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A Renieri

Showing results (41-50 of 106) with videos related to

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Clinical Genetics|February 28, 2004
Chromosome 2 deletion encompassing the MAP2 gene in a patient with autism and Rett-like featuresC Pescucci, I Meloni, M Bruttini, et al.
Nephron|January 1, 1994
Variability of clinical phenotype in a large Alport family with Gly 1143 Ser change of collagen alpha 5(IV)-chainA Renieri, M Meroni, A Sessa, et al.
International Journal of Cancer|April 1, 1993
Epstein-Barr virus and gastric cancer: data and unanswered questionsL Leoncini, C Vindigni, T Megha, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|January 1, 1994
De-novo COL4A5 gene mutations in Alport's syndromeL Massella, G Rizzoni, R De Blasis, et al.
Physical Review. E, Statistical, Nonlinear, and Soft Matter Physics|April 20, 2004
Saturation and electron-beam lifetime in a storage ring free-electron laserR Bartolini, G Dattoli, L Giannessi, et al.
American Journal of Human Genetics|September 14, 2000
A mutation in the rett syndrome gene, MECP2, causes X-linked mental retardation and progressive spasticity in malesI Meloni, M Bruttini, I Longo, et al.
European Journal of Human Genetics : EJHG|June 15, 2000
Preserved speech variant is allelic of classic Rett syndromeC De Bona, M Zappella, G Hayek, et al.
European Neurology|September 28, 1998
CAG repeat expansion in an italian family with spinocerebellar ataxia type 2 (SCA2): a clinical and genetic studyA Malandrini, L Galli, M Villanova, et al.
Human Genetics|October 1, 1993
Small frameshift deletions within the COL4A5 gene in juvenile-onset Alport syndromeA Renieri, M Seri, L Galli, et al.
Nephron|January 1, 1995
Renal transplantation from living donor parents in two brothers with Alport syndrome. Can asymptomatic female carriers of the Alport gene be accepted as kidney donors?A Sessa, A Pietrucci, S Carozzi, et al.
Pageof 11

Showing results (41-50 of 106) with videos related to

Sort By:
Pageof 11
Clinical Genetics|February 28, 2004
Chromosome 2 deletion encompassing the MAP2 gene in a patient with autism and Rett-like featuresC Pescucci, I Meloni, M Bruttini, et al.
Nephron|January 1, 1994
Variability of clinical phenotype in a large Alport family with Gly 1143 Ser change of collagen alpha 5(IV)-chainA Renieri, M Meroni, A Sessa, et al.
International Journal of Cancer|April 1, 1993
Epstein-Barr virus and gastric cancer: data and unanswered questionsL Leoncini, C Vindigni, T Megha, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|January 1, 1994
De-novo COL4A5 gene mutations in Alport's syndromeL Massella, G Rizzoni, R De Blasis, et al.
Physical Review. E, Statistical, Nonlinear, and Soft Matter Physics|April 20, 2004
Saturation and electron-beam lifetime in a storage ring free-electron laserR Bartolini, G Dattoli, L Giannessi, et al.
American Journal of Human Genetics|September 14, 2000
A mutation in the rett syndrome gene, MECP2, causes X-linked mental retardation and progressive spasticity in malesI Meloni, M Bruttini, I Longo, et al.
European Journal of Human Genetics : EJHG|June 15, 2000
Preserved speech variant is allelic of classic Rett syndromeC De Bona, M Zappella, G Hayek, et al.
European Neurology|September 28, 1998
CAG repeat expansion in an italian family with spinocerebellar ataxia type 2 (SCA2): a clinical and genetic studyA Malandrini, L Galli, M Villanova, et al.
Human Genetics|October 1, 1993
Small frameshift deletions within the COL4A5 gene in juvenile-onset Alport syndromeA Renieri, M Seri, L Galli, et al.
Nephron|January 1, 1995
Renal transplantation from living donor parents in two brothers with Alport syndrome. Can asymptomatic female carriers of the Alport gene be accepted as kidney donors?A Sessa, A Pietrucci, S Carozzi, et al.
Pageof 11