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 1.644
EU - Europa 418
AS - Asia 187
OC - Oceania 6
Continente sconosciuto - Info sul continente non disponibili 2
SA - Sud America 1
Totale 2.258
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Nazione #
US - Stati Uniti d'America 1.639
FI - Finlandia 170
SG - Singapore 144
DE - Germania 136
IT - Italia 34
CN - Cina 32
BE - Belgio 23
CZ - Repubblica Ceca 21
FR - Francia 7
CA - Canada 5
GB - Regno Unito 5
NL - Olanda 5
SA - Arabia Saudita 5
AU - Australia 4
RU - Federazione Russa 4
AT - Austria 3
PL - Polonia 3
A2 - ???statistics.table.value.countryCode.A2??? 2
HK - Hong Kong 2
IL - Israele 2
NZ - Nuova Zelanda 2
AE - Emirati Arabi Uniti 1
CL - Cile 1
DK - Danimarca 1
ES - Italia 1
IN - India 1
NO - Norvegia 1
RO - Romania 1
RS - Serbia 1
SE - Svezia 1
UA - Ucraina 1
Totale 2.258
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Città #
Chandler 580
Helsinki 170
Singapore 130
Ashburn 114
Lawrence 107
Princeton 107
Munich 91
Las Vegas 44
Hanover 39
Boardman 23
Brussels 23
Brno 20
Miami 16
Seattle 10
Genoa 9
Atlanta 7
Shanghai 4
Milan 3
Paris 3
Toronto 3
Andover 2
Cambridge 2
Guangzhou 2
Hong Kong 2
Nanyang 2
Novokuznetsk 2
Perugia 2
Piscataway 2
Roubaix 2
Weston-super-Mare 2
Zhengzhou 2
Al Ain City 1
Augusta 1
Beijing 1
Belgrade 1
Buffalo 1
Clifton 1
Cupertino 1
Den Haag 1
Dunedin 1
Florence 1
Hamm 1
Harbin 1
Iesi 1
Jiangmen 1
Lanzhou 1
Madrid 1
Nanchang 1
Nanning 1
Ningde 1
Olomouc 1
Qinhuangdao 1
Raanana 1
Riyadh 1
Rizhao 1
Rome 1
Santa Clara 1
Siena 1
Stockholm 1
Suri 1
Sydney 1
Tel Aviv 1
Trumbull 1
Varese 1
Vergiate 1
Weihai 1
Totale 1.560
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Nome #
A Novel KCNA2 Variant in a Patient with Non-Progressive Congenital Ataxia and Epilepsy: Functional Characterization and Sensitivity to 4-Aminopyridine 73
Altered functional properties of a missense variant in the TRESK K+ channel (KCNK18) associated with migraine and intellectual disability 65
Clinical and Functional Study of a De Novo Variant in the PVP Motif of Kv1.1 Channel Associated with Epilepsy, Developmental Delay and Ataxia 64
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 60
A novel KCNA1 mutation in a patient with paroxysmal ataxia, myokymia, painful contractures and metabolic dysfunctions 59
Adrenergic Stimulation of Tissue-type Plasminogen Activator Release in a Model of Vascular Perfusion in Rats 33
A channelopathy mutation in the voltage-sensor discloses contributions of a conserved phenylalanine to gating properties of Kv1.1 channels and ataxia 32
Identification of a New de Novo Mutation Underlying Regressive Episodic Ataxia Type I 31
Differential pH-sensitivity of Kir4.1 and Kir4.2 and modulation by heteropolymerisation with Kir5.1 29
5-HT2 receptors-mediated modulation of voltage-gated K+ channels and neurophysiopathological correlates 29
Fotorecettori ed Epitelio Pigmentato della Retina; Meccanismi di Trasduzione e Rinnovamento 28
Lethal digenic mutations in the K+channels kir4.1 (KCNJ10) and SLACK (KCNT1) associated with severe-disabling seizures and neurodevelopmental delay 28
Localization and Age Dependent Expression of the Inward Rectifier K+ Channel Kir 5.1 in a Mammalian Reproductive System 28
Reconciling the discrepancies on the involvement of large-conductance Ca(2+)-activated K channels in glioblastoma cell migration 27
De novo point mutations in patients diagnosed with ataxic cerebral palsy 27
Dexamethasone in Glioblastoma Multiforme Therapy: Mechanisms and Controversies 27
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 27
Genetic inactivation of Kcnj16 identifies Kir5.1 as an important determinant of neuronal PCO2/pH sensitivity 27
Effect of Aspirin on the Fibrinolytic Response in Perfused Rat Hindquarters 27
The Episodic Ataxia Type 1 Mutation F184C Alters the Zn2+ Modulation of the Human Kv1.4-Kv1.1/Kvbeta1 Channel 26
Amiloride Inhibits Tissue-Type Plasminogen Activator (t-PA) Release from Vascular Endothelium 26
