MASTRANGELO, Mario
 Distribuzione geografica
Continente #
NA - Nord America 4.226
EU - Europa 2.044
AS - Asia 1.003
SA - Sud America 57
AF - Africa 15
OC - Oceania 13
Continente sconosciuto - Info sul continente non disponibili 2
Totale 7.360
Nazione #
US - Stati Uniti d'America 4.139
IT - Italia 1.002
SG - Singapore 457
UA - Ucraina 301
IN - India 235
CN - Cina 231
SE - Svezia 192
FI - Finlandia 132
GB - Regno Unito 87
CA - Canada 79
DE - Germania 61
AR - Argentina 48
FR - Francia 44
IE - Irlanda 37
RU - Federazione Russa 37
NL - Olanda 34
ID - Indonesia 30
BG - Bulgaria 29
BE - Belgio 26
AU - Australia 13
ES - Italia 9
CH - Svizzera 8
JP - Giappone 8
IR - Iran 7
RO - Romania 7
RS - Serbia 7
PL - Polonia 6
TG - Togo 6
TR - Turchia 6
BR - Brasile 5
KR - Corea 5
MX - Messico 5
TW - Taiwan 5
EG - Egitto 4
HK - Hong Kong 4
IL - Israele 4
PT - Portogallo 4
AL - Albania 3
AT - Austria 3
BZ - Belize 3
CL - Cile 3
CZ - Repubblica Ceca 3
IQ - Iraq 3
LT - Lituania 3
VN - Vietnam 3
ZA - Sudafrica 3
EU - Europa 2
GR - Grecia 2
PH - Filippine 2
SK - Slovacchia (Repubblica Slovacca) 2
CO - Colombia 1
DK - Danimarca 1
EE - Estonia 1
HU - Ungheria 1
JO - Giordania 1
KG - Kirghizistan 1
MK - Macedonia 1
NO - Norvegia 1
PS - Palestinian Territory 1
SC - Seychelles 1
TN - Tunisia 1
Totale 7.360
Città #
Fairfield 521
Chandler 325
Rome 281
Singapore 275
Woodbridge 262
Ashburn 247
Houston 213
Seattle 212
Secaucus 181
Wilmington 174
Cambridge 144
Beijing 142
Ann Arbor 140
Santa Clara 134
Princeton 130
New York 110
Jacksonville 100
Plano 93
San Paolo di Civitate 69
Millbury 59
Lawrence 56
Boardman 55
Dearborn 50
Torre del Greco 49
Boston 46
Ottawa 45
San Diego 41
Helsinki 40
Dublin 37
Federal 37
Andover 35
Milan 33
Sofia 29
Jakarta 28
Norwalk 27
Toronto 23
Brussels 22
Falls Church 18
Moscow 18
Fremont 17
Naples 14
Des Moines 13
Florence 13
Lappeenranta 11
Turin 10
Auburn Hills 9
Bühl 9
Civitanova Marche 9
Falkenstein 9
Pozzolengo 9
Salò 9
Hefei 8
Phoenix 8
Bologna 7
Bremen 7
Fasano 7
Kunming 7
London 7
Mannheim 7
Nanjing 7
Ravenna 7
Cagliari 6
Lomé 6
Melbourne 6
Palermo 6
San Mateo 6
Chicago 5
Cipolletti 5
Frankfurt am Main 5
Jinan 5
Miami 5
Nanchang 5
Padova 5
Pamplona 5
Redmond 5
Redwood City 5
San Jose 5
Southend 5
Stockholm 5
Venezia 5
Bari 4
Bern 4
Hangzhou 4
Little Rock 4
Los Angeles 4
Mumbai 4
Needham 4
Polignano a Mare 4
Radomsko 4
St Louis 4
Torino 4
Véry 4
Waanrode 4
Angri 3
Belize City 3
Brno 3
Cairo 3
Cinisello Balsamo 3
Dallas 3
Fongshan District 3
Totale 4.878
Nome #
The impact of next generation sequencing in the diagnostic work-up of pediatric epilepsies: a single centre observational cohort study 309
MALFORMAZIONE DI CHIARI DI TIPO I E POLIMICROGIRIA PERISILVIANA BILATERALE 163
Pyridoxine-5'-phosphate oxidase (pnpo) deficiency. clinical and biochemical alterations associated with the c.347g>a (pp. arg116gln) mutation 116
Biochemical data from the characterization of a new pathogenic mutation of human pyridoxine-5'-phosphate oxidase (PNPO) 115
Acute diplopia in the pediatric Emergency Department. A cohort multicenter Italian study 108
EMIMEGALOENCEFALIA E SINDROME DI PROTEUS: PRESENTAZIONE DI UN CASO 107
