Università LUM Giuseppe Degennaro - sito della Ricerca Institutional Research Information System

D'ADAMO, MARIA CRISTINA 
 Distribuzione geografica
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Continente #
NA - Nord America 3.815
AS - Asia 1.321
EU - Europa 920
Continente sconosciuto - Info sul continente non disponibili 168
SA - Sud America 91
AF - Africa 73
OC - Oceania 6
Totale 6.394
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Nazione #
US - Stati Uniti d'America 3.751
SG - Singapore 640
CN - Cina 524
DE - Germania 377
FI - Finlandia 170
IT - Italia 109
FR - Francia 67
BR - Brasile 66
MA - Marocco 57
GB - Regno Unito 43
HK - Hong Kong 40
VN - Vietnam 38
CA - Canada 29
PL - Polonia 29
BE - Belgio 26
CZ - Repubblica Ceca 21
NL - Olanda 20
IN - India 16
MX - Messico 16
SA - Arabia Saudita 12
EE - Estonia 11
JP - Giappone 10
PK - Pakistan 10
RU - Federazione Russa 9
ZA - Sudafrica 9
BD - Bangladesh 7
HN - Honduras 7
ES - Italia 6
ID - Indonesia 6
JM - Giamaica 6
SE - Svezia 6
AR - Argentina 5
CO - Colombia 5
EC - Ecuador 5
RO - Romania 5
AU - Australia 4
IE - Irlanda 4
LT - Lituania 4
AE - Emirati Arabi Uniti 3
AT - Austria 3
IL - Israele 3
IQ - Iraq 3
PE - Perù 3
A2 - ???statistics.table.value.countryCode.A2??? 2
AZ - Azerbaigian 2
BO - Bolivia 2
CH - Svizzera 2
CL - Cile 2
CR - Costa Rica 2
EG - Egitto 2
NP - Nepal 2
NZ - Nuova Zelanda 2
TR - Turchia 2
VE - Venezuela 2
BG - Bulgaria 1
CI - Costa d'Avorio 1
DK - Danimarca 1
DM - Dominica 1
ET - Etiopia 1
GT - Guatemala 1
HU - Ungheria 1
KE - Kenya 1
KW - Kuwait 1
LB - Libano 1
MD - Moldavia 1
MK - Macedonia 1
MU - Mauritius 1
NI - Nicaragua 1
NO - Norvegia 1
PY - Paraguay 1
RS - Serbia 1
SV - El Salvador 1
TN - Tunisia 1
UA - Ucraina 1
UZ - Uzbekistan 1
Totale 6.228
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Città #
Chandler 580
Dallas 432
Ashburn 397
San Jose 391
Singapore 281
Frankfurt am Main 226
Helsinki 170
The Dalles 124
Hefei 122
Princeton 108
Lawrence 107
Munich 97
Cranberry Township 92
Beijing 68
Council Bluffs 62
Casablanca 56
Santa Clara 48
Las Vegas 45
Hong Kong 40
Hanover 39
Los Angeles 29
Columbus 26
Brussels 25
Brooklyn 24
Warsaw 24
Boardman 23
Seattle 23
Hillsboro 22
New York 22
Miami 21
Brno 20
San Francisco 19
Oxnard 16
Phoenix 16
Ho Chi Minh City 15
Atlanta 14
Boston 12
São Paulo 12
Genoa 11
Mexico City 10
Milan 10
Islamabad 9
Tokyo 9
Paris 8
Amsterdam 7
Chicago 7
Manchester 7
New Orleans 7
Barnet 6
Guangzhou 6
Hanoi 6
London 6
Montreal 6
Stockholm 6
Toronto 6
Bologna 5
Brasília 5
Charlotte 5
Johannesburg 5
Philadelphia 5
Queens 5
Riyadh 5
Rome 5
Roubaix 5
Shanghai 5
Bari 4
Bexley 4
Buffalo 4
Houston 4
Kingston 4
Limburg an der Lahn 4
Monte 4
Mumbai 4
Newark 4
Palermo 4
Reston 4
San Pedro Sula 4
Washington 4
Birmingham 3
Da Nang 3
Dublin 3
Laredo 3
Perugia 3
Pittsburgh 3
Poplar 3
Savannah 3
St Petersburg 3
Syracuse 3
Varese 3
Al Ain City 2
Andover 2
Augusta 2
Baku 2
Belo Horizonte 2
Brighton 2
Cambridge 2
Campobasso 2
Cape Town 2
Chennai 2
Cincinnati 2
Totale 4.132
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Nome #
Zinc Ion Dyshomeostasis in Autism Spectrum Disorder 197
A Novel KCNA2 Variant in a Patient with Non-Progressive Congenital Ataxia and Epilepsy: Functional Characterization and Sensitivity to 4-Aminopyridine 156
Update on the implication of potassium channels in autism: K(+) channelautism spectrum disorder 130
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 113
