Zobrazeno 1 - 10
of 1 421
pro vyhledávání: '"Canatan D"'
Autor:
TUBA, TOLA, ALANOĞLU, EMİNE GÜÇHAN, POLAT, MÜMİN, ÖĞÜT, SERDAL, canatan, duran, KİŞİOĞLU, AHMET NESİMİ, ÖNEM, EBRU, KAYA, SELÇUK, ADİLOĞLU, ALİ KUDRET
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______1865::81abb2a726fceed36d7003fa6918f7a0
http://acikerisim.sdu.edu.tr/xmlui/handle/123456789/79045
http://acikerisim.sdu.edu.tr/xmlui/handle/123456789/79045
Autor:
Sümter H; Uşak Training and Research Hospital, Clinic of Hematology, Uşak, Türkiye, Mızrak S; Uşak University Faculty of Medicine, Department of Biochemistry, Uşak, Türkiye, Ceylaner S; Intergen Genetics and Rare Diseases Diagnosis Center, Ankara, Türkiye, Canatan D; Antalya Genetic Assessment Center, Antalya, Türkiye; Antalya Bilim University, Antalya, Türkiye
Publikováno v:
Turkish journal of haematology : official journal of Turkish Society of Haematology [Turk J Haematol] 2023 Aug 31; Vol. 40 (3), pp. 234-235. Date of Electronic Publication: 2023 Jul 31.
Autor:
Kendir-Demirkol Y; Department of Pediatrics, Süleyman Demirel University Faculty of Medicine, Isparta, Türkiye., Jenny LA; Department of Ophthalmology, Columbia University Medical Center, New York, United States., Demirkol A; Department of Ophtalmology, Süleyman Demirel University Faculty of Medicine, Isparta, Turkiye., Özen M; Department of Pediatric Infectious Diseases, Süleyman Demirel University Faculty of Medicine, Isparta, Türkiye., Ayata A; Department of Pediatric Oncology, Süleyman Demirel University Faculty of Medicine, Isparta, Türkiye., Canatan D; Department of Pediatric Hematology, Süleyman Demirel University Faculty of Medicine, Isparta, Türkiye.
Publikováno v:
Turkish archives of pediatrics [Turk Arch Pediatr] 2023 May; Vol. 58 (3), pp. 298-301.
Autor:
Canatan D; Vocational School of Health Services of Antalya Bilim University -Antalya Turkey Medical Director of Antalya Genetic Diseases Assessment Center Çıplaklı Mah. Akdeniz Bulvarı No:290 A Döşemealtı/Antalya . durancanatan@gmail.com., Sonmez Y; yoncasonmez@yahoo.com., Yılmaz O; Akdeniz University Genetic Department. yilmazozle@gmail.com., Coşkun HŞ; Akdeniz University, Faculty of Medicine, Department of Medical Oncology- Antalya- Turkey. hs.coskun@yahoo.com., Göksu SS; Akdeniz University, Faculty of Medicine, Department of Medical Oncology- Antalya- Turkey. semasezgingoksu@gmail.com., Uçar S; Akdeniz University, Faculty of Medicine, Department of Medical Oncology- Antalya- Turkey. seldacakal@gmail.com., Aktekin MR; Akdeniz University, Faculty of Medicine, Department of Public Health - Antalya- Turkey. mehmetaktekin1@gmail.com.
Publikováno v:
Acta bio-medica : Atenei Parmensis [Acta Biomed] 2023 Feb 13; Vol. 94 (1), pp. e2023045. Date of Electronic Publication: 2023 Feb 13.
Background: Data on the prevalence and type of endocrine disorders in β-thalassemia intermedia (β-TI) patients are scarce. This multicenter study was designed to determine the prevalence of endocrine complications and the associated risk factors in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::84a01e57a24fec7463df58e1e55d2eae
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3078628
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3078628
A review of the literature on COVID-19 pandemic in patients with thalassemias is presented. Globally, the prevalence of COVID-19 among β-thalassemia patients seems to be lower than in general population; associated co-morbidities aggravated the seve
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::873f86de0fe2d1013f35746b3f21149a
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3120729
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3120729
Background: More than five decades ago, thalassemia major (TDT) was fatal in the first decade of life. Survival and quality of life have improved progressively thanks to the implementation of a significant advance in diagnostic and therapeutic method
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::2ebb147fe7f1ce452b0304f114f58418
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3121897
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3121897
Background: Transfusion-dependent β-thalassemia (TDT) is associated with several complications necessitating a multidisciplinary approach for diagnosis, treatment and follow-up. Hypogonadism in female TDT patients is one of the most common endocrine
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::01eb85d3cd9d8bc5dcf442ad05767fe7
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3122761
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3122761
Changes in thyroid function and thyroid function tests occur in patients with β-thalassemia major (TM). The frequency of hypothyroidism in TM patients ranges from 4% to 29 % in different reports. The wide variation has been attributed to several fac
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::c9d3f89984b350e02add9dfdcb30ed9e
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3106560
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3106560