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Results: 1-25/26
Authors:
Tekin, D
Yavuzer, S
Tekin, M
Akar, N
Cin, S
Citation: D. Tekin et al., Possible effects of antioxidant status on increased platelet aggregation in childhood iron-deficiency anemia, PEDIATR INT, 43(1), 2001, pp. 74-77
Authors:
Cakar, N
Yalcinkaya, F
Ozkaya, N
Tekin, M
Akar, N
Kocak, H
Misirlioglu, M
Akar, E
Tumer, N
Citation: N. Cakar et al., Familial Mediterranean fever (FMF)-associated amyloidosis in childhood. Clinical features, course and outcome, CLIN EXP RH, 19(5), 2001, pp. S63-S67
Authors:
Tekin, M
Akar, N
Cin, S
Blanton, SH
Xia, XJ
Liu, XZ
Nance, WE
Pandya, A
Citation: M. Tekin et al., Connexin 26 (GJB2) mutations in the Turkish population: implications for the origin and high frequency of the 35delG mutation in Caucasians, HUM GENET, 108(5), 2001, pp. 385-389
Authors:
Tekin, M
Jackson-Cook, C
Pandya, A
Citation: M. Tekin et al., De novo inverted tandem duplication of the short arm of chromosome 12 in apatient with microblepharon, AM J MED G, 104(1), 2001, pp. 42-46
Authors:
Tekin, M
Arnos, KS
Pandya, A
Citation: M. Tekin et al., Advances in hereditary deafness, LANCET, 358(9287), 2001, pp. 1082-1090
Authors:
Tekin, M
Bodurtha, JN
Nance, WE
Pandya, A
Citation: M. Tekin et al., Waardenburg syndrome type 3 (Klein-Waardenburg syndrome) segregating with a heterozygous deletion in box domain of PAX3: a simple variant or a true syndrome, CLIN GENET, 60(4), 2001, pp. 301-304
Authors:
Tekin, M
Arnos, KS
Xia, XJ
Oelrich, MK
Liu, XZ
Nance, WE
Pandya, A
Citation: M. Tekin et al., W44C mutation in the connexin 26 gene associated with dominant non-syndromic deafness, CLIN GENET, 59(4), 2001, pp. 269-273
Authors:
Yalcinkaya, F
Cakar, N
Misirlioglu, M
Tumer, N
Akar, N
Tekin, M
Tastan, H
Kocak, H
Ozkaya, N
Elhan, AH
Citation: F. Yalcinkaya et al., Genotype-phenotype correlation in a large group of Turkish patients with familial Mediterranean fever: evidence for mutation-independent amyloidosis.(vol 39, pg 67, 2000), RHEUMATOLOG, 39(10), 2000, pp. 1170-1170
Authors:
Yalcinkaya, F
Cakar, N
Misirlioglu, M
Tumer, N
Akar, N
Tekin, M
Tastan, H
Kocak, H
Ozkaya, N
Elhan, AH
Citation: F. Yalcinkaya et al., Genotype-phenotype correlation in a large group of Turkish patients with familial Mediterranean fever: evidence for mutation-independent amyloidosis, RHEUMATOLOG, 39(1), 2000, pp. 67-72
Authors:
Yalcinkaya, F
Tekin, M
Cakar, N
Akar, E
Akar, N
Tumer, N
Citation: F. Yalcinkaya et al., Familial Mediterranean fever and systemic amyloidosis in untreated Turkishpatients, QJM-MON J A, 93(10), 2000, pp. 681-684
Authors:
Buller, A
Pandya, A
Jackson-Cook, C
Bodurtha, J
Tekin, M
Wilkinson, DS
Garrett, CT
Ferreira-Gonzalez, A
Citation: A. Buller et al., Validation of a multiplex methylation-sensitive PCR assay for the diagnosis of Prader-Willi and Angelman's syndromes, MOL DIAGN, 5(3), 2000, pp. 239-243
