D'ADAMO, MARIA CRISTINA 
 Distribuzione geografica
Continente #
NA - Nord America 1.608
EU - Europa 248
AS - Asia 6
OC - Oceania 3
Continente sconosciuto - Info sul continente non disponibili 2
SA - Sud America 1
Totale 1.868
Nazione #
US - Stati Uniti d'America 1.604
DE - Germania 127
BE - Belgio 52
IT - Italia 22
FI - Finlandia 15
CZ - Repubblica Ceca 5
FR - Francia 5
CA - Canada 4
GB - Regno Unito 4
RU - Federazione Russa 4
AT - Austria 3
NL - Olanda 3
PL - Polonia 3
A2 - ???statistics.table.value.countryCode.A2??? 2
IL - Israele 2
NZ - Nuova Zelanda 2
SG - Singapore 2
AE - Emirati Arabi Uniti 1
AU - Australia 1
CL - Cile 1
IN - India 1
NO - Norvegia 1
RO - Romania 1
RS - Serbia 1
SE - Svezia 1
UA - Ucraina 1
Totale 1.868
Città #
Chandler 580
Ashburn 114
Lawrence 107
Princeton 107
Munich 67
Brussels 52
Las Vegas 44
Hanover 39
Miami 16
Seelze 16
Helsinki 15
Seattle 10
Brno 5
Genoa 5
Toronto 3
Andover 2
Boardman 2
Cambridge 2
Milan 2
Novokuznetsk 2
Paris 2
Perugia 2
Roubaix 2
Weston-super-Mare 2
Al Ain City 1
Augusta 1
Belgrade 1
Cupertino 1
Den Haag 1
Dunedin 1
Florence 1
Raanana 1
Rome 1
Siena 1
Stockholm 1
Suri 1
Sydney 1
Tel Aviv 1
Trumbull 1
Varese 1
Totale 1.214
Nome #
Clinical and Functional Study of a De Novo Variant in the PVP Motif of Kv1.1 Channel Associated with Epilepsy, Developmental Delay and Ataxia 29
Differential pH-sensitivity of Kir4.1 and Kir4.2 and modulation by heteropolymerisation with Kir5.1 29
Identification of a New de Novo Mutation Underlying Regressive Episodic Ataxia Type I 29
Association of A Novel Splice Site Mutation in P/Q-Type Calcium Channels with Childhood Epilepsy and Late-Onset Slowly Progressive Non-Episodic Cerebellar Ataxia 28
A Novel KCNA2 Variant in a Patient with Non-Progressive Congenital Ataxia and Epilepsy: Functional Characterization and Sensitivity to 4-Aminopyridine 28
The Episodic Ataxia Type 1 Mutation F184C Alters the Zn2+ Modulation of the Human Kv1.4-Kv1.1/Kvbeta1 Channel 27
Fotorecettori ed Epitelio Pigmentato della Retina; Meccanismi di Trasduzione e Rinnovamento 26
De novo point mutations in patients diagnosed with ataxic cerebral palsy 26
Localization and Age Dependent Expression of the Inward Rectifier K+ Channel Kir 5.1 in a Mammalian Reproductive System 26
Genetic inactivation of Kcnj16 identifies Kir5.1 as an important determinant of neuronal PCO2/pH sensitivity 26
Altered functional properties of a missense variant in the TRESK K+ channel (KCNK18) associated with migraine and intellectual disability 26
Lethal digenic mutations in the K+channels kir4.1 (KCNJ10) and SLACK (KCNT1) associated with severe-disabling seizures and neurodevelopmental delay 25
A channelopathy mutation in the voltage-sensor discloses contributions of a conserved phenylalanine to gating properties of Kv1.1 channels and ataxia 25
Dexamethasone in Glioblastoma Multiforme Therapy: Mechanisms and Controversies 25
Genetic investigation of children with ataxia using exome sequencing 24
Murine Models of EA1 24
Mutations in KCNA1 affect stoichiometry and fast inactivation of heteromeric K+ channels 24
Publisher Correction: Thymosin α1 represents a potential potent single-molecule-based therapy for cystic fibrosis 24
5-HT2 receptors-mediated modulation of voltage-gated K+ channels and neurophysiopathological correlates 24
Episodic ataxia type 1 mutations cause loss-of-function impairments of heteromeric channels formed by the Kv1.4 and Kv1.1 subunits 24
Reconciling the discrepancies on the involvement of large-conductance Ca(2+)-activated K channels in glioblastoma cell migration 23
Genetically-induced abnormalities of Kir2.1 channels: implications for short QT3 syndrome and autism/epilepsy phenotype 23
Amiloride Inhibits Tissue-Type Plasminogen Activator (t-PA) Release from Vascular Endothelium 23
Role of RPTPα and Tyrosine Phosphorylation in the Serotonergic Inhibition of Voltage-Dependent Potassium Channels 23
The Response of Vascular Fibrinolysis to the Adrenergic Stimulation is Abnormal in Aged Rats 23
Effect of Aspirin on the Fibrinolytic Response in Perfused Rat Hindquarters 23
