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Nereo Bresolin

Showing results (101-110 of 346) with videos related to

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Journal of Neurology|March 15, 2005
Association of neuronal nitric oxide synthase C276T polymorphism with Alzheimer's diseaseDaniela Galimberti, Eliana Venturelli, Alberto Gatti, et al.
Neurology Research International|November 14, 2013
Optic neuritis as isolated manifestation of leptomeningeal carcinomatosis: a case report and systematic review of ocular manifestations of neoplastic meningitisSilvia Lanfranconi, Paola Basilico, Ilaria Trezzi, et al.
BMC Evolutionary Biology|June 3, 2009
A complex selection signature at the human AVPR1B geneRachele Cagliani, Matteo Fumagalli, Uberto Pozzoli, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|September 19, 2008
Charcot-Marie-Tooth type 1a in a child with Long QT syndromeLuciana Losito, Marta De Rinaldis, Leonarda Gennaro, et al.
Archives of Neurology|November 16, 2005
Muscle coenzyme Q10 level in statin-related myopathyCostanza Lamperti, Ali B Naini, Valeria Lucchini, et al.
Journal of Cardiovascular Medicine (Hagerstown, Md.)|February 28, 2008
Migraine, stroke and patent foramen ovale: a dangerous trio?Gianfranco Butera, Elio Agostoni, Giuseppe Biondi-Zoccai, et al.
Human Genetics|May 1, 2004
An intragenic deletion/inversion event in the DMD gene determines a novel exon creation and results in a BMD phenotypeRachele Cagliani, Manuela Sironi, Emma Ciafaloni, et al.
Muscle & Nerve|August 20, 2004
Developmental and tissue-specific regulation of a novel dysferlin isoformSabrina Salani, Sabrina Lucchiari, Francesco Fortunato, et al.
Cellular and Molecular Life Sciences : CMLS|March 4, 2020
Current understanding of and emerging treatment options for spinal muscular atrophy with respiratory distress type 1 (SMARD1)Martina G L Perego, Noemi Galli, Monica Nizzardo, et al.
Ageing Research Reviews|September 24, 2020
Insights into disease mechanisms and potential therapeutics for C9orf72-related amyotrophic lateral sclerosis/frontotemporal dementiaDelia Gagliardi, Gianluca Costamagna, Michela Taiana, et al.
Pageof 35

Showing results (101-110 of 346) with videos related to

Sort By:
Pageof 35
Journal of Neurology|March 15, 2005
Association of neuronal nitric oxide synthase C276T polymorphism with Alzheimer's diseaseDaniela Galimberti, Eliana Venturelli, Alberto Gatti, et al.
Neurology Research International|November 14, 2013
Optic neuritis as isolated manifestation of leptomeningeal carcinomatosis: a case report and systematic review of ocular manifestations of neoplastic meningitisSilvia Lanfranconi, Paola Basilico, Ilaria Trezzi, et al.
BMC Evolutionary Biology|June 3, 2009
A complex selection signature at the human AVPR1B geneRachele Cagliani, Matteo Fumagalli, Uberto Pozzoli, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|September 19, 2008
Charcot-Marie-Tooth type 1a in a child with Long QT syndromeLuciana Losito, Marta De Rinaldis, Leonarda Gennaro, et al.
Archives of Neurology|November 16, 2005
Muscle coenzyme Q10 level in statin-related myopathyCostanza Lamperti, Ali B Naini, Valeria Lucchini, et al.
Journal of Cardiovascular Medicine (Hagerstown, Md.)|February 28, 2008
Migraine, stroke and patent foramen ovale: a dangerous trio?Gianfranco Butera, Elio Agostoni, Giuseppe Biondi-Zoccai, et al.
Human Genetics|May 1, 2004
An intragenic deletion/inversion event in the DMD gene determines a novel exon creation and results in a BMD phenotypeRachele Cagliani, Manuela Sironi, Emma Ciafaloni, et al.
Muscle & Nerve|August 20, 2004
Developmental and tissue-specific regulation of a novel dysferlin isoformSabrina Salani, Sabrina Lucchiari, Francesco Fortunato, et al.
Cellular and Molecular Life Sciences : CMLS|March 4, 2020
Current understanding of and emerging treatment options for spinal muscular atrophy with respiratory distress type 1 (SMARD1)Martina G L Perego, Noemi Galli, Monica Nizzardo, et al.
Ageing Research Reviews|September 24, 2020
Insights into disease mechanisms and potential therapeutics for C9orf72-related amyotrophic lateral sclerosis/frontotemporal dementiaDelia Gagliardi, Gianluca Costamagna, Michela Taiana, et al.
Pageof 35