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Genetic disorders of mitochondrial fatty acid oxidation
C. A. Stanley,
D. E. Hale
Resultado de la investigación
:
Review article
›
revisión exhaustiva
28
Citas (Scopus)
Información general
Huella
Huella
Profundice en los temas de investigación de 'Genetic disorders of mitochondrial fatty acid oxidation'. En conjunto forman una huella única.
Clasificar por
Ponderación
Alfabéticamente
Medicine and Dentistry
Cardiology
20%
Cardiomyopathy
20%
Child
20%
Childbirth
20%
Combination Therapy
20%
Diagnosis
20%
Diagnostic Procedure
20%
Differential Diagnosis
20%
Diseases
100%
Endocrinology
20%
Enzyme
20%
Fatty Acid Oxidation
60%
Genetic Disorder
60%
Hypoglycemia
20%
Infant
20%
Medium-Chain Acyl-Coenzyme A Dehydrogenase Deficiency
20%
Metabolism
40%
Muscle Weakness
20%
Neurology
20%
Pediatrician
20%
Phenotype
20%
Recognition
20%
Reye Syndrome
20%
Skeletal Muscle
20%
Sudden Infant Death Syndrome
20%
Biochemistry, Genetics and Molecular Biology
Beta Oxidation
60%
Birth
20%
Genetic Disorder
40%
Genetics
40%
Lysozyme
20%
Medium-Chain Acyl-Coenzyme A Dehydrogenase Deficiency
20%
Metabolic Pathway
40%
Phenotype
20%
Recognition
20%
Skeletal Muscle
20%
Neuroscience
Cardiomyopathy
20%
Differential Diagnosis
20%
Endocrinology
20%
Enzymes
20%
Familiarity
20%
Gastroenterology
20%
Hypoglycemia
20%
Phenotype
20%
Recognition
20%
Reye Syndrome
20%
Skeletal Muscle
20%
Immunology and Microbiology
Birth
20%
Fatty Acid Oxidation
60%
Metabolism
40%
Phenotype
20%
Recognition
20%
Skeletal Muscle
20%
Pharmacology, Toxicology and Pharmaceutical Science
Medium Chain Acyl Coenzyme A Dehydrogenase Deficiency
20%
Sudden Infant Death Syndrome
20%