Search research articles
Contact Us
Filters
Showing results (11-20 of 19) with videos related to
Page
of 2
Sort By:
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 transplant
Theresa 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 Kingdom
Alexandra 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 regimen
Kanchan 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 Kingdom
Alexandra 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 programmes
Daniel 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 correlation
Pamela 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 fission
Rojeen Shahni, Catherine M Cale, Glenn Anderson, et al.
American Journal of Human Genetics
|
January 31, 2017
Mutations in EXTL3 Cause Neuro-immuno-skeletal Dysplasia Syndrome
Machteld M Oud, Paul Tuijnenburg, Maja Hempel, et al.
The Journal of Clinical Investigation
|
March 28, 2023
Human inherited complete STAT2 deficiency underlies inflammatory viral diseases
Giorgia Bucciol, Leen Moens, Masato Ogishi, et al.
Page
of 2
Search research articles
Search
Showing results (11-20 of 19) with videos related to
Sort By:
Page
of 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 transplant
Theresa 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 Kingdom
Alexandra 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 regimen
Kanchan 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 Kingdom
Alexandra 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 programmes
Daniel 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 correlation
Pamela 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 fission
Rojeen Shahni, Catherine M Cale, Glenn Anderson, et al.
American Journal of Human Genetics
|
January 31, 2017
Mutations in EXTL3 Cause Neuro-immuno-skeletal Dysplasia Syndrome
Machteld M Oud, Paul Tuijnenburg, Maja Hempel, et al.
The Journal of Clinical Investigation
|
March 28, 2023
Human inherited complete STAT2 deficiency underlies inflammatory viral diseases
Giorgia Bucciol, Leen Moens, Masato Ogishi, et al.
Page
of 2