Eur J Immunol. 1992. PMID: 1425927

3

[Determination of the frequency of the A2m (2) allele of immunoglobin A in the Tunisian population by RFLP analysis].

Fakhfakh F, Rouis S, Makni H, Ayadi H. Fakhfakh F, et al. Rev Fr Transfus Hemobiol. 1991 Dec;34(6):441-7. doi: 10.1016/s1140-4639(05)80138-8. Rev Fr Transfus Hemobiol. 1991. PMID: 1685319 French.

4

[Alpha heavy chain disease. Molecular analysis of a new case].

Fakhfakh F, Mihaesco E, Ayadi H, Brouet JC, Tsapis A. Fakhfakh F, et al. Presse Med. 1993 Jun 19;22(22):1047-51. Presse Med. 1993. PMID: 8415447 French.

5

Antibody epitopes probed by immunoselected phage-display library peptides in members of a family with various rheumatic manifestations.

Fakhfakh F, Ayadi H, Bahloul Z, Jarraya A, Sioud M, Zouali M. Fakhfakh F, et al. Clin Exp Rheumatol. 1996 Nov-Dec;14(6):607-11. Clin Exp Rheumatol. 1996. PMID: 8978954

6

Polymorphism of the human immunoglobulin heavy chain locus in rheumatoid arthritis.

Fakhfakh F, Ayadi H, Maalej A, Bahloul Z, Jarraya A, Zouali M. Fakhfakh F, et al. Autoimmunity. 1997;25(2):109-16. doi: 10.3109/08916939708996277. Autoimmunity. 1997. PMID: 9189012 Free article.

7

[Molecular analysis of ten families with Duchenne muscular atrophy].

Fakhfakh F, Mhiri C, Triki C, Ayadi H. Fakhfakh F, et al. Tunis Med. 1996 Mar;74(3):113-8. Tunis Med. 1996. PMID: 9507291 French. No abstract available.

8

[Hemoglobin beta S haplotype in the Kebili region (southern Tunisia)].

Frikha M, Fakhfakh F, Mseddi S, Gargouri J, Ghali L, Labiadh Z, Harrabi M, Souissi T, Ayadi H. Frikha M, et al. Among authors: fakhfakh f. Transfus Clin Biol. 1998 Apr;5(2):166-72. doi: 10.1016/s1246-7820(98)80006-2. Transfus Clin Biol. 1998. PMID: 9618841 French.

9

Analysis of immunoglobulin VH and TCR cbeta polymorphisms in a large family with thyroid autoimmune disorder.

Fakhfakh F, Maalej A, Makni H, Abid M, Jouida J, Zouali M, Ayadi H. Fakhfakh F, et al. Exp Clin Immunogenet. 1999;16(4):185-91. doi: 10.1159/000019110. Exp Clin Immunogenet. 1999. PMID: 10575272

10

New FKRP mutations causing congenital muscular dystrophy associated with mental retardation and central nervous system abnormalities. Identification of a founder mutation in Tunisian families.

Louhichi N, Triki C, Quijano-Roy S, Richard P, Makri S, Méziou M, Estournet B, Mrad S, Romero NB, Ayadi H, Guicheney P, Fakhfakh F. Louhichi N, et al. Among authors: fakhfakh f. Neurogenetics. 2004 Feb;5(1):27-34. doi: 10.1007/s10048-003-0165-9. Epub 2003 Dec 2. Neurogenetics. 2004. PMID: 14652796 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

177 results

Search Page

Filters