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ABOUT JoVE

Overview Leadership Blog JoVE Help Center

AUTHORS

Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

LIBRARIANS

Testimonials Subscriptions Access Resources Library Advisory Board FAQ

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JoVE Journal Methods Collections JoVE Encyclopedia of Experiments Archive

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R A Maselli

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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.

Muscle & Nerve|October 27, 1997

Cluster of wound botulism in California: clinical, electrophysiologic, and pathologic studyR A Maselli, W Ellis, R N Mandler, et al.

Neurology|July 27, 2001

Presynaptic congenital myasthenic syndrome due to quantal release deficiencyR A Maselli, D Z Kong, C M Bowe, et al.

Clinical Genetics|December 24, 2010

Congenital myasthenic syndrome associated with epidermolysis bullosa caused by homozygous mutations in PLEC1 and CHRNER A Maselli, J Arredondo, O Cagney, et al.

Clinical Genetics|March 16, 2013

Exome sequencing detection of two untranslated GFPT1 mutations in a family with limb-girdle myastheniaR A Maselli, J Arredondo, J Nguyen, et al.

Pageof 4

Search research articles

Showing results (31-40 of 35) with videos related to

Sort By:

Pageof 4

You have reached the last page of results.This site can display upto 35 results.

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.

Muscle & Nerve|October 27, 1997

Cluster of wound botulism in California: clinical, electrophysiologic, and pathologic studyR A Maselli, W Ellis, R N Mandler, et al.

Neurology|July 27, 2001

Presynaptic congenital myasthenic syndrome due to quantal release deficiencyR A Maselli, D Z Kong, C M Bowe, et al.

Clinical Genetics|December 24, 2010

Congenital myasthenic syndrome associated with epidermolysis bullosa caused by homozygous mutations in PLEC1 and CHRNER A Maselli, J Arredondo, O Cagney, et al.

Clinical Genetics|March 16, 2013

Exome sequencing detection of two untranslated GFPT1 mutations in a family with limb-girdle myastheniaR A Maselli, J Arredondo, J Nguyen, et al.

Pageof 4