Hypercoagulable State in Aged Rats 22
Adrenergic Stimulation of Tissue-type Plasminogen Activator Release in a Model of Vascular Perfusion in Rats 22
Author Correction: Thymosin α1 represents a potential potent single-molecule-based therapy for cystic fibrosis 22
Antithrombotic Activity of Dermatan Sulphates, Heparin and their Combination in an Animal Model of Arterial Thrombosis 22
Gain-of-function defects of astrocytic Kir4.1 channels in children with autism spectrum disorders and epilepsy 22
Novel phenotype associated with a mutation in the KCNA1(Kv1.1) gene 22
Copertina della rivista scientifica: Neuroscience 21
ERG channels regulate the excitability of medial vestibular neurons 21
Differential pH-sensitivity of Kir4.1 and Kir4.2 and Modulation by Heteropolymerisation with Kir5.1. 21
The role of ion channels in the hypoxia-induced aggressiveness of glioblastoma 21
A method to identify tissue cell subpopulations with distinct multi-molecular profiles from data on co-localization of two markers at a time: the case of sensory ganglia 21
A Calsequestrin-1 mutation associated with a skeletal muscle disease alters sarcoplasmic Ca2+ release 21
A novel KCNA1 mutation in a patient with paroxysmal ataxia, myokymia, painful contractures and metabolic dysfunctions 21
The neurobiology of episodic ataxia type 1: a Shaker-like K+ channel disorder 20
Thrombotic Tendency in Spontaneously Hypercholesterolemic Rats 20
The Episodic Ataxia Type 1 Mutation F184C Alters the Zn2+ Modulation of the Human Kv1.4-Kv1.1/Kvbeta1 Channel 20
Changes in Primary Hemostasis During Thrombus Formation in a Model of Artherial Thrombosis in Rats 20
Different Response of Vascular Fibrinolysis to Adrenergic Stimulation in Young and Aged Rats 20
Update on the implication of potassium channels in autism: K(+) channelautism spectrum disorder 20
KCNA4 deficiency leads to a syndrome of abnormal striatum, congenital cataract and intellectual disability 20
Thymosin α1 represents a potential potent single-molecule-based therapy for cystic fibrosis 20
An Episodic Ataxia Type-1 (EA1) mutation in the S1 segment sensitises the hKv1.1 potassium channel to extracellular Zn2+ 20
Kv1.1 knock-in ataxic mice exhibit spontaneous myokymic activity exacerbated by fatigue, ischemia and low temperature 20
Kcnj16 (Kir5.1) Gene Ablation Causes Subfertility and Increases the Prevalence of Morphologically Abnormal Spermatozoa 20
KCNK18 Biallelic Variants Associated with Intellectual Disability and Neurodevelopmental Disorders Alter TRESK Channel Activity 20
The Role of alfa-adrenergic Receptors in the Acute Release of Tissue-Type Plasminogen Activator (t-PA) in a Model of Vascular Perfusion in Rats 19
Cathepsin G, a Polymorphonuclear Leucocyte Protease, Affects Endothelial Monolayer Integrity Both in Vivo and ex Vivo 19
Identification and functional characterization of a novel mutation in the KCNA1 gene of a Sicilian family affected by episodic ataxia type 1 19
Role of the vascular wall in the thrombotic Tendency of Hypercholesterolemic Rats 19
Contributions of the central hydrophobic residue in the PXP motif of Voltage-Dependent K+ Channels to S6 flexibility and Gating Properties 19
Changes of the Hemostatic Balance in a Model of Aging in Rats 19
Changes in Primary Hemostasis and Blood Coagulation During the Formation of an Arterial Thrombus in Rats 19
Neutrophil Derived Cathepsin G Induce Potentially Thrombogenic Changes in Human Endothelial Cells: a scanning electron microscopy study in static and dynamic conditions 19
Episodic Ataxia Type 1 Mutations Affect Fast Inactivation of K+ Channels by a Reduction in Either Subunit Surface Expression or Affinity for Inactivation Domain 19
Musculoskeletal Features without Ataxia Associated with a Novel de novo Mutation in KCNA1 Impairing the Voltage Sensitivity of Kv1.1 Channel 19
The CaMKII/MLC1 Axis Confers Ca2+-Dependence to Volume-Regulated Anion Channels (VRAC) in Astrocytes 18
Episodic ataxia type-1 mutations in the hKv1.1 citoplasmic pore region alter the gating properties of the channels. 18
