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A Sangalli

Showing results (1-10 of 21) with videos related to

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Molecular and Cellular Probes|May 15, 2002
Rapid and efficient genotype analysis of the COL1a1 Sp1 binding site dimorphism, a genetic marker for bone mineral densityS Mirandola, A Sangalli, M Mottes
American Journal of Medical Genetics|January 15, 1993
Haplotype analysis of collagen type I genes in the general population and in osteogenesis imperfecta familiesM Mottes, A Sangalli, P F Pignatti
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|July 14, 2001
Stickler syndrome and vitreoretinal degeneration: correlation between locus mutation and vitreous phenotype. Apropos of a caseF Parentin, A Sangalli, M Mottes, et al.
European Annals of Allergy and Clinical Immunology|December 14, 2022
Acetylsalicylic acid desensitization in an allergic pregnant woman post-vascular scaffolds implantationF Rivolta, A Chiei Gallo, A Sangalli, et al.
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|June 12, 2017
A novel mutation in ABCD1 unveils different clinical phenotypes in a family with adrenoleukodystrophyM Margoni, F Soli, A Sangalli, et al.
European Annals of Allergy and Clinical Immunology|February 13, 2024
Clavulanic acid sensitization seems more involved in cutaneous than systemic reactions in amoxicillinclavulanate drug reactionsF Rivolta, C Cappelletti, A Sangalli, et al.
The Journal of Biological Chemistry|May 20, 1994
Substitution of an aspartic acid for glycine 700 in the alpha 2(I) chain of type I collagen in a recurrent lethal type II osteogenesis imperfecta dramatically affects the mineralization of boneL Cohen-Solal, L Zylberberg, A Sangalli, et al.
Human Gene Therapy|October 6, 1998
Transduced fibroblasts and metachromatic leukodystrophy lymphocytes transfer arylsulfatase A to myelinating glia and deficient cells in vitroA Sangalli, C Taveggia, A Salviati, et al.
American Journal of Medical Genetics|January 9, 2001
Autosomal dominant benign recurrent intrahepatic cholestasis (BRIC) unlinked to 18q21 and 2q24A Floreani, M Molaro, M Mottes, et al.
The International Journal of Biochemistry & Cell Biology|November 24, 2018
RNA-binding proteins RBM20 and PTBP1 regulate the alternative splicing of FHOD3P Lorenzi, A Sangalli, S Fochi, et al.
Pageof 3

Showing results (1-10 of 21) with videos related to

Sort By:
Pageof 3
Molecular and Cellular Probes|May 15, 2002
Rapid and efficient genotype analysis of the COL1a1 Sp1 binding site dimorphism, a genetic marker for bone mineral densityS Mirandola, A Sangalli, M Mottes
American Journal of Medical Genetics|January 15, 1993
Haplotype analysis of collagen type I genes in the general population and in osteogenesis imperfecta familiesM Mottes, A Sangalli, P F Pignatti
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|July 14, 2001
Stickler syndrome and vitreoretinal degeneration: correlation between locus mutation and vitreous phenotype. Apropos of a caseF Parentin, A Sangalli, M Mottes, et al.
European Annals of Allergy and Clinical Immunology|December 14, 2022
Acetylsalicylic acid desensitization in an allergic pregnant woman post-vascular scaffolds implantationF Rivolta, A Chiei Gallo, A Sangalli, et al.
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|June 12, 2017
A novel mutation in ABCD1 unveils different clinical phenotypes in a family with adrenoleukodystrophyM Margoni, F Soli, A Sangalli, et al.
European Annals of Allergy and Clinical Immunology|February 13, 2024
Clavulanic acid sensitization seems more involved in cutaneous than systemic reactions in amoxicillinclavulanate drug reactionsF Rivolta, C Cappelletti, A Sangalli, et al.
The Journal of Biological Chemistry|May 20, 1994
Substitution of an aspartic acid for glycine 700 in the alpha 2(I) chain of type I collagen in a recurrent lethal type II osteogenesis imperfecta dramatically affects the mineralization of boneL Cohen-Solal, L Zylberberg, A Sangalli, et al.
Human Gene Therapy|October 6, 1998
Transduced fibroblasts and metachromatic leukodystrophy lymphocytes transfer arylsulfatase A to myelinating glia and deficient cells in vitroA Sangalli, C Taveggia, A Salviati, et al.
American Journal of Medical Genetics|January 9, 2001
Autosomal dominant benign recurrent intrahepatic cholestasis (BRIC) unlinked to 18q21 and 2q24A Floreani, M Molaro, M Mottes, et al.
The International Journal of Biochemistry & Cell Biology|November 24, 2018
RNA-binding proteins RBM20 and PTBP1 regulate the alternative splicing of FHOD3P Lorenzi, A Sangalli, S Fochi, et al.
Pageof 3