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Reha Artan
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Journal Articles

Novel immunodeficiency caused by homozygous mutation in solute carrier family 19 member 1, which encodes the reduced folate carrier

Akira Shiraishi, Vedat Uygun, Nigel Sharfe, Serap Beldar, Mark G. F. Sun, Harjit Dadi, Linda Vong, Michelle Maxson, Neslihan E. Karaca, Süleyman Mevlitoğlu, Sergio Grinstein, Reha Artan, Daniele Merico, Chaim M. Roifman
Journal: Blood
Blood (2023) 141 (26): 3226–3230.
https://doi.org/10.1182/blood.2022017968
Published: 2023
Includes: Supplemental data
Journal Articles

von Willebrand Disease in Children with Glycogen Storage Disease Type Ia.

Aygen Yilmaz, MD, Reha Artan, MD, Mustafa Akcam, MD, Alphan Kupesiz, MD, M. Akif Yesilipek, MD
Journal: Blood
Blood (2004) 104 (11): 3988.
https://doi.org/10.1182/blood.V104.11.3988.3988
Published: 2004