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Catherine M Cale

Showing results (11-20 of 19) with videos related to

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Neuropediatrics|February 12, 2013
Cognitive ability in children with chronic granulomatous disease: a comparison of those managed conservatively with those who have undergone hematopoietic stem cell transplantTheresa S Cole, Fiona McKendrick, Andrew J Cant, et al.
Journal of Clinical Immunology|March 15, 2019
Health-Related Quality of Life and Emotional Health in X-Linked Carriers of Chronic Granulomatous Disease in the United KingdomAlexandra C Battersby, Helen Braggins, Mark S Pearce, et al.
Blood|September 16, 2004
Improved survival after unrelated donor bone marrow transplantation in children with primary immunodeficiency using a reduced-intensity conditioning regimenKanchan Rao, Persis J Amrolia, Alison Jones, et al.
The Journal of Allergy and Clinical Immunology|March 28, 2017
Inflammatory and autoimmune manifestations in X-linked carriers of chronic granulomatous disease in the United KingdomAlexandra C Battersby, Helen Braggins, Mark S Pearce, et al.
British Journal of Haematology|June 14, 2016
Post-thaw viability of cryopreserved peripheral blood stem cells (PBSC) does not guarantee functional activity: important implications for quality assurance of stem cell transplant programmesDaniel A Morgenstern, Gulrukh Ahsan, Margaret Brocklesby, et al.
Clinical Immunology (Orlando, Fla.)|November 16, 2013
The many faces of Artemis-deficient combined immunodeficiency - Two patients with DCLRE1C mutations and a systematic literature review of genotype-phenotype correlationPamela P Lee, Lisa Woodbine, Kimberly C Gilmour, et al.
Brain : a Journal of Neurology|July 1, 2015
Signal transducer and activator of transcription 2 deficiency is a novel disorder of mitochondrial fissionRojeen Shahni, Catherine M Cale, Glenn Anderson, et al.
American Journal of Human Genetics|January 31, 2017
Mutations in EXTL3 Cause Neuro-immuno-skeletal Dysplasia SyndromeMachteld M Oud, Paul Tuijnenburg, Maja Hempel, et al.
The Journal of Clinical Investigation|March 28, 2023
Human inherited complete STAT2 deficiency underlies inflammatory viral diseasesGiorgia Bucciol, Leen Moens, Masato Ogishi, et al.
Pageof 2

Showing results (11-20 of 19) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 19 results.
Neuropediatrics|February 12, 2013
Cognitive ability in children with chronic granulomatous disease: a comparison of those managed conservatively with those who have undergone hematopoietic stem cell transplantTheresa S Cole, Fiona McKendrick, Andrew J Cant, et al.
Journal of Clinical Immunology|March 15, 2019
Health-Related Quality of Life and Emotional Health in X-Linked Carriers of Chronic Granulomatous Disease in the United KingdomAlexandra C Battersby, Helen Braggins, Mark S Pearce, et al.
Blood|September 16, 2004
Improved survival after unrelated donor bone marrow transplantation in children with primary immunodeficiency using a reduced-intensity conditioning regimenKanchan Rao, Persis J Amrolia, Alison Jones, et al.
The Journal of Allergy and Clinical Immunology|March 28, 2017
Inflammatory and autoimmune manifestations in X-linked carriers of chronic granulomatous disease in the United KingdomAlexandra C Battersby, Helen Braggins, Mark S Pearce, et al.
British Journal of Haematology|June 14, 2016
Post-thaw viability of cryopreserved peripheral blood stem cells (PBSC) does not guarantee functional activity: important implications for quality assurance of stem cell transplant programmesDaniel A Morgenstern, Gulrukh Ahsan, Margaret Brocklesby, et al.
Clinical Immunology (Orlando, Fla.)|November 16, 2013
The many faces of Artemis-deficient combined immunodeficiency - Two patients with DCLRE1C mutations and a systematic literature review of genotype-phenotype correlationPamela P Lee, Lisa Woodbine, Kimberly C Gilmour, et al.
Brain : a Journal of Neurology|July 1, 2015
Signal transducer and activator of transcription 2 deficiency is a novel disorder of mitochondrial fissionRojeen Shahni, Catherine M Cale, Glenn Anderson, et al.
American Journal of Human Genetics|January 31, 2017
Mutations in EXTL3 Cause Neuro-immuno-skeletal Dysplasia SyndromeMachteld M Oud, Paul Tuijnenburg, Maja Hempel, et al.
The Journal of Clinical Investigation|March 28, 2023
Human inherited complete STAT2 deficiency underlies inflammatory viral diseasesGiorgia Bucciol, Leen Moens, Masato Ogishi, et al.
Pageof 2