Citation Impact
Citing Papers
International consensus guidance for management of myasthenia gravis
2016 Standout
Epigenetic regulation of hypoxic sensing disrupts cardiorespiratory homeostasis
2012 StandoutNobel
The Epidemiology of Neuromuscular Disorders: A Comprehensive Overview of the Literature
2015
Ultrastructural Characterization of the Lower Motor System in a Mouse Model of Krabbe Disease
2016 Standout
Mechanisms of Thrombus Formation
2008 Standout
Enzymatic synthesis of capsaicin analogs and their effect on the T-type Ca2+ channels
2007
Neuropathy Target Esterase Gene Mutations Cause Motor Neuron Disease
2008
Cardiac manifestations of myotonic dystrophy type 1
2011
Antithrombotic Therapy for VTE Disease
2016 Standout
Voltage-gated calcium channels and pain
2006
Antithrombotic Therapy for VTE Disease
2012 Standout
The early-onset torsion dystonia gene (DYT1) encodes an ATP-binding protein
1997 Standout
Executive Summary
2012 Standout
Mechanism of Neuromuscular Dysfunction in Krabbe Disease
2015
Mortality in myotonic dystrophy patients in the area of prophylactic pacing devices
2010
From Ionic Currents to Molecular Mechanisms
2000 Standout
Ion Channel Mutations in Periodic Paralysis and Related Myotonic Diseasesa
1993
Hypokalemic periodic paralysis mutations: Confirmation of mutation and analysis of founder effect
1996
Hypoxia‐inducible factor 1 mediates increased expression of NADPH oxidase‐2 in response to intermittent hypoxia
2011 StandoutNobel
Myotonia Fluctuans
1994
Cellular and Molecular Mechanisms of Pain
2009 StandoutNobel
The evolution of infrahissian conduction time in myotonic dystrophy patients: clinical implications
2011
Investigation of Notch3 as a candidate gene for bipolar disorder using brain hyperintensities as an endophenotype
2002
Mutation in the S4 segment of the adult skeletal sodium channel gene in an Italian Paramyotonia Congenita (PC) family
1994
Antithrombotic Therapy in Neonates and Children
2008
Antithrombotic Therapy in Neonates and Children
2012
The Endophenotype Concept in Psychiatry: Etymology and Strategic Intentions
2003 Standout
High levels of somatic DNA diversity at the myotonic dystrophy type 1 locus are driven by ultra-frequent expansion and contraction mutations
2012
DNA‐Templated Organic Synthesis: Nature's Strategy for Controlling Chemical Reactivity Applied to Synthetic Molecules
2004 Standout
International Union of Pharmacology. XLVII. Nomenclature and Structure-Function Relationships of Voltage-Gated Sodium Channels
2005 Standout
NADPH Oxidase-Dependent Regulation of T-Type Ca2+Channels and Ryanodine Receptors Mediate the Augmented Exocytosis of Catecholamines from Intermittent Hypoxia-Treated Neonatal Rat Chromaffin Cells
2010
Diagnosis, Treatment, and Long-Term Management of Kawasaki Disease: A Scientific Statement for Health Professionals From the American Heart Association
2017 Standout
Recent advances in the study on capsaicinoids and capsinoids
2010 Standout
Physiological Implications of Hydrogen Sulfide: A Whiff Exploration That Blossomed
2012 Standout
Sodium Channel Defects in Myotonia and Periodic Paralysis
1996
Molecular Physiology of Low-Voltage-Activated T-type Calcium Channels
2003
Adaptive and Maladaptive Cardiorespiratory Responses to Continuous and Intermittent Hypoxia Mediated by Hypoxia-Inducible Factors 1 and 2
2012 StandoutNobel
2015 ESC Guidelines for the management of patients with ventricular arrhythmias and the prevention of sudden cardiac death
2015 Standout
Independent origin of identical beta cardiac myosin heavy-chain mutations in hypertrophic cardiomyopathy.
1993
Management of Massive and Submassive Pulmonary Embolism, Iliofemoral Deep Vein Thrombosis, and Chronic Thromboembolic Pulmonary Hypertension
2011 Standout
Neural Science
2000 StandoutNobel
Diagnosis and Management of Cerebral Venous Thrombosis
2011 Standout
Neuropathology of degenerative cell death in Caenorhabditis elegans.
1997 StandoutNobel
Aromatic Sulfonyl Fluorides Covalently Kinetically Stabilize Transthyretin to Prevent Amyloidogenesis while Affording a Fluorescent Conjugate
2013 StandoutNobel
Hypokalemic periodic paralysis and the dihydropyridine receptor (CACNL1A3): genotype/phenotype correlations for two predominant mutations and evidence for the absence of a founder effect in 16 caucasian families.
1995
Extrahelical (CAG)/(CTG) triplet repeat elements support proliferating cell nuclear antigen loading and MutLα endonuclease activation
2013 StandoutNobel
The Emergence of Modern Neuroscience: Some Implications for Neurology and Psychiatry
2000 StandoutNobel
Improving the Fidelity of Thermus Thermophilus DNA Ligase
1996
Phospholipase A2Enzymes: Physical Structure, Biological Function, Disease Implication, Chemical Inhibition, and Therapeutic Intervention
2011 Standout
Bisaryloxime Ethers as Potent Inhibitors of Transthyretin Amyloid Fibril Formation
2005 StandoutNobel
Neuropathology of Degenerative Cell Death inCaenorhabditis elegans
1997 StandoutNobel
Hematological Problems in Pediatric Intensive Care
2013 Standout
Works of S. Todorović being referenced
Troyer Syndrome
2019
Survival and mortality of myotonic dystrophy type 1 (Steinert's disease) in the population of Belgrade
2006
Epidemiology of Charcot-Marie-Tooth Disease in the Population of Belgrade, Serbia
2011
Association of Krabbe leukodystrophy and congenital fiber type disproportion
1996
The Role of T-Type Calcium Channels in Epilepsy and Pain
2006
The Recurrence Risk of Ischemic Stroke in Childhood
2004
Cav3.2 Channel Is a Molecular Substrate for Inhibition of T-Type Calcium Currents in Rat Sensory Neurons by Nitrous Oxide
2001
Molecular genetic and genetic correlations in sodium channelopathies: lack of founder effect and evidence for a second gene.
1993
Hyperkalemic periodic paralysis
1993