Altered functional properties of a missense variant in the TRESK K+ channel (KCNK18) associated with migraine and intellectual disability 102
A novel KCNA1 mutation in a patient with paroxysmal ataxia, myokymia, painful contractures and metabolic dysfunctions 98
Clinical and Functional Study of a De Novo Variant in the PVP Motif of Kv1.1 Channel Associated with Epilepsy, Developmental Delay and Ataxia 92
A Calsequestrin-1 mutation associated with a skeletal muscle disease alters sarcoplasmic Ca2+ release 79
Fotorecettori ed Epitelio Pigmentato della Retina; Meccanismi di Trasduzione e Rinnovamento 76
Adrenergic Stimulation of Tissue-type Plasminogen Activator Release in a Model of Vascular Perfusion in Rats 76
Autism with Seizures and Intellectual Disability: Possible Causative Role of Gain-of-Function of the Inwardly-Rectifying K+ Channel Kir4.1 73
A channelopathy mutation in the voltage-sensor discloses contributions of a conserved phenylalanine to gating properties of Kv1.1 channels and ataxia 71
5-HT2 receptors-mediated modulation of voltage-gated K+ channels and neurophysiopathological correlates 71
Amiloride Inhibits Tissue-Type Plasminogen Activator (t-PA) Release from Vascular Endothelium 69
Animal Models of Episodic Ataxia Type 1 (EA1) 67
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 66
An Episodic Ataxia Type-1 (EA1) mutation in the S1 segment sensitises the hKv1.1 potassium channel to extracellular Zn2+ 65
Mutations in the KCNA1 Gene Associated with Episodic Ataxia Type-1 Syndrome Impair Heteromeric Voltage-Gated K+ Channel Function 64
Antithrombotic Activity of Dermatan Sulphates, Heparin and their Combination in an Animal Model of Arterial Thrombosis 64
Kcnj16 (Kir5.1) Gene Ablation Causes Subfertility and Increases the Prevalence of Morphologically Abnormal Spermatozoa 64
Reconciling the discrepancies on the involvement of large-conductance Ca(2+)-activated K channels in glioblastoma cell migration 63
Identification of a New de Novo Mutation Underlying Regressive Episodic Ataxia Type I 63
Author Correction: Thymosin α1 represents a potential potent single-molecule-based therapy for cystic fibrosis 63
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. 63
An activator of voltage-gated K+channels Kv1.1 as a therapeutic candidate for episodic ataxia type 1 62
Differential pH-sensitivity of Kir4.1 and Kir4.2 and modulation by heteropolymerisation with Kir5.1 62
A Novel KCNA1 Mutation Identified in an Italian Family Affected by Episodic Ataxia Type 1 62
Localization and Age Dependent Expression of the Inward Rectifier K+ Channel Kir 5.1 in a Mammalian Reproductive System 61
KCNK18 Biallelic Variants Associated with Intellectual Disability and Neurodevelopmental Disorders Alter TRESK Channel Activity 61
Lethal digenic mutations in the K+channels kir4.1 (KCNJ10) and SLACK (KCNT1) associated with severe-disabling seizures and neurodevelopmental delay 58
Dexamethasone in Glioblastoma Multiforme Therapy: Mechanisms and Controversies 58
Abnormal Vascular Response to Fibrinolytic Stimulation inAged Rats 58
Episodic ataxia type-1 mutations in the hKv1.1 citoplasmic pore region alter the gating properties of the channels. 57
Kv1.1 knock-in ataxic mice exhibit spontaneous myokymic activity exacerbated by fatigue, ischemia and low temperature 57
The emerging role of the inwardly rectifying K+channels in autism spectrum disorders andepilepsy 57
Episodic ataxia type 1 mutations cause loss-of-function impairments of heteromeric channels formed by the Kv1.4 and Kv1.1 subunits 57
