Mansour I - Search Results

1

Effects of a short-term calcium and vitamin D treatment on serum cytokines, bone markers, insulin and lipid concentrations in healthy post-menopausal women.

Gannagé-Yared MH, Azoury M, Mansour I, Baddoura R, Halaby G, Naaman R. Gannagé-Yared MH, et al. Among authors: mansour i. J Endocrinol Invest. 2003 Aug;26(8):748-53. doi: 10.1007/BF03347358. J Endocrinol Invest. 2003. PMID: 14669830 Clinical Trial.

2

Panel-reactive antibodies using complement-dependent cytotoxicity, flow cytometry, and ELISA in patients awaiting renal transplantation or transplanted patients: a comparative study.

Mansour I, Messaed C, Azoury M, Klayme S, Naaman R. Mansour I, et al. Transplant Proc. 2001 Aug;33(5):2844-7. doi: 10.1016/s0041-1345(01)02214-x. Transplant Proc. 2001. PMID: 11498183 No abstract available.

3

Weak association between HLA-B27 and the spondylarthropathies in Lebanon.

Awadia H, Baddoura R, Naman R, Klayme S, Mansour I, Tamouza R, Marzais F, Raffoux C, Toubert A, Charron D. Awadia H, et al. Among authors: mansour i. Arthritis Rheum. 1997 Feb;40(2):388-9. doi: 10.1002/art.1780400226. Arthritis Rheum. 1997. PMID: 9041952 No abstract available.

4

A new HLA-B*27 allele (B*2719) identified in a Lebanese patient affected with ankylosing spondylitis.

Tamouza R, Mansour I, Bouguacha N, Klayme S, Djouadi K, Laoussadi S, Azoury M, Dulphy N, Ramasawmy R, Krishnamoorthy R, Toubert A, Naman R, Charron D. Tamouza R, et al. Among authors: mansour i. Tissue Antigens. 2001 Jul;58(1):30-3. doi: 10.1034/j.1399-0039.2001.580105.x. Tissue Antigens. 2001. PMID: 11580853

5

HLA phenotype polymorphism in the Lebanese population.

Mansour I, Klaymé S, Naman R, Loiselet J, Hallé L, Kaplan C. Mansour I, et al. Transfus Clin Biol. 1996;3(5):289-95. doi: 10.1016/s1246-7820(96)80019-x. Transfus Clin Biol. 1996. PMID: 8950804 Clinical Trial.

6

[Hepatitis C virus in hemodialysis patients and blood donors in Lebanon].

Naman RE, Mansour I, Klayme S, Khalil G. Naman RE, et al. Among authors: mansour i. J Med Liban. 1996;44(1):4-9. J Med Liban. 1996. PMID: 8965318 French.

7

Genetic screening of fourteen mutations in Jordanian familial Mediterranean fever patients.

Medlej-Hashim M, Rawashdeh M, Chouery E, Mansour I, Delague V, Lefranc G, Naman R, Loiselet J, Mégarbané A. Medlej-Hashim M, et al. Among authors: mansour i. Hum Mutat. 2000 Apr;15(4):384. doi: 10.1002/(SICI)1098-1004(200004)15:4<384::AID-HUMU19>3.0.CO;2-U. Hum Mutat. 2000. PMID: 10737992

8

Familial Mediterranean fever in Lebanon: mutation spectrum, evidence for cases in Maronites, Greek orthodoxes, Greek catholics, Syriacs and Chiites and for an association between amyloidosis and M694V and M694I mutations.

Mansour I, Delague V, Cazeneuve C, Dodé C, Chouery E, Pêcheux C, Medlej-Hashim M, Salem N, El Zein L, Levan-Petit I, Lefranc G, Goossens M, Delpech M, Amselem S, Loiselet J, Grateau G, Mégarbane A, Naman R. Mansour I, et al. Eur J Hum Genet. 2001 Jan;9(1):51-5. doi: 10.1038/sj.ejhg.5200574. Eur J Hum Genet. 2001. PMID: 11175300

9

Asymptomatic deficiency in the peptide transporter associated to antigen processing (TAP).

de la Salle H, Saulquin X, Mansour I, Klayme S, Fricker D, Zimmer J, Cazenave JP, Hanau D, Bonneville M, Houssaint E, Lefranc G, Naman R. de la Salle H, et al. Among authors: mansour i. Clin Exp Immunol. 2002 Jun;128(3):525-31. doi: 10.1046/j.1365-2249.2002.01862.x. Clin Exp Immunol. 2002. PMID: 12067308 Free PMC article.

10

Familial Mediterranean Fever: association of elevated IgD plasma levels with specific MEFV mutations.

Medlej-Hashim M, Petit I, Adib S, Chouery E, Salem N, Delague V, Rawashdeh M, Mansour I, Lefranc G, Naman R, Loiselet J, Lecron JC, Serre JL, Mégarbané A. Medlej-Hashim M, et al. Among authors: mansour i. Eur J Hum Genet. 2001 Nov;9(11):849-54. doi: 10.1038/sj.ejhg.5200725. Eur J Hum Genet. 2001. PMID: 11781702

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