Zobrazeno 1 - 10
of 215
pro vyhledávání: '"Mualla Cetin"'
Autor:
Elisa Fermo, Cristina Vercellati, Anna Paola Marcello, Anna Zaninoni, Selin Aytac, Mualla Cetin, Ilaria Capolsini, Maddalena Casale, Sabrina Paci, Alberto Zanella, Wilma Barcellini, Paola Bianchi
Publikováno v:
Frontiers in Physiology, Vol 10 (2019)
Glucose-6-phosphate isomerase (GPI, EC 5.3.1.9) is a dimeric enzyme that catalyzes the reversible isomerization of glucose-6-phosphate to fructose-6-phosphate, the second reaction step of glycolysis. GPI deficiency, transmitted as an autosomal recess
Externí odkaz:
https://doaj.org/article/947e2996a8d84b9bbc80d5007230ad12
Autor:
Burcin Beken, Selin Aytac, Gunay Balta, Baris Kuskonmaz, Duygu Uckan, Sule Unal, Mualla Cetin, Fatma Gumruk
Publikováno v:
Haematologica, Vol 103, Iss 2 (2018)
Familial hemophagocytic lymphohistiocytosis is an autosomal recessive, life-threatening condition characterized by defective immune response. A retrospective analysis was performed on 57 patients diagnosed with familial hemophagocytic lymphohistiocyt
Externí odkaz:
https://doaj.org/article/b5ff11a0fc9d4473a9225a7780271ba8
Publikováno v:
Turkish Journal of Hematology, Vol 32, Iss 4, Pp 317-322 (2015)
INTRODUCTION: Transcobalamin II deficiency is one of the rare causes of inherited vitamin B12 disorders in which the patients have characteristically normal or high vitamin B12 levels related to the transport defect of vitamin B12 into the cell, endi
Externí odkaz:
https://doaj.org/article/acf8edcd3d2c45dd8ca63f7fd186db9f
Autor:
Mualla Cetin, Kamile Arıkan, Mehmet Ceyhan, Fatma Gumruk, Selin Aytac, Ateş Kara, Eda Karadag-Oncel, Ali Bülent Cengiz
Publikováno v:
Laboratory Medicine. 52:477-484
Objective To investigate the value of presepsin and proadrenomedullin (proADM) as new markers for febrile neutropenia, by comparing them with conventional markers. Methods Plasma specimens for presepsin, proADM, C-reactive protein (CRP), and procalci
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ab813209cf890201b68f8023cd7e684d
https://doi.org/10.1093/labmed/lmab002
https://doi.org/10.1093/labmed/lmab002
Publikováno v:
Perceptual and Motor Skills. 128:1091-1106
Children with acute leukemia (ALL) often suffer from several disease and treatment related side-effects during treatment. The aim of the present study was to determine the gross and fine motor functioning and basic cognitive performance of children (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8356b82f6528f17476a93ddb65f224c5
https://doi.org/10.1177/00315125211002065
https://doi.org/10.1177/00315125211002065
Autor:
Ali Bülent Cengiz, Fahriye Duygu Cetinkaya, Yasemin Ozsurekci, Kamile Arıkan, Mualla Cetin, Mehmet Ceyhan, Ateş Kara, Ayşe Büyükcam, Selin Aytac
Publikováno v:
Journal of Pediatric Hematology/Oncology. 43:e613-e618
Background Invasive fungal infections (IFIs) are a leading cause of morbidity and death in immunocompromised patients. Data on efficacy and pharmacokinetics of posaconazole in pediatric patients are rare (1 to 5). Herein, we retrospectively analyzed
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3a7f4b94d99955e86448fcb1c115834f
https://doi.org/10.1097/mph.0000000000002080
https://doi.org/10.1097/mph.0000000000002080
Autor:
Sule Unal, Mualla Cetin, Baris Kuskonmaz, İnci Yaman Bajin, Kader Karli Oguz, Fatma Gumruk, Selin Aytac, Selin Ardalı
Publikováno v:
Acta Medica. 51:43-48
In this case report; a 12-year-old male with ALL who developed transient left hemiparesis associated with dysphasia and central facial paralysis 14 days after high dose methotrexate (5g/m2) and intrathecal MTX (12 mg, according to age) treatment has
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::04abd9eb04823600dad8472c6f69812a
https://doi.org/10.32552/2020.actamedica.405
https://doi.org/10.32552/2020.actamedica.405
Autor:
Ezgi Deniz Batu, Deniz Cagdas Ayvaz, Hatice Asuman Özkara, Ekim Z. Taskiran, Omer Karadag, Ilhan Tezcan, Mualla Cetin, Sule Unal, Hafize Emine Sönmez, Yelda Bilginer, Naz Guleray, Seza Ozen, Abdulsamet Erden, Fatma Gumruk
Publikováno v:
The Journal of Rheumatology. 47:117-125
Objective.Deficiency of adenosine deaminase 2 (DADA2) is an autosomal recessive autoinflammatory disorder associated with ADA2 mutations. We aimed to investigate the characteristics and ADA2 enzyme activities of patients with DADA2 compared to non-DA
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::049cafbcbee17a980a573e7e222d7aca
https://doi.org/10.3899/jrheum.181384
https://doi.org/10.3899/jrheum.181384
Publikováno v:
Acta Oncologica Turcica. 52:424-431
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8dd2c361fffc802fc925b873485d4298
https://doi.org/10.5505/aot.2019.86648
https://doi.org/10.5505/aot.2019.86648
Publikováno v:
Acta Oncologica Turcica. 52:53-57
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7232f6ff95e781531d471307b2836031
https://doi.org/10.5505/aot.2019.16362
https://doi.org/10.5505/aot.2019.16362