AAAAAA
Results:
1-11
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Results: 11
Authors:
Anlar, B
Alikasifoglu, M
Kose, G
Guven, A
Gurer, Y
Yakut, A
Citation: B. Anlar et al., Tumor necrosis factor-alpha gene polymorphisms in children with multiple sclerosis, NEUROPEDIAT, 32(4), 2001, pp. 214-216
Authors:
Alikasifoglu, M
Cullu, F
Kutlu, T
Arvas, A
Tastan, Y
Erginoz, E
Kaypmaz, A
Tumay, G
Citation: M. Alikasifoglu et al., Comparison study of the immunogenicity of different types and dosages of recombinant hepatitis B vaccine in healthy neonates, J TROP PEDI, 47(1), 2001, pp. 60-62
Authors:
Vencovsky, J
Jarosova, K
Ruzickova, S
Nemcova, D
Niederlova, J
Ozen, S
Alikasifoglu, M
Bakkaloglu, A
Ollier, WER
Mageed, RA
Citation: J. Vencovsky et al., Higher frequency of allele 2 of the interleukin-1 receptor antagonist genein patients with juvenile idiopathic arthritis, ARTH RHEUM, 44(10), 2001, pp. 2387-2391
Authors:
Tuncbilek, E
Alikasifoglu, M
Aktas, D
Duman, F
Yanik, H
Anar, B
Oostra, B
Willemsen, R
Citation: E. Tuncbilek et al., Screening for the fragile X syndrome among mentally retarded males by hairroot analysis, AM J MED G, 95(2), 2000, pp. 105-107
Authors:
Tokgozoglu, S
Alikasifoglu, M
Unsal, I
Atalar, E
Aytemir, K
Ozer, N
Ovunc, K
Usal, O
Kes, S
Tuncbilek, E
Citation: S. Tokgozoglu et al., Methylene tetrahydrofolate reductase genotype and the risk and extent of coronary artery disease in a population with low plasma folate, HEART, 81(5), 1999, pp. 518-522
Authors:
Boduroglu, K
Alikasifoglu, M
Anar, B
Tuncbilek, E
Citation: K. Boduroglu et al., Association of the 677C -> T mutation on the methylenetetrahydrofolate reductase gene in turkish patients with neural tube defects, J CHILD NEU, 14(3), 1999, pp. 159-161
Authors:
Ozen, S
Alikasifoglu, M
Saatci, U
Bakkaloglu, A
Besbas, N
Kara, N
Kocak, H
Erbas, B
Unsal, I
Tuncbilek, E
Citation: S. Ozen et al., Implications of certain genetic polymorphisms in scarring in vesicoureteric reflux: Importance of ACE polymorphism, AM J KIDNEY, 34(1), 1999, pp. 140-145
Authors:
Alikasifoglu, M
Topaloglu, H
Tuncbilek, E
Ceviz, M
Anar, B
Demir, E
Ozme, S
Citation: M. Alikasifoglu et al., Clinical and genetic correlate in childhood onset Friedreich ataxia, NEUROPEDIAT, 30(2), 1999, pp. 72-76
Authors:
Tuncbilek, E
Alikasifoglu, M
Boduroglu, K
Aktas, D
Anar, B
Citation: E. Tuncbilek et al., Frequency of fragile X syndrome among Turkish patients with mental retardation of unknown etiology, AM J MED G, 84(3), 1999, pp. 202-203
Authors:
Erbas, T
Alikasifoglu, M
Aksoyek, S
Unsal, I
Gedik, O
Tuncbilek, E
Citation: T. Erbas et al., Effects of angiotensin-converting enzyme gene polymorphism on the left-ventricular function and mass in patients with acromegaly, CARDIOLOGY, 92(4), 1999, pp. 226-231
Authors:
Koc, A
Pronk, JC
Alikasifoglu, M
Joenje, H
Altay, C
Citation: A. Koc et al., Variable pathogenicity of exon 43del (FAA) in four Fanconi anaemia patients within a consanguineous family, BR J HAEM, 104(1), 1999, pp. 127-130
Risultati:
1-11
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