Actual insights into the clinical management of febrile seizures 102
PRICKLE1-related early onset epileptic encephalopathy 99
Management of Neurological Emergencies in Children: An Updated Overview 97
Lennox-Gastaut Syndrome: A State of the Art Review. 94
STUPOR AND FAST ACTIVITY ON ELECTROENCEPHALOGRAPHY IN A CHILD TREATED WITH VALPROATE 92
Report of two never treated adult sisters with aromatic L-amino Acid decarboxylase deficiency: a portrait of the natural history of the disease or an expanding phenotype? 90
Corrigendum to “Pyridoxine-5′-phosphate oxidase (Pnpo) deficiency: Clinical and biochemical alterations associated with the C.347g > A (P.·Arg116gln) mutation” [Mol. Genet. Metab. 122/1–2 (2017) 135–142] 89
POSSIBLE ASSOCIATIONS OF POLYMORPHISMS IN THE METABOTROPIC GLUTAMATE RECEPTOR TYPE 3 GENE (GRM3) WITH ABSENCE EPILEPSY 88
Bilateral (opercular and paracentral lobular) polymicrogyria and neurofibromatosis type 1 86
Novel Genes of Early-Onset Epileptic Encephalopathies: From Genotype to Phenotypes. 84
Minor head trauma in the pediatric emergency department: decision making nodes 82
Progressive myoclonus epilepsy and ceroidolipofuscinosis 14. The multifaceted phenotypic spectrum of KCTD7-related disorders 80
The outcome of white matter abnormalities in early treated phenylketonuric patients. A retrospective longitudinal long-term study 80
ANIDROSI E IPERTERMIA IN BAMBINO IN TRATTAMENTO CON TOPIRAMATO 79
Epilepsy in children with type 1 diabetes mellitus: Pathophysiological basis and clinical hallmarks. 79
Bilateral perysilvian polymicrogyria in Chiari I malformation 78
TUMURI NEUROEPITELIALI DISEMBRIOBLASTICI (DNET) IN ETA’ PEDIATRICA 77
SCHIZENCEFALIA PARIETALE SINISTRA E POLIMICROGIRIA PARIETO – OCCIPITALE BILATERALE 77
Pyridoxine-dependent epilepsies: an observational study on clinical, diagnostic, therapeutic and prognostic features in a pediatric cohort. 77
PANENCEFALITE SUBACUTA SCLEROSANTE: UN CASO PEDIATRICO 76
ADEM E SCLEROSI MULTIPLA: QUALI SONO I CONFINI?” 75
Neuromotor and cognitive outcomes of early treatment in tyrosine hydroxylase deficiency type b 72
Photosensitivity as an early marker of epileptic and developmental encephalopathies 71
A new form of cerebral folate deficiency with severe self-injurious behaviour 70
New trends in neuronal migration disorders 70
Complex epileptic (Foix-Chavany-Marie like) syndrome in a child with neurofibromatosis type 1 (nf1) and bilateral (opercular and paracentral) polymicrogyria 70
SINCOPI IN ETA’ PEDIATRICA: LA NOSTRA ESPERIENZA CLINICA 69
Broadening phenotype of adenylosuccinate lyase deficiency: A novel clinical pattern resembling neuronal ceroid lipofuscinosis 69
Mitochondrial Neurogastrointestinal Encephalomyopathy: Novel Pathogenic Mutations in Thymidine Phosphorylase Gene in Two Italian Brothers 68
A diagnostic algorithm for the evaluation of early onset genetic-metabolic epileptic encephalopathies 68
LA SINDROME DI OHTAHARA: NUOVE ACQUISIZIONI EZIOPATOGENETICHE 67
Eponym: Rasmussen syndrome 67
Teaching Video NeuroImages: Clinical course of infantile ascending hereditary spastic paralysis 66