Cardiac Structural Alteration and Thrombotic Tendency in Spontaneously Hypercholestreolemic Rat 18
Modulation of delayed rectifier K+ channels by 5HT2c receptors 18
A Novel KCNA1 Mutation Identified in an Italian Family Affected by Episodic Ataxia Type 1 18
Episodic Ataxia Type 1 Mutations in the KCNA1 Gene Impair the Fast Inactivation Properties of the Human K+ Channels Kv1.4-1.1/Kvbeta1.1 and Kv1.4-1.1/Kvbeta1.2. 18
Experimental arterial thrombosis in genetically or diet induced hyperlipidemia in rats--role of vitamin K-dependent clotting factors and prevention by low-intensity oral anticoagulation 18
Episodic Ataxia Type 1 Mutation F184C Alters Zn2+-Induced Modulation of the Human Potassium Channel Kv1.4-Kv1.1/Kvbeta1.1 18
Morphological and Homeostatic Changes in Rats with Abdominal Arterial Prosthesis 17
New insights into the pathogenesis and therapeutics of episodic ataxia type 1 17
pH-Dependence of the Inwardly Rectifying Potassium Channel Kir5.1 and Localisation in Renal Tubular Epithelia 17
Gain-of-Function of the Inwardly-Rectifying K+ Channel Kir4.1 Contributes to Autism with Seizures and Intellectual Disability 17
Commentary: A channelopathy mutation in the voltage-sensor discloses contributions of a conserved phenylalanine to gating properties of Kv1.1 channels and ataxia 17
Abnormal Vascular Response to Fibrinolytic Stimulation inAged Rats 17
Electromechanical coupling of the Kv1.1 voltage-gated K+ channel is fine-tuned by the simplest amino acid residue in the S4-S5 linker 17
Role of inwardly-rectifying potassium channels Kir5.1 in learning and memory processes in a mouse knock-out model 16
Copertina della rivista The Journal of Physiology 16
Vascular Fibrinolysis in Aging: Enhanced Response to Adrenergic Stimulation 16
Episodic Ataxia Type 1 16
Mutations in KCNA1 gene associated with episodic ataxia type-1 sindrome impair heteromeric voltage-gated K+ channel function 16
Mutations in the KCNA1 Gene Associated with Episodic Ataxia Type-1 Syndrome Impair Heteromeric Voltage-Gated K+ Channel Function 16
Expression in e.coli and purification of recombinant fragments of wild type and mutant human prion protein 16
Autism with Seizures and Intellectual Disability: Possible Causative Role of Gain-of-Function of the Inwardly-Rectifying K+ Channel Kir4.1 16
The emerging role of the inwardly rectifying K+channels in autism spectrum disorders andepilepsy 16
Electromechanical coupling of the Kv1.1 voltage-gated K+ channel is fine-tuned by the simplest amino acid residue in the S4-S5 linker 16
Animal Models of Episodic Ataxia Type 1 (EA1) 15
ERG channels modulate the medial vestibular neurons processing of temporal information 15
Role of the S1 segment in the voltage-dependent gating of Kv1.1 channels revealed by naturally occurring pathogenic mutations. 15
Episodic Ataxias as Ion Channel Diseases 14
Identification of a heteromeric interaction which influences the rectification, gating and pH-sensitivity of Kir4.1/Kir5.1 potassium channels 14
Functional Characterization of an Episodic Ataxia Type-1 Mutation Occurring in the S1 Segment of hKv1.1 Channels. 14
Gating properties of human heteromeric voltage-gated potassium channels and effects of episodic ataxia type-1 mutations. 13
Ion Channels Involvement in Neurodevelopmental Disorders 13
Kv1.1 Channelopathies: Pathophysiological Mechanisms and Therapeutic Approaches 13
Voltage-gated calcium channels modulate synaptic transmission at vestibular neurons 9
Enhanced Vascular Plasminogen Activator (t-PA) Release by Epinephrine in Aged Rats 9
Functional Properties of Voltage-Gated Potassium Channels Probed with Methanethiosulfonate Reagents. 8
Effects of Episodic Ataxia-Associated Mutations on hKv1.4-1.1/Kvbeta1 channels 8
Effects of dyslipidemia on t-PA release in rats 8
Totale 1.957
Categoria #
all - tutte 25.267
article - articoli 0
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 25.267


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022181 0 0 0 0 0 0 96 16 28 31 4 6
2022/20231.392 218 25 4 218 152 235 2 102 219 68 125 24
2023/2024452 36 80 36 32 106 79 10 1 72 0 0 0
Totale 2.025