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A Ferlini

Showing results (71-80 of 88) with videos related to

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Neuroscience|October 18, 2008
A novel KCNA1 mutation identified in an Italian family affected by episodic ataxia type 1P Imbrici, F Gualandi, M C D'Adamo, et al.
Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis|December 3, 2003
Atypical familial motor neuropathy in patients with mutant TTR Ile68LeuF Salvi, C Scaglione, R Michelucci, et al.
Orphanet Journal of Rare Diseases|September 30, 2016
Rett syndrome: a wide clinical and autonomic pictureG Pini, S Bigoni, L Congiu, et al.
Journal of Medical Genetics|February 1, 1997
Refinement of the laminin alpha2 chain locus to human chromosome 6q2 in severe and mild merosin deficient congenital muscular dystrophyI S Naom, M D'Alessandro, H Topaloglu, et al.
Biochimica Et Biophysica Acta|June 8, 2014
Defective collagen VI α6 chain expression in the skeletal muscle of patients with collagen VI-related myopathiesF Tagliavini, C Pellegrini, F Sardone, et al.
American Journal of Medical Genetics|September 20, 2002
Exploring the clinical and epidemiological complexity of GJB2-linked deafnessF Gualandi, A Ravani, A Berto, et al.
Gene Therapy|November 13, 2009
Dystrophin restoration in skeletal, heart and skin arrector pili smooth muscle of mdx mice by ZM2 NP-AON complexesA Ferlini, P Sabatelli, M Fabris, et al.
Neuromuscular Disorders : NMD|March 8, 2013
Duchenne muscular dystrophy and epilepsyM Pane, S Messina, C Bruno, et al.
Heart (British Cardiac Society)|February 21, 1998
Dystrophin gene abnormalities in two patients with idiopathic dilated cardiomyopathyF Muntoni, A Di Lenarda, M Porcu, et al.
Biochimica Et Biophysica Acta. Gene Regulatory Mechanisms|November 4, 2020
Corrigendum to: "Transcriptional and epigenetic analyses of the DMD locus reveal novel cis-acting DNA elements that govern muscle dystrophin expression". [Biochim. Biophys. Acta Gene Regul. Mech. 2017 Nov;1860(11):1138-1147.]S Gherardi, M Bovolenta, C Passarelli, et al.
Pageof 9

Showing results (71-80 of 88) with videos related to

Sort By:
Pageof 9
Neuroscience|October 18, 2008
A novel KCNA1 mutation identified in an Italian family affected by episodic ataxia type 1P Imbrici, F Gualandi, M C D'Adamo, et al.
Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis|December 3, 2003
Atypical familial motor neuropathy in patients with mutant TTR Ile68LeuF Salvi, C Scaglione, R Michelucci, et al.
Orphanet Journal of Rare Diseases|September 30, 2016
Rett syndrome: a wide clinical and autonomic pictureG Pini, S Bigoni, L Congiu, et al.
Journal of Medical Genetics|February 1, 1997
Refinement of the laminin alpha2 chain locus to human chromosome 6q2 in severe and mild merosin deficient congenital muscular dystrophyI S Naom, M D'Alessandro, H Topaloglu, et al.
Biochimica Et Biophysica Acta|June 8, 2014
Defective collagen VI α6 chain expression in the skeletal muscle of patients with collagen VI-related myopathiesF Tagliavini, C Pellegrini, F Sardone, et al.
American Journal of Medical Genetics|September 20, 2002
Exploring the clinical and epidemiological complexity of GJB2-linked deafnessF Gualandi, A Ravani, A Berto, et al.
Gene Therapy|November 13, 2009
Dystrophin restoration in skeletal, heart and skin arrector pili smooth muscle of mdx mice by ZM2 NP-AON complexesA Ferlini, P Sabatelli, M Fabris, et al.
Neuromuscular Disorders : NMD|March 8, 2013
Duchenne muscular dystrophy and epilepsyM Pane, S Messina, C Bruno, et al.
Heart (British Cardiac Society)|February 21, 1998
Dystrophin gene abnormalities in two patients with idiopathic dilated cardiomyopathyF Muntoni, A Di Lenarda, M Porcu, et al.
Biochimica Et Biophysica Acta. Gene Regulatory Mechanisms|November 4, 2020
Corrigendum to: "Transcriptional and epigenetic analyses of the DMD locus reveal novel cis-acting DNA elements that govern muscle dystrophin expression". [Biochim. Biophys. Acta Gene Regul. Mech. 2017 Nov;1860(11):1138-1147.]S Gherardi, M Bovolenta, C Passarelli, et al.
Pageof 9