Consensus guideline for the diagnosis and treatment of aromatic l-amino acid decarboxylase (AADC) deficiency 66
NEUROLOGICAL “SOFT SIGNS” IN CHILDREN AND ADOLESCENTS 65
A novel developmental encephalopathy with epilepsy and hyperkinetic movement disorders associated with a deletion of the sodium channel gene cluster on chromosome 2q24.3 64
TRATTAMENTO CON INFUSIONE CONTINUA DI ALFA INTERFERON PER VIA INTRATECALE TRAMITE POMPA D’ INFUSIONE LOMBARE NELLA PANENCEFALITE SUBACUTA SCLEROSANTE: PRESENTAZIONE DI UN CASO CLINICO 64
Genes of Early-Onset Epileptic Encephalopathies: From Genotype to Phenotype 63
Transdermal rotigotine in the treatment of aromatic L-amino acid decarboxylase deficiency 63
Genetic background of febrile seizures 60
The International Working Group on Neurotransmitter related Disorders (iNTD): A worldwide research project focused on primary and secondary neurotransmitter disorders 60
POLIMORFISMI DI SINGOLI NUCLEOTIDI (SNPS) DEL GENE CODIFICANTE PER IL RECETTORE METABOTROPO PER IL GLUTAMMATO DI TIPO 3 (GRM3) IN BAMBINI CON ASSENZE: UN POSSIBILE LINK PATOGENETICO? 59
MEGACISTERNA MAGNA E DISTURBI DEL LINGUAGGIO 59
AADC deficiency from infancy to adulthood: Symptoms and developmental outcome in an international cohort of 63 patients 59
TSC1 as a Novel Gene for Sleep-Related Hypermotor Epilepsy: A Child with a Mild Phenotype of Tuberous Sclerosis 59
Early-onset hereditary neuropathy with liability to pressure palsy 59
Inborn errors of creatine metabolism and epilepsy 58
ENCEFALITE DI RASMUSSEN 57
Stupor and fast activity on electroencephalography in a child treated with valproate. 57
Suggestive Seizure Induction technique in a pediatric PNES population related to neurocognitive and psychological profile: a pilot study. 55
RUOLO DELLA DTI NELLA DEFINIZIONE DELLE PATOLOGIE EPILETTICHE 53
Ap1s2-truncating variant in a patient with severe neurodevelopmental disorder and cerebral folate deficiency 53
PHENOTYIPING AND DIAGNOSTIC TIMING IN NGS-DIAGNOSED GENETIC DEVELOPMENTAL ENCEPHALOPATHIES WITH EPILEPSY AND MOVEMENT DISORDERS 53
UN CASO DI MALATTIA DI KAWASAKY 52
STROKE IN ETA’ PEDIATRICA: VALUTAZIONE DEI FATTORI DI RISCHIO E PRESENTAZIONE DI UNA CASISTICA 52
Clinical approach to neurodegenerative disorders in childhood: an updated overview. 52
Update on the treatment of vitamin B6 dependent epilepsies 52
ENCEFALITE DI RASMUSSEN: PRESENTAZIONE DI UN CASO CLINICO 51
STATO EMICRANICO E PUPILLA DI ADIE IN ETÀ PEDIATRICA 51
Diagnostic work-up and therapeutic options in management of pediatric status epilepticus 51
Other single-gene disorders 51
SINTOMI NEUROLOGICI DI ALLARME IN ETA’ EVOLUTIVA 50
Assessment of intellectual impairment, health-related quality of life, and behavioral phenotype in patients with neurotransmitter related disorders: data from the iNTD registry 50
GLUT1 DEFICIENCY: A MILD PHENOTYPE IN A 4 YEARS OLD FEMALE WITH EARLY ONSET ABSENCES AND ATAXIA 49
The spectrum of movement disorders under 3 years of agein inherited disorders of monoamine metabolism 49
EMIMEGALOENCEFALIA E SINDROME DI PROTEUS: PRESENTAZIONE DI UN CASO CLINICO 49
Acute ischemic stroke in childhood: a comprehensive review 49
