carnitine has been researched along with Glycogenosis in 14 studies
| Excerpt | Relevance | Reference |
|---|---|---|
| "Metabolic myopathies are disorders of muscle energy production that result in skeletal muscle dysfunction." | 2.39 | Metabolic myopathies. ( Barohn, R; Haller, RG; Martin, A, 1994) |
| "Epidemiology of muscular dystrophies has been important in the prevention of these diseases." | 1.26 | [Muscular diseases: epidemiology of progressive muscular dystrophies]. ( Armani, M; Schergna, E, 1981) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 13 (92.86) | 18.7374 |
| 1990's | 1 (7.14) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Deufel, T | 1 |
| Paetzke, I | 1 |
| Pongratz, D | 1 |
| Hübner, G | 1 |
| Wieland, OH | 1 |
| Gamstorp, I | 1 |
| Kachaner, J | 1 |
| Batisse, A | 1 |
| Fermont, L | 1 |
| Piechaud, JF | 1 |
| Ribierre, M | 1 |
| Schergna, E | 1 |
| Armani, M | 1 |
| Gilly, R | 1 |
| Carrier, H | 1 |
| Lamit, J | 1 |
| Armbrustmacher, VW | 1 |
| Griffin, JL | 1 |
| Buxton, PH | 1 |
| Martin, A | 1 |
| Haller, RG | 1 |
| Barohn, R | 1 |
| Claireaux, AE | 1 |
| Lake, BD | 1 |
| Somer, H | 1 |
| Cornelio, F | 1 |
| Di Donato, S | 1 |
| Sahgal, V | 1 |
| Solomon, R | 1 |
| Sugie, H | 1 |
| Kobayashi, J | 1 |
| Sugie, Y | 1 |
| Ichimura, M | 1 |
| Miyamoto, R | 1 |
| Ito, T | 1 |
| Shimizu, K | 1 |
| Igarashi, Y | 1 |
| Maaswinkel-Mooy, PD | 1 |
| Poorthuis, BJ | 1 |
| van Gelderen, HH | 1 |
| van de Kamp, JJ | 1 |
4 reviews available for carnitine and Glycogenosis
| Article | Year |
|---|---|
Non-dystrophic, myogenic myopathies with onset in infancy or childhood. A review of some characteristic syndromes.
Topics: Carnitine; Carnitine O-Palmitoyltransferase; Child; Child, Preschool; Dermatomyositis; Endocrine Sys | 1982 |
Pathology of muscle.
Topics: Adult; Carnitine; Carnitine O-Palmitoyltransferase; Child; Child, Preschool; Denervation; Female; Gl | 1980 |
Metabolic myopathies.
Topics: Carnitine; Energy Metabolism; Exercise Test; Glycogen Storage Disease; Humans; Magnetic Resonance Sp | 1994 |
[Metabolic myopathies].
Topics: Carnitine; Carnitine O-Palmitoyltransferase; Glycogen; Glycogen Storage Disease; Humans; Mitochondri | 1979 |
10 other studies available for carnitine and Glycogenosis
| Article | Year |
|---|---|
[Diagnostic significance of muscle biopsies in metabolic myopathies. II. Clinical biochemistry].
Topics: Adult; Biopsy; Carnitine; Diagnosis, Differential; Electrophoresis, Polyacrylamide Gel; Glycogen Sto | 1984 |
["Metabolic" myocardiopathies in childhood (author's transl)].
Topics: Cardiomyopathies; Carnitine; Diabetes Mellitus; Echocardiography; Glycogen Storage Disease; Humans; | 1981 |
[Muscular diseases: epidemiology of progressive muscular dystrophies].
Topics: Adenosine Monophosphate; Carnitine; Carnitine O-Palmitoyltransferase; Consanguinity; Dietary Fats; G | 1981 |
[Congenital myopathy with lipid and glycogen overload of muscle fiber and partial deficit of carnitine].
Topics: Carnitine; Glycogen Storage Disease; Glycogen Storage Disease Type I; Humans; Infant; Lipidoses; Mal | 1980 |
Pathology of inflammatory and metabolic myopathies.
Topics: AMP Deaminase; Carnitine; Carnitine O-Palmitoyltransferase; Glycogen Storage Disease; Humans; Lipido | 1981 |
Muscle disorders in the floppy child.
Topics: Biopsy; Carnitine; Child; Glycogen Storage Disease; Humans; Infant; Muscles; Muscular Atrophy; Muscu | 1978 |
Myopathies due to enzyme deficiencies.
Topics: Adult; Carnitine; Carnitine O-Palmitoyltransferase; Enzymes; Female; Glucan 1,4-alpha-Glucosidase; G | 1985 |
Metabolic response to exercise and muscle disease.
Topics: Adenosine Triphosphatases; Calcium; Carnitine; Carnitine O-Palmitoyltransferase; Female; Glycogen; G | 1986 |
Infantile muscle glycogen storage disease: phosphoglucomutase deficiency with decreased muscle and serum carnitine levels.
Topics: Carnitine; Glycogen Storage Disease; Humans; Infant; Male; Muscles; Phosphoglucomutase | 1988 |
Dicarboxylicaciduria and secondary carnitine deficiency in glycogenosis type IV.
Topics: Carnitine; Dicarboxylic Acids; Glycogen Storage Disease; Glycogen Storage Disease Type IV; Humans; I | 1987 |