Tuba Hilkay Karapinar (Tuba H Karapınar, Tuba Hilkay Karapınar)

Publication Activity (10 Years)

Years Active: 2019-2022
Publications (10 Years): 3

Top Topics

Pulmonary Embolism

Chemotherapy Induced

Genome Wide Identification

Top Venues

Sisli Etfal Hastanesi tip bulteni

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

Pediatric blood & cancer

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

Publications

Işık Odaman Al, Yeşim Oymak, Filiz Hazan, Semra Gürsoy, Tülay Öztürk Atasoy, Özlem Bağ, Salih Özmen, Nurgul Karakaya, Tuba Hilkay Karapinar
A Neonatal Case of Infantile Malignant Osteopetrosis Presenting with Thrombocytopenia and Hypotonicity: A Novel Mutation in Chloride Voltage-Gated Channel 7 Gene. Sisli Etfal Hastanesi tip bulteni 56 (1) (2022)
Emine Zengin, Nazan Sarper, Arzu Yazal Erdem, Işık Odaman Al, Melike Sezgin Evim, Hüsniye Neşe Yaralı, Fatma Burcu Belen, Arzu Akçay, Ayşen Türedi Yıldırım, Tuba Hilkay Karapinar, Adalet Meral Güneş, Hale Ören, Lale Olcay, Birol Baytan, Hüseyin Gülen, Gülyüz Öztürk, Mehmet Fatih Orhan, Yeşim Oymak, Sibel Akpınar, Özlem Tüfekçi, Meryem Albayrak, Burçak Tatlı Güneş, Aylin Canpolat, Namık Özbek
Thrombolysis with Systemic Recombinant Tissue Plasminogen Activator in Children: A Multicenter Retrospective Study Turkish journal of haematology : official journal of Turkish Society of Haematology 38 (4) (2021)
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)