Diagnostic Approach in Infants and Children with Mitochondrial Diseases
Mitochondrial diseases are a heterogeneous group of disorders affecting energy production in the human body. The diagnosis of mitochondrial diseases represents a challenge to clinicians, especially for pediatric cases, which show enormous variation in clinical presentations, as well as biochemical a...
Main Author: | Ching-Shiang Chi |
---|---|
Format: | Article |
Language: | English |
Published: |
Elsevier
2015-02-01
|
Series: | Pediatrics and Neonatology |
Subjects: | |
Online Access: | http://www.sciencedirect.com/science/article/pii/S1875957214000990 |
Similar Items
-
Diagnostic value of blood coenzyme Qlo levels in children with mitochondrial diseases
by: E. A. Nikolaeva, et al.
Published: (2016-03-01) -
Diagnostics and prevention of nuclear-encoded mitochondrial diseases in infants
by: E. A. Nikolaeva
Published: (2016-03-01) -
Kawasaki disease in infants
by: Jung Sook Yeom, et al.
Published: (2013-09-01) -
Role of mitochondrial genetics in complex diseases
by: Namrata Londhe, et al.
Published: (2016-01-01) -
Accessibility of Early Infant Diagnostic Services by Under-5 Years and HIV Exposed Children in Muheza District, North-East Tanzania
by: Veneranda M. Bwana, et al.
Published: (2018-05-01)