Zobrazeno 1 - 10
of 1 571
pro vyhledávání: '"Sami Ulus"'
Autor:
ÖNER, Nergiz, ANKARA DR. SAMİ ULUS KADIN DOĞUM ÇOCUK SAĞLIĞI VE HASTALIKLARI SAĞLIK UYGULAMA VE ARAŞTIRMA MERKEZİ, ÖZEK, Gülcihan, EGE ÜNİVERSİTESİ, EGE TIP FAKÜLTESİ
Publikováno v:
Volume: 29, Issue: 1 47-51
SDÜ Tıp Fakültesi Dergisi
SDÜ Tıp Fakültesi Dergisi
AmaçVitamin B12 eksikliği çocukluk çağında sık görülen birdurumdur ve eksikliğine bağlı olarak çeşitli nörolojik,hematolojik ve dermatolojik bulgular görülebilmektedir.Çalışmanın amacı B12 vitamini eksikliği tanısıalan çocuk
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______1865::8bebbf014d952d63f87a411a8d0a7a4e
http://acikerisim.sdu.edu.tr/xmlui/handle/123456789/96240
http://acikerisim.sdu.edu.tr/xmlui/handle/123456789/96240
Autor:
Sonay Aydin, Erdem Fatihoglu, Erzincan Universitesi Tip Fakultesi, Radyoloji Ana Bilim Dali, Erzincan, Turkiye, Sami Ulus Egitim ve Arastirma Hastanesi, Radyoloji Klinigi, Ankara, Turkiye
Publikováno v:
Archives of Basic and Clinical Research. 2:33-36
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4d1503cfe9cf512d10f45da720e23d92
https://doi.org/10.5152/abcr.2020.19002
https://doi.org/10.5152/abcr.2020.19002
Publikováno v:
Archives of Basic and Clinical Research. 1:1-4
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::81ab285118aaaa4266f3aece490c42b2
https://doi.org/10.5152/abcr.2019.01
https://doi.org/10.5152/abcr.2019.01
Autor:
Fehime Kara Eroglu, Sami Ulus Maternity Rheumatology, Fatma Yazılıtaş, Çiğdem Üner, Mehmet Bülbül, Nilüfer Arda, Deniz Karakaya, Eda Didem Kurt Şükür, Evrim Kargın Çakıcı, Gökçe Can, Tülin Güngör, Evra Çelikkaya
Publikováno v:
Turkish Journal of Nephrology. 28:250-256
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d0526c90ebe7d09421720ed81b46fa7e
https://doi.org/10.5152/turkjnephrol.2019.3664
https://doi.org/10.5152/turkjnephrol.2019.3664
Publikováno v:
Archives of Basic and Clinical Research. 2:111-112
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0431e039c12afd88daf059708f73ef05
https://doi.org/10.5152/abcr.2020.19001
https://doi.org/10.5152/abcr.2020.19001
Autor:
Sami Ulus, Pamir Isik, Ayhan Yaman, Selmin Karademir, Ali Bay, Semra Çetinkaya, Abdurrahman Kara, Nese Yarali, Serdar Ozkasap, Bahattin Tunç
Publikováno v:
International Journal of Hematology and Oncology. 23:193-199
Even the life span has prolonged for the last 40 years, increase in frequently seen complications with increasing age negatively affect the life quality of thalassemia patients. In our study, complications encountered in 67 s-thalassemia patients who
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2200af4c56d464493f909ec80069eca0
https://doi.org/10.4999/uhod.12005
https://doi.org/10.4999/uhod.12005
Autor:
Senem Ozgur, Ahmet Metin Hasçiçek, Hasmet Sarici, Tolga Karakan, Cem Nedim Yücetürk, Musa Ekici, Berat Cem Ozgur, Asim Ozayar, Sami Ulus
Publikováno v:
Pediatrics Research International Journal. :1-6
Objective: Nocturnal enuresis is a common problem among children. This multifactorial disease is a source of stress of the families. Therefore, it is important how to approach the disorder, plan the treatment in order to provide a satisfactory cure r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7a6364a735228e889c91deb4395d28f0
https://doi.org/10.5171/2013.318022
https://doi.org/10.5171/2013.318022
Autor:
Sami Ulus, Zehra Aycan
Publikováno v:
Journal of Clinical Research in Pediatric Endocrinology. 1
Obesity is defined as a condition where a pathological excess of body fat is present in an individual. Obesity develops when there is a discrepancy between energy intake and energy output. During its development the original steady-state is disturbed
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2e607626d928a37aff7d71158354767d
https://doi.org/10.4008/jcrpe.v1i1.25
https://doi.org/10.4008/jcrpe.v1i1.25
Autor:
Kasapkara, Çigdem Seher, Nuoffer, Jean Marc, Baysoy, Gökhan, Aldudak, Bedri, Özbek, Mehmet Nuri, Akcaboy, Meltem, Largiadèr, Carlo R.
