carnitine has been researched along with Hemiplegia in 3 studies
Hemiplegia: Severe or complete loss of motor function on one side of the body. This condition is usually caused by BRAIN DISEASES that are localized to the cerebral hemisphere opposite to the side of weakness. Less frequently, BRAIN STEM lesions; cervical SPINAL CORD DISEASES; PERIPHERAL NERVOUS SYSTEM DISEASES; and other conditions may manifest as hemiplegia. The term hemiparesis (see PARESIS) refers to mild to moderate weakness involving one side of the body.
Excerpt | Relevance | Reference |
---|---|---|
"L-Carnitine deficiency is a rare metabolic disorder leading to cerebral infarctions, as seen in our five patients, and should be considered in the differential diagnosis of children who have had a stroke, particularly when associated with hypoglycemia and myopathy." | 3.69 | MR in children with L-carnitine deficiency. ( Barrow, M; Castillo, M; Mukherji, SK; Smith, M; Thompson, JE, 1996) |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 3 (100.00) | 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 |
---|---|
Vallée, L | 1 |
Fontaine, M | 1 |
Nuyts, JP | 1 |
Ricart, G | 1 |
Krivosic, I | 1 |
Divry, P | 1 |
Vianey-Saban, C | 1 |
Lhermitte, M | 1 |
Vamecq, J | 1 |
Thompson, JE | 1 |
Smith, M | 1 |
Castillo, M | 1 |
Barrow, M | 1 |
Mukherji, SK | 1 |
Steen, C | 1 |
Baumgartner, ER | 1 |
Duran, M | 1 |
Lehnert, W | 1 |
Suormala, T | 1 |
Fingerhut, R | 1 |
Stehn, M | 1 |
Kohlschütter, A | 1 |
3 other studies available for carnitine and Hemiplegia
Article | Year |
---|---|
Stroke, hemiparesis and deficient mitochondrial beta-oxidation.
Topics: Carnitine; Cerebrovascular Disorders; Child, Preschool; Fatty Acid Desaturases; Glutarates; Hemipleg | 1994 |
MR in children with L-carnitine deficiency.
Topics: Adolescent; Carnitine; Cause of Death; Cerebral Hemorrhage; Cerebral Infarction; Cerebral Ventricles | 1996 |
Metabolic stroke in isolated 3-methylcrotonyl-CoA carboxylase deficiency.
Topics: Amino Acid Metabolism, Inborn Errors; Carbon-Carbon Ligases; Carnitine; Diet, Protein-Restricted; Fa | 1999 |