Autism with Seizures and Intellectual Disability: Possible Causative Role of Gain-of-Function of the Inwardly-Rectifying K+ Channel Kir4.1 26
Genetic investigation of children with ataxia using exome sequencing 25
Murine Models of EA1 25
A Calsequestrin-1 mutation associated with a skeletal muscle disease alters sarcoplasmic Ca2+ release 25
Episodic ataxia type 1 mutations cause loss-of-function impairments of heteromeric channels formed by the Kv1.4 and Kv1.1 subunits 25
Kcnj16 (Kir5.1) Gene Ablation Causes Subfertility and Increases the Prevalence of Morphologically Abnormal Spermatozoa 25
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
Genetically-induced abnormalities of Kir2.1 channels: implications for short QT3 syndrome and autism/epilepsy phenotype 24
Author Correction: Thymosin α1 represents a potential potent single-molecule-based therapy for cystic fibrosis 24
Antithrombotic Activity of Dermatan Sulphates, Heparin and their Combination in an Animal Model of Arterial Thrombosis 24
Animal Models of Episodic Ataxia Type 1 (EA1) 23
Role of RPTPα and Tyrosine Phosphorylation in the Serotonergic Inhibition of Voltage-Dependent Potassium Channels 23
Update on the implication of potassium channels in autism: K(+) channelautism spectrum disorder 23
A Novel KCNA1 Mutation Identified in an Italian Family Affected by Episodic Ataxia Type 1 23
An Episodic Ataxia Type-1 (EA1) mutation in the S1 segment sensitises the hKv1.1 potassium channel to extracellular Zn2+ 23
Gain-of-function defects of astrocytic Kir4.1 channels in children with autism spectrum disorders and epilepsy 23
Novel phenotype associated with a mutation in the KCNA1(Kv1.1) gene 23
Copertina della rivista scientifica: Neuroscience 22
ERG channels regulate the excitability of medial vestibular neurons 22
Hypercoagulable State in Aged Rats 22
Differential pH-sensitivity of Kir4.1 and Kir4.2 and Modulation by Heteropolymerisation with Kir5.1. 22
Different Response of Vascular Fibrinolysis to Adrenergic Stimulation in Young and Aged Rats 22
Thymosin α1 represents a potential potent single-molecule-based therapy for cystic fibrosis 22
KCNK18 Biallelic Variants Associated with Intellectual Disability and Neurodevelopmental Disorders Alter TRESK Channel Activity 22
Musculoskeletal Features without Ataxia Associated with a Novel de novo Mutation in KCNA1 Impairing the Voltage Sensitivity of Kv1.1 Channel 22
Thrombotic Tendency in Spontaneously Hypercholesterolemic Rats 21
The Episodic Ataxia Type 1 Mutation F184C Alters the Zn2+ Modulation of the Human Kv1.4-Kv1.1/Kvbeta1 Channel 21
The Response of Vascular Fibrinolysis to the Adrenergic Stimulation is Abnormal in Aged Rats 21
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. 21
KCNA4 deficiency leads to a syndrome of abnormal striatum, congenital cataract and intellectual disability 21
Episodic Ataxia Type 1 Mutation F184C Alters Zn2+-Induced Modulation of the Human Potassium Channel Kv1.4-Kv1.1/Kvbeta1.1 21
Episodic Ataxia Type 1 Mutations Affect Fast Inactivation of K+ Channels by a Reduction in Either Subunit Surface Expression or Affinity for Inactivation Domain 21
The neurobiology of episodic ataxia type 1: a Shaker-like K+ channel disorder 20
Identification and functional characterization of a novel mutation in the KCNA1 gene of a Sicilian family affected by episodic ataxia type 1 20
Role of the vascular wall in the thrombotic Tendency of Hypercholesterolemic Rats 20
Changes in Primary Hemostasis During Thrombus Formation in a Model of Artherial Thrombosis in Rats 20
Contributions of the central hydrophobic residue in the PXP motif of Voltage-Dependent K+ Channels to S6 flexibility and Gating Properties 20
Mutations in the KCNA1 Gene Associated with Episodic Ataxia Type-1 Syndrome Impair Heteromeric Voltage-Gated K+ Channel Function 20
The role of ion channels in the hypoxia-induced aggressiveness of glioblastoma 20
