Nazan Sarper (N Sarper)

Publication Activity (10 Years)

Years Active: 2021-2024
Publications (10 Years): 14

Top Topics

Botulinum Toxin

Top Venues

Haemophilia : the official journal of the World Federation of Hemophilia

European journal of haematology

Journal of pediatric genetics

Turkish journal of medical sciences

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

Publications

Christian Pfrepper, Paolo Radossi, Jerzy Windyga, Kaan Kavakli, Roger E G Schutgens, Nazan Sarper, Joan Gu, Kayode Badejo, Nisha Jain
Recombinant porcine factor VIII in patients with congenital haemophilia A with inhibitors undergoing surgery: Phase 3, single-arm, open-label study. Haemophilia : the official journal of the World Federation of Hemophilia 30 (2) (2024)
Christian Pfrepper, Paolo Radossi, Jerzy Windyga, Kaan Kavakli, Roger E G Schutgens, Nazan Sarper, Joan Gu, Kayode Badejo, Nisha Jain
Recombinant porcine factor VIII in patients with congenital haemophilia A with inhibitors undergoing surgery: Phase 3, single-arm, open-label study. Haemophilia : the official journal of the World Federation of Hemophilia 30 (2) (2024)
Esra Isik, Yesim Aydinok, Canan Albayrak, Basak Durmus, Zeynep Karakas, Mehmet Fatih Orhan, Nazan Sarper, Sultan Aydin Köker, Selma Unal, Yeşim Oymak, Nihal Karadaş, Ayşen Türedi Yıldırım, Davut Albayrak, Funda Tayfun Küpesiz, Deniz Tuğcu, Serap Karaman, Mahmut Töbü, Ekrem Ünal, Alper Ozcan, Sule Unal, Tekin Aksu, Ayşegül Ünüvar, Mustafa Bilici, Fatih Mehmet Azık, Yilmaz Ay, Sema Aylan Gelen, Emine Zengin, Esin Albudak, Ibrahim Eker, Taner Karakaya, Ozgur Cogulu, Ferda Özkınay, Tahir Atik
Identification of the molecular etiology in rare congenital hemolytic anemias using next-generation sequencing with exome-based copy number variant analysis. European journal of haematology (2024)
Christian Pfrepper, Paolo Radossi, Jerzy Windyga, Kaan Kavakli, Roger E G Schutgens, Nazan Sarper, Joan Gu, Kayode Badejo, Nisha Jain
Recombinant porcine factor VIII in patients with congenital haemophilia A with inhibitors undergoing surgery: Phase 3, single-arm, open-label study. Haemophilia : the official journal of the World Federation of Hemophilia (2024)
Christian Pfrepper, Paolo Radossi, Jerzy Windyga, Kaan Kavakli, Roger E G Schutgens, Nazan Sarper, Joan Gu, Kayode Badejo, Nisha Jain
Recombinant porcine factor VIII in patients with congenital haemophilia A with inhibitors undergoing surgery: Phase 3, single-arm, open-label study. Haemophilia : the official journal of the World Federation of Hemophilia (2024)
Esra Isik, Yesim Aydinok, Canan Albayrak, Basak Durmus, Zeynep Karakas, Mehmet Fatih Orhan, Nazan Sarper, Sultan Aydin Köker, Selma Unal, Yeşim Oymak, Nihal Karadaş, Ayşen Türedi Yıldırım, Davut Albayrak, Funda Tayfun Küpesiz, Deniz Tuğcu, Serap Karaman, Mahmut Töbü, Ekrem Ünal, Alper Ozcan, Sule Unal, Tekin Aksu, Ayşegül Ünüvar, Mustafa Bilici, Fatih Mehmet Azık, Yilmaz Ay, Sema Aylan Gelen, Emine Zengin, Esin Albudak, Ibrahim Eker, Taner Karakaya, Ozgur Cogulu, Ferda Özkınay, Tahir Atik
Identification of the molecular etiology in rare congenital hemolytic anemias using next-generation sequencing with exome-based copy number variant analysis. European journal of haematology 113 (1) (2024)