Actual insights into treatable inborn errors of metabolism causing epilepsy 48
DISPLASIA FRONTONASALE, SINDROME DI CHIARI DI TIPO I E POLIMICROGIRIA: UNA NUOVA ASSOCIAZIONE 46
TERAPIA DELL’ EPILESSIA 46
POLYMICROGYRIA ASSOCIATED WITH NEUROFIBROMATOSIS TYPE 1 46
The natural history of l-aminoacid decarboxylase (AADC) deficiency: report of two never treated adult patients. 46
Epilepsy in kcnh1-related syndromes 46
Consensus guideline for the diagnosis and treatment of tetrahydrobiopterin (BH4) deficiencies 46
White matter involvement and neurocognitive outcome in phenylketonuric (PKU) patients with and without BH4/sapropterin dihydrochloride supplementation 45
LEISHMANIOSI VISCERALE E SUPERINFEZIONI: UN CASO PEDIATRICO 43
ESORDIO PEDIATRICO PRECOCE IN UN CASO DI NEUROPATIA EREDITARIA CON IPERSENSIBILITA’ ALLA PRESSIONE (HNPP) 43
Compound heterozygosis in AADC deficiency: A complex phenotype dissected through comparison among heterodimeric and homodimeric AADC proteins 43
I DISTURBI DELLA DEAMBULAZIONE 42
LONG TERM OUTCOME IN TYROSINE HYDROXYLASE DEFICIENCY- TYPE B: A FIFTEEN YEARS FOLLOW UP IN A MALE PATIENT 42
EARLY ONSET PARKINSONISM: A NEW CLINICAL AND BIOCHEMICAL PHENOTYPE 42
Insights into the expanding phenotypic spectrum of inherited disorders of biogenic amines 42
Expanding the genetic and phenotypic spectrum of CHD2-related disease: From early neurodevelopmental disorders to adult-onset epilepsy 42
Fenotipo epilettico e gestione terapeutica in un paziente con deficit di succinico semialdeide deidrogenasi: evoluzione dall’ infanzia all’ età adulta 42
UTILIZZO DELLE IMMUNOGLOBULINE NELLA MIELITE TRASVERSA: PRESENTAZIONE DI UN CASO 40
Neurodevelopmental Impairment As the Main Phenotypic Hallmark Associated with the Translocation t(7;10)(7p22.3;q26.11) 40
Contemporary onset of atypical chronic inflammatory demyelinating polyradiculoneuropathy and type 1 diabetes in an adolescent 40
Successful pregnancy in a patient with l-amino acid decarboxylase deficiency. therapeutic management and clinical outcome 38
null 38
KCNQ2 encephalopathy manifesting with Rett-like features A follow-up into adulthood 38
Early post-cooling brain magnetic resonance for the prediction of neurodevelopmental outcome in newborns with hypoxic-ischemic encephalopathy 38
Stroke and stroke-like episodes in inborn errors of metabolism: Pathophysiological and clinical implications 38
LOSS OF CONTINUITY OF CARE IN PEDIATRIC NEUROLOGY SERVICES DURING COVID-19 LOCKDOWN: AN ADDITIONAL STRESSOR FOR PARENTS 38
Generation of an induced pluripotent stem cell line CSSi015-A (9553), carrying a point mutation c.2915C > T in the human calcium sensing receptor (CasR) gene 37
Totale 6.555
Categoria #
all - tutte 25.139
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 25.139


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020702 0 0 0 0 0 0 121 177 107 189 78 30
2020/2021632 85 64 54 62 14 56 49 65 44 75 56 8
2021/20221.208 15 76 152 35 165 41 30 135 98 72 169 220
2022/20231.267 233 199 75 153 158 109 31 103 106 16 65 19
2023/20241.189 50 100 37 79 142 166 70 238 16 113 81 97
2024/2025872 83 99 150 151 159 230 0 0 0 0 0 0
Totale 7.765