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Biochimica Et Biophysica Acta
|
September 27, 2002
A replicating module as the unit of mitochondrial structure and functioning
Roderick A Capaldi, Robert Aggeler, Robert Gilkerson, et al.
Clinical Chemistry
|
July 11, 2013
High-throughput immunoassay for the biochemical diagnosis of Friedreich ataxia in dried blood spots and whole blood
Devin Oglesbee, Charles Kroll, Oleksandr Gakh, et al.
Clinical Chemistry
|
September 3, 2010
Determination of total homocysteine, methylmalonic acid, and 2-methylcitric acid in dried blood spots by tandem mass spectrometry
Coleman T Turgeon, Mark J Magera, Carla D Cuthbert, et al.
American Journal of Medical Genetics. Part A
|
September 26, 2024
Case Report of Friedreich's Ataxia and ALG1 -Related Biochemical Abnormalities in a Patient With Progressive Spastic Paraplegia
Aisling Quinlan, Lance Rodan, Elizabeth Barkoudah, et al.
Journal of Psychiatric Research
|
October 23, 2016
Mitochondrial DNA sequence data reveals association of haplogroup U with psychosis in bipolar disorder
Mark A Frye, Euijung Ryu, Malik Nassan, et al.
Stem Cells (Dayton, Ohio)
|
April 5, 2013
Disease-causing mitochondrial heteroplasmy segregated within induced pluripotent stem cell clones derived from a patient with MELAS
Clifford D L Folmes, Almudena Martinez-Fernandez, Ester Perales-Clemente, et al.
Clinical Chemistry
|
September 6, 2005
Automated spectrophotometric analysis of mitochondrial respiratory chain complex enzyme activities in cultured skin fibroblasts
Karen A Kramer, Devin Oglesbee, Stacy J Hartman, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
November 3, 2017
Moonlighting newborn screening markers: the incidental discovery of a second-tier test for Pompe disease
Silvia Tortorelli, Jason S Eckerman, Joseph J Orsini, et al.
Journal of Inherited Metabolic Disease
|
September 25, 2023
A new test method for biochemical analysis of plasmalogens in dried blood spots and erythrocytes from patients with peroxisomal disorders
Peter J Wegwerth, Amy L White, Stephanie D Stoway, et al.
Molecular Genetics and Metabolism
|
June 18, 2020
Laboratory monitoring of patients with hereditary tyrosinemia type I
Matthew J Schultz, Brian C Netzel, Rani H Singh, et al.
Page
of 10
Search research articles
Search
Showing results (51-60 of 99) with videos related to
Sort By:
Page
of 10
Biochimica Et Biophysica Acta
|
September 27, 2002
A replicating module as the unit of mitochondrial structure and functioning
Roderick A Capaldi, Robert Aggeler, Robert Gilkerson, et al.
Clinical Chemistry
|
July 11, 2013
High-throughput immunoassay for the biochemical diagnosis of Friedreich ataxia in dried blood spots and whole blood
Devin Oglesbee, Charles Kroll, Oleksandr Gakh, et al.
Clinical Chemistry
|
September 3, 2010
Determination of total homocysteine, methylmalonic acid, and 2-methylcitric acid in dried blood spots by tandem mass spectrometry
Coleman T Turgeon, Mark J Magera, Carla D Cuthbert, et al.
American Journal of Medical Genetics. Part A
|
September 26, 2024
Case Report of Friedreich's Ataxia and ALG1 -Related Biochemical Abnormalities in a Patient With Progressive Spastic Paraplegia
Aisling Quinlan, Lance Rodan, Elizabeth Barkoudah, et al.
Journal of Psychiatric Research
|
October 23, 2016
Mitochondrial DNA sequence data reveals association of haplogroup U with psychosis in bipolar disorder
Mark A Frye, Euijung Ryu, Malik Nassan, et al.
Stem Cells (Dayton, Ohio)
|
April 5, 2013
Disease-causing mitochondrial heteroplasmy segregated within induced pluripotent stem cell clones derived from a patient with MELAS
Clifford D L Folmes, Almudena Martinez-Fernandez, Ester Perales-Clemente, et al.
Clinical Chemistry
|
September 6, 2005
Automated spectrophotometric analysis of mitochondrial respiratory chain complex enzyme activities in cultured skin fibroblasts
Karen A Kramer, Devin Oglesbee, Stacy J Hartman, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
November 3, 2017
Moonlighting newborn screening markers: the incidental discovery of a second-tier test for Pompe disease
Silvia Tortorelli, Jason S Eckerman, Joseph J Orsini, et al.
Journal of Inherited Metabolic Disease
|
September 25, 2023
A new test method for biochemical analysis of plasmalogens in dried blood spots and erythrocytes from patients with peroxisomal disorders
Peter J Wegwerth, Amy L White, Stephanie D Stoway, et al.
Molecular Genetics and Metabolism
|
June 18, 2020
Laboratory monitoring of patients with hereditary tyrosinemia type I
Matthew J Schultz, Brian C Netzel, Rani H Singh, et al.
Page
of 10