Publikováno v:
Kasapkara, Çigdem Seher; Nuoffer, Jean Marc; Baysoy, Gökhan; Aldudak, Bedri; Özbek, Mehmet Nuri; Akcaboy, Meltem; Largiadèr, Carlo R. (2019). Lethal Very Long-Chain Acyl-Coa Dehydrogenase Deficiency with A Novel Mutation. Gazi medical journal, 30(3), pp. 323-324. Gazi University Faculty of Medicine 10.12996/GMJ.2019.83
WOS: 000472585000023 Very long chain acyl-CoA dehydrogenase deficiency is an autosomal recessive genetic disorder in which the first step in the mitochondrial beta-oxidation of fatty acids for 14-20 carbons is defective. Clinical presentation is hete
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4f61b3f2381dae1f0c89d0ee34912bb7
Autor:
Cindy S. Ma, Jean-Laurent Casanova, Monika Schmidt, Federico Mele, Gaspard Kerner, James P. Di Santo, Cecilia S. Lindestam Arlehamn, Avneet Heer, Lluis Quintana-Murci, Alessandro Sette, Bernhard Fleckenstein, Tomi Lazarov, Sandra Jovic, Natalie Wong, Stéphanie Boisson-Dupuis, Daniela Latorre, Julia K. Joseph, Bertrand Boisson, Rubén Martínez-Barricarte, Caner Aytekin, Danielle T. Avery, Aydan Ikinciogullari, Figen Dogu, Jean-François Emile, Etienne Patin, Federica Sallusto, Yoann Seeleuthner, Yuval Itan, Laurent Abel, Franck Rapaport, Alejandro Nieto-Patlán, Frederic Geissmann, Satoshi Okada, Fabienne Jabot-Hanin, Stuart G. Tangye, Esther van de Vosse, Geetha Rao, Elissa K. Deenick, Jacinta Bustamante, Mélanie Migaud, Caroline Deswarte, Mohammed Reza Bloursaz, Laura Surace, Benedetta Bigio, Davood Mansouri, Anne Puel, Payam Tabarsi, Xiao-Fei Kong, Gönül Tanır, Vanessa L. Bryant, Noé Ramírez-Alejo, Seyed Alireza Mahdaviani, Janet Markle
Publikováno v:
Science Immunology
Science Immunology, 2018, 3 (30), pp.eaau6759. ⟨10.1126/sciimmunol.aau6759⟩
Science Immunology, American Association for the Advancement of Science, 2018, 3 (30), pp.eaau6759. ⟨10.1126/sciimmunol.aau6759⟩
Science Immunology, 2018, 3 (30), pp.eaau6759. ⟨10.1126/sciimmunol.aau6759⟩
Science Immunology, American Association for the Advancement of Science, 2018, 3 (30), pp.eaau6759. ⟨10.1126/sciimmunol.aau6759⟩
International audience; Hundreds of patients with autosomal recessive, complete IL-12p40 or IL-12Rβ1 deficiency have been diagnosed over the last 20 years. They typically suffer from invasive mycobacteriosis and, occasionally, from mucocutaneous can
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::12b2d54fb97a024a1be58ace641d7fed
https://doi.org/10.1126/sciimmunol.aau6759
https://doi.org/10.1126/sciimmunol.aau6759