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Carlo Minetti

Showing results (31-40 of 190) with videos related to

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Neuromuscular Disorders : NMD|February 4, 2009
White matter lesions in spastic paraplegia with mutations in SPG5/CYP7B1Roberta Biancheri, Marianna Ciccolella, Andrea Rossi, et al.
Epilepsia|March 24, 2011
Natural history and long-term evolution in families with autosomal dominant cortical tremor, myoclonus, and epilepsyAntonietta Coppola, Lia Santulli, Luigi Del Gaudio, et al.
Epilepsia|January 19, 2006
A novel SCN2A mutation in family with benign familial infantile seizuresPasquale Striano, Laura Bordo, Maria Luisa Lispi, et al.
American Journal of Medical Genetics. Part A|December 19, 2018
Primary muscle involvement in a 15-year-old girl with the recurrent homozygous c.362dupC variant in FKBP14Marco Castori, Chiara Fiorillo, Emanuele Agolini, et al.
International Journal of Molecular Sciences|August 23, 2020
eATP/P2X7R Axis: An Orchestrated Pathway Triggering Inflammasome Activation in Muscle DiseasesChiara Panicucci, Lizzia Raffaghello, Santina Bruzzone, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 26, 2011
A proof-of-concept trial of the whey protein alfa-lactalbumin in chronic cortical myoclonusLuca Errichiello, Marianna Pezzella, Lia Santulli, et al.
Cell Cycle (Georgetown, Tex.)|November 19, 2005
Caveolin-1-deficient mice have an increased mammary stem cell population with upregulation of Wnt/beta-catenin signalingFederica Sotgia, Terence M Williams, Alex W Cohen, et al.
Neurology|July 21, 2010
Lesional reflex epilepsy associated with the thought of foodPasquale Striano, Carlo Minetti, Federico Zara, et al.
Journal of Neuroimmunology|May 12, 2009
Autoantibodies to glutamic acid decarboxylase (GAD) in focal and generalized epilepsy: A study on 233 patientsLuca Errichiello, Giuseppe Perruolo, Angelo Pascarella, et al.
Seizure|April 25, 2018
Erratum to "De novo 12q22.q23.3 duplication associated with temporal lobe epilepsy" [Seizure 57 (2018) 63-65]Maria Stella Vari, Monica Traverso, Tommaso Bellini, et al.
Pageof 19

Showing results (31-40 of 190) with videos related to

Sort By:
Pageof 19
Neuromuscular Disorders : NMD|February 4, 2009
White matter lesions in spastic paraplegia with mutations in SPG5/CYP7B1Roberta Biancheri, Marianna Ciccolella, Andrea Rossi, et al.
Epilepsia|March 24, 2011
Natural history and long-term evolution in families with autosomal dominant cortical tremor, myoclonus, and epilepsyAntonietta Coppola, Lia Santulli, Luigi Del Gaudio, et al.
Epilepsia|January 19, 2006
A novel SCN2A mutation in family with benign familial infantile seizuresPasquale Striano, Laura Bordo, Maria Luisa Lispi, et al.
American Journal of Medical Genetics. Part A|December 19, 2018
Primary muscle involvement in a 15-year-old girl with the recurrent homozygous c.362dupC variant in FKBP14Marco Castori, Chiara Fiorillo, Emanuele Agolini, et al.
International Journal of Molecular Sciences|August 23, 2020
eATP/P2X7R Axis: An Orchestrated Pathway Triggering Inflammasome Activation in Muscle DiseasesChiara Panicucci, Lizzia Raffaghello, Santina Bruzzone, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 26, 2011
A proof-of-concept trial of the whey protein alfa-lactalbumin in chronic cortical myoclonusLuca Errichiello, Marianna Pezzella, Lia Santulli, et al.
Cell Cycle (Georgetown, Tex.)|November 19, 2005
Caveolin-1-deficient mice have an increased mammary stem cell population with upregulation of Wnt/beta-catenin signalingFederica Sotgia, Terence M Williams, Alex W Cohen, et al.
Neurology|July 21, 2010
Lesional reflex epilepsy associated with the thought of foodPasquale Striano, Carlo Minetti, Federico Zara, et al.
Journal of Neuroimmunology|May 12, 2009
Autoantibodies to glutamic acid decarboxylase (GAD) in focal and generalized epilepsy: A study on 233 patientsLuca Errichiello, Giuseppe Perruolo, Angelo Pascarella, et al.
Seizure|April 25, 2018
Erratum to "De novo 12q22.q23.3 duplication associated with temporal lobe epilepsy" [Seizure 57 (2018) 63-65]Maria Stella Vari, Monica Traverso, Tommaso Bellini, et al.
Pageof 19