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G Novelli

Showing results (201-210 of 330) with videos related to

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Transplantation Proceedings|May 31, 2011
Management of sepsis during MARS treatment in acute on chronic liver failureG Novelli, V Morabito, F Pugliese, et al.
The Turkish Journal of Pediatrics|October 1, 1996
RFLP discordance in a PKU family due to a deletion in the PAH geneP Bosco, N Ceratto, F Cali, et al.
The European Respiratory Journal|July 2, 2011
Rescue of murine silica-induced lung injury and fibrosis by human embryonic stem cellsP Spitalieri, M C Quitadamo, A Orlandi, et al.
Cytogenetics and Cell Genetics|January 1, 1996
Assignment of the hexokinase type 3 gene (HK3) to human chromosome band 5q35.3 by somatic cell hybrids and in situ hybridizationA Colosimo, G Calabrese, M Gennarelli, et al.
American Journal of Medical Genetics|July 3, 1995
Two pedigrees of autosomal dominant atrioventricular canal defect (AVCD): exclusion from the critical region on 8pF Amati, A Mari, R Mingarelli, et al.
Annals of Human Genetics|December 16, 2004
Characterization of the loricrin (LOR) gene as a positional candidate for the PSORS4 psoriasis susceptibility locusE Giardina, F Capon, M C De Rosa, et al.
Human Genetics|April 6, 1999
Genomic structure, promoter characterisation and mutational analysis of the S100A7 gene: exclusion of a candidate for familial psoriasis susceptibilityS Semprini, F Capon, S Bovolenta, et al.
Transplantation Proceedings|February 1, 1996
Multiple organ harvesting: evolution of surgical technique--personal experienceD Alfani, P Berloco, P Bruzzone, et al.
Genomics|May 1, 1991
The search for south European cystic fibrosis mutations: identification of two new mutations, four variants, and intronic sequencesP Gasparini, V Nunes, A Savoia, et al.
American Journal of Human Genetics|September 14, 2000
Mapping a dominant form of multinodular goiter to chromosome Xp22F Capon, A Tacconelli, E Giardina, et al.
Pageof 33

Showing results (201-210 of 330) with videos related to

Sort By:
Pageof 33
Transplantation Proceedings|May 31, 2011
Management of sepsis during MARS treatment in acute on chronic liver failureG Novelli, V Morabito, F Pugliese, et al.
The Turkish Journal of Pediatrics|October 1, 1996
RFLP discordance in a PKU family due to a deletion in the PAH geneP Bosco, N Ceratto, F Cali, et al.
The European Respiratory Journal|July 2, 2011
Rescue of murine silica-induced lung injury and fibrosis by human embryonic stem cellsP Spitalieri, M C Quitadamo, A Orlandi, et al.
Cytogenetics and Cell Genetics|January 1, 1996
Assignment of the hexokinase type 3 gene (HK3) to human chromosome band 5q35.3 by somatic cell hybrids and in situ hybridizationA Colosimo, G Calabrese, M Gennarelli, et al.
American Journal of Medical Genetics|July 3, 1995
Two pedigrees of autosomal dominant atrioventricular canal defect (AVCD): exclusion from the critical region on 8pF Amati, A Mari, R Mingarelli, et al.
Annals of Human Genetics|December 16, 2004
Characterization of the loricrin (LOR) gene as a positional candidate for the PSORS4 psoriasis susceptibility locusE Giardina, F Capon, M C De Rosa, et al.
Human Genetics|April 6, 1999
Genomic structure, promoter characterisation and mutational analysis of the S100A7 gene: exclusion of a candidate for familial psoriasis susceptibilityS Semprini, F Capon, S Bovolenta, et al.
Transplantation Proceedings|February 1, 1996
Multiple organ harvesting: evolution of surgical technique--personal experienceD Alfani, P Berloco, P Bruzzone, et al.
Genomics|May 1, 1991
The search for south European cystic fibrosis mutations: identification of two new mutations, four variants, and intronic sequencesP Gasparini, V Nunes, A Savoia, et al.
American Journal of Human Genetics|September 14, 2000
Mapping a dominant form of multinodular goiter to chromosome Xp22F Capon, A Tacconelli, E Giardina, et al.
Pageof 33