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Showing results (61-70 of 103) with videos related to
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Clinical Genetics
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July 11, 1998
Murine MPS I: insights into the pathogenesis of Hurler syndrome
C Russell, G Hendson, G Jevon, et al.
Neuropediatrics
|
July 4, 2007
Isolated sulfite oxidase deficiency in the newborn: lactic acidaemia and leukoencephalopathy
S N Basheer, P J Waters, C W Lam, et al.
Acta Paediatrica (Oslo, Norway : 1992)
|
April 5, 2020
Split-week gestational age model provides valuable information on outcomes in extremely preterm infants
Sumesh Thomas, Jessie van Dyk, Hussein Zein, et al.
Children (Basel, Switzerland)
|
September 28, 2021
Does a Split-Week Gestational Age Model Provide Valuable Information on Neurodevelopmental Outcomes in Extremely Preterm Infants?
Elizabeth Asztalos, Alberto Nettel Aguirre, Leonora Hendson, et al.
Pathology, Research and Practice
|
September 7, 2015
Assessing the accuracy of death records and pre-mortem clinical diagnoses in children diagnosed with brain tumors: A retrospective chart review of children in British Columbia, Canada
Haroon Hasan, Glenda Hendson, A Fuchsia Howard, et al.
American Journal of Medical Genetics. Part A
|
November 1, 2022
Lethal respiratory course and additional features expand the phenotypic spectrum of PIEZO2-related distal arthrogryposis type 5
Agata Oliwa, Glenda Hendson, Cheryl Longman, et al.
Human Pathology
|
March 13, 1998
Absence of detectable EWS/FLI1 expression after therapy-induced neural differentiation in Ewing sarcoma
S R Knezevich, G Hendson, J A Mathers, et al.
Cancer
|
April 5, 2007
Intracystic bleomycin therapy for craniopharyngioma in children: the Canadian experience
Juliette Hukin, Paul Steinbok, Lucie Lafay-Cousin, et al.
Molecular Genetics and Metabolism Reports
|
February 7, 2019
Congenital lactic acidosis, cerebral cysts and pulmonary hypertension in an infant with FOXRED1 related complex I deficiency
Delia Apatean, Bojana Rakic, Catherine Brunel-Guitton, et al.
Molecular Genetics and Metabolism Reports
|
May 9, 2019
Congenital lactic acidosis, cerebral cysts and pulmonary hypertension in an infant with FOXRED1 related complex 1 deficiency
Delia Apatean, Bojana Rakic, Catherine Brunel-Guitton, et al.
Page
of 11
Search research articles
Search
Showing results (61-70 of 103) with videos related to
Sort By:
Page
of 11
Clinical Genetics
|
July 11, 1998
Murine MPS I: insights into the pathogenesis of Hurler syndrome
C Russell, G Hendson, G Jevon, et al.
Neuropediatrics
|
July 4, 2007
Isolated sulfite oxidase deficiency in the newborn: lactic acidaemia and leukoencephalopathy
S N Basheer, P J Waters, C W Lam, et al.
Acta Paediatrica (Oslo, Norway : 1992)
|
April 5, 2020
Split-week gestational age model provides valuable information on outcomes in extremely preterm infants
Sumesh Thomas, Jessie van Dyk, Hussein Zein, et al.
Children (Basel, Switzerland)
|
September 28, 2021
Does a Split-Week Gestational Age Model Provide Valuable Information on Neurodevelopmental Outcomes in Extremely Preterm Infants?
Elizabeth Asztalos, Alberto Nettel Aguirre, Leonora Hendson, et al.
Pathology, Research and Practice
|
September 7, 2015
Assessing the accuracy of death records and pre-mortem clinical diagnoses in children diagnosed with brain tumors: A retrospective chart review of children in British Columbia, Canada
Haroon Hasan, Glenda Hendson, A Fuchsia Howard, et al.
American Journal of Medical Genetics. Part A
|
November 1, 2022
Lethal respiratory course and additional features expand the phenotypic spectrum of PIEZO2-related distal arthrogryposis type 5
Agata Oliwa, Glenda Hendson, Cheryl Longman, et al.
Human Pathology
|
March 13, 1998
Absence of detectable EWS/FLI1 expression after therapy-induced neural differentiation in Ewing sarcoma
S R Knezevich, G Hendson, J A Mathers, et al.
Cancer
|
April 5, 2007
Intracystic bleomycin therapy for craniopharyngioma in children: the Canadian experience
Juliette Hukin, Paul Steinbok, Lucie Lafay-Cousin, et al.
Molecular Genetics and Metabolism Reports
|
February 7, 2019
Congenital lactic acidosis, cerebral cysts and pulmonary hypertension in an infant with FOXRED1 related complex I deficiency
Delia Apatean, Bojana Rakic, Catherine Brunel-Guitton, et al.
Molecular Genetics and Metabolism Reports
|
May 9, 2019
Congenital lactic acidosis, cerebral cysts and pulmonary hypertension in an infant with FOXRED1 related complex 1 deficiency
Delia Apatean, Bojana Rakic, Catherine Brunel-Guitton, et al.
Page
of 11