Corry M R Weemaes - JoVE Visualize

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Blood|October 31, 2002

Radiosensitive SCID patients with Artemis gene mutations show a complete B-cell differentiation arrest at the pre-B-cell receptor checkpoint in bone marrowJeroen G Noordzij, Nicole S Verkaik, Mirjam van der Burg, et al.

The Journal of Allergy and Clinical Immunology|April 10, 2013

Antibody deficiency in patients with ataxia telangiectasia is caused by disturbed B- and T-cell homeostasis and reduced immune repertoire diversityGertjan J Driessen, Hanna Ijspeert, Corry M R Weemaes, et al.

Journal of Clinical Immunology|August 21, 2024

Allogeneic Hematopoietic Stem Cell Transplantation in Immunodeficiency-Centromeric Instability-Facial Dysmorphism (ICF) Syndrome: an EBMT/ESID Inborn Errors Working Party StudyDagmar Berghuis, Lubna S Mehyar, Rolla Abu-Arja, et al.

Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America|March 7, 2002

Results of 2 years of treatment with protease-inhibitor--containing antiretroviral therapy in dutch children infected with human immunodeficiency virus type 1Annemarie M C van Rossum, Sibyl P M Geelen, Nico G Hartwig, et al.

Movement Disorders : Official Journal of the Movement Disorder Society|September 13, 2021

Nicotinamide Riboside Improves Ataxia Scores and Immunoglobulin Levels in Ataxia TelangiectasiaStefanie J G Veenhuis, Nienke J H van Os, Anjo J W M Janssen, et al.

Clinical Immunology (Orlando, Fla.)|January 28, 2017

Ataxia-telangiectasia: Immunodeficiency and survivalNienke J H van Os, Anne F M Jansen, Marcel van Deuren, et al.

European Journal of Human Genetics : EJHG|March 15, 2013

Heterogeneous clinical presentation in ICF syndrome: correlation with underlying gene defectsCorry M R Weemaes, Maarten J D van Tol, Jun Wang, et al.

Human Mutation|January 4, 2012

Presence of ATM protein and residual kinase activity correlates with the phenotype in ataxia-telangiectasia: a genotype-phenotype studyMijke M M Verhagen, James I Last, Frans B L Hogervorst, et al.

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Showing results (21-30 of 28) with videos related to

Sort By:

Pageof 3

You have reached the last page of results.This site can display upto 28 results.

Blood|October 31, 2002

Radiosensitive SCID patients with Artemis gene mutations show a complete B-cell differentiation arrest at the pre-B-cell receptor checkpoint in bone marrowJeroen G Noordzij, Nicole S Verkaik, Mirjam van der Burg, et al.

The Journal of Allergy and Clinical Immunology|April 10, 2013

Antibody deficiency in patients with ataxia telangiectasia is caused by disturbed B- and T-cell homeostasis and reduced immune repertoire diversityGertjan J Driessen, Hanna Ijspeert, Corry M R Weemaes, et al.

Journal of Clinical Immunology|August 21, 2024

Allogeneic Hematopoietic Stem Cell Transplantation in Immunodeficiency-Centromeric Instability-Facial Dysmorphism (ICF) Syndrome: an EBMT/ESID Inborn Errors Working Party StudyDagmar Berghuis, Lubna S Mehyar, Rolla Abu-Arja, et al.

Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America|March 7, 2002

Results of 2 years of treatment with protease-inhibitor--containing antiretroviral therapy in dutch children infected with human immunodeficiency virus type 1Annemarie M C van Rossum, Sibyl P M Geelen, Nico G Hartwig, et al.

Movement Disorders : Official Journal of the Movement Disorder Society|September 13, 2021

Nicotinamide Riboside Improves Ataxia Scores and Immunoglobulin Levels in Ataxia TelangiectasiaStefanie J G Veenhuis, Nienke J H van Os, Anjo J W M Janssen, et al.

Clinical Immunology (Orlando, Fla.)|January 28, 2017

Ataxia-telangiectasia: Immunodeficiency and survivalNienke J H van Os, Anne F M Jansen, Marcel van Deuren, et al.

European Journal of Human Genetics : EJHG|March 15, 2013

Heterogeneous clinical presentation in ICF syndrome: correlation with underlying gene defectsCorry M R Weemaes, Maarten J D van Tol, Jun Wang, et al.

Human Mutation|January 4, 2012

Presence of ATM protein and residual kinase activity correlates with the phenotype in ataxia-telangiectasia: a genotype-phenotype studyMijke M M Verhagen, James I Last, Frans B L Hogervorst, et al.

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