nad has been researched along with Amyotonia Congenita in 10 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 10 (100.00) | 18.7374 |
| 1990's | 0 (0.00) | 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 |
|---|---|
| Csenkér, E; Diószeghy, P; Mechler, F; Molnár, L | 1 |
| Coquillat, G; Marescaux, C; Micheletti, G; Rohmer, F; Walter, P; Warter, JM | 1 |
| Clark, JB; Land, JM; Morgan-Hughes, JA | 1 |
| Duncan, ID; Griffiths, IR; McQueen, A | 1 |
| Siemes, H | 1 |
| Coërs, C; Telerman-Toppet, N | 1 |
| Copeland, W; Kelly, S; Smith, RO | 1 |
| Dubowitz, V; Gallup, B; Strugalska-Cynowska, H | 1 |
| Ionescu, V; Radu, H | 1 |
| Bojinov, S; Lolova, I | 1 |
10 other study(ies) available for nad and Amyotonia Congenita
| Article | Year |
|---|---|
Carbohydrate metabolites in the blood and CSF of patients with neuromuscular disorders.
Topics: Blood Glucose; Brain Chemistry; Glucose; Humans; Lactates; NAD; Neuromuscular Diseases; Pyruvates; Pyruvic Acid | 1981 |
[An autosomal recessive syndrome with myopathy and central and peripheral nervous system involvement (author's transl)].
Topics: Adenosine Triphosphatases; Adolescent; Adult; Central Nervous System; Chromosome Aberrations; Chromosome Disorders; Female; Histocytochemistry; Humans; Male; Microscopy, Electron; Muscles; NAD; Neuromuscular Diseases; Pedigree; Peripheral Nerves | 1981 |
Mitochondrial myopathy. Biochemical studies revealing a deficiency of NADH--cytochrome b reductase activity.
Topics: Adult; Cytochrome Reductases; Humans; Lactates; Male; Mitochondria, Muscle; Muscular Atrophy; NAD; NADH Dehydrogenase; Neuromuscular Diseases; Physical Exertion | 1981 |
A myopathy associated with myotonia in the dog.
Topics: Animals; Cell Nucleus; Connective Tissue; Dog Diseases; Dogs; Histocytochemistry; Hyalin; Muscles; Muscular Diseases; Myotonia; NAD; Necrosis; Neuromuscular Diseases; Regeneration; Succinate Dehydrogenase | 1975 |
[Mitochondrial myopathies and encephalomyopathies. Neuromuscular and central nervous system diseases caused by defects in mitochondrial oxidative metabolism].
Topics: Brain; Brain Diseases, Metabolic; Carnitine O-Acetyltransferase; Child; Citric Acid Cycle; Cytochromes; Energy Metabolism; Enzymes; Humans; Lactates; Lactic Acid; Mitochondria, Muscle; Muscles; NAD; Neuromuscular Diseases; Pyruvate Dehydrogenase Complex Deficiency Disease; Pyruvates; Pyruvic Acid; Succinates; Succinic Acid | 1985 |
A third muscle fibre type related to collateral reinnervation in motor neurone and peripheral nerve diseases (preliminary report).
Topics: Adenosine Triphosphatases; Dihydrolipoamide Dehydrogenase; Humans; Motor Neurons; Myofibrils; NAD; Nerve Regeneration; Neuromuscular Diseases; Peripheral Nervous System Diseases; Staining and Labeling | 1971 |
A fluorescent spot test for creatine kinase.
Topics: Buffers; Chemical Phenomena; Chemistry; Clinical Enzyme Tests; Clinical Laboratory Techniques; Creatine Kinase; Female; Fluorescence; Humans; Indicators and Reagents; Male; Mass Screening; Muscular Diseases; Muscular Dystrophies; NAD; Neuromuscular Diseases; Spectrophotometry; Time Factors | 1968 |
Histochemical studies on normal and diseased human and chick muscle in tissue culture.
Topics: Adenosine Triphosphatases; Adolescent; Adult; Aged; Animals; Cell Differentiation; Chick Embryo; Child; Child, Preschool; Culture Techniques; Female; Glucosyltransferases; Glycogen; Histocytochemistry; Humans; Infant; Infant, Newborn; Male; Middle Aged; Muscles; Myofibrils; Myosins; NAD; Neuromuscular Diseases; Species Specificity | 1972 |
Nemaline (neuro) myopathy. Rod-like bodies and type I fibre atrophy in a case of congenital hypotonia with denervation.
Topics: Adenosine Triphosphatases; Child, Preschool; Dihydrolipoamide Dehydrogenase; Electromyography; Female; Humans; Muscle Contraction; Muscles; Myofibrils; Myosins; NAD; Neuromuscular Diseases | 1972 |
Some nonspecific morphological changes in neuromuscular diseases.
Topics: Acid Phosphatase; Adenosine Triphosphatases; Adult; Alkaline Phosphatase; Amyotrophic Lateral Sclerosis; Biopsy; Child, Preschool; Dihydrolipoamide Dehydrogenase; Esterases; Glucosyltransferases; Glucuronidase; Glycerolphosphate Dehydrogenase; Histocytochemistry; Humans; L-Lactate Dehydrogenase; Muscle Denervation; Muscles; Muscular Atrophy; Muscular Dystrophies; Myositis; Myotonic Dystrophy; NAD; Neuromuscular Diseases; Succinate Dehydrogenase | 1973 |