Publications by authors named "Michael Seleman"

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A novel truncating mutation in MYD88 in a patient with BCG adenitis, neutropenia and delayed umbilical cord separation.
Craig D Platt, Fatima Zaman, Jacqueline G Wallace, Michael Seleman, Janet Chou

Clin Immunol· October 2019

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A monoallelic activating mutation in RAC2 resulting in a combined immunodeficiency.
Vassilios Lougaris, Janet Chou, Abdallah Beano, Jacqueline G Wallace, Manuela Baronio, Michael Seleman

J Allergy Clin Immunol· April 2019

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Novel biallelic TRNT1 mutations resulting in sideroblastic anemia, combined B and T cell defects, hypogammaglobulinemia, recurrent infections, hypertrophic cardiomyopathy and developmental delay.
Vassilios Lougaris, Janet Chou, Manuela Baronio, Luisa Gazzurelli, Tiziana Lorenzini, Michael Seleman

Clin Immunol· March 2018

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A novel mutation in the JH4 domain of JAK3 causing severe combined immunodeficiency complicated by vertebral osteomyelitis.
Farah Qamar, Samina Junejo, Sonia Qureshi, Michael Seleman, Wayne Bainter

Clin Immunol· October 2017

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Uses of Next-Generation Sequencing Technologies for the Diagnosis of Primary Immunodeficiencies.
Michael Seleman, Rodrigo Hoyos-Bachiloglu, Raif S Geha, Janet Chou

Front Immunol· July 2017

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