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Naschla Kohistani
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Journal Articles

A Rare Case of Congenital Atransferrinemia: International Collaboration for Genetic Diagnosis

Hanan Nazir, MD, Murtadha K. Al-Khabori, MD MSc, FRCPC, Naschla Kohistani, MD, Jacek Puchalka, PhD, Christoph Klein, MD PhD
Journal: Blood
Blood (2014) 124 (21): 4883.
https://doi.org/10.1182/blood.V124.21.4883.4883
Published: 2014
Journal Articles

Inherited biallelic CSF3R mutations in severe congenital neutropenia

Alexa Triot, Päivi M. Järvinen, Juan I. Arostegui, Dhaarini Murugan, Naschla Kohistani, José Luis Dapena Díaz, Tomas Racek, Jacek Puchałka, E. Michael Gertz, Alejandro A. Schäffer, Daniel Kotlarz, Dietmar Pfeifer, Cristina Díaz de Heredia Rubio, Mehmet Akif Ozdemir, Turkan Patiroglu, Musa Karakukcu, José Sánchez de Toledo Codina, Jordi Yagüe, Ivo P. Touw, Ekrem Unal, Christoph Klein
Journal: Blood
Blood (2014) 123 (24): 3811–3817.
https://doi.org/10.1182/blood-2013-11-535419
Published: 2014
Includes: Supplemental data
Journal Articles

Inherited Biallelic Loss-Of-Function Mutations In CSF3R Define a Novel Type Of Severe Congenital Neutropenia With Full Myeloid Cell Maturation and Refractoriness To RhG-CSF

Alexa Triot, Päivi M Järvinen, Juan I. Arostegui, MD, Tomas Racek, PhD, Jacek Puchalka, Jose Luis Dapena Díaz, MD, Naschla Kohistani, MD, E. Michael Gertz, PhD, Alejandro A. Schäffer, Cristina Díaz de Heredia Rubio, MD, Mehmet A. Ozdemir, MD, Turkan Patiroglu, MD, Musa Karakukcu, MD, José Sanchez de Toledo Codina, MD, Jordi Yagüe, MD, PhD, Ekrem Unal, Christoph Klein, MD PhD
Journal: Blood
Blood (2013) 122 (21): 1025.
https://doi.org/10.1182/blood.V122.21.1025.1025
Published: 2013
Journal Articles

Novel NGS-Based Platforms For Molecular Diagnosis Of Severe Congenital Neutropenia

Tomas Racek, PhD, Jacek Puchalka, PhD, Naschla Kohistani, MD, Christoph Klein, MD PhD
Journal: Blood
Blood (2013) 122 (21): 1034.
https://doi.org/10.1182/blood.V122.21.1034.1034
Published: 2013