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Archives of Neurology
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April 1, 1972
Comparative study of acid maltase deficiency. Biochemical differences between infantile, childhood, and adult types
C Angelini, A G Engel
Journal of Neurology
|
November 14, 1997
Long-term cyclosporine treatment in a group of severe myasthenia gravis patients
D M Bonifati, C Angelini
Lancet (London, England)
|
July 10, 1976
Letter: Duchenne carrier detection
G 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 muscle
C 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-oxidation
C 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 report
G Groppo, C Angelini, A Bertone
Acta Neurologica
|
January 1, 1976
[Polyneuropathies due to adhesives. Histopathological and ultrastructural studies]
N Rizzuto, H Terzian, C Angelini
Page
of 54
Search research articles
Search
Showing results (21-30 of 531) with videos related to
Sort By:
Page
of 54
Archives of Neurology
|
April 1, 1972
Comparative study of acid maltase deficiency. Biochemical differences between infantile, childhood, and adult types
C Angelini, A G Engel
Journal of Neurology
|
November 14, 1997
Long-term cyclosporine treatment in a group of severe myasthenia gravis patients
D M Bonifati, C Angelini
Lancet (London, England)
|
July 10, 1976
Letter: Duchenne carrier detection
G 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 muscle
C 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-oxidation
C 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 report
G Groppo, C Angelini, A Bertone
Acta Neurologica
|
January 1, 1976
[Polyneuropathies due to adhesives. Histopathological and ultrastructural studies]
N Rizzuto, H Terzian, C Angelini
Page
of 54