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Journal of Inherited Metabolic Disease
|
January 27, 2005
Lipid-storage myopathy and respiratory insufficiency due to ETFQO mutations in a patient with late-onset multiple acyl-CoA dehydrogenation deficiency
R K J Olsen, M Pourfarzam, A A M Morris, et al.
Developmental Medicine and Child Neurology
|
August 15, 2006
Pyruvate dehydrogenase E3 binding protein (protein X) deficiency
R M Brown, R A Head, A A M Morris, et al.
The American Journal of Pathology
|
July 8, 1999
Mitochondrial DNA depletion syndrome is expressed in amniotic fluid cell cultures
J C Blake, J W Taanman, A M Morris, et al.
European Journal of Human Genetics : EJHG
|
April 1, 2004
A novel point mutation in the mitochondrial tRNA(Trp) gene produces a neurogastrointestinal syndrome
Katharina Maniura-Weber, Robert W Taylor, Margaret A Johnson, et al.
Journal of Inherited Metabolic Disease
|
March 17, 2025
Cystathionine β-Synthase Deficiency in the E-HOD Registry-Part II: Dietary and Pharmacological Treatment
Andrew A M Morris, Jitka Sokolová, Markéta Pavlíková, et al.
Journal of Inherited Metabolic Disease
|
December 9, 2020
Cystathionine β-synthase deficiency in the E-HOD registry-part I: pyridoxine responsiveness as a determinant of biochemical and clinical phenotype at diagnosis
Viktor Kožich, Jitka Sokolová, Andrew A M Morris, et al.
Neuroepidemiology
|
September 11, 2002
Annualized incidence and spectrum of illness from an outbreak investigation of Bell's palsy
A M Morris, S L Deeks, M D Hill, et al.
Human Mutation
|
October 2, 2008
Analysis of mutant DNA polymerase gamma in patients with mitochondrial DNA depletion
Jan-Willem Taanman, Shamima Rahman, Alistair T Pagnamenta, et al.
American Journal of Medical Genetics. Part A
|
April 12, 2026
A Diagnostic Conundrum in Fumarase Deficiency: Expanding the Clinical and Genetic Spectrum in a Cohort of Pediatric and Adult Patients
Siew Li Ting, John Bassett, Jonathan Meyer, et al.
American Journal of Respiratory and Critical Care Medicine
|
August 10, 2000
Permanent declines in pulmonary function following pneumonia in human immunodeficiency virus-infected persons. The Pulmonary Complications of HIV Infection Study Group
A M Morris, L Huang, P Bacchetti, et al.
Page
of 13
Search research articles
Search
Showing results (91-100 of 127) with videos related to
Sort By:
Page
of 13
Journal of Inherited Metabolic Disease
|
January 27, 2005
Lipid-storage myopathy and respiratory insufficiency due to ETFQO mutations in a patient with late-onset multiple acyl-CoA dehydrogenation deficiency
R K J Olsen, M Pourfarzam, A A M Morris, et al.
Developmental Medicine and Child Neurology
|
August 15, 2006
Pyruvate dehydrogenase E3 binding protein (protein X) deficiency
R M Brown, R A Head, A A M Morris, et al.
The American Journal of Pathology
|
July 8, 1999
Mitochondrial DNA depletion syndrome is expressed in amniotic fluid cell cultures
J C Blake, J W Taanman, A M Morris, et al.
European Journal of Human Genetics : EJHG
|
April 1, 2004
A novel point mutation in the mitochondrial tRNA(Trp) gene produces a neurogastrointestinal syndrome
Katharina Maniura-Weber, Robert W Taylor, Margaret A Johnson, et al.
Journal of Inherited Metabolic Disease
|
March 17, 2025
Cystathionine β-Synthase Deficiency in the E-HOD Registry-Part II: Dietary and Pharmacological Treatment
Andrew A M Morris, Jitka Sokolová, Markéta Pavlíková, et al.
Journal of Inherited Metabolic Disease
|
December 9, 2020
Cystathionine β-synthase deficiency in the E-HOD registry-part I: pyridoxine responsiveness as a determinant of biochemical and clinical phenotype at diagnosis
Viktor Kožich, Jitka Sokolová, Andrew A M Morris, et al.
Neuroepidemiology
|
September 11, 2002
Annualized incidence and spectrum of illness from an outbreak investigation of Bell's palsy
A M Morris, S L Deeks, M D Hill, et al.
Human Mutation
|
October 2, 2008
Analysis of mutant DNA polymerase gamma in patients with mitochondrial DNA depletion
Jan-Willem Taanman, Shamima Rahman, Alistair T Pagnamenta, et al.
American Journal of Medical Genetics. Part A
|
April 12, 2026
A Diagnostic Conundrum in Fumarase Deficiency: Expanding the Clinical and Genetic Spectrum in a Cohort of Pediatric and Adult Patients
Siew Li Ting, John Bassett, Jonathan Meyer, et al.
American Journal of Respiratory and Critical Care Medicine
|
August 10, 2000
Permanent declines in pulmonary function following pneumonia in human immunodeficiency virus-infected persons. The Pulmonary Complications of HIV Infection Study Group
A M Morris, L Huang, P Bacchetti, et al.
Page
of 13