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A Ferlini

Showing results (51-60 of 88) with videos related to

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Clinical Genetics|November 1, 1983
Incidence of classic PKU in Italy estimated from consanguineous marriages and from neonatal screeningG Romeo, P Menozzi, A Ferlini, et al.
Journal of Community Genetics|March 5, 2022
Communicating the diagnosis of Klinefelter syndrome to children and adolescents: when, how, and who?L Aliberti, I Gagliardi, S Bigoni, et al.
Medical Oncology and Tumor Pharmacotherapy|January 1, 1989
Clinical and immunological assessment in HIV+ subjects receiving inosine-pranobex. A randomised, multicentric studyC De Simone, F Albertini, M Almaviva, et al.
Neuropediatrics|August 1, 1997
Expression of laminin chains in skin in merosin-deficient congenital muscular dystrophyC A Sewry, M D'Alessandro, L A Wilson, et al.
American Journal of Medical Genetics|January 2, 1995
Androgen receptor gene (CAG)n repeat analysis in the differential diagnosis between Kennedy disease and other motoneuron disordersA Ferlini, M C Patrosso, D Guidetti, et al.
European Journal of Pediatrics|May 1, 1988
Italian experience regarding the prevention of Duchenne and Becker muscular dystrophiesG Romeo, M Devoto, N Archidiacono, et al.
American Journal of Human Genetics|May 1, 1983
Incidence of Friedreich ataxia in Italy estimated from consanguineous marriagesG Romeo, P Menozzi, A Ferlini, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|November 24, 2011
Clinical, morphological and genetic studies in a cohort of 21 patients with myofibrillar myopathyG Vattemi, M Neri, S Piffer, et al.
Neurology|October 26, 1999
Transthyretin amyloidosis and superficial siderosis of the CNSM Mascalchi, F Salvi, M G Pirini, et al.
Human Genetics|April 1, 1997
The role of immunocytochemistry and linkage analysis in the prenatal diagnosis of merosin-deficient congenital muscular dystrophyI Naom, M D'Alessandro, C Sewry, et al.
Pageof 9

Showing results (51-60 of 88) with videos related to

Sort By:
Pageof 9
Clinical Genetics|November 1, 1983
Incidence of classic PKU in Italy estimated from consanguineous marriages and from neonatal screeningG Romeo, P Menozzi, A Ferlini, et al.
Journal of Community Genetics|March 5, 2022
Communicating the diagnosis of Klinefelter syndrome to children and adolescents: when, how, and who?L Aliberti, I Gagliardi, S Bigoni, et al.
Medical Oncology and Tumor Pharmacotherapy|January 1, 1989
Clinical and immunological assessment in HIV+ subjects receiving inosine-pranobex. A randomised, multicentric studyC De Simone, F Albertini, M Almaviva, et al.
Neuropediatrics|August 1, 1997
Expression of laminin chains in skin in merosin-deficient congenital muscular dystrophyC A Sewry, M D'Alessandro, L A Wilson, et al.
American Journal of Medical Genetics|January 2, 1995
Androgen receptor gene (CAG)n repeat analysis in the differential diagnosis between Kennedy disease and other motoneuron disordersA Ferlini, M C Patrosso, D Guidetti, et al.
European Journal of Pediatrics|May 1, 1988
Italian experience regarding the prevention of Duchenne and Becker muscular dystrophiesG Romeo, M Devoto, N Archidiacono, et al.
American Journal of Human Genetics|May 1, 1983
Incidence of Friedreich ataxia in Italy estimated from consanguineous marriagesG Romeo, P Menozzi, A Ferlini, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|November 24, 2011
Clinical, morphological and genetic studies in a cohort of 21 patients with myofibrillar myopathyG Vattemi, M Neri, S Piffer, et al.
Neurology|October 26, 1999
Transthyretin amyloidosis and superficial siderosis of the CNSM Mascalchi, F Salvi, M G Pirini, et al.
Human Genetics|April 1, 1997
The role of immunocytochemistry and linkage analysis in the prenatal diagnosis of merosin-deficient congenital muscular dystrophyI Naom, M D'Alessandro, C Sewry, et al.
Pageof 9