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G Andria

Showing results (21-30 of 137) with videos related to

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Biochimica Et Biophysica Acta|August 9, 1972
Enzymic activities of the brush border membrane of rat intestine hydrolyzing -naphthylamides of amino acids, leucinamide and dipeptidesS Auricchio, M Pierro, G Andria, et al.
Journal Francais D'Ophtalmologie|January 1, 1980
[Juvenilis macular degeneration in a family affected by cystinuria]G M Greco, A Magli, G Bonavolonta, et al.
Journal of Medical Genetics|December 1, 1983
Severe cardiac anomalies in sibs with Larsen syndromeP Strisciuglio, G Sebastio, G Andria, et al.
Advances in Experimental Medicine and Biology|January 1, 1977
On the mechanism of renaturation of proteins containing disulfide bondsH Taniuchi, A S Acharya, G Andria, et al.
European Journal of Pediatrics|September 1, 1984
Steroid sulphatase deficiency and hypogonadismG Andria, A Ballabio, G Parenti, et al.
Clinical Genetics|April 1, 1988
A simplified test to detect PKU heterozygotes by discriminant analysis in mentally retarded children and their mothersR Sartorio, L Greco, R Carrozzo, et al.
American Journal of Human Genetics|December 1, 1996
A 68-bp insertion found in a homocystinuric patient is a common variant and is skipped by alternative splicing of the cystathionine beta-synthase mRNAM P Sperandeo, R de Franchis, G Andria, et al.
Clinical Genetics|May 1, 1996
A mild form of Roberts/SC phocomelia syndrome with asymmetrical reduction of the upper limbsD Concolino, D Sperlì, R Cinti, et al.
Journal of Medical Genetics|October 1, 1993
Long survival of a patient with Marshall-Smith syndrome without respiratory complicationsD Sperli, D Concolino, C Barbato, et al.
Pediatric Research|February 1, 1973
Enzymatic activity hydrolyzing -glutamyl- -naphthylamide in human intestine during adult and fetal lifeS Auricchio, F Ciccimarra, A Vegnente, et al.
Pageof 14

Showing results (21-30 of 137) with videos related to

Sort By:
Pageof 14
Biochimica Et Biophysica Acta|August 9, 1972
Enzymic activities of the brush border membrane of rat intestine hydrolyzing -naphthylamides of amino acids, leucinamide and dipeptidesS Auricchio, M Pierro, G Andria, et al.
Journal Francais D'Ophtalmologie|January 1, 1980
[Juvenilis macular degeneration in a family affected by cystinuria]G M Greco, A Magli, G Bonavolonta, et al.
Journal of Medical Genetics|December 1, 1983
Severe cardiac anomalies in sibs with Larsen syndromeP Strisciuglio, G Sebastio, G Andria, et al.
Advances in Experimental Medicine and Biology|January 1, 1977
On the mechanism of renaturation of proteins containing disulfide bondsH Taniuchi, A S Acharya, G Andria, et al.
European Journal of Pediatrics|September 1, 1984
Steroid sulphatase deficiency and hypogonadismG Andria, A Ballabio, G Parenti, et al.
Clinical Genetics|April 1, 1988
A simplified test to detect PKU heterozygotes by discriminant analysis in mentally retarded children and their mothersR Sartorio, L Greco, R Carrozzo, et al.
American Journal of Human Genetics|December 1, 1996
A 68-bp insertion found in a homocystinuric patient is a common variant and is skipped by alternative splicing of the cystathionine beta-synthase mRNAM P Sperandeo, R de Franchis, G Andria, et al.
Clinical Genetics|May 1, 1996
A mild form of Roberts/SC phocomelia syndrome with asymmetrical reduction of the upper limbsD Concolino, D Sperlì, R Cinti, et al.
Journal of Medical Genetics|October 1, 1993
Long survival of a patient with Marshall-Smith syndrome without respiratory complicationsD Sperli, D Concolino, C Barbato, et al.
Pediatric Research|February 1, 1973
Enzymatic activity hydrolyzing -glutamyl- -naphthylamide in human intestine during adult and fetal lifeS Auricchio, F Ciccimarra, A Vegnente, et al.
Pageof 14