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G R Villani

Showing results (1-10 of 21) with videos related to

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Human Mutation|April 17, 1999
Two novel mutations of the arylsulfatase B gene in two Italian patients with severe form of mucopolysaccharidosis. Mutations in brief no. 127. OnlineG R Villani, N Balzano, P Di Natale
Biochimica Et Biophysica Acta|June 6, 2000
Expression of five iduronate-2-sulfatase site-directed mutationsG R Villani, A Daniele, N Balzano, et al.
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics|January 1, 1996
[Mutation analysis in Hunter patients]G R Villani, N Balzano, M Grosso, et al.
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics|January 1, 1996
[Mucopolysaccharidosis II (Hunter syndrome): identification of the carrier state of the disease by means of mutation analysis]N Balzano, G R Villani, G Coppa, et al.
Human Mutation|April 29, 1998
Identification of molecular defects in Italian Sanfilippo A patients including 13 novel mutationsP Di Natale, N Balzano, S Esposito, et al.
Pediatric Neurology|October 6, 2001
Extraneurologic symptoms as presenting signs of Sanfilippo diseaseR Barone, A Fiumara, G R Villani, et al.
Human Mutation|April 24, 1999
Detection of four novel mutations in the iduronate-2-sulfatase gene. Mutations in brief no. 123. OnlineN Balzano, G R Villani, M Grosso, et al.
International Journal of Molecular Medicine|September 24, 1999
Bone marrow transplantation in a Hunter patient with P266H mutationG V Coppa, O Gabrielli, R Cordiali, et al.
Toxicology|January 1, 1992
Effect of avarol and avarone on in vitro-induced microsomal lipid peroxidationM A Belisario, M Maturo, R Pecce, et al.
Biochimica Et Biophysica Acta|February 26, 1999
Maroteaux-lamy syndrome: five novel mutations and their structural localizationG R Villani, N Balzano, D Vitale, et al.
Pageof 3

Showing results (1-10 of 21) with videos related to

Sort By:
Pageof 3
Human Mutation|April 17, 1999
Two novel mutations of the arylsulfatase B gene in two Italian patients with severe form of mucopolysaccharidosis. Mutations in brief no. 127. OnlineG R Villani, N Balzano, P Di Natale
Biochimica Et Biophysica Acta|June 6, 2000
Expression of five iduronate-2-sulfatase site-directed mutationsG R Villani, A Daniele, N Balzano, et al.
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics|January 1, 1996
[Mutation analysis in Hunter patients]G R Villani, N Balzano, M Grosso, et al.
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics|January 1, 1996
[Mucopolysaccharidosis II (Hunter syndrome): identification of the carrier state of the disease by means of mutation analysis]N Balzano, G R Villani, G Coppa, et al.
Human Mutation|April 29, 1998
Identification of molecular defects in Italian Sanfilippo A patients including 13 novel mutationsP Di Natale, N Balzano, S Esposito, et al.
Pediatric Neurology|October 6, 2001
Extraneurologic symptoms as presenting signs of Sanfilippo diseaseR Barone, A Fiumara, G R Villani, et al.
Human Mutation|April 24, 1999
Detection of four novel mutations in the iduronate-2-sulfatase gene. Mutations in brief no. 123. OnlineN Balzano, G R Villani, M Grosso, et al.
International Journal of Molecular Medicine|September 24, 1999
Bone marrow transplantation in a Hunter patient with P266H mutationG V Coppa, O Gabrielli, R Cordiali, et al.
Toxicology|January 1, 1992
Effect of avarol and avarone on in vitro-induced microsomal lipid peroxidationM A Belisario, M Maturo, R Pecce, et al.
Biochimica Et Biophysica Acta|February 26, 1999
Maroteaux-lamy syndrome: five novel mutations and their structural localizationG R Villani, N Balzano, D Vitale, et al.
Pageof 3