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Human Mutation
|
December 8, 2004
Molecular and muscle pathology in a series of caveolinopathy patients
Luigi Fulizio, Anna Chiara Nascimbeni, Marina Fanin, et al.
Neuropathology and Applied Neurobiology
|
July 22, 2014
Familial polyglucosan body myopathy with unusual phenotype
Marina Fanin, Anna Chiara Nascimbeni, Marco Savarese, et al.
Neurological Research
|
September 3, 2010
Genotype-phenotype correlations in a large series of patients with muscle type CPT II deficiency
Angelica Anichini, Marina Fanin, Christine Vianey-Saban, et al.
BMC Medicine
|
April 9, 2009
Different atrophy-hypertrophy transcription pathways in muscles affected by severe and mild spinal muscular atrophy
Caterina Millino, Marina Fanin, Andrea Vettori, et al.
The American Journal of Cardiology
|
November 15, 2011
Sudden death associated with danon disease in women
Daniela Miani, Matthew Taylor, Luisa Mestroni, et al.
Muscle & Nerve
|
December 10, 2014
Incomplete penetrance in limb-girdle muscular dystrophy type 1F
Marina Fanin, Enrico Peterle, Chiara Fritegotto, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
March 28, 2009
Comparative transcriptional and biochemical studies in muscle of myotonic dystrophies (DM1 and DM2)
Sergio Salvatori, Sandra Furlan, Marina Fanin, et al.
Ultrastructural Pathology
|
June 24, 2010
The role of ultrastructural examination in storage diseases
Valentina Papa, Lucia Tarantino, Paola Preda, et al.
Journal of Neurology
|
November 20, 2010
Comparison of muscle ultrastructure in myasthenia gravis with anti-MuSK and anti-AChR antibodies
Giovanna Cenacchi, Valentina Papa, Papa Valentina, et al.
Scientific Reports
|
September 2, 2016
Functional changes in Becker muscular dystrophy: implications for clinical trials in dystrophinopathies
Luca Bello, Paola Campadello, Andrea Barp, et al.
Page
of 6
Search research articles
Search
Showing results (31-40 of 56) with videos related to
Sort By:
Page
of 6
Human Mutation
|
December 8, 2004
Molecular and muscle pathology in a series of caveolinopathy patients
Luigi Fulizio, Anna Chiara Nascimbeni, Marina Fanin, et al.
Neuropathology and Applied Neurobiology
|
July 22, 2014
Familial polyglucosan body myopathy with unusual phenotype
Marina Fanin, Anna Chiara Nascimbeni, Marco Savarese, et al.
Neurological Research
|
September 3, 2010
Genotype-phenotype correlations in a large series of patients with muscle type CPT II deficiency
Angelica Anichini, Marina Fanin, Christine Vianey-Saban, et al.
BMC Medicine
|
April 9, 2009
Different atrophy-hypertrophy transcription pathways in muscles affected by severe and mild spinal muscular atrophy
Caterina Millino, Marina Fanin, Andrea Vettori, et al.
The American Journal of Cardiology
|
November 15, 2011
Sudden death associated with danon disease in women
Daniela Miani, Matthew Taylor, Luisa Mestroni, et al.
Muscle & Nerve
|
December 10, 2014
Incomplete penetrance in limb-girdle muscular dystrophy type 1F
Marina Fanin, Enrico Peterle, Chiara Fritegotto, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
March 28, 2009
Comparative transcriptional and biochemical studies in muscle of myotonic dystrophies (DM1 and DM2)
Sergio Salvatori, Sandra Furlan, Marina Fanin, et al.
Ultrastructural Pathology
|
June 24, 2010
The role of ultrastructural examination in storage diseases
Valentina Papa, Lucia Tarantino, Paola Preda, et al.
Journal of Neurology
|
November 20, 2010
Comparison of muscle ultrastructure in myasthenia gravis with anti-MuSK and anti-AChR antibodies
Giovanna Cenacchi, Valentina Papa, Papa Valentina, et al.
Scientific Reports
|
September 2, 2016
Functional changes in Becker muscular dystrophy: implications for clinical trials in dystrophinopathies
Luca Bello, Paola Campadello, Andrea Barp, et al.
Page
of 6