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1-17
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Results: 17
Authors:
Yenicesu, I
Uckan, D
Cetin, M
Tuncer, AM
Tezcan, I
Gurgey, A
Citation: I. Yenicesu et al., Evaluation of coagulation in pediatric bone marrow transplantation patients, PEDIAT TRAN, 5(6), 2001, pp. 430-433
Authors:
Uckan, D
Cetin, M
Haliloglu, M
Ciftci, AO
Tuncer, MA
Tezcan, I
Citation: D. Uckan et al., Pneumatosis intestinalis in an infant undergoing bone marrow transplantation for Wiskott-Aldrich syndrome, PEDIAT TRAN, 5(5), 2001, pp. 370-373
Authors:
Sobacchi, C
Frattini, A
Orchard, P
Porras, O
Tezcan, I
Andolina, M
Babul-Hirji, R
Baric, I
Canham, N
Chitayat, D
Dupuis-Girod, S
Ellis, I
Etzioni, A
Fasth, A
Fisher, A
Gerritsen, B
Gulino, V
Horwitz, E
Klamroth, V
Lanino, E
Mirolo, M
Musio, A
Matthijs, G
Nonomaya, S
Notarangelo, LD
Ochs, HD
Furga, AS
Valiaho, J
van Hove, JLK
Vihinen, M
Vujic, D
Vezzoni, P
Villa, A
Citation: C. Sobacchi et al., The mutational spectrum of human malignant autosomal recessive osteopetrosis, HUM MOL GEN, 10(17), 2001, pp. 1767-1773
Authors:
Shi, YQ
Li, L
Sanal, O
Tezcan, I
Emery, GC
Blattmann, H
Crompton, NEA
Citation: Yq. Shi et al., High levels of delayed radiation-induced apoptosis observed in lymphoblastoid cell lines from ataxia-telangiectasia patients, INT J RAD O, 49(2), 2001, pp. 555-559
Authors:
Uckan, D
Hicsonmez, G
Tunc, B
Cetin, M
Tezcan, I
Tuncer, M
Citation: D. Uckan et al., The analysis of eosinophil and lymphocyte phenotype following single dose of high-dose methylprednisolone in two siblings with marked hypereosinophilia, CLIN LAB H, 23(1), 2001, pp. 33-37
Authors:
Moshous, D
Callebaut, I
de Chasseval, R
Corneo, B
Cavazzana-Calvo, M
Le Deist, F
Tezcan, I
Sanal, O
Bertrand, Y
Philippe, N
Fischer, A
de Villartay, JP
Citation: D. Moshous et al., Artemis, a novel DNA double-strand break repair/V(D)J recombination protein, is mutated in human severe combined immune deficiency, CELL, 105(2), 2001, pp. 177-186
Authors:
Kilic, SS
Tezcan, I
Sanal, O
Metin, A
Ersoy, F
Citation: Ss. Kilic et al., Transient hypogammaglobulinemia of infancy: Clinical and immunologic features of 40 new cases, PEDIATR INT, 42(6), 2000, pp. 647-650
Authors:
Pastural, E
Ersoy, F
Yalman, N
Wulffraat, N
Grillo, E
Ozkinay, F
Tezcan, I
Gedikoglu, G
Philippe, N
Fischer, A
de St Basile, G
Citation: E. Pastural et al., Two genes are responsible for Griscelli syndrome at the same 15q21 locus, GENOMICS, 63(3), 2000, pp. 299-306
Authors:
Yetgin, S
Olcay, L
Yel, L
Tuncer, M
Tezcan, I
Erdemli, E
Oner, AF
Behm, FG
Citation: S. Yetgin et al., T-ALL with monoclonal gammopathy and hairy cell features, AM J HEMAT, 65(2), 2000, pp. 166-170
Authors:
Sanal, O
Morgan, G
Gocmen, A
Novelli, V
Klein, N
Tezcan, I
Ersoy, F
Berkel, AI
Yel, L
Citation: O. Sanal et al., Isolated cutaneous response to granulocyte-monocyte colony stimulating factor in fatal idiopathic disseminated Bacillus-Calmette-Guerin infection, EUR J PED, 159(3), 2000, pp. 149-152
Authors:
Sanal, O
Yel, L
Kucukali, T
Gilbert-Barnes, E
Tardieu, M
Tezcan, I
Ersoy, F
Metin, A
de Saint Basile, G
Citation: O. Sanal et al., An allelic variant of Griscelli disease: presentation with severe hypotonia, mental-motor retardation, and hypopigmentation consistent with Elejalde syndrome (neuroectodermal melanolysosomal disorder), J NEUROL, 247(7), 2000, pp. 570-572
Authors:
Revy, P
Muto, T
Levy, Y
Geissmann, F
Plebani, A
Sanal, O
Catalan, N
Forveille, M
Dufourcq-Lagelouse, R
Gennery, A
Tezcan, I
Ersoy, F
Kayserili, H
Ugazio, AG
Brousse, N
Muramatsu, M
Notarangelo, LD
Kinoshita, K
Honjo, T
Fischer, A
Durandy, A
Citation: P. Revy et al., Activation-induced cytidine deaminase (AID) deficiency causes the autosomal recessive form of the hyper-IgM syndrome (HIGM2), CELL, 102(5), 2000, pp. 565-575
Authors:
Metin, A
Sanal, O
Ersoy, F
Tezcan, I
Berkel, AI
Irkec, C
Citation: A. Metin et al., Polymorphism of the fourth component of complement in Turks, HUMAN BIOL, 72(3), 2000, pp. 527-533
Authors:
Kilic, SS
Ersoy, F
Sanal, O
Turkbay, D
Tezcan, I
Citation: Ss. Kilic et al., Alopecia universalis in a patient with common variable immunodeficiency, PEDIAT DERM, 16(4), 1999, pp. 305-307
Authors:
Sanal, O
Ersoy, F
Yel, L
Tezcan, I
Metin, A
Ozyurek, H
Gariboglu, S
Fikrig, S
Berkel, AI
Rijkers, GT
Zegers, BJM
Citation: O. Sanal et al., Impaired IgG antibody production to pneumococcal polysaccharides in patients with ataxia-telangiectasia, J CLIN IMM, 19(5), 1999, pp. 326-334
Authors:
Tezcan, I
Sanal, O
Ersoy, F
Uckan, D
Kilic, S
Metin, A
Cetin, M
Akun, R
Oner, C
Tuncer, AM
Citation: I. Tezcan et al., Successful bone marrow transplantation in a case of Griscelli disease which presented in accelerated phase with neurological involvement, BONE MAR TR, 24(8), 1999, pp. 931-933
Authors:
Godthelp, BC
van Eggermond, MCJA
Peijnenburg, A
Tezcan, I
van Lierde, S
van Tol, MJD
Vossen, JM
van den Elsen, PJ
Citation: Bc. Godthelp et al., Incomplete T-cell immune reconstitution in two major histocompatibility complex class II-deficiency/bare lymphocyte syndrome patients after HLA-identical sibling bone marrow transplantation, BLOOD, 94(1), 1999, pp. 348-358
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