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I Dianzani

Showing results (1-10 of 80) with videos related to

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Haematologica|November 1, 1996
Diamond-Blackfan anemia: a congenital defect in erythropoiesisI Dianzani, E Garelli, U Ramenghi
Paediatric Drugs|October 7, 2000
Diamond-Blackfan Anaemia: an overviewI Dianzani, E Garelli, U Ramenghi
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics|July 1, 1984
[Wolfram's syndrome. Presentation of a case]F Cerutti, R Balboni, I Dianzani, et al.
The Biochemical Journal|December 17, 1998
Diminished expression of phosphatidylethanolamine N-methyltransferase 2 during hepatocarcinogenesisL Tessitore, I Dianzani, Z Cui, et al.
European Journal of Pediatrics|June 1, 1996
Phenotyping of phenylketonuric patients by oral phenylalanine loadingA Ponzone, M Spada, L de Sanctis, et al.
British Journal of Haematology|September 1, 1991
A spontaneous mutation causing unstable Hb Hammersmith: detection of the beta 42 TTT----TCT change by CCM and direct sequencingI Dianzani, S Ramus, R G Cotton, et al.
Trends in Genetics : TIG|December 1, 1993
Dilemmas and progress in mutation detectionI Dianzani, C Camaschella, A Ponzone, et al.
Diabetes Care|January 1, 1984
Insulin-dependent diabetes mellitus and maternal ageF Cerutti, R Balboni, I Dianzani, et al.
Human Genetics|June 1, 1993
A frequent EcoRI polymorphism in the bcl-2 geneP Ghia, I Dianzani, A Serra, et al.
Advances in Experimental Medicine and Biology|January 1, 1993
The spectrum of mutations in dihydropteridine reductase deficiencyP M Smooker, D W Howells, I Dianzani, et al.
Pageof 8

Showing results (1-10 of 80) with videos related to

Sort By:
Pageof 8
Haematologica|November 1, 1996
Diamond-Blackfan anemia: a congenital defect in erythropoiesisI Dianzani, E Garelli, U Ramenghi
Paediatric Drugs|October 7, 2000
Diamond-Blackfan Anaemia: an overviewI Dianzani, E Garelli, U Ramenghi
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics|July 1, 1984
[Wolfram's syndrome. Presentation of a case]F Cerutti, R Balboni, I Dianzani, et al.
The Biochemical Journal|December 17, 1998
Diminished expression of phosphatidylethanolamine N-methyltransferase 2 during hepatocarcinogenesisL Tessitore, I Dianzani, Z Cui, et al.
European Journal of Pediatrics|June 1, 1996
Phenotyping of phenylketonuric patients by oral phenylalanine loadingA Ponzone, M Spada, L de Sanctis, et al.
British Journal of Haematology|September 1, 1991
A spontaneous mutation causing unstable Hb Hammersmith: detection of the beta 42 TTT----TCT change by CCM and direct sequencingI Dianzani, S Ramus, R G Cotton, et al.
Trends in Genetics : TIG|December 1, 1993
Dilemmas and progress in mutation detectionI Dianzani, C Camaschella, A Ponzone, et al.
Diabetes Care|January 1, 1984
Insulin-dependent diabetes mellitus and maternal ageF Cerutti, R Balboni, I Dianzani, et al.
Human Genetics|June 1, 1993
A frequent EcoRI polymorphism in the bcl-2 geneP Ghia, I Dianzani, A Serra, et al.
Advances in Experimental Medicine and Biology|January 1, 1993
The spectrum of mutations in dihydropteridine reductase deficiencyP M Smooker, D W Howells, I Dianzani, et al.
Pageof 8