Pathology of Mitochondrial Encephalomyopathies
The role of the muscle biopsy, histochemistry, electronmicroscopy, measurement of respiratory chain enzymes, and genetic studies in the diagnosis of mitochondrial cytopathies (MC) is reviewed by researchers at the University of Calgary and Alberta Children's Hospital, Canada.
Saved in:
Main Author: | J Gordon Millichap (Author) |
---|---|
Format: | Book |
Published: |
Pediatric Neurology Briefs Publishers,
2005-08-01T00:00:00Z.
|
Subjects: | |
Online Access: | Connect to this object online. |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Mitochondrial Encephalomyopathies: Incidence & DNA
by: J Gordon Millichap
Published: (2001) -
Mitochondrial Encephalomyopathy Associated with Pyruvate Dehydrogenase Complex Deficiency: Eight Clinical Cases
by: Ekaterina A. Nikolaeva, et al.
Published: (2021) -
Novel compound heterozygous TARS2 variants in a Chinese family with mitochondrial encephalomyopathy: a case report
by: Xiaojing Li, et al.
Published: (2020) -
Case Report: A Novel Intronic Mutation in AIFM1 Associated With Fatal Encephalomyopathy and Mitochondrial Disease in Infant
by: Qi Peng, et al.
Published: (2022) -
Clinical Value of Magnetic Resonance Spectroscopy in the Initial Evaluation of Patients with Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-Like Episodes
by: Hyunjoo Lee, et al.
Published: (2021)