Authors:
Tekin, M
Ohle, C
Johnson, DE
Christmas, JT
Bodurtha, J
Citation: M. Tekin et al., Counseling dilemmas in EEC syndrome, GEN COUNSEL, 11(1), 2000, pp. 19-24
Authors:
Tekin, M
Ellison, J
Citation: M. Tekin et J. Ellison, Oromandibular-limb hypogenesis spectrum and maternal lithium use, CLIN DYSMOR, 9(2), 2000, pp. 139-141
Authors:
Akar, N
Tekin, M
Uysal, Z
Uzunali, O
Citation: N. Akar et al., Effect of desferrioxamine on urinary copper and zinc excretion in beta-thalassemia major patients, J TR EL EXP, 13(2), 2000, pp. 195-198
Authors:
Tekin, M
Yalcinkaya, F
Tumer, N
Akar, N
Misirlioglu, M
Cakar, N
Citation: M. Tekin et al., Clinical, laboratory and molecular characteristics of children with Familial Mediterranean Fever-associated vasculitis, ACT PAEDIAT, 89(2), 2000, pp. 177-182
Authors:
Tekin, M
Ng, J
Bodurtha, J
Citation: M. Tekin et al., A 17-month-old with extreme prenatal-onset growth delay, EUR J PED, 159(12), 2000, pp. 926-928
Authors:
Tekin, M
Mutlu, C
Paparella, MM
Schachern, PA
Jaisinghani, VJ
Le, CT
Citation: M. Tekin et al., Tympanic membrane and middle ear pathologic correlates in mucoid otitis media, OTO H N SUR, 123(3), 2000, pp. 258-262
Authors:
Mutlu, C
Tekin, M
Paparella, MM
Schachern, PA
Citation: C. Mutlu et al., Bone dust in the middle ear, AM J OTOL, 21(2), 2000, pp. 286-287
Authors:
Tekin, M
Jackson-Cook, C
Buller, A
Ferreira-Gonzalez, A
Pandya, A
Garrett, CT
Bodurtha, J
Citation: M. Tekin et al., Fluorescence in situ hybridization detectable mosaicism for Angelman syndrome with biparental methylation, AM J MED G, 95(2), 2000, pp. 145-149
Authors:
Tekin, M
Tutar, E
Arsan, S
Atay, G
Bodurtha, J
Citation: M. Tekin et al., Ophthalmo-acromelic syndrome: Report and review, AM J MED G, 90(2), 2000, pp. 150-154
Authors:
Tekin, M
Yalcinkaya, F
Cakar, N
Akar, N
Misirlioglu, M
Tastan, H
Tumer, N
Citation: M. Tekin et al., MEFV mutations in multiplex families with familial Mediterranean fever: isa particular genotype necessary for amyloidosis?, CLIN GENET, 57(6), 2000, pp. 430-434
Authors:
Tekin, M
Yalcinkaya, F
Tumer, N
Cakar, N
Kocak, H
Ozkaya, N
Gencgonul, H
Citation: M. Tekin et al., Familial Mediterranean fever - renal involvement by diseases other than amyloid, NEPH DIAL T, 14(2), 1999, pp. 475-479
Authors:
Tekin, M
Yalcinkaya, F
Tumer, N
Cakar, N
Kocak, H
Citation: M. Tekin et al., Familial Mediterranean fever and acute rheumatic fever: A pathogenetic relationship?, CLIN RHEUMA, 18(6), 1999, pp. 446-449
Authors:
Tekin, M
Bodurtha, J
Ciftci, E
Arsan, S
Citation: M. Tekin et al., Further family with possible autosomal recessive inheritance of Adams-Oliver syndrome, AM J MED G, 86(1), 1999, pp. 90-91
Authors:
Pasin, M
Yavuzer, S
Tekin, M
Akar, N
Violi, F
Citation: M. Pasin et al., Oxygen free radical-dependent increased platelet function in beta-thalassemia major patients, THROMB RES, 92(6), 1998, pp. 283-286