Citation Impact
Citing Papers
Reactive oxygen species, toxicity, oxidative stress, and antioxidants: chronic diseases and aging
2023 Standout
Development of lipophilic cations as therapies for disorders due to mitochondrial dysfunction
2001
Structure of a mammalian ryanodine receptor
2014 StandoutNatureNobel
Structural Basis for Gating and Activation of RyR1
2016 StandoutNobel
Population frequencies of inherited neuromuscular diseases—A world survey
1991 Standout
Oxidative stress, aging, and diseases
2018 Standout
ETFDH mutations as a major cause of riboflavin-responsive multiple acyl-CoA dehydrogenation deficiency
2007
Skeletal Muscle Fatigue: Cellular Mechanisms
2008 Standout
Myonuclear domains in muscle adaptation and disease
1999
Ca2+ channels and skeletal muscle diseases
2010
Ryanodine Receptors: Allosteric Ion Channel Giants
2014
Exercise-Induced Oxidative Stress: Cellular Mechanisms and Impact on Muscle Force Production
2008 Standout
A Capacitative Calcium Current in Cultured Skeletal Muscle Cells Is Mediated by the Calcium-specific Leak Channel and Inhibited by Dihydropyridine Compounds
1996
Calcium's Role in Mechanotransduction during Muscle Development
2014 Standout
Oxidative Stress Hypothesis in Alzheimer's Disease
1997 Standout
A genome-wide association study of meat and carcass traits in Australian cattle1
2011 Standout
Coenzyme Q<sub>10</sub> Therapy
2014
Does impairment of energy metabolism result in excitotoxic neuronal death in neurodegenerative illnesses?
1992
Expression of human IAP-like protein in skeletal muscle: a possible explanation for the rare incidence of muscle fiber apoptosis in T-cell mediated inflammatory myopathies
2000
Autophagic and apoptotic features during programmed cell death in the fat body of the tobacco hornworm (Manduca sexta)
2004
Calcium entry through stretch-inactivated ion channels in mdx myotubes
1990 Nature
Cardiopulmonary Support in Duchenne Muscular Dystrophy
2006
Rhabdomyolysis and Acute Kidney Injury
2009 Standout
Coenzyme Q10 as a therapy for mitochondrial disease
2014
Calcium channels in neurological disease
1997
Mitochondrial Encephalopathy, Lactic Acidosis, and Strokelike Episodes
2008
The muscular dystrophies
2002 Standout
A Metachromatic Dye-Atpase Method for The Simultaneous Identification of Skeletal Muscle Fiber Types I, IIA, IIB and IIC
1990
Exon skipping and dystrophin restoration in patients with Duchenne muscular dystrophy after systemic phosphorodiamidate morpholino oligomer treatment: an open-label, phase 2, dose-escalation study
2011 Standout
Postulated Role of Interdomain Interaction within the Ryanodine Receptor in Ca2+ Channel Regulation
2000
Prostate-specific deletion of the murine Pten tumor suppressor gene leads to metastatic prostate cancer
2003 Standout
Endurance exercise performance: the physiology of champions
2007 Standout
Prevalence of Muscular Dystrophies: A Systematic Literature Review
2014 Standout
Mitochondria: In Sickness and in Health
2012 Standout
Store-Operated Calcium Channels
2005 Standout
Therapeutic approaches for muscle wasting disorders
2006
Clinical and genetic issues in familial dilated cardiomyopathy
2005
The Role of Inflammation in Age-Related Sarcopenia
2017
Mitochondria‐associated apoptotic signalling in denervated rat skeletal muscle
2005
The Dystrophinopathies: An Alternative to the Structural Hypothesis
1998
Calpains Are Activated in Necrotic Fibers from mdx Dystrophic Mice
1995
Effects of Coenzyme Q10 in Early Parkinson Disease
2002
Undetectable dystrophin can still result in a relatively benign phenotype of dystrophinopathy
1999
The Human Gene Map for Performance and Health-Related Fitness Phenotypes
2006
The Pore Structure of the Closed RyR1 Channel
2005
The epidemiology of Parkinson's disease: risk factors and prevention
2016 Standout
Courtship and Other Behaviors Affected by a Heat-Sensitive, Molecularly Novel Mutation in the cacophony Calcium-Channel Gene of Drosophila
2002 StandoutNobel
Classification of the cardiomyopathies: a position statement from the european society of cardiology working group on myocardial and pericardial diseases
2007 Standout
Transcriptional co-activator PGC-1α drives the formation of slow-twitch muscle fibres
2002 StandoutNature
Neurological diseases caused by ion-channel mutations
2000
Microbubble Stability is a Major Determinant of the Efficiency of Ultrasound and Microbubble Mediated in vivo Gene Transfer
2009 StandoutNobel
Hematopoietic and nonhematopoietic potentials of Hoechstlow/side population cells isolated from adult rat kidney
2004 StandoutNobel
Autophagy in cell death: an innocent convict?
2005 Standout
Mitochondria: The Next (Neurode)Generation
2011
Repertoires of Autophagy in the Pathogenesis of Ocular Diseases
2015 Standout
ACTN3 Genotype Is Associated with Human Elite Athletic Performance
2003 Standout
Rhabdomyolysis: A review
2002
Grandpa and I have Dystrophinopathy?: Approach to Asymptomatic HyperCKemia
2006
Physiological Roles of Mitochondrial Reactive Oxygen Species
2012 Standout
Calcium Influx through Calcium Leak Channels Is Responsible for the Elevated Levels of Calcium-dependent Proteolysis in Dystrophic Myotubes
2000
Polymyositis and dermatomyositis
2003 Standout
Critical evaluation of cytosolic calcium determination in resting muscle fibres from normal and dystrophic (mdx) mice
1993
The role of Ca2+ ions in excitation-contraction coupling of skeletal muscle fibres
1995
Inflammageing: chronic inflammation in ageing, cardiovascular disease, and frailty
2018 Standout
Cellular and molecular diversities of mammalian skeletal muscle fibers
1990
Oxidative damage and mitochondrial decay in aging.
