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Mualla Çetin

Hacettepe University

27H指数
189论文数
2.7K被引数
收录论文 19
发表时间
Clinical and Molecular Spectrum of Glucose-6-Phosphate Isomerase Deficiency. Report of 12 New Cases
err2019-05-07
err20
errOAAI
errFermo, Elisa; Vercellati, Cristina; Marcello, Anna Paola; Zaninoni, Anna; Aytac, Selin; Cetin, Mualla; Capolsini, Ilaria; Casale, Maddalena; Paci, Sabrina; Zanella, Alberto; Barcellini, Wilma; Bianchi, Paola
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A Monogenic Disease with a Variety of Phenotypes: Deficiency of Adenosine Deaminase 2
err2019-05-01
err79
PREAI
errOzen, Seza; Batu, Ezgi Deniz; Taskiran, Ekim Z.; Ozkara, Hatice Asuman; Unal, Sule; Guleray, Naz; Erden, Abdulsamet; Karadag, Omer; Gumruk, Fatma; Cetin, Mualla; Sonmez, Hafize Emine; Bilginer, Yelda; Ayvaz, Deniz Cagdas; Tezcan, Ilhan
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The clinical and laboratory evaluation of familial hemophagocytic lymphohistiocytosis and the importance of hepatic and spinal cord involvement: a single center experience
err2017-11-16
err17
errOAAI
errBeken, Burcin; Aytac, Selin; Balta, Gunay; Kuskonmaz, Baris; Uckan, Duygu; Unal, Sule; Cetin, Mualla; Gumruk, Fatma
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Generalized lichen nitidus associated with neurofibromatosis type 1 and juvenile myelomonocytic leukemia
err2016-10-05
err3
PREAI
errDogan, Sibel; Memis, Pelin; Ersoy-Evans, Sibel; Gokoz, Ozay; Tavil, Betul; Cetin, Mualla
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Early-onset chronic axonal neuropathy, strokes, and hemolysis Inherited CD59 deficiency
err2015-03-24
err34
PREAI
errHaliloglu, Goknur; Maluenda, Jerome; Sayinbatur, Bahattin; Aumont, Cedric; Temucin, Cagri; Tavil, Betul; Cetin, Mualla; Oguz, Kader K.; Gut, Ivo; Picard, Veronique; Melki, Judith; Topaloglu, Haluk
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Biochemical markers of glucose metabolism may be used to estimate the degree and progression of iron overload in the liver and pancreas of patients with β-thalassemia major
err2015-03-06
err18
PREAI
errBas, Munevver; Gumruk, Fatma; Gonc, Nazli; Cetin, Mualla; Tuncer, Murat; Hazirolan, Tuncay; Yildirim, Gokce; Karabulut, Erdem; Unal, Sule
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Kindlin-3-independent adhesion of neutrophils from patients with leukocyte adhesion deficiency type III
err2014-04-01
err12
errOAAI
errvan de Vijver, Edith; Tool, Anton T. J.; Sanal, Ozden; Cetin, Mualla; Unal, Sule; Aytac, Selin; Seeger, Karl; Pagliara, Daria; Rutella, Sergio; van den Berg, Timo K.; Kuijpers, Taco W.
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Atypical combined immunodeficiency due to Artemis defect: A case presenting as hyperimmunoglobulin M syndrome and with LGLL由于Artemis缺陷引起的非典型联合免疫缺陷: 一例表现为高免疫球蛋白M综合征和LGLL的病例
err2013-12-01
err24
PREAI
errBajin, Inci Yaman; Ayyaz, Deniz Cagdas; Unal, Sule; Ozgur, Tuba Turul; Cetin, Mualla; Gumruk, Fatma; Tezcan, Ilhan; de Villartay, Jean-Pierre; Sanal, Ozden
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Medical management of moyamoya disease and recurrent stroke in an infant with Majewski osteodysplastic primordial dwarfism type II (MOPD II)
err2012-04-17
err13
PREAI
errKilic, Esra; Utine, Eda; Unal, Sule; Haliloglu, Goknur; Oguz, Kader Karli; Cetin, Mualla; Boduroglu, Koray; Alanay, Yasemin
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Serological response to influenza vaccine after hematopoetic stem cell transplantation
err2010-01-30
err18
PREAI
errYalcin, S. Songuel; Kondolot, Meda; Albayrak, Nurhan; Altas, A. Basak; Karacan, Yasemin; Kuskonmaz, Baris; Aksu, Salih; Cetin, Mualla; Goker, Hakan; Yurdakok, Kadriye; Uckan, Duygu
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Hemophagocytosis associated with leukemia: a striking association with juvenile myelomonocytic leukemia与白血病相关的噬血细胞症: 与青少年粒单核细胞白血病的惊人联系
err2009-10-02
err13
PREAI
errUnal, Sule; Cetin, Mualla; Kutlay, Nuket Yurur; Elmas, Selin Aytac; Gumruk, Fatma; Tukun, Ajlan; Tuncer, Murat; Gurgey, Aytemiz
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Alternative algorithm for L-asparaginase allergy in children with acute lymphoblastic leukemia
err2009-04-01
err40
PREAI
errSoyer, Ozge Uysal; Aytac, Selin; Tuncer, Ayfer; Cetin, Mualla; Yetgin, Sevgi; Sekerel, Bulent Enis
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Diamond-Blackfan anemia associated with β-thalassemia trait
err2006-01-01
err4
errOAAI
errTavil, B; Çetin, M; Kuskonmaz, B; Gümrük, F
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Hereditary juvenile cobalamin deficiency caused by mutations in the intrinsic factor gene
err2005-02-28
err71
errOAAI
errTanner, SM; Li, ZY; Perko, JD; Öner, C; Çetin, M; Altay, Ç; Yurtsever, Z; David, KL; Faivre, L; Ismail, EA; Gräsbeck, R; de la Chapelle, A
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Genetically heterogeneous selective intestinal malabsorption of vitamin B12:: Founder effects, consanguinity, and high clinical awareness explain aggregations in Scandinavia and the Middle East
err2004-03-03
err67
errOAAI
errTanner, SM; Li, ZY; Bisson, R; Acar, C; Öner, C; Öner, R; Çetin, M; Abdelaal, MA; Ismail, EA; Lissens, W; Krahe, R; Broch, H; Gräsbeck, R; de la Chapelle, A
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