Genetic inactivation of Kcnj16 identifies Kir5.1 as an important determinant of neuronal PCO2/pH sensitivity 56
Effect of Aspirin on the Fibrinolytic Response in Perfused Rat Hindquarters 56
Hypercoagulable State in Aged Rats 55
Genetically-induced abnormalities of Kir2.1 channels: implications for short QT3 syndrome and autism/epilepsy phenotype 55
Gain-of-function defects of astrocytic Kir4.1 channels in children with autism spectrum disorders and epilepsy 54
Novel phenotype associated with a mutation in the KCNA1(Kv1.1) gene 54
Kv1.1 Channelopathies: Pathophysiological Mechanisms and Therapeutic Approaches 54
Antithrombotic activity of dermatan sulphates, heparins and their combination in an animal model of arterial thrombosis 53
Genetic investigation of children with ataxia using exome sequencing 53
The CaMKII/MLC1 Axis Confers Ca2+-Dependence to Volume-Regulated Anion Channels (VRAC) in Astrocytes 52
Mutations in KCNA1 affect stoichiometry and fast inactivation of heteromeric K+ channels 52
Thymosin α1 represents a potential potent single-molecule-based therapy for cystic fibrosis 52
Musculoskeletal Features without Ataxia Associated with a Novel de novo Mutation in KCNA1 Impairing the Voltage Sensitivity of Kv1.1 Channel 52
Role of RPTPα and Tyrosine Phosphorylation in the Serotonergic Inhibition of Voltage-Dependent Potassium Channels 51
Publisher Correction: Thymosin α1 represents a potential potent single-molecule-based therapy for cystic fibrosis 50
Episodic Ataxia Type 1 Mutations Affect Fast Inactivation of K+ Channels by a Reduction in Either Subunit Surface Expression or Affinity for Inactivation Domain 50
Copertina della rivista scientifica: Neuroscience 49
Changes in Primary Hemostasis During Thrombus Formation in a Model of Artherial Thrombosis in Rats 49
Contributions of the central hydrophobic residue in the PXP motif of Voltage-Dependent K+ Channels to S6 flexibility and Gating Properties 49
Modulation of delayed rectifier K+ channels by 5HT2c receptors 49
New insights into the pathogenesis and therapeutics of episodic ataxia type 1 49
Electromechanical coupling of the Kv1.1 voltage-gated K+ channel is fine-tuned by the simplest amino acid residue in the S4-S5 linker 49
The Episodic Ataxia Type 1 Mutation F184C Alters the Zn2+ Modulation of the Human Kv1.4-Kv1.1/Kvbeta1 Channel 48
Different Response of Vascular Fibrinolysis to Adrenergic Stimulation in Young and Aged Rats 48
De novo point mutations in patients diagnosed with ataxic cerebral palsy 48
KCNA4 deficiency leads to a syndrome of abnormal striatum, congenital cataract and intellectual disability 48
Gain-of-Function of the Inwardly-Rectifying K+ Channel Kir4.1 Contributes to Autism with Seizures and Intellectual Disability 48
Role of the vascular wall in the thrombotic Tendency of Hypercholesterolemic Rats 47
Neutrophil Derived Cathepsin G Induce Potentially Thrombogenic Changes in Human Endothelial Cells: a scanning electron microscopy study in static and dynamic conditions 47
Ion Channels Involvement in Neurodevelopmental Disorders 47
Electromechanical coupling of the Kv1.1 voltage-gated K+ channel is fine-tuned by the simplest amino acid residue in the S4-S5 linker 47
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 46
Cardiac Structural Alteration and Thrombotic Tendency in Spontaneously Hypercholestreolemic Rat 46
The Episodic Ataxia Type 1 Mutation F184C Alters the Zn2+ Modulation of the Human Kv1.4-Kv1.1/Kvbeta1 Channel 46