1994 Standout
A Validated Whole-Genome Association Study of Efficient Food Conversion in Cattle
2007
Oxidation of the skeletal muscle Ca2+release channel alters calmodulin binding
1999
Supramolecular Hydrogelators and Hydrogels: From Soft Matter to Molecular Biomaterials
2015 Standout
Alzheimer's disease
1998 Standout
The muscular dystrophies
2012
2011 ACCF/AHA Guideline for the Diagnosis and Treatment of Hypertrophic Cardiomyopathy
2011 Standout
Mitochondrial Reactive Oxygen Species (ROS) and ROS-Induced ROS Release
2014 Standout
The Calpain System
2003 Standout
Calcium Ion in Skeletal Muscle: Its Crucial Role for Muscle Function, Plasticity, and Disease
2000
PTEN and Myotubularin: Novel Phosphoinositide Phosphatases
2001
The `Spectraplakins': cytoskeletal giants with characteristics of both spectrin and plakin families
2002
The structure of the ankyrin-binding site of β-spectrin reveals how tandem spectrin-repeats generate unique ligand-binding properties
2009 StandoutNobel
Fiber Types in Mammalian Skeletal Muscles
2011 Standout
Contemporary Definitions and Classification of the Cardiomyopathies
2006 Standout
Membrane potential, resting calcium and calcium transients in isolated muscle fibres from normal and dystrophic mice.
1993
Function and Genetics of Dystrophin and Dystrophin-Related Proteins in Muscle
2002
Raised intracellular [Ca2+] abolishes excitation‐contraction coupling in skeletal muscle fibres of rat and toad.
1995
Testosterone-induced increase in muscle size in healthy young men is associated with muscle fiber hypertrophy
2002 Standout
Increased calcium influx in dystrophic muscle.
1991
Voltage-sensor sodium channel mutations cause hypokalemic periodic paralysis type 2 by enhanced inactivation and reduced current
2000
Natural product and natural product derived drugs in clinical trials
2014 Standout
Pharmacology of the Na v 1.1 domain IV voltage sensor reveals coupling between inactivation gating processes
2017 StandoutNobel
Clinical Approach to Genetic Cardiomyopathy in Children
1996
Sertoli-Sertoli and Sertoli-Germ Cell Interactions and Their Significance in Germ Cell Movement in the Seminiferous Epithelium during Spermatogenesis
2004 Standout
Increased Activity of Calcium Leak Channels in Myotubes of Duchenne Human and mdx Mouse Origin
1990 Science
Satellite Cells and the Muscle Stem Cell Niche
2013 Standout
Cellular and Molecular Regulation of Muscle Regeneration
2004 Standout
The Emergence of Modern Neuroscience: Some Implications for Neurology and Psychiatry
2000 StandoutNobel
Molecular Mechanisms of Myocardial Remodeling
1999 Standout
Ribosome Biogenesis: Emerging Evidence for a Central Role in the Regulation of Skeletal Muscle Mass
2014 Standout
Dysregulation of the TSC-mTOR pathway in human disease
2004 Standout
Exercise metabolism in Duchenne muscular dystrophy: a biochemical and [31P]-nuclear magnetic resonance study ofmdxmice
1993
Creatine and Creatinine Metabolism
2000 Standout
A critical evaluation of resting intracellular free calcium regulation in dystrophic mdx muscle
1996
Works of C. Doriguzzi being referenced
Centronuclear myopathy: clinical, morphological and genetic characters a review of 288 cases
1991
Muscle apoptosis in humans occurs in normal and denervated muscle, but not in myotonic dystrophy, dystrophinopathies or inflammatory disease
1997
Mutations in the ryanodine receptor gene in central core disease and malignant hyperthermia
1993
Systematic use of dystrophin testing in muscle biopsies: results in 201 cases
1997
Dilating cardiomyopathy as the expression of Xp21 Becker type muscular dystrophy
1992
Alpha-Sarcoglycan Deficiency Featuring Exercise Intolerance and Myoglobinuria
2002
Exercise intolerance and recurrent myoglobinuria as the only expression of Xp21 Becker type muscular dystrophy
1993
Absence of dystrophin in two patients with Becker type Xp21 muscular dystrophy
1992
Ubidecarenone in the treatment of mitochondrial myopathies: a multi-center double-blind trial
1990
Lipid Storage Myopathy in Multiple Acyl-CoA Dehydrogenase Deficiency: An Adult Case
1992
A new method for myofibrillar Ca++-ATPase reaction based on the use of metachromatic dyes: Its advantages in muscle fibre typing
1983
A new mtDNA mutation associated with a progressive encephalopathy and cytochrome c oxidase deficiency
2000
Unusual expression and very mild course of Xp21 muscular dystrophy (Becker type) in a 60‐year‐old man with 26 percent deletion of the dystrophin gene
1994
Interictal conduction slowing in muscle fibers in hypokalemic periodic paralysis
1983
Dystrophinopathy expressing as either cardiomyopathy or Becker dystrophy in the same family
2000
Free cytoplasmic Ca ++ at rest and after cholinergic stimulus is increased in cultured muscle cells from Duchenne muscular dystrophy patients
1988
Epidemiology of Duchenne muscular dystrophy in the province of Turin
1981