Advanced filters
De novo CXCR4 Mutation in WHIM Syndrome: Report of a 4-Year-Old Case without Wart and Myelokathexis
Shayan Roshdi, Sepideh Shahkarami, Samaneh Zoghi, Elham Rayzan, Rasol Molatefi, Meino Rohlfs, Christoph Klein, Nima Rezaei
Published: 2025-03-12
HMGB1 Polymorphisms in Acute Lymphoblastic Leukemia
Elham Rayzan, Saeed Farajzadeh Valilou, Sara Hemmati, Amin Sadeghi, Hamid Farajifard, Sepideh Shahkarami, Nima Rezaei
Published: 2025-02-24
A Novel Homozygous RAB27A Mutation is Associated with Griscelli Syndrom type II and Less Severe Presentations
Mostafa Kamali, Sepideh Shahkarami, Elham Rayzan, Iraj Mohammazadeh, Meino Rohlfs, Christoph Klein, Nima Rezaei
Published: 2024-06-22
Congenital Cardiac Defects in G6PC3 Deficiency: Report of a Mutation and a Literature Review
Mahsima Shabani, Elham Rayzan, Ido Somekh, Christoph Klein, Nima Rezaei
Published: 2025-03-15
1 - 4 of 4 items