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M Di Rocco

Showing results (81-90 of 115) with videos related to

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European Journal of Pediatrics|April 1, 1988
Glycogen storage disease: recommendations for treatmentJ Fernandes, J V Leonard, S W Moses, et al.
The American Journal of Pathology|June 1, 1995
Abnormal morphology of fibrillin microfibrils in fibroblast cultures from patients with neonatal Marfan syndromeM Godfrey, M Raghunath, J Cisler, et al.
Transplantation Proceedings|February 1, 1997
Comparison between HLA class I PCR-ARMS and serologic typing in cadaveric kidney transplantationD Adorno, A Canossi, F Papola, et al.
Neuropediatrics|September 3, 2005
Different molecular mechanisms leading to white matter hypomyelination in infantile onset lysosomal disordersM Di Rocco, A Rossi, G Parenti, et al.
Journal of Medical Genetics|December 5, 2006
Molecular characterisation of six patients with prolidase deficiency: identification of the first small duplication in the prolidase gene and of a mutation generating symptomatic and asymptomatic outcomes within the same familyA Lupi, A Rossi, E Campari, et al.
Transplant International : Official Journal of the European Society for Organ Transplantation|December 9, 2000
HLA class I residue mismatch and renal graft outcomeA Piazza, A Canossi, O Buonomo, et al.
Child: Care, Health and Development|April 21, 2005
Nevoid Basal Cell Carcinoma Syndrome in infants: improving diagnosisL Pastorino, R Cusano, C Baldo, et al.
Neuropediatrics|June 24, 2010
Cognitive profile in spastic paraplegia with thin corpus callosum and mutations in SPG11L Siri, F M Battaglia, A Tessa, et al.
Journal of Inherited Metabolic Disease|January 26, 2006
Congenital disorder of glycosylation (CDG) Ig: report on a patient and review of the literatureM Di Rocco, T Hennet, C E Grubenmann, et al.
Oncogene|April 25, 2012
ADAR2-editing activity inhibits glioblastoma growth through the modulation of the CDC14B/Skp2/p21/p27 axisF Galeano, C Rossetti, S Tomaselli, et al.
Pageof 12

Showing results (81-90 of 115) with videos related to

Sort By:
Pageof 12
European Journal of Pediatrics|April 1, 1988
Glycogen storage disease: recommendations for treatmentJ Fernandes, J V Leonard, S W Moses, et al.
The American Journal of Pathology|June 1, 1995
Abnormal morphology of fibrillin microfibrils in fibroblast cultures from patients with neonatal Marfan syndromeM Godfrey, M Raghunath, J Cisler, et al.
Transplantation Proceedings|February 1, 1997
Comparison between HLA class I PCR-ARMS and serologic typing in cadaveric kidney transplantationD Adorno, A Canossi, F Papola, et al.
Neuropediatrics|September 3, 2005
Different molecular mechanisms leading to white matter hypomyelination in infantile onset lysosomal disordersM Di Rocco, A Rossi, G Parenti, et al.
Journal of Medical Genetics|December 5, 2006
Molecular characterisation of six patients with prolidase deficiency: identification of the first small duplication in the prolidase gene and of a mutation generating symptomatic and asymptomatic outcomes within the same familyA Lupi, A Rossi, E Campari, et al.
Transplant International : Official Journal of the European Society for Organ Transplantation|December 9, 2000
HLA class I residue mismatch and renal graft outcomeA Piazza, A Canossi, O Buonomo, et al.
Child: Care, Health and Development|April 21, 2005
Nevoid Basal Cell Carcinoma Syndrome in infants: improving diagnosisL Pastorino, R Cusano, C Baldo, et al.
Neuropediatrics|June 24, 2010
Cognitive profile in spastic paraplegia with thin corpus callosum and mutations in SPG11L Siri, F M Battaglia, A Tessa, et al.
Journal of Inherited Metabolic Disease|January 26, 2006
Congenital disorder of glycosylation (CDG) Ig: report on a patient and review of the literatureM Di Rocco, T Hennet, C E Grubenmann, et al.
Oncogene|April 25, 2012
ADAR2-editing activity inhibits glioblastoma growth through the modulation of the CDC14B/Skp2/p21/p27 axisF Galeano, C Rossetti, S Tomaselli, et al.
Pageof 12