Naman R - Search Results

1

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. Among authors: naman r. Eur J Hum Genet. 2001 Jan;9(1):51-5. doi: 10.1038/sj.ejhg.5200574. Eur J Hum Genet. 2001. PMID: 11175300

2

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: naman r. 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

3

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: naman r. Eur J Hum Genet. 2001 Nov;9(11):849-54. doi: 10.1038/sj.ejhg.5200725. Eur J Hum Genet. 2001. PMID: 11781702

4

Familial Mediterranean fever: the potential for misdiagnosis of E148V using the E148Q usual RFLP detection method.

Medlej-Hashim M, Salem N, Chouery E, Rawashdeh M, Delague V, Haffar M, Mansour I, Naman R, Lefranc G, Loiselet J, Mégarbané A. Medlej-Hashim M, et al. Among authors: naman r. Clin Genet. 2002 Jan;61(1):71-3. doi: 10.1034/j.1399-0004.2002.10114.x. Clin Genet. 2002. PMID: 11903360 No abstract available.

5

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

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

6

HLA phenotype polymorphism in the Lebanese population.

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

7

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: naman r. Arthritis Rheum. 1997 Feb;40(2):388-9. doi: 10.1002/art.1780400226. Arthritis Rheum. 1997. PMID: 9041952 No abstract available.

8

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: naman r. 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.

9

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: naman r. Tissue Antigens. 2001 Jul;58(1):30-3. doi: 10.1034/j.1399-0039.2001.580105.x. Tissue Antigens. 2001. PMID: 11580853

10

Genotypes of hepatitis C virus (HCV) among positive Lebanese patients: comparison of data with that from other Middle Eastern countries.

Sharara AI, Ramia S, Ramlawi F, Fares JE, Klayme S, Naman R. Sharara AI, et al. Among authors: naman r. Epidemiol Infect. 2007 Apr;135(3):427-32. doi: 10.1017/S0950268806006911. Epub 2006 Jul 19. Epidemiol Infect. 2007. PMID: 16848924 Free PMC article.

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