Canan Albayrak

<i>SNX10</i> mutations define a subgroup of human autosomal recessive osteopetrosis with variable clinical severity

Alessandra Pangrazio, Anders Fasth, Andrea Sbardellati et al. · Journal of Bone and Mineral Research · 2012 · 70 citations · Full text

Medicine, Genetics, Molecular Genetics +14

Marked overlap of four genetic syndromes with dyskeratosis congenita confounds clinical diagnosis

A. J. Walne, Laura C. Collopy, Shirleny Cardoso et al. · Haematologica · 2016 · 45 citations · Full text

Life Sciences, Dermatology, Genetics +13

Invasive Fungal Infections in Children With Hematologic and Malignant Diseases

Sevinç Nursev Özsevik, Gülnar Şensoy, Canan Albayrak et al. · Journal of Pediatric Hematology/Oncology · 2014 · 37 citations

Medicine, Infectious Diseases, Pediatrics +16

Once‐weekly prophylaxis with glycoPEGylated recombinant factor VIII (N8‐GP) in severe haemophilia A: Safety and efficacy results from pathfinder 2 (randomized phase III trial)

Nicola Curry, Canan Albayrak, Miguel A. Escobar et al. · Haemophilia · 2019 · 36 citations · Full text

Medicine, Hematology, Pharmacotherapy +17

Thalassemia-free and graft-versus-host-free survival: outcomes of hematopoietic stem cell transplantation for thalassemia major, Turkish experience

M. Akif Yeşilipek, Vedat Uygun, Alphan Küpesiz et al. · Bone Marrow Transplantation · 2022 · 29 citations

Medicine, Hematology, Surgery +16