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C Angelini

Showing results (1-10 of 531) with videos related to

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Journal of Neurology|November 26, 1976
Lipid storage myopathies. A review of metabolic defect and of treatmentC Angelini
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|June 9, 2005
Limb-girdle muscular dystrophies: heterogeneity of clinical phenotypes and pathogenetic mechanismsC Angelini
Acta Neurologica|October 1, 1989
[Alterations of mitochondria in metabolic diseases. Carnitine deficiency, carnitine palmitoyltransferase deficiency and beta oxidation]C Angelini
Bailliere'S Clinical Endocrinology and Metabolism|September 1, 1990
Defects of fatty-acid oxidation in muscleC Angelini
Lancet (London, England)|September 20, 1975
Letter: Carnitine deficiencyC Angelini
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|February 15, 2011
State of the art in muscle glycogenosesC Angelini
Rivista Siciliana Della Tubercolosi E Delle Malattie Dell'Apparato Respiratorio|February 19, 2014
[On 2 cases of Friedreich's disease with electrocardiographic changes and hypopotassemia]C ANGELINI
Rivista Di Patologia Nervosa E Mentale|June 1, 1970
[Thyrotoxic and hypothyroid myopathy. Biochemical and histopathological study]C Angelini
Neuromuscular Disorders : NMD|July 17, 1999
Infantile lipid storage myopathy with nocturnal hypoventilation shows abnormal low-affinity muscle carnitine uptake in vitroL Vergani, C Angelini
Today'S OR Nurse|June 1, 1984
Putting the bite on mandibular deficiencyC Angelini, M Schmidt
Pageof 54

Showing results (1-10 of 531) with videos related to

Sort By:
Pageof 54
Journal of Neurology|November 26, 1976
Lipid storage myopathies. A review of metabolic defect and of treatmentC Angelini
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|June 9, 2005
Limb-girdle muscular dystrophies: heterogeneity of clinical phenotypes and pathogenetic mechanismsC Angelini
Acta Neurologica|October 1, 1989
[Alterations of mitochondria in metabolic diseases. Carnitine deficiency, carnitine palmitoyltransferase deficiency and beta oxidation]C Angelini
Bailliere'S Clinical Endocrinology and Metabolism|September 1, 1990
Defects of fatty-acid oxidation in muscleC Angelini
Lancet (London, England)|September 20, 1975
Letter: Carnitine deficiencyC Angelini
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|February 15, 2011
State of the art in muscle glycogenosesC Angelini
Rivista Siciliana Della Tubercolosi E Delle Malattie Dell'Apparato Respiratorio|February 19, 2014
[On 2 cases of Friedreich's disease with electrocardiographic changes and hypopotassemia]C ANGELINI
Rivista Di Patologia Nervosa E Mentale|June 1, 1970
[Thyrotoxic and hypothyroid myopathy. Biochemical and histopathological study]C Angelini
Neuromuscular Disorders : NMD|July 17, 1999
Infantile lipid storage myopathy with nocturnal hypoventilation shows abnormal low-affinity muscle carnitine uptake in vitroL Vergani, C Angelini
Today'S OR Nurse|June 1, 1984
Putting the bite on mandibular deficiencyC Angelini, M Schmidt
Pageof 54