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Levocarnitine

Known as: 3-Carboxy-2-hydroxy-N,N,N-trimethyl-1-propanaminium hydroxide, inner salt, Vitamin BT, Levocarnitina 
A form of carnitine, which is a substance made in muscle and liver tissue and found in certain foods, such as meat, poultry, fish, and some dairy… 
National Institutes of Health

Related topics

Related topics

19 relations
Carboxymethylcellulose Sodium 5 MG/ML / Glycerin 9 MG/ML Ophthalmic SolutionDeficiency DiseasesDrug AllergyHYDROXYCUT ADVANCED WEIGHT LOSS FORMULA, EPHEDRA-FREE

Narrower (4)

Carni Q-Gel ForteCarnitorLEVOCARNITINE HYDROCHLORIDELEVOCARNITINE TARTRATE

Broader (1)

Carnitine

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Review
2013
Review
2013
The SLC22 family with transporters of organic cations, anions and zwitterions.
Review
2010
Review
2010
Pharmacological Treatment of Painful HIV-Associated Sensory Neuropathy: A Systematic Review and Meta-Analysis of Randomised Controlled Trials
Background Significant pain from HIV-associated sensory neuropathy (HIV-SN) affects ∼40% of HIV infected individuals treated with… 
Review
2008
Review
2008
Cellular Stress Response: A Novel Target for Chemoprevention and Nutritional Neuroprotection in Aging, Neurodegenerative Disorders and Longevity
The predominant molecular symptom of aging is the accumulation of altered gene products. Moreover, several conditions including… 
Review
2007
Review
2007
The Effects and Mechanisms of Mitochondrial Nutrient α-Lipoic Acid on Improving Age-Associated Mitochondrial and Cognitive Dysfunction: An Overview
We have identified a group of nutrients that can directly or indirectly protect mitochondria from oxidative damage and improve… 
Highly Cited
2006
Highly Cited
2006
Natural History, Outcome, and Treatment Efficacy in Children and Adults with Glutaryl-CoA Dehydrogenase Deficiency
Glutaryl-CoA dehydrogenase (GCDH) deficiency is a rare inborn disorder of l-lysine, l-hydroxylysine, and l-tryptophan metabolism… 
Review
1997
Review
1997
Glucose metabolism in the ischemic heart.
A number of clinical trials are presently evaluating whether stimulating glucose metabolism is an effective therapeutic approach… 
Highly Cited
1996
Highly Cited
1996
Clinical course, early diagnosis, treatment, and prevention of disease in glutaryl-CoA dehydrogenase deficiency.
BACKGROUND Glutaryl-CoA dehydrogenase deficiency (GDD) is a recessively inherited neurometabolic disorder associated with… 
Highly Cited
1990
Highly Cited
1990
Radioisotopic assays of CoASH and carnitine and their acetylated forms in human skeletal muscle.
Highly Cited
1975
Highly Cited
1975
The syndrome of systemic carnitine deficiency
An 11 -year-old boy had had recurrent episodes of hepatic and cerebral dysfunction and underdeveloped musculature. Overt weakness… 
Highly Cited
1974
Highly Cited
1974
Carnitine levels in human serum in health and disease.
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