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C Angelini

Showing results (21-30 of 531) with videos related to

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Archives of Neurology|April 1, 1972
Comparative study of acid maltase deficiency. Biochemical differences between infantile, childhood, and adult typesC Angelini, A G Engel
Journal of Neurology|November 14, 1997
Long-term cyclosporine treatment in a group of severe myasthenia gravis patientsD M Bonifati, C Angelini
Lancet (London, England)|July 10, 1976
Letter: Duchenne carrier detectionG A Danieli, C Angelini
Archives of Biochemistry and Biophysics|May 1, 1973
Subcellular distribution of acid and neutral alpha-glucosidases in normal, acid maltase deficient, and myophosphorylase deficient human skeletal muscleC Angelini, A G Engel
La Nouvelle Presse Medicale|February 21, 1981
[Systemic carnitine deficiency: its place in Reye's syndrome (author's transl)]P Chapoy, C Angelini, S Cederbaum
Acta Neurologica|November 1, 1970
[Behavior of serum isoenzymes of lactic dehydrogenase in various muscular diseases]C Angelini, G Cazzato, P Fardin
Rivista Di Patologia Nervosa E Mentale|May 1, 1981
[Report of two patients with fibromuscular dysplasia of the internal carotid artery (author's transl)]C Angelini, N Brunoro, V Gallucci
Critical Reviews in Clinical Laboratory Sciences|January 1, 1992
Clinical and biochemical aspects of carnitine deficiency and insufficiency: transport defects and inborn errors of beta-oxidationC Angelini, L Vergani, A Martinuzzi
Italian Journal of Orthopaedics and Traumatology|January 1, 1992
Percutaneous pinning of displaced supracondylar fractures of the humerus in children. Case reportG Groppo, C Angelini, A Bertone
Acta Neurologica|January 1, 1976
[Polyneuropathies due to adhesives. Histopathological and ultrastructural studies]N Rizzuto, H Terzian, C Angelini
Pageof 54

Showing results (21-30 of 531) with videos related to

Sort By:
Pageof 54
Archives of Neurology|April 1, 1972
Comparative study of acid maltase deficiency. Biochemical differences between infantile, childhood, and adult typesC Angelini, A G Engel
Journal of Neurology|November 14, 1997
Long-term cyclosporine treatment in a group of severe myasthenia gravis patientsD M Bonifati, C Angelini
Lancet (London, England)|July 10, 1976
Letter: Duchenne carrier detectionG A Danieli, C Angelini
Archives of Biochemistry and Biophysics|May 1, 1973
Subcellular distribution of acid and neutral alpha-glucosidases in normal, acid maltase deficient, and myophosphorylase deficient human skeletal muscleC Angelini, A G Engel
La Nouvelle Presse Medicale|February 21, 1981
[Systemic carnitine deficiency: its place in Reye's syndrome (author's transl)]P Chapoy, C Angelini, S Cederbaum
Acta Neurologica|November 1, 1970
[Behavior of serum isoenzymes of lactic dehydrogenase in various muscular diseases]C Angelini, G Cazzato, P Fardin
Rivista Di Patologia Nervosa E Mentale|May 1, 1981
[Report of two patients with fibromuscular dysplasia of the internal carotid artery (author's transl)]C Angelini, N Brunoro, V Gallucci
Critical Reviews in Clinical Laboratory Sciences|January 1, 1992
Clinical and biochemical aspects of carnitine deficiency and insufficiency: transport defects and inborn errors of beta-oxidationC Angelini, L Vergani, A Martinuzzi
Italian Journal of Orthopaedics and Traumatology|January 1, 1992
Percutaneous pinning of displaced supracondylar fractures of the humerus in children. Case reportG Groppo, C Angelini, A Bertone
Acta Neurologica|January 1, 1976
[Polyneuropathies due to adhesives. Histopathological and ultrastructural studies]N Rizzuto, H Terzian, C Angelini
Pageof 54