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Morten Duno

Showing results (41-50 of 108) with videos related to

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Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|August 19, 2022
Biochemical and clinical manifestations in adults with hypophosphatasia: a national cross-sectional studyNicola Hepp, Anja Lisbeth Frederiksen, Morten Duno, et al.
Journal of Neurology|May 15, 2013
Anoctamin 5 muscular dystrophy in Denmark: prevalence, genotypes, phenotypes, cardiac findings, and muscle protein expressionNanna Witting, Morten Duno, Helle Petri, et al.
Cardiology|January 30, 2010
Genetic variation in the inwardly rectifying K channel subunits KCNJ3 (GIRK1) and KCNJ5 (GIRK4) in patients with sinus node dysfunctionHaya N Holmegard, Juliane Theilade, Marianne Benn, et al.
Parkinsonism & Related Disorders|May 13, 2014
Atypical Friedreich ataxia in patients with FXN p.R165P point mutation or comorbid hemochromatosisEmil Ygland, Franco Taroni, Cinzia Gellera, et al.
American Journal of Human Genetics|August 2, 2007
Deficiency of the alpha subunit of succinate-coenzyme A ligase causes fatal infantile lactic acidosis with mitochondrial DNA depletionElsebet Ostergaard, Ernst Christensen, Elisabeth Kristensen, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|October 9, 2013
Alternating hemiplegia of childhood in Denmark: clinical manifestations and ATP1A3 mutation statusChristina E Hoei-Hansen, Christine Í Dali, Troels J B Lyngbye, et al.
Clinical Case Reports|October 21, 2016
Asymptomatic parental mosaicism for osteogenesis imperfecta associated with a new splice site mutation in <i>COL1A2</i>Anja Lisbeth Frederiksen, Morten Duno, Iben B G Johnsen, et al.
JIMD Reports|June 26, 2015
Exercise Intolerance and Myoglobinuria Associated with a Novel Maternally Inherited MT-ND1 MutationJabin Rafiq, Morten Duno, Elsebet Østergaard, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|December 4, 2014
A mitochondrial tRNA(Met) mutation causing developmental delay, exercise intolerance and limb girdle phenotype with onset in early childhoodAlfred Peter Born, Morten Duno, Jabin Rafiq, et al.
Human Mutation|June 20, 2020
A single c.1715G>C calpain 3 gene variant causes dominant calpainopathy with loss of calpain 3 expression and activityJohn Vissing, Julia R Dahlqvist, Carinne Roudaut, et al.
Pageof 11

Showing results (41-50 of 108) with videos related to

Sort By:
Pageof 11
Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|August 19, 2022
Biochemical and clinical manifestations in adults with hypophosphatasia: a national cross-sectional studyNicola Hepp, Anja Lisbeth Frederiksen, Morten Duno, et al.
Journal of Neurology|May 15, 2013
Anoctamin 5 muscular dystrophy in Denmark: prevalence, genotypes, phenotypes, cardiac findings, and muscle protein expressionNanna Witting, Morten Duno, Helle Petri, et al.
Cardiology|January 30, 2010
Genetic variation in the inwardly rectifying K channel subunits KCNJ3 (GIRK1) and KCNJ5 (GIRK4) in patients with sinus node dysfunctionHaya N Holmegard, Juliane Theilade, Marianne Benn, et al.
Parkinsonism & Related Disorders|May 13, 2014
Atypical Friedreich ataxia in patients with FXN p.R165P point mutation or comorbid hemochromatosisEmil Ygland, Franco Taroni, Cinzia Gellera, et al.
American Journal of Human Genetics|August 2, 2007
Deficiency of the alpha subunit of succinate-coenzyme A ligase causes fatal infantile lactic acidosis with mitochondrial DNA depletionElsebet Ostergaard, Ernst Christensen, Elisabeth Kristensen, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|October 9, 2013
Alternating hemiplegia of childhood in Denmark: clinical manifestations and ATP1A3 mutation statusChristina E Hoei-Hansen, Christine Í Dali, Troels J B Lyngbye, et al.
Clinical Case Reports|October 21, 2016
Asymptomatic parental mosaicism for osteogenesis imperfecta associated with a new splice site mutation in <i>COL1A2</i>Anja Lisbeth Frederiksen, Morten Duno, Iben B G Johnsen, et al.
JIMD Reports|June 26, 2015
Exercise Intolerance and Myoglobinuria Associated with a Novel Maternally Inherited MT-ND1 MutationJabin Rafiq, Morten Duno, Elsebet Østergaard, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|December 4, 2014
A mitochondrial tRNA(Met) mutation causing developmental delay, exercise intolerance and limb girdle phenotype with onset in early childhoodAlfred Peter Born, Morten Duno, Jabin Rafiq, et al.
Human Mutation|June 20, 2020
A single c.1715G>C calpain 3 gene variant causes dominant calpainopathy with loss of calpain 3 expression and activityJohn Vissing, Julia R Dahlqvist, Carinne Roudaut, et al.
Pageof 11