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Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke
|
January 10, 2004
[The genetic basis of muscle disease]
Laurence Bindoff, Nils Erik Gilhus
Thyroid : Official Journal of the American Thyroid Association
|
February 13, 2002
Thyrotoxicosis and paraparesis in a young woman: case report and review of the literature
Gunnar Mellgren, Inger Hjørdis Bleskestad, Sylvi Aanderud, et al.
Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke
|
June 27, 2002
[Thyrotoxic periodic paralysis--an unusual complication of hyperthyroidism]
Gunnar Mellgren, Pål Ivar Holm, Ernst Asbjørn Lien, et al.
Muscle & Nerve
|
November 26, 2003
Late-onset mitochondrial disorder with electromyographic evidence of myotonia
Mathew L P Howse, Theresa M Wardell, Christopher J Fisher, et al.
Mitochondrion
|
October 2, 2010
Predicting the contribution of novel POLG mutations to human disease through analysis in yeast model
Enrico Baruffini, Rita Horvath, Cristina Dallabona, et al.
Diabetes Care
|
June 12, 2008
Neurological features and enzyme therapy in patients with endocrine and exocrine pancreas dysfunction due to CEL mutations
Mette Vesterhus, Helge Raeder, Harald Aurlien, et al.
Plos One
|
January 28, 2014
Spastic paraplegia type 7 is associated with multiple mitochondrial DNA deletions
Iselin Marie Wedding, Jeanette Koht, Gia Tuong Tran, et al.
Mitochondrion
|
November 6, 2007
Liver mtDNA content increases during development: a comparison of methods and the importance of age- and tissue-specific controls for the diagnosis of mtDNA depletion
Karl J Morten, Neil Ashley, Frits Wijburg, et al.
Journal of Inherited Metabolic Disease
|
August 29, 2020
Diagnostic value of serum biomarkers FGF21 and GDF15 compared to muscle sample in mitochondrial disease
Jenni M Lehtonen, Mari Auranen, Niklas Darin, et al.
Annals of Clinical and Translational Neurology
|
April 29, 2020
Global FKRP Registry: observations in more than 300 patients with Limb Girdle Muscular Dystrophy R9
Lindsay B Murphy, Olivia Schreiber-Katz, Karen Rafferty, et al.
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Showing results (1-10 of 13) with videos related to
Sort By:
Page
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Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke
|
January 10, 2004
[The genetic basis of muscle disease]
Laurence Bindoff, Nils Erik Gilhus
Thyroid : Official Journal of the American Thyroid Association
|
February 13, 2002
Thyrotoxicosis and paraparesis in a young woman: case report and review of the literature
Gunnar Mellgren, Inger Hjørdis Bleskestad, Sylvi Aanderud, et al.
Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke
|
June 27, 2002
[Thyrotoxic periodic paralysis--an unusual complication of hyperthyroidism]
Gunnar Mellgren, Pål Ivar Holm, Ernst Asbjørn Lien, et al.
Muscle & Nerve
|
November 26, 2003
Late-onset mitochondrial disorder with electromyographic evidence of myotonia
Mathew L P Howse, Theresa M Wardell, Christopher J Fisher, et al.
Mitochondrion
|
October 2, 2010
Predicting the contribution of novel POLG mutations to human disease through analysis in yeast model
Enrico Baruffini, Rita Horvath, Cristina Dallabona, et al.
Diabetes Care
|
June 12, 2008
Neurological features and enzyme therapy in patients with endocrine and exocrine pancreas dysfunction due to CEL mutations
Mette Vesterhus, Helge Raeder, Harald Aurlien, et al.
Plos One
|
January 28, 2014
Spastic paraplegia type 7 is associated with multiple mitochondrial DNA deletions
Iselin Marie Wedding, Jeanette Koht, Gia Tuong Tran, et al.
Mitochondrion
|
November 6, 2007
Liver mtDNA content increases during development: a comparison of methods and the importance of age- and tissue-specific controls for the diagnosis of mtDNA depletion
Karl J Morten, Neil Ashley, Frits Wijburg, et al.
Journal of Inherited Metabolic Disease
|
August 29, 2020
Diagnostic value of serum biomarkers FGF21 and GDF15 compared to muscle sample in mitochondrial disease
Jenni M Lehtonen, Mari Auranen, Niklas Darin, et al.
Annals of Clinical and Translational Neurology
|
April 29, 2020
Global FKRP Registry: observations in more than 300 patients with Limb Girdle Muscular Dystrophy R9
Lindsay B Murphy, Olivia Schreiber-Katz, Karen Rafferty, et al.
Page
of 2