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American Journal of Otolaryngology
|
April 16, 2022
Impact of intraoperative ischemia time on acute complications of head and neck microvascular free tissue transfer: A systematic review and meta-analysis
Stephen F Politano, Divya Balchander, Claudia I Cabrera, et al.
European Journal of Human Genetics : EJHG
|
April 28, 2011
Muscular dystrophy with marked Dysferlin deficiency is consistently caused by primary dysferlin gene mutations
Mafalda Cacciottolo, Gelsomina Numitone, Stefania Aurino, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology
|
February 25, 2015
Far field R-wave sensing in Myotonic Dystrophy type 1: right atrial appendage versus Bachmann's bundle region lead placement
Vincenzo Russo, Gerardo Nigro, Andrea Antonio Papa, et al.
Nature Genetics
|
October 1, 1996
Autosomal recessive limb-girdle muscular dystrophy, LGMD2F, is caused by a mutation in the delta-sarcoglycan gene
V Nigro, E de Sá Moreira, G Piluso, et al.
Neuropediatrics
|
February 16, 2024
PGAP2-Related Hyperphosphatasia-Mental Retardation Syndrome: Report of a Novel Patient, Toward a Broadening of Phenotypic Spectrum and Therapeutic Perspectives
Annalisa Saracino, Martina Totaro, Davide Politano, et al.
Neurology. Genetics
|
May 18, 2026
<i>KIF5C</i>-Related Neurodevelopmental Disorder: Three New Cases and Additional Neuroradiologic Insights
Davide Politano, Simone Gana, Simona Orcesi, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology
|
July 17, 2019
Cardiac diseases as a predictor warning of hereditary muscle diseases. The case of laminopathies
Paola D'Ambrosio, Roberta Petillo, Annalaura Torella, et al.
European Heart Journal
|
March 27, 2003
A preliminary randomized study of growth hormone administration in Becker and Duchenne muscular dystrophies
Antonio Cittadini, Lucia Ines Comi, Salvatore Longobardi, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology
|
May 29, 2009
Analysis of Single Nucleotide Polymorphisms (SNPs) of the small-conductance calcium activated potassium channel (SK3) gene as genetic modifier of the cardiac phenotype in myotonic dystrophy type 1 patients
F Rinaldi, A Botta, L Vallo, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
November 24, 2006
High plasma creatine kinase: review of the literature and proposal for a diagnostic algorithm
L Morandi, C Angelini, A Prelle, et al.
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of 64
Search research articles
Search
Showing results (401-410 of 638) with videos related to
Sort By:
Page
of 64
American Journal of Otolaryngology
|
April 16, 2022
Impact of intraoperative ischemia time on acute complications of head and neck microvascular free tissue transfer: A systematic review and meta-analysis
Stephen F Politano, Divya Balchander, Claudia I Cabrera, et al.
European Journal of Human Genetics : EJHG
|
April 28, 2011
Muscular dystrophy with marked Dysferlin deficiency is consistently caused by primary dysferlin gene mutations
Mafalda Cacciottolo, Gelsomina Numitone, Stefania Aurino, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology
|
February 25, 2015
Far field R-wave sensing in Myotonic Dystrophy type 1: right atrial appendage versus Bachmann's bundle region lead placement
Vincenzo Russo, Gerardo Nigro, Andrea Antonio Papa, et al.
Nature Genetics
|
October 1, 1996
Autosomal recessive limb-girdle muscular dystrophy, LGMD2F, is caused by a mutation in the delta-sarcoglycan gene
V Nigro, E de Sá Moreira, G Piluso, et al.
Neuropediatrics
|
February 16, 2024
PGAP2-Related Hyperphosphatasia-Mental Retardation Syndrome: Report of a Novel Patient, Toward a Broadening of Phenotypic Spectrum and Therapeutic Perspectives
Annalisa Saracino, Martina Totaro, Davide Politano, et al.
Neurology. Genetics
|
May 18, 2026
<i>KIF5C</i>-Related Neurodevelopmental Disorder: Three New Cases and Additional Neuroradiologic Insights
Davide Politano, Simone Gana, Simona Orcesi, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology
|
July 17, 2019
Cardiac diseases as a predictor warning of hereditary muscle diseases. The case of laminopathies
Paola D'Ambrosio, Roberta Petillo, Annalaura Torella, et al.
European Heart Journal
|
March 27, 2003
A preliminary randomized study of growth hormone administration in Becker and Duchenne muscular dystrophies
Antonio Cittadini, Lucia Ines Comi, Salvatore Longobardi, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology
|
May 29, 2009
Analysis of Single Nucleotide Polymorphisms (SNPs) of the small-conductance calcium activated potassium channel (SK3) gene as genetic modifier of the cardiac phenotype in myotonic dystrophy type 1 patients
F Rinaldi, A Botta, L Vallo, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
November 24, 2006
High plasma creatine kinase: review of the literature and proposal for a diagnostic algorithm
L Morandi, C Angelini, A Prelle, et al.
Page
of 64