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P Di Natale

Showing results (41-50 of 72) with videos related to

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Clinical Genetics|June 1, 1979
Sanfilippo B syndrome (MPS III B): mild and severe forms within the same sibshipG Andria, P Di Natale, E Del Giudice, 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.
Prenatal Diagnosis|October 1, 1987
First-trimester prenatal diagnosis of Sanfilippo C diseaseP Di Natale, N Pannone, G D'Argenio, 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.
Biochimica Et Biophysica Acta|December 4, 2001
The effect of four mutations on the expression of iduronate-2-sulfatase in mucopolysaccharidosis type IIG Bonuccelli, P Di Natale, F Corsolini, et al.
Genomics|June 1, 1993
Cloning and characterization of the cDNA for the murine iduronate sulfatase geneA Daniele, C J Faust, G E Herman, et al.
European Journal of Medical Genetics|July 1, 2008
Precocious puberty in Sanfilippo IIIA disease: diagnosis and follow-up of two new casesD Concolino, G Muzzi, L Pisaturo, 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.
Human Mutation|January 1, 1997
Mucopolysaccharidosis type II: identification of six novel mutations in Italian patientsG R Villani, N Balzano, M Grosso, et al.
Prenatal Diagnosis|October 16, 1999
Prenatal diagnosis of sanfilippo type A syndrome in a family with S66W mutant alleleP Di Natale, G R Villani, S Esposito, et al.
Pageof 8

Showing results (41-50 of 72) with videos related to

Sort By:
Pageof 8
Clinical Genetics|June 1, 1979
Sanfilippo B syndrome (MPS III B): mild and severe forms within the same sibshipG Andria, P Di Natale, E Del Giudice, 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.
Prenatal Diagnosis|October 1, 1987
First-trimester prenatal diagnosis of Sanfilippo C diseaseP Di Natale, N Pannone, G D'Argenio, 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.
Biochimica Et Biophysica Acta|December 4, 2001
The effect of four mutations on the expression of iduronate-2-sulfatase in mucopolysaccharidosis type IIG Bonuccelli, P Di Natale, F Corsolini, et al.
Genomics|June 1, 1993
Cloning and characterization of the cDNA for the murine iduronate sulfatase geneA Daniele, C J Faust, G E Herman, et al.
European Journal of Medical Genetics|July 1, 2008
Precocious puberty in Sanfilippo IIIA disease: diagnosis and follow-up of two new casesD Concolino, G Muzzi, L Pisaturo, 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.
Human Mutation|January 1, 1997
Mucopolysaccharidosis type II: identification of six novel mutations in Italian patientsG R Villani, N Balzano, M Grosso, et al.
Prenatal Diagnosis|October 16, 1999
Prenatal diagnosis of sanfilippo type A syndrome in a family with S66W mutant alleleP Di Natale, G R Villani, S Esposito, et al.
Pageof 8