Parminder Singh, Kishore Gollapalli, Stefano Mangiola, Daniela Schranner, Mohd Aslam Yusuf, Manish Chamoli, Sting L Shi, Bruno Lopes-Bastos, Tripti Nair, Annett Riermeier, Elena M Vayndorf, Judy Z Wu, Aishwarya Nilakhe, Christina Q Nguyen, Michael Muir, Michael G Kiflezghi, Anna Foulger, Alex Junker, Jack Devine, Kunal Sharan, Shankar J Chinta, Swati Rajput, Anand Rane, Philipp Baumert, Martin Schönfelder, Francescopaolo Iavarone, Giorgia di Lorenzo, Swati Kumari, Alka Gupta, Rajesh Sarkar, Costerwell Khyriem, Amanpreet S Chawla, Ankur Sharma, Nazan Sarper, Sanjeev K Kanojiya, Bichitra Kumar Biswal, Carmine Settembre, Nagarajan Perumal, Kimara L Targoff, Martin Picard, Sarika Gupta, Vidya Velagapudi, Anthony T Papenfuss, Alaattin Kaya, Miguel Godinho Ferreira, Brian Keith Kennedy, Julie K Andersen, Gordon J Lithgow, Abdullah Mahmood Ali, Arnab Mukhopadhyay, Aarno Palotie, Gabi Kastenmüller, Matt Kaeberlein, Henning Wackerhage, Bhupinder Pal, Vijay K Yadav
Taurine deficiency as a driver of aging. Science (New York, N.Y.) 380 (6649) (2023)
Nazan Sarper, Intzi Tachsin, Sema Aylan Gelen, Emine Zengin
The outcome in pediatric acute myeloblastic leukemia; results of the first-line treatment and contribution of hematopoietic stem cell transplantation to survival of relapsed patients. Turkish journal of medical sciences 54 (2) (2023)
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)
Berkay Saraymen, Sabahattin Muhtaroglu, Mustafa Yavuz Köker, Nazan Sarper, Emine Zengin, Canan Albayrak, Davut Albayrak, Osman Bülent Zülfikar, Başak Koç Şenol, Esma Bentli, Semih Yılmaz, Aysun Çetin, Bülent Eser, Mustafa Çetin
Flow cytometric analysis of platelet surface glycoproteins in the diagnosis of thirty-two Turkish patients with Glanzmann thrombasthenia: a multicenter experience Turkish journal of medical sciences 51 (4) (2021)
Sema Aylan Gelen, Bulent Kara, Isil Eser Şimsek, Mesut Gungor, Emine Zengin, Nazan Sarper
Autoimmune Hemolytic Anemia Due to Spondyloenchondrodysplasia with Spastic Paraparesis and Intracranial Calcification due to Mutation in ACP5 . Journal of pediatric genetics 13 (1) (2021)
Sema Aylan Gelen, Bulent Kara, Isil Eser Şimsek, Mesut Gungor, Emine Zengin, Nazan Sarper
Autoimmune Hemolytic Anemia Due to Spondyloenchondrodysplasia with Spastic Paraparesis and Intracranial Calcification due to Mutation in ACP5 . Journal of pediatric genetics 13 (1) (2021)
Sema Aylan Gelen, Nazan Sarper, Emine Zengin, Intzi Tachsin, Mehmet Azizoğlu
Clinical Characteristics of Pediatric Patients with Congenital Erythrocytosis: A Single-Center Study. Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion 38 (2) (2021)
Mustafa Yavuz Köker, Nazan Sarper, Canan Albayrak, Osman Bülent Zülfikar, Emine Zengin, Berkay Saraymen, Davut Albayrak, Başak Koç Şenol, Hüseyin Avcılar, Musa Karakukcu, Christophe Chenet, F Bianchi, Alexandre G De Brevern, Rachel Petermann, Vincent Jallu
New αIIbβ3 variants in 28 Turkish Glanzmann patients; Structural hypothesis for complex activation by residues variations in I-EGF domains. Platelets (2021)