Zobrazeno 1 - 10
of 72
pro vyhledávání: '"Umran CaliSkan"'
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 8, Iss 5, Pp QD01-QD02 (2014)
Glomus tumours (GTs) primarily arise from glomus bodies that are located in the dermis layer of skin. However, they can be encountered ectopically in most parts of the body. As a result of researches done in a 17-month-old male patient who prssented
Externí odkaz:
https://doaj.org/article/cd2b867ee44a4d98bfa11d1a0531962e
Autor:
Alphan Kupesiz, Mehmet Sönmez, Bulent Zulfikar, Hüseyin Tokgöz, Süha Süreyya Özbek, Turgut Seber, İpek Tamsel, Burcu Özkan, Can Çevikol, Basak Koc, Fahri Şahin, İlgen Şaşmaz, Zuhal Mehrekula, Kaan Kavakli, Demet Aydoğdu, S. Aytac, Polat Koşucu, Gülen Tüysüz, Tugana Akbas, Can Balkan, Ali Bülent Antmen, Taner Arpaci, Umran Caliskan, Berna Oguz, Mesut Bulakci
Publikováno v:
Turkish Journal of Hematology
Turkish Journal of Hematology, Vol 38, Iss 2, Pp 101-110 (2021)
Turkish Journal of Hematology, Vol 38, Iss 2, Pp 101-110 (2021)
This study aimed to observe the preventive effect of prophylactic treatment on joint health in people with hemophilia (PwH) and to investigate the importance of integration of ultrasonographic examination into clinical and radiological evaluation of
Autor:
Jacqueline Halton, Leonardo R Brandão, Matteo Luciani, Lisa Bomgaars, Elizabeth Chalmers, Lesley G Mitchell, Ildar Nurmeev, Anjali Sharathkumar, Pavel Svirin, Kirill Gorbatikov, Igor Tartakovsky, Monika Simetzberger, Fenglei Huang, Zhichao Sun, Jörg Kreuzer, Savion Gropper, Paul Reilly, Martina Brueckmann, Manuela Albisetti, Asiya Safina, Ondrej Zapletal, Tomas Kuhn, Tomas Votava, Judy Felgenhauer, Ali Amid, Paola Saracco, Csongor Kiss, Susan Halimeh, Madlen Reschke, Beate Wulff, Michele David, Zbynek Novak, Inna Trunina, Tony Frisk, Heidi Glosli, Andreas Groll, Olga Lvova, Ilgen Sasmaz, Darintr Sosothikul, Virginija Zilinskaite, Erin Cockrell, Valeriy Digtyar, Ivana Hadacova, Sauli Palmu, Anjali Pawar, Joyce Maria Annichino Bizzacchi, Umran Caliskan, Tiraje Celkan, Dmytro Dmytriiev, Colleen Harkins Druzgal, Graciela Onelda Elena, Antonis Kattamis, Ramazan Kaan Kavakli, Christoph Male, Nihal Ozdemir, An Van Damme, Tatiana Zvereva, Aanen Aarli, Rogelio Alejandro Paredes Aguilera, Selin Aytac, Jorge Carneiro, Antonio Chistolini, Maria Gabriela Mazzucconi, Fernando Corrales-Medina, Francis Couturaud, Stacey E Croteau, Cameron Trenor III, Michael Damgaard, Natalia Dixon, Anna Galustyan, Jiri Hak, Marianne Hoffmann, Alphan Kupesiz, Veerle Labarque, Christel van Geet, Ming-Chih Lin, Yun-Ching Fu, Sandra Loggetto, Veerle Mondelaers, Irena Odri-Komazec, Shoshana Revel-Vilk, Julian Sevilla, Luciano Fuzzato Silva, José Kerr Saraiva, Fernando Felix Montes Tapia, Wendy Woods-Swafford
Publikováno v:
The Lancet. Haematology, Vol. 8, no.1, p. e22-e33 (2021)
BACKGROUND: Dabigatran etexilate is a direct oral anticoagulant with potential to overcome the limitations of standard of care in children with venous thromboembolism. The aims of this clinical trial were to study the appropriateness of a paediatric
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2e6576a5afe58bf10852f806c3c8eb49
https://hdl.handle.net/2078.1/260410
https://hdl.handle.net/2078.1/260410
Autor:
Talia Ileri, Yesim Aydinok, Ezgi Paslı Uysalol, Aydan Akdeniz, Mustafa Buyukavci, Naci Tiftik, Mehmet Akin, Berna Atabay, Akif Yesilipek, Yeşim Oymak, Turkan Patiroglu, Güçhan Alanoğlu, Arzu Akcay, Özcan Bör, Canan Vergin, Gonul Aydogan, Hüseyin Tokgöz, Sule Unal, Zeynep Karakas, Adalet Meral Güneş, Nur Soyer, Meral Türker, Elif Güler Kazanci, Mediha Akcan, Banu Oflaz, Nihal Karadaş, Selda Kahraman, Yurdanur Kilinç, Murat Söker, Süheyla Ocak, Melike Sezgin Evim, Didem Atay, Selma Unal, Umran Caliskan, Ali Bay, E. Unal
Publikováno v:
Turkish Journal of Hematology
Turkish Journal of Hematology, Vol 35, Iss 1, Pp 12-18 (2018)
Turkish Journal of Hematology, Vol 35, Iss 1, Pp 12-18 (2018)
WOS: 000426572200002
PubMed ID: 28404539
Objective: The Turkish Society of Pediatric Hematology set up a National Hemoglobinopathy Registry to demonstrate the demographic and disease characteristics of patients and assess the efficacy of a
PubMed ID: 28404539
Objective: The Turkish Society of Pediatric Hematology set up a National Hemoglobinopathy Registry to demonstrate the demographic and disease characteristics of patients and assess the efficacy of a
