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Results: 1-9 |
Results: 9
Effect of inhaled steroid therapy on distribution of Tc-99m DTPA radioaerosol in asthmatic children
Authors: Yuksel, H Yuksel, D Demir, E Tanac, R Kayaliodlu, M
Citation: H. Yuksel et al., Effect of inhaled steroid therapy on distribution of Tc-99m DTPA radioaerosol in asthmatic children, ALL ASTH P, 21(6), 2000, pp. 361-365
The gene encoding gigaxonin, a new member of the cytoskeletal BTB/kelch repeat family, is mutated in giant axonal neuropathy
Authors: Bomont, P Cavalier, L Blondeau, F Hamida, CB Belal, S Tazir, M Demir, E Topaloglu, H Korinthenberg, R Tuysuz, B Landrieu, P Hentati, F Koenig, M
Citation: P. Bomont et al., The gene encoding gigaxonin, a new member of the cytoskeletal BTB/kelch repeat family, is mutated in giant axonal neuropathy, NAT GENET, 26(3), 2000, pp. 370-374
Giant axonal neuropathy locus refinement to a < 590 kb critical interval
Authors: Cavalier, L BenHamida, C Amouri, R Belal, S Bomont, P Lagarde, N Gressin, L Callen, D Demir, E Topaloglu, H Landrieu, P Ioos, C Ben Hamida, M Koenig, M Hentati, F
Citation: L. Cavalier et al., Giant axonal neuropathy locus refinement to a < 590 kb critical interval, EUR J HUM G, 8(7), 2000, pp. 527-534
Weight gain associated with valproate in childhood
Authors: Demir, E Aysun, S
Citation: E. Demir et S. Aysun, Weight gain associated with valproate in childhood, PED NEUROL, 22(5), 2000, pp. 361-364
Effect of alendronate treatment on the clinical picture and bone turnover markers in chronic idiopathic hyperphosphatasia
Authors: Demir, E Bereket, A Ozkan, B Topcu, M
Citation: E. Demir et al., Effect of alendronate treatment on the clinical picture and bone turnover markers in chronic idiopathic hyperphosphatasia, J PED END M, 13(2), 2000, pp. 217-221
A cross section of autosomal recessive limb-girdle muscular dystrophies in38 families
Authors: Dincer, P Akcoren, Z Demir, E Richard, I Sancak, O Kale, G Ozme, S Karaduman, A Tan, E Urtizberea, JA Beckmann, JS Topaloglu, H
Citation: P. Dincer et al., A cross section of autosomal recessive limb-girdle muscular dystrophies in38 families, J MED GENET, 37(5), 2000, pp. 361-367
Genotype-phenotype correlation in three homozygotes and nine compound heterozygotes for the cystic fibrosis mutation 2183AA -> G shows a severe phenotype
Authors: Kilinc, MO Ninis, VN Tolun, A Estivill, X Casals, T Savov, A Dagli, E Karakoc, F Demirkol, M Huner, G Ozkinay, F Demir, E Seculi, JL Pena, J Bousono, C Ferrer-Calvete, J Calvo, C Glover, G Kremenski, I
Citation: Mo. Kilinc et al., Genotype-phenotype correlation in three homozygotes and nine compound heterozygotes for the cystic fibrosis mutation 2183AA -> G shows a severe phenotype, J MED GENET, 37(4), 2000, pp. 307-309
Sublingual immunotherapy and influence on urinary leukotrienes in seasonalpediatric allergy
Authors: Yuksel, H Tanac, R Gousseinov, A Demir, E
Citation: H. Yuksel et al., Sublingual immunotherapy and influence on urinary leukotrienes in seasonalpediatric allergy, J INVES ALL, 9(5), 1999, pp. 305-313
Clinical and genetic correlate in childhood onset Friedreich ataxia
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
Risultati: 1-9 |