Murine Models of EA1 46
Vascular Fibrinolysis in Aging: Enhanced Response to Adrenergic Stimulation 46
Changes in Primary Hemostasis and Blood Coagulation During the Formation of an Arterial Thrombus in Rats 46
Copertina della rivista The Journal of Physiology 45
ERG channels regulate the excitability of medial vestibular neurons 45
Gating properties of human heteromeric voltage-gated potassium channels and effects of episodic ataxia type-1 mutations. 45
Changes of the Hemostatic Balance in a Model of Aging in Rats 45
Expression in e.coli and purification of recombinant fragments of wild type and mutant human prion protein 45
Role of the S1 segment in the voltage-dependent gating of Kv1.1 channels revealed by naturally occurring pathogenic mutations. 44
The Response of Vascular Fibrinolysis to the Adrenergic Stimulation is Abnormal in Aged Rats 44
Amiloride inhibits tissue-type plasminogen activator (t-PA) release from vascular endothelium 43
Role of inwardly-rectifying potassium channels Kir5.1 in learning and memory processes in a mouse knock-out model 43
Functional Properties of Voltage-Gated Potassium Channels Probed with Methanethiosulfonate Reagents. 43
Episodic Ataxia Type 1 43
Mutations in KCNA1 gene associated with episodic ataxia type-1 sindrome impair heteromeric voltage-gated K+ channel function 43
Differential pH-sensitivity of Kir4.1 and Kir4.2 and Modulation by Heteropolymerisation with Kir5.1. 43
The role of ion channels in the hypoxia-induced aggressiveness of glioblastoma 43
K+ channelepsy: progress in the neurobiology of potassium channels and epilepsy 43
Functional Characterization of an Episodic Ataxia Type-1 Mutation Occurring in the S1 Segment of hKv1.1 Channels. 43
Episodic Ataxia Type 1 Mutation F184C Alters Zn2+-Induced Modulation of the Human Potassium Channel Kv1.4-Kv1.1/Kvbeta1.1 43
pH-Dependence of the Inwardly Rectifying Potassium Channel Kir5.1 and Localisation in Renal Tubular Epithelia 43
The neurobiology of episodic ataxia type 1: a Shaker-like K+ channel disorder 42
Thrombotic Tendency in Spontaneously Hypercholesterolemic Rats 42
Identification and functional characterization of a novel mutation in the KCNA1 gene of a Sicilian family affected by episodic ataxia type 1 42
Morphological and Homeostatic Changes in Rats with Abdominal Arterial Prosthesis 42
Commentary: A channelopathy mutation in the voltage-sensor discloses contributions of a conserved phenylalanine to gating properties of Kv1.1 channels and ataxia 42
ERG channels modulate the medial vestibular neurons processing of temporal information 41
Cathepsin G, a Polymorphonuclear Leucocyte Protease, Affects Endothelial Monolayer Integrity Both in Vivo and ex Vivo 38
Identification of a heteromeric interaction which influences the rectification, gating and pH-sensitivity of Kir4.1/Kir5.1 potassium channels 38
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 38
Totale 5.753
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Categoria #
all - tutte 75.246
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 75.246
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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
2022/20231.360 218 25 4 218 152 235 2 101 214 63 123 5
2023/2024483 33 79 34 29 96 79 10 1 72 7 0 43
2024/2025815 18 15 15 165 110 70 12 19 189 14 90 98
2025/20263.007 143 461 263 266 193 73 583 199 215 394 86 131
2026/2027548 43 129 181 195 0 0 0 0 0 0 0 0
Totale 6.394