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F Piccolo

Showing results (11-20 of 32) with videos related to

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Pediatrie|July 1, 1981
[Persistent idiopathic lactic acidosis in a child (association with obesity and glucose intolerance]L Chini, B Bacchielli, F Mancini, et al.
Neuroepidemiology|January 1, 1995
Frequency of duplication at 17p11.2 in families of northeast Italy with Charcot-Marie-Tooth disease type 1M L Mostacciuolo, F Schiavon, C Angelini, et al.
Developmental Medicine and Child Neurology|December 11, 1997
Absence of alpha-sarcoglycan and novel missense mutations in the alpha-sarcoglycan gene in a young British girl with muscular dystrophyR M Quinlivan, S A Robb, C Sewry, et al.
The Journal of Applied Psychology|September 14, 2011
Explaining the justice-performance relationship: trust as exchange deepener or trust as uncertainty reducer?Jason A Colquitt, Jeffery A Lepine, Ronald F Piccolo, et al.
Arthritis and Rheumatism|June 1, 1990
Inflammation and cartilage metabolism in rheumatoid arthritis. Studies of the blood markers hyaluronic acid, orosomucoid, and keratan sulfateA R Poole, J Witter, N Roberts, et al.
Minerva Pediatrica|June 30, 2005
[Depressive symptoms and low self-esteem in obese children and adolescents]S Cortese, M Cuzzolaro, C Maffeis, et al.
Child'S Brain|January 1, 1982
Medical therapy of true precocious puberty due to hamartoma of the tuber cinereum. A report of 2 casesF Piccolo, S Conti, L Bozzao, et al.
Neuromuscular Disorders : NMD|December 1, 1996
Abnormalities in alpha-, beta- and gamma-sarcoglycan in patients with limb-girdle muscular dystrophyC A Sewry, J Taylor, L V Anderson, et al.
Nature Genetics|June 1, 1995
Primary adhalinopathy: a common cause of autosomal recessive muscular dystrophy of variable severityF Piccolo, S L Roberds, M Jeanpierre, et al.
Acta Paediatrica Scandinavica|May 1, 1980
Albright's hereditary osteodystrophyB Boscherini, G Coen, G Bianchini, et al.
Pageof 4

Showing results (11-20 of 32) with videos related to

Sort By:
Pageof 4
Pediatrie|July 1, 1981
[Persistent idiopathic lactic acidosis in a child (association with obesity and glucose intolerance]L Chini, B Bacchielli, F Mancini, et al.
Neuroepidemiology|January 1, 1995
Frequency of duplication at 17p11.2 in families of northeast Italy with Charcot-Marie-Tooth disease type 1M L Mostacciuolo, F Schiavon, C Angelini, et al.
Developmental Medicine and Child Neurology|December 11, 1997
Absence of alpha-sarcoglycan and novel missense mutations in the alpha-sarcoglycan gene in a young British girl with muscular dystrophyR M Quinlivan, S A Robb, C Sewry, et al.
The Journal of Applied Psychology|September 14, 2011
Explaining the justice-performance relationship: trust as exchange deepener or trust as uncertainty reducer?Jason A Colquitt, Jeffery A Lepine, Ronald F Piccolo, et al.
Arthritis and Rheumatism|June 1, 1990
Inflammation and cartilage metabolism in rheumatoid arthritis. Studies of the blood markers hyaluronic acid, orosomucoid, and keratan sulfateA R Poole, J Witter, N Roberts, et al.
Minerva Pediatrica|June 30, 2005
[Depressive symptoms and low self-esteem in obese children and adolescents]S Cortese, M Cuzzolaro, C Maffeis, et al.
Child'S Brain|January 1, 1982
Medical therapy of true precocious puberty due to hamartoma of the tuber cinereum. A report of 2 casesF Piccolo, S Conti, L Bozzao, et al.
Neuromuscular Disorders : NMD|December 1, 1996
Abnormalities in alpha-, beta- and gamma-sarcoglycan in patients with limb-girdle muscular dystrophyC A Sewry, J Taylor, L V Anderson, et al.
Nature Genetics|June 1, 1995
Primary adhalinopathy: a common cause of autosomal recessive muscular dystrophy of variable severityF Piccolo, S L Roberds, M Jeanpierre, et al.
Acta Paediatrica Scandinavica|May 1, 1980
Albright's hereditary osteodystrophyB Boscherini, G Coen, G Bianchini, et al.
Pageof 4