Objectives: The common data elements (CDE) project was developed by the National Institute of Neurological Disorders and Stroke (NINDS) to provide clinical researchers with tools to improve data quality and allow for harmonization of data collected in different research studies. CDEs have been created for several neurological diseases; the aim of this project was to develop CDEs specifically curated for mitochondrial disease (Mito) to enhance clinical research. Methods: Nine working groups (WGs), composed of international mitochondrial disease experts, provided recommendations for Mito clinical research. They initially reviewed existing NINDS CDEs and instruments, and developed new data elements or instruments when needed. Recommendations w...
Human mitochondrial DNA (mtDNA) encodes a set of 37 genes which are essential structural and functio...
Objectives: These European Federation of Neurological Sciences (EFNS) guidelines are designed to pro...
MSeqDR is the Mitochondrial Disease Sequence Data Resource, a centralized and comprehensive genome a...
OBJECTIVES: The common data elements (CDE) project was developed by the National Institute of Neurol...
Mitochondrial biology is integral to our fundamental understanding of human health and many diseases...
Primary mitochondrial diseases (PMD) are genetic disorders with extensive clinical and molecular het...
Aim: The North American Mitochondrial Disease Consortium (NAMDC) comprises a network of 17 clinical ...
Success rates for genomic analyses of highly heterogeneous disorders can be greatly improved if a la...
The success of whole exome sequencing (WES) for highly heterogeneous disorders, such as mitochondria...
textabstractSuccess rates for genomic analyses of highly heterogeneous disorders can be greatly impr...
Contains fulltext : 152487.pdf (publisher's version ) (Closed access
Human mitochondrial DNA (mtDNA) encodes a set of 37 genes which are essential structural and functio...
Objectives: These European Federation of Neurological Sciences (EFNS) guidelines are designed to pro...
MSeqDR is the Mitochondrial Disease Sequence Data Resource, a centralized and comprehensive genome a...
OBJECTIVES: The common data elements (CDE) project was developed by the National Institute of Neurol...
Mitochondrial biology is integral to our fundamental understanding of human health and many diseases...
Primary mitochondrial diseases (PMD) are genetic disorders with extensive clinical and molecular het...
Aim: The North American Mitochondrial Disease Consortium (NAMDC) comprises a network of 17 clinical ...
Success rates for genomic analyses of highly heterogeneous disorders can be greatly improved if a la...
The success of whole exome sequencing (WES) for highly heterogeneous disorders, such as mitochondria...
textabstractSuccess rates for genomic analyses of highly heterogeneous disorders can be greatly impr...
Contains fulltext : 152487.pdf (publisher's version ) (Closed access
Human mitochondrial DNA (mtDNA) encodes a set of 37 genes which are essential structural and functio...
Objectives: These European Federation of Neurological Sciences (EFNS) guidelines are designed to pro...
MSeqDR is the Mitochondrial Disease Sequence Data Resource, a centralized and comprehensive genome a...