Gül Nihal Özdemir (Nihal Özdemir, Nihal Ozdemir)

Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2018-2022
Publications (10 Years): 11

Top Topics

St Elevation Myocardial Infarction

Acute Lymphoblastic Leukemia

Radiation Therapy

Top Venues

Pediatric blood & cancer

Turkish journal of haematology : official journal of Turkish Society of Haematology

Turkish archives of pediatrics

Journal of clinical research in pediatric endocrinology

This page only lists publications with an associated author ORCID identifier.

Publications

Gül Nihal Özdemir, Eren Gündüz
Gaucher Disease for Hematologists Turkish journal of haematology : official journal of Turkish Society of Haematology 39 (2) (2022)
Eren Gündüz, Hakkı Onur Kırkızlar, Elif Gülsüm Ümit, Sedanur Karaman Gulsaran, Vildan Özkocamaz, Fahir Özkalemkaş, Omer Candar, Tuğrul Elverdi, Selin Kucukyurt, Semra Paydaş, Özcan Çeneli, Senem Maral, Senem Maral, Ömer Ekinci, Yıldız İpek, Cem Kiş, Zeynep Tuğba Güven, Aydan Akdeniz, Tülin Tiraje Celkan, Ayşe Hilal Eroğlu Küçükdiler, Gülsüm Akgün Çağlıyan, Ceyda Özçelik Şengöz, Ayşe Karataş, Tuba Bulduk, Alper Özcan, Fatma Burcu Belen, Aylin Canbolat, İbrahim Kartal, Hale Ören, Ersin Töret, Gül Nihal Özdemir, Şule Mine Bakanay Öztürk
Castleman Disease: A Multicenter Case Series from Turkey Turkish journal of haematology : official journal of Turkish Society of Haematology 39 (2) (2022)
Akihiro Hoshino, David Boutboul, Yuan Zhang, Hye Sun Kuehn, Jerôme Hadjadj, Gül Nihal Özdemir, Tiraje Celkan, Christoph Walz, Capucine Picard, Christelle Lenoir, Nizar Mahlaoui, Christoph Klein, Xiao P Peng, Antoine Azar, Erin Reigh, Morgane Cheminant, Alain Fischer, Frédéric Rieux-Laucat, Isabelle Callebaut, Fabian H Hauck, Joshua Milner, Sergio D Rosenzweig, Sylvain Latour
Gain-of-function IKZF1 variants in humans cause immune dysregulation associated with abnormal T/B cell late differentiation. Science immunology 7 (69) (2022)
Rejin Kebudi, Nilgün Kurucu, Deniz Tuğcu, Şadan Hacısalihoğlu, Tunç Fışgın, Süheyla Ocak, Gülnur Tokuç, Gül Nihal Özdemir, Ceyhun Bozkurt, Dilek İnce, Seda Aras, Ali Ayçiçek, Başak Adaklı Aksoy, Nihal Karadaş, Gülyüz Öztürk, Mehmet Fatih Orhan, Eda Ataseven, Sinan Akbayram, Ebru Yılmaz, Özlem Tüfekçi, Sema Vural, Arzu Akyay, Aylin Canbolat Ayhan, Suar Çakı Kılıç, Veysiye Hülya Uzel, Yeter Düzenli, Elif Güler Kazancı, Can Acıpayam, Murat Elli, Atilla Tanyeli, Zeynep Karakas, Ayper Somer, Ateş Kara
COVID-19 infection in children with cancer and stem cell transplant recipients in Turkey: A nationwide study. Pediatric blood & cancer 68 (6) (2021)
Mehmet Akif Kılıç, Gül Nihal Özdemir, Tuba Nur Tahtakesen, Ezgi Paslı Uysalol, Cengiz Bayram, Ali Ayçiçek, Gönül Aydoğan
Glucose 6 phosphate dehydrogenase deficiency: A single-center experience. Turkish archives of pediatrics 56 (3) (2021)
Eren Gündüz, Gül Nihal Özdemir, Şule Mine Bakanay Öztürk, Sema Karakuş
A Rare Lymphoproliferative Disease: Castleman Disease Turkish journal of haematology : official journal of Turkish Society of Haematology 38 (4) (2021)
Evrim Cifci Sunamak, Gül Nihal Özdemir, Tiraje Celkan
Posterior reversible encephalopathy syndrome in children with acute lymphoblastic leukemia: Experience of a single center using BFM protocols. Pediatric blood & cancer 66 (6) (2019)
Rejin Kebudi, Gül Nihal Özdemir
Changes in hepatitis B antibody status after chemotherapy in children with cancer. Pediatric blood & cancer 67 (4) (2019)
Deniz Yilmaz Karapinar, Türkan Patıroğlu, Ayşe Metin, Ümran Çalışkan, Tiraje Celkan, Barış Yılmaz, Zeynep Karakaş, Tuba Hilkay Karapinar, Burcu Akıncı, Ferda Özkınay, Hüseyin Onay, Mehmet Akif Yeşilipek, Himmet Haluk Akar, Gülen Tüysüz, Hüseyin Tokgöz, Gül Nihal Özdemir, Ayça Kiykim, Serap Karaman, Yurdanur Kılınç, Yeşim Oymak, Alphan Küpesiz, Lale Olcay, Zuhal Keskin Yıldırım, Gönül Aydoğan, Müge Gökçe, Talia İleri, Yusuf Ziya Aral, Ali Bay, Berna Atabay, Zuhre Kaya, Murat Söker, Nihal Karadaş, Uğur Özbek, Bilge Özsait Selçuk, Hamiyet Hekimci Özdemir, Vedat Uygun, Gülsün Tezcan Karasu, Şebnem Yılmaz
Homozygous c.130-131 ins A (pW44X) mutation in the HAX1 gene as the most common cause of congenital neutropenia in Turkey: Report from the Turkish Severe Congenital Neutropenia Registry. Pediatric blood & cancer 66 (10) (2019)
Melek Yıldız, Gül Nihal Özdemir, Hasan Önal, Başak Koç Şenol, Beyza Eliuz-Tipici, Osman Bülent Zülfikar
Evaluation of Unfavorable Cardiovascular and Metabolic Risk Factors in Children and Young Adults with Haemophilia Journal of clinical research in pediatric endocrinology 11 (2) (2018)
Munevver Sari, Cemil Izgi, Gokhan Kahveci, Alev Kılıcgedik, Zubeyde Bayram, Suzan Hatipoglu, Selcuk Pala, Gül Nihal Özdemir
Infarction of the septomarginal band and tricuspid papillary muscle rupture related to alcohol septal ablation for hypertrophic cardiomyopathy. Echocardiography (Mount Kisco, N.Y.) 35 (6) (2018)