Management of Children with Glycogen Storage Disease (Liver Involvement Forms). Best Practice Guidelines
Glycogen storage disease is the hereditary carbohydrate metabolism pathology which is caused by mutations in various genes encoding enzymes responsible for glycogenesis and glycogenolysis. Excessive glycogen deposition in various tissues cells (mostly in liver and muscles) occurs due to enzyme defec...
Main Authors: | Alexander A. Baranov, Leyla S. Namazova-Baranova, Andrey N. Surkov, Olga S. Gundobina, Elena A. Vishneva, Tea V. Margieva, Nato D. Vashakmadze, Liliya R. Selimzyanova |
---|---|
Format: | Article |
Language: | English |
Published: |
Paediatrician Publishers, LLC
2020-09-01
|
Series: | Pediatričeskaâ Farmakologiâ |
Subjects: | |
Online Access: | https://www.pedpharma.ru/jour/article/view/1883 |
Similar Items
-
Oral Manifestations in Patients with Glycogen Storage Disease: A Systematic Review of the Literature
by: Antonio Romano, et al.
Published: (2020-09-01) -
GLYCOGENOSIS IN CHILDREN: MODERN ASPECTS (PART I)
by: A. N. Surkov
Published: (2012-03-01) -
Novel GYS2 mutations in a Japanese patient with glycogen storage disease type 0a
by: Hiroyuki Iijima, et al.
Published: (2021-03-01) -
Skeletal muscle metabolism during prolonged exercise in Pompe disease
by: Nicolai Preisler, et al.
Published: (2017-07-01) -
Computed Tomography and Magnetic Resonance Imaging Features of Primary and Secondary Hepatic Glycogenosis
by: Zhi-yuan Chen, et al.
Published: (2018-11-01)