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Annals of Clinical and Translational Neurology
|
June 7, 2024
Epidemiology and natural history of POLG disease in Norway: a nationwide cohort study
Erle Kristensen, Linda Mathisen, Siren Berland, et al.
Seizure
|
June 28, 2024
Refractory and super-refractory status epilepticus in children and adolescents: A population-based study
Seline W Hepsø, Maya Lee, Kristoffer Noszka, et al.
Mitochondrion
|
September 25, 2020
Mental health and health related quality of life in mitochondrial POLG disease
Omar Hikmat, Bente Johanne Vederhus, Merete Roineland Benestad, 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.
Epilepsia
|
June 20, 2018
Elevated cerebrospinal fluid protein in POLG-related epilepsy: Diagnostic and prognostic implications
Omar Hikmat, Karin Naess, Martin Engvall, et al.
Journal of Medical Genetics
|
December 7, 2021
Phenotypic spectrum and clinical course of single large-scale mitochondrial DNA deletion disease in the paediatric population: a multicentre study
Kristoffer Björkman, John Vissing, Elsebet Østergaard, et al.
Kidney Diseases (Basel, Switzerland)
|
May 9, 2022
Renal Phenotype in Mitochondrial Diseases: A Multicenter Study
Maria Parasyri, Per Brandström, Johanna Uusimaa, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
September 20, 2018
Correction: The clinical spectrum and natural history of early-onset diseases due to DNA polymerase gamma mutations
Omar Hikmat, Charalampos Tzoulis, Wui K Chong, et al.
Journal of Inherited Metabolic Disease
|
May 12, 2020
Simplifying the clinical classification of polymerase gamma (POLG) disease based on age of onset; studies using a cohort of 155 cases
Omar Hikmat, Karin Naess, Martin Engvall, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
May 5, 2017
The clinical spectrum and natural history of early-onset diseases due to DNA polymerase gamma mutations
Omar Hikmat, Charalampos Tzoulis, Wui K Chong, et al.
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of 3
Search research articles
Search
Showing results (11-20 of 29) with videos related to
Sort By:
Page
of 3
Annals of Clinical and Translational Neurology
|
June 7, 2024
Epidemiology and natural history of POLG disease in Norway: a nationwide cohort study
Erle Kristensen, Linda Mathisen, Siren Berland, et al.
Seizure
|
June 28, 2024
Refractory and super-refractory status epilepticus in children and adolescents: A population-based study
Seline W Hepsø, Maya Lee, Kristoffer Noszka, et al.
Mitochondrion
|
September 25, 2020
Mental health and health related quality of life in mitochondrial POLG disease
Omar Hikmat, Bente Johanne Vederhus, Merete Roineland Benestad, 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.
Epilepsia
|
June 20, 2018
Elevated cerebrospinal fluid protein in POLG-related epilepsy: Diagnostic and prognostic implications
Omar Hikmat, Karin Naess, Martin Engvall, et al.
Journal of Medical Genetics
|
December 7, 2021
Phenotypic spectrum and clinical course of single large-scale mitochondrial DNA deletion disease in the paediatric population: a multicentre study
Kristoffer Björkman, John Vissing, Elsebet Østergaard, et al.
Kidney Diseases (Basel, Switzerland)
|
May 9, 2022
Renal Phenotype in Mitochondrial Diseases: A Multicenter Study
Maria Parasyri, Per Brandström, Johanna Uusimaa, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
September 20, 2018
Correction: The clinical spectrum and natural history of early-onset diseases due to DNA polymerase gamma mutations
Omar Hikmat, Charalampos Tzoulis, Wui K Chong, et al.
Journal of Inherited Metabolic Disease
|
May 12, 2020
Simplifying the clinical classification of polymerase gamma (POLG) disease based on age of onset; studies using a cohort of 155 cases
Omar Hikmat, Karin Naess, Martin Engvall, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
May 5, 2017
The clinical spectrum and natural history of early-onset diseases due to DNA polymerase gamma mutations
Omar Hikmat, Charalampos Tzoulis, Wui K Chong, et al.
Page
of 3