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A Maselli

Showing results (101-110 of 130) with videos related to

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Annals of the New York Academy of Sciences|June 21, 1993
Effector mechanisms of myasthenic antibodiesD P Richman, R L Wollmann, R A Maselli, et al.
Muscle & Nerve|May 26, 2021
Dominant and recessive congenital myasthenic syndromes caused by SYT2 mutationsRicardo A Maselli, David T Wei, Trent S Hodgson, et al.
La Radiologia Medica|November 1, 1994
[The magnetic resonance imaging of abdominal aortic aneurysms]F Barzi, P Panzarola, L Regi, et al.
Annals of the New York Academy of Sciences|July 21, 1998
Antibody effector mechanisms in myasthenia gravis. The complement hypothesisD P Richman, M A Agius, C A Kirvan, et al.
Muscle & Nerve|November 1, 1993
Neuromuscular transmission in amyotrophic lateral sclerosisR A Maselli, R L Wollman, C Leung, et al.
Human Molecular Genetics|April 8, 2010
Mutations in MUSK causing congenital myasthenic syndrome impair MuSK-Dok-7 interactionRicardo A Maselli, Juan Arredondo, Orla Cagney, et al.
Journal of Biological Regulators and Homeostatic Agents|April 9, 2008
Quality of life in non-allergic rhinitis depends on the predominant inflammatory cell typeM Gelardi, A Maselli Del Giudice, M L Fiorella, et al.
BMC Medical Genomics|August 12, 2024
Congenital myasthenic syndrome secondary to pathogenic variants in the SLC5A7 gene: report of two casesJavier A Muntadas, Martin R Hyland, Maria Del Rosario Ortolá Martínez, et al.
Neuromolecular Medicine|July 14, 2012
Dominantly inherited myotonia congenita resulting from a mutation that increases open probability of the muscle chloride channel CLC-1David P Richman, Yawei Yu, Ting-Ting Lee, et al.
Journal of Medical Genetics|March 3, 2009
Mutations in LAMB2 causing a severe form of synaptic congenital myasthenic syndromeR A Maselli, J J Ng, J A Anderson, et al.
Pageof 13

Showing results (101-110 of 130) with videos related to

Sort By:
Pageof 13
Annals of the New York Academy of Sciences|June 21, 1993
Effector mechanisms of myasthenic antibodiesD P Richman, R L Wollmann, R A Maselli, et al.
Muscle & Nerve|May 26, 2021
Dominant and recessive congenital myasthenic syndromes caused by SYT2 mutationsRicardo A Maselli, David T Wei, Trent S Hodgson, et al.
La Radiologia Medica|November 1, 1994
[The magnetic resonance imaging of abdominal aortic aneurysms]F Barzi, P Panzarola, L Regi, et al.
Annals of the New York Academy of Sciences|July 21, 1998
Antibody effector mechanisms in myasthenia gravis. The complement hypothesisD P Richman, M A Agius, C A Kirvan, et al.
Muscle & Nerve|November 1, 1993
Neuromuscular transmission in amyotrophic lateral sclerosisR A Maselli, R L Wollman, C Leung, et al.
Human Molecular Genetics|April 8, 2010
Mutations in MUSK causing congenital myasthenic syndrome impair MuSK-Dok-7 interactionRicardo A Maselli, Juan Arredondo, Orla Cagney, et al.
Journal of Biological Regulators and Homeostatic Agents|April 9, 2008
Quality of life in non-allergic rhinitis depends on the predominant inflammatory cell typeM Gelardi, A Maselli Del Giudice, M L Fiorella, et al.
BMC Medical Genomics|August 12, 2024
Congenital myasthenic syndrome secondary to pathogenic variants in the SLC5A7 gene: report of two casesJavier A Muntadas, Martin R Hyland, Maria Del Rosario Ortolá Martínez, et al.
Neuromolecular Medicine|July 14, 2012
Dominantly inherited myotonia congenita resulting from a mutation that increases open probability of the muscle chloride channel CLC-1David P Richman, Yawei Yu, Ting-Ting Lee, et al.
Journal of Medical Genetics|March 3, 2009
Mutations in LAMB2 causing a severe form of synaptic congenital myasthenic syndromeR A Maselli, J J Ng, J A Anderson, et al.
Pageof 13