Changes in Primary Hemostasis and Blood Coagulation During the Formation of an Arterial Thrombus in Rats 20
Kv1.1 knock-in ataxic mice exhibit spontaneous myokymic activity exacerbated by fatigue, ischemia and low temperature 20
Abnormal Vascular Response to Fibrinolytic Stimulation inAged Rats 20
The CaMKII/MLC1 Axis Confers Ca2+-Dependence to Volume-Regulated Anion Channels (VRAC) in Astrocytes 19
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
Cardiac Structural Alteration and Thrombotic Tendency in Spontaneously Hypercholestreolemic Rat 19
Changes of the Hemostatic Balance in a Model of Aging 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
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 19
The emerging role of the inwardly rectifying K+channels in autism spectrum disorders andepilepsy 19
Electromechanical coupling of the Kv1.1 voltage-gated K+ channel is fine-tuned by the simplest amino acid residue in the S4-S5 linker 19
Episodic ataxia type-1 mutations in the hKv1.1 citoplasmic pore region alter the gating properties of the channels. 18
Role of inwardly-rectifying potassium channels Kir5.1 in learning and memory processes in a mouse knock-out model 18
Morphological and Homeostatic Changes in Rats with Abdominal Arterial Prosthesis 18
New insights into the pathogenesis and therapeutics of episodic ataxia type 1 18
pH-Dependence of the Inwardly Rectifying Potassium Channel Kir5.1 and Localisation in Renal Tubular Epithelia 18
Gain-of-Function of the Inwardly-Rectifying K+ Channel Kir4.1 Contributes to Autism with Seizures and Intellectual Disability 18
Commentary: A channelopathy mutation in the voltage-sensor discloses contributions of a conserved phenylalanine to gating properties of Kv1.1 channels and ataxia 18
Electromechanical coupling of the Kv1.1 voltage-gated K+ channel is fine-tuned by the simplest amino acid residue in the S4-S5 linker 18
Episodic Ataxia Type 1 17
Modulation of delayed rectifier K+ channels by 5HT2c receptors 17
Expression in e.coli and purification of recombinant fragments of wild type and mutant human prion protein 17
Functional Characterization of an Episodic Ataxia Type-1 Mutation Occurring in the S1 Segment of hKv1.1 Channels. 17
Copertina della rivista The Journal of Physiology 16
Cathepsin G, a Polymorphonuclear Leucocyte Protease, Affects Endothelial Monolayer Integrity Both in Vivo and ex Vivo 16
Vascular Fibrinolysis in Aging: Enhanced Response to Adrenergic Stimulation 16
Mutations in KCNA1 gene associated with episodic ataxia type-1 sindrome impair heteromeric voltage-gated K+ channel function 16
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
Identification of a heteromeric interaction which influences the rectification, gating and pH-sensitivity of Kir4.1/Kir5.1 potassium channels 15
Ion Channels Involvement in Neurodevelopmental Disorders 15
Episodic Ataxias as Ion Channel Diseases 14
Gating properties of human heteromeric voltage-gated potassium channels and effects of episodic ataxia type-1 mutations. 14
Kv1.1 Channelopathies: Pathophysiological Mechanisms and Therapeutic Approaches 14
Voltage-gated calcium channels modulate synaptic transmission at vestibular neurons 11
Integrative analysis of long isoform sequencing and functional data identifies distinct cortical layer neuronal subtypes derived from human iPSCs 10
Enhanced Vascular Plasminogen Activator (t-PA) Release by Epinephrine in Aged Rats 10
Functional Properties of Voltage-Gated Potassium Channels Probed with Methanethiosulfonate Reagents. 9
Effects of Episodic Ataxia-Associated Mutations on hKv1.4-1.1/Kvbeta1 channels 9
Totale 2.307
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Categoria #
all - tutte 39.124
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 39.124
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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
2024/2025393 18 15 15 165 110 70 0 0 0 0 0 0
Totale 2.417