Search research articles
Contact Us
Filters
Showing results (21-30 of 82) with videos related to
Page
of 9
Sort By:
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
July 4, 2024
Fabry disease Enzyme Enhancement on migalastat Study: FEES
Mathura Kugan, Simona D'Amore, Udita Mitra-Royhurst, et al.
The Journal of Clinical Endocrinology and Metabolism
|
July 12, 2016
Defining the Newborn Blood Spot Screening Reference Interval for TSH: Impact of Ethnicity
Catherine Peters, Ivan Brooke, Simon Heales, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
January 26, 2022
Cerebellar and Midbrain Lysosomal Enzyme Deficiency in Isolated Dystonia
Sebastian R Schreglmann, Derek Burke, Amit Batla, et al.
Journal of Neurochemistry
|
January 10, 2008
Glutamate induces release of glutathione from cultured rat astrocytes--a possible neuroprotective mechanism?
João Frade, Simon Pope, Maike Schmidt, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology
|
April 7, 2007
(6R)-5,6,7,8-tetrahydro-L-biopterin and its stereoisomer prevent ischemia reperfusion injury in human forearm
Lila Mayahi, Simon Heales, David Owen, et al.
Journal of Neurochemistry
|
April 19, 2008
Myelin-induced microglial neurotoxicity can be controlled by microglial metabotropic glutamate receptors
Fleur Pinteaux-Jones, Ioanna G Sevastou, Victoria A H Fry, et al.
Cardiovascular Research
|
August 15, 2002
GTP cyclohydrolase I gene transfer augments intracellular tetrahydrobiopterin in human endothelial cells: effects on nitric oxide synthase activity, protein levels and dimerisation
Shijie Cai, Nicholas J Alp, Denise McDonald, et al.
Mechanisms of Ageing and Development
|
November 24, 2007
Rapid neonatal weight gain in rats results in a renal ubiquinone (CoQ) deficiency associated with premature death
Piran Shelley, Jane Tarry-Adkins, Malgorzata Martin-Gronert, et al.
Journal of Inherited Metabolic Disease
|
January 18, 2015
Bi-allelic CLPB mutations cause cataract, renal cysts, nephrocalcinosis and 3-methylglutaconic aciduria, a novel disorder of mitochondrial protein disaggregation
Marta Kanabus, Rojeen Shahni, José W Saldanha, et al.
Journal of Inherited Metabolic Disease
|
June 21, 2011
Urine analysis of glucose tetrasaccharide by HPLC; a useful marker for the investigation of patients with Pompe and other glycogen storage diseases
Victoria Manwaring, Helen Prunty, Katie Bainbridge, et al.
Page
of 9
Search research articles
Search
Showing results (21-30 of 82) with videos related to
Sort By:
Page
of 9
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
July 4, 2024
Fabry disease Enzyme Enhancement on migalastat Study: FEES
Mathura Kugan, Simona D'Amore, Udita Mitra-Royhurst, et al.
The Journal of Clinical Endocrinology and Metabolism
|
July 12, 2016
Defining the Newborn Blood Spot Screening Reference Interval for TSH: Impact of Ethnicity
Catherine Peters, Ivan Brooke, Simon Heales, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
January 26, 2022
Cerebellar and Midbrain Lysosomal Enzyme Deficiency in Isolated Dystonia
Sebastian R Schreglmann, Derek Burke, Amit Batla, et al.
Journal of Neurochemistry
|
January 10, 2008
Glutamate induces release of glutathione from cultured rat astrocytes--a possible neuroprotective mechanism?
João Frade, Simon Pope, Maike Schmidt, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology
|
April 7, 2007
(6R)-5,6,7,8-tetrahydro-L-biopterin and its stereoisomer prevent ischemia reperfusion injury in human forearm
Lila Mayahi, Simon Heales, David Owen, et al.
Journal of Neurochemistry
|
April 19, 2008
Myelin-induced microglial neurotoxicity can be controlled by microglial metabotropic glutamate receptors
Fleur Pinteaux-Jones, Ioanna G Sevastou, Victoria A H Fry, et al.
Cardiovascular Research
|
August 15, 2002
GTP cyclohydrolase I gene transfer augments intracellular tetrahydrobiopterin in human endothelial cells: effects on nitric oxide synthase activity, protein levels and dimerisation
Shijie Cai, Nicholas J Alp, Denise McDonald, et al.
Mechanisms of Ageing and Development
|
November 24, 2007
Rapid neonatal weight gain in rats results in a renal ubiquinone (CoQ) deficiency associated with premature death
Piran Shelley, Jane Tarry-Adkins, Malgorzata Martin-Gronert, et al.
Journal of Inherited Metabolic Disease
|
January 18, 2015
Bi-allelic CLPB mutations cause cataract, renal cysts, nephrocalcinosis and 3-methylglutaconic aciduria, a novel disorder of mitochondrial protein disaggregation
Marta Kanabus, Rojeen Shahni, José W Saldanha, et al.
Journal of Inherited Metabolic Disease
|
June 21, 2011
Urine analysis of glucose tetrasaccharide by HPLC; a useful marker for the investigation of patients with Pompe and other glycogen storage diseases
Victoria Manwaring, Helen Prunty, Katie Bainbridge, et al.
Page
of 9