Autor:
Özlem Tüfekçi, Hüseyin Tokgöz, Serap Karaman, Yılmaz Bengoa Ş, Gulsun Karasu, Davut Albayrak, Musa Karakukcu, Hale Ören, Yılmaz Karapınar D, Alphan Kupesiz, Ünal İnce E, Nazan Sarper, Canan Albayrak, T. Karapınar, Emel Ünal, Gül Nihal Özdemir, Neşe Yaralı, Uygun, Haldun Öniz, Namik Ozbek, Kaçar D, Canan Vergin, Umran Caliskan, Talia Ileri, Idil Yenicesu, Mehmet Akif Yesilipek, Erol Erduran, Ülker Koçak, Adalet Meral Güneş, Ahmet Koç, Birol Baytan, Zühre Kaya, Turkan Patiroglu, Berna Atabay, Tiraje Celkan, Mehmet Ertem, Sezgin Evim M
Publikováno v:
Turkish Journal of Hematology. 35:27-34
OBJECTIVE This study aimed to define the status of juvenile myelomonocytic leukemia (JMML) patients in Turkey in terms of time of diagnosis, clinical characteristics, mutational studies, clinical course, and treatment strategies. MATERIALS AND METHOD
Publikováno v:
European Journal of Ophthalmology. 31:NP106-NP108
Purpose: To describe a case of traumatic hyphema in a patient with severe hemophilia A. Case: We present a case of a 16-year-old boy with severe hemophilia A who presented to our ophthalmology department with total hyphema and elevated intraocular pr
Publikováno v:
Volume: 5, Issue: 1 24-30
Family Practice and Palliative Care
Family Practice and Palliative Care, Vol 5, Iss 1, Pp 24-30 (2020)
Family Practice and Palliative Care
Family Practice and Palliative Care, Vol 5, Iss 1, Pp 24-30 (2020)
Introduction: Malignant and chronic diseases in children affect all family members economically and psychologically and can cause serious adjustment problems and psychological disorders. This study is aimed to compare the depression/anxiety levels an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fbb614e3aa14b8c434a53d6a51185fc1
https://dergipark.org.tr/tr/pub/fppc/issue/52039/562433
https://dergipark.org.tr/tr/pub/fppc/issue/52039/562433
Autor:
Diyar Z. Akkaynak, Yeşim Oymak, Gonul Aydogan, Tuğba Gürleyen Eren, Gülsün Karasu, Bahattin Tunç, Fatma Gumruk, Selma Unal, Umran Caliskan, Turkan Patiroglu, Adalet Meral Güneş, Zafer Salcioglu, Ahmet Koç, Yusuf Ziya Aral, Yasemin Isik Balci, Mehmet Akin, Aylin Canbolat Ayhan, Vedat Uygun, Osman Alphan Küpesiz, Gönül Oktay, Canan Vergin, Betül Biner, İlgen Şaşmaz, Mehmet Ertem, Hilmi Apak, Emine Türkkan, Yıldız Yildirmak, Cetin Timur, Elif Güler Kazanci, Gülersu Irken, Ülker Koçak, Murat Söker, Erdal Kurtoğlu, Mehmet Akif Yesilipek, Bülent Antmen, Zeynep Karakas
PubMedID: 30300449 Objectives: To evaluate the long-term efficacy and safety of deferasirox therapy in a large observational cohort of children with transfusion-dependent thalassemia (TDT) and sickle cell anemia (SCA) in Turkey. Methods: This was a m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1b5a731b446ddb4e25ef6dbad909d7cf
Autor:
Gülen Tüysüz, Lale Olcay, Ferda Ozkinay, Murat Söker, Hüseyin Onay, Turkan Patiroglu, Ugur Ozbek, Şebnem Yılmaz, Ali Bay, Tiraje Celkan, Hamiyet Hekimci Özdemir, Zeynep Karakas, Nihal Karadaş, Mehmet Akif Yesilipek, Hüseyin Tokgöz, Gonul Aydogan, Talia Ileri, Baris Yilmaz, Yeşim Oymak, Serap Karaman, Zuhal Keskin Yildirim, Vedat Uygun, Umran Caliskan, Berna Atabay, Burcu Akıncı, Ayse Metin, Tuba Hilkay Karapınar, Yusuf Ziya Aral, Müge Gökçe, Zühre Kaya, Ayca Kiykim, Gülsün Karasu, Bilge Özsait Selçuk, Alphan Kupesiz, H. Haluk Akar, Deniz Yilmaz Karapinar, Yurdanur Kilinç, Gül Nihal Özdemir
WOS: 000478208700001
PubMed ID: 31321910
Background Severe congenital neutropenia is a rare disease, and autosomal dominantly inherited ELANE mutation is the most frequently observed genetic defect in the registries from North America and W
PubMed ID: 31321910
Background Severe congenital neutropenia is a rare disease, and autosomal dominantly inherited ELANE mutation is the most frequently observed genetic defect in the registries from North America and W
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3957b5a6f3bf8948d4de62234d0e2999
https://hdl.handle.net/20.500.12605/15940
https://hdl.handle.net/20.500.12605/15940
Autor:
Hüseyin Tokgöz, Umran Caliskan
Publikováno v:
International Journal of Hematology and Oncology. 26:1-6
The aim of the study is to present the experience of children diagnosed with Langerhans cell histiocytosis (LCH) at our center. Medical records of children with LCH were screened in terms of gender, age at diagnosis, clinical findings, risk groups, t