PRATICO', ANDREA DOMENICO
 Distribuzione geografica
Continente #
AS - Asia 1.223
NA - Nord America 848
EU - Europa 501
SA - Sud America 356
AF - Africa 24
OC - Oceania 2
Totale 2.954
Nazione #
US - Stati Uniti d'America 816
SG - Singapore 560
HK - Hong Kong 531
BR - Brasile 330
IE - Irlanda 173
IT - Italia 88
DE - Germania 81
TR - Turchia 51
FR - Francia 49
GB - Regno Unito 26
AT - Austria 20
CA - Canada 14
IN - India 14
FI - Finlandia 11
MX - Messico 11
AR - Argentina 10
NL - Olanda 10
BD - Bangladesh 9
UZ - Uzbekistan 9
RU - Federazione Russa 8
PL - Polonia 7
ES - Italia 6
ZA - Sudafrica 6
IQ - Iraq 5
UA - Ucraina 5
AE - Emirati Arabi Uniti 4
CO - Colombia 4
JM - Giamaica 4
JP - Giappone 4
KE - Kenya 4
MA - Marocco 4
TN - Tunisia 4
JO - Giordania 3
LA - Repubblica Popolare Democratica del Laos 3
LT - Lituania 3
PK - Pakistan 3
RO - Romania 3
VE - Venezuela 3
VN - Vietnam 3
AL - Albania 2
AM - Armenia 2
AZ - Azerbaigian 2
BO - Bolivia 2
BW - Botswana 2
CL - Cile 2
EG - Egitto 2
KW - Kuwait 2
KZ - Kazakistan 2
LV - Lettonia 2
NP - Nepal 2
PE - Perù 2
PH - Filippine 2
SA - Arabia Saudita 2
SE - Svezia 2
AU - Australia 1
BE - Belgio 1
BH - Bahrain 1
CR - Costa Rica 1
DK - Danimarca 1
EC - Ecuador 1
EE - Estonia 1
GA - Gabon 1
GE - Georgia 1
HN - Honduras 1
ID - Indonesia 1
IL - Israele 1
KG - Kirghizistan 1
LB - Libano 1
LK - Sri Lanka 1
NO - Norvegia 1
NR - Nauru 1
PT - Portogallo 1
PY - Paraguay 1
QA - Qatar 1
SC - Seychelles 1
SY - Repubblica araba siriana 1
TJ - Tagikistan 1
TT - Trinidad e Tobago 1
UY - Uruguay 1
Totale 2.954
Città #
Hong Kong 531
Singapore 261
Santa Clara 200
Dublin 173
Dallas 159
The Dalles 158
Istanbul 47
Munich 32
São Paulo 29
Los Angeles 27
Assago 16
Düsseldorf 14
Frankfurt am Main 13
Ashburn 12
Catania 12
San Francisco 11
Chicago 10
Rome 10
Rio de Janeiro 9
Tashkent 9
Boston 8
Mexico City 8
New York 8
Turku 8
Curitiba 7
Palermo 7
Artena 6
Atlanta 6
Brasília 6
Brooklyn 6
Chennai 6
Lauterbourg 6
Portsmouth 6
Seattle 6
Vienna 6
Amsterdam 5
Bari 5
Belo Horizonte 5
Caxias do Sul 5
Duque de Caxias 5
Falkenstein 5
Roubaix 5
Uberlândia 5
Bexley 4
Manchester 4
Milan 4
Newark 4
Porto Alegre 4
Praia Grande 4
Ribeirão Preto 4
Salt Lake City 4
São José dos Campos 4
Tokyo 4
Wroclaw 4
Amman 3
Ankara 3
Boardman 3
Buenos Aires 3
Charlotte 3
Dubai 3
Helsinki 3
Juiz de Fora 3
Kingston 3
Limeira 3
Mauá 3
Medellín 3
Minneapolis 3
Montreal 3
Nairobi 3
Naples 3
New Delhi 3
Niterói 3
Phoenix 3
Ribeirão das Neves 3
Santa Luzia 3
Santo André 3
São Bernardo do Campo 3
São Sebastião do Paraíso 3
Tramandaí 3
Vientiane 3
Warsaw 3
Aparecida de Goiânia 2
Araranguá 2
Athens 2
Barquisimeto 2
Bauru 2
Belém 2
Bologna 2
Brumadinho 2
Calgary 2
Cape Town 2
Capivari 2
Cariacica 2
Cincinnati 2
Contagem 2
Curvelo 2
Delhi 2
Denver 2
Dhaka 2
Dourados 2
Totale 2.036
Nome #
An 11-year follow-up of neonatal onset bath-induced alternating hemiplegia of childhood in monozygotic twins 42
KCNT1-Related Epilepsy: A Review 37
A neurocutaneous phenotype with paired hypo- and hyperpigmented macules, microcephaly and stunted growth as prominent features 35
Neonatal seizures as onset of Inborn Errors of Metabolism (IEMs): from diagnosis to treatment. A systematic review 34
Congenital generalized hypertrichosis: the skin as a clue to complex malformation syndromes 31
Focal Cortical Dysplasia: Diagnosis, Classification, and Treatment Options 31
A child with rhombencephalosynapsis, agenesis of the trigeminal ganglion and optic coloboma (without alopecia): A variant of the cerebellotrigeminal dermal dysplasia? 30
Anomalies of the Craniocervical Junction (Chiari Malformations) 29
HyperCKemia as a biomarker for muscular diseases 28
Cutis Tricolor 27
Manuale di Pediatria, quinta edizione. Capitolo 2 "Anamnesi ed esame obiettivo". Capitolo 29 "Malattie Neurologiche" 25
Pediatric Lemierre's Syndrome: A Comprehensive Literature Review 25
Neurocutaneous syndromes in art and antiquities 24
Nevus Sebaceous Syndrome 24
Anomalies of the Mesenchyme (Meninges and Skull)-Defects of Neural Tube Closure: Cephalocele and Other Calvarial and Skull Base Defects; Intracranial Lipomas; Arachnoid Cysts; Nonsyndromic and Syndromic Craniosynostoses 24
A child with congenital heart disease and situs viscerum inversus 24
A clinical review on megalencephaly: A large brain as a possible sign of cerebral impairment 23
Schizencephaly: Etiopathogenesis, Classification, Therapeutic, and Rehabilitative Approach 23
Lissencephaly, Pachygyrias, Band Heterotopias, RELN Pathway, and ARX Mutations (Incomplete Neuron Migration) 23
Aicardi-Goutières Syndrome Type 2: A Report on Two Cases with Different Phenotypes Caused by RNASEH2B Gene Mutations 23
Infantile spasms in the setting of Sturge-Weber syndrome 22
Wyburn-Mason Syndrome 22
WDR45 gene and its role in pediatric epilepsies 22
Zespół padaczkowy z drgawkami połowiczymi i porażeniem połowiczym. Wyniki badania za pomocaogonek rezonansu magnetycznego u trzyletniego chłopca. Hemiconvulsion-hemiplegia-epilepsy syndrome. Magnetic resonance findings in a 3-year-old boy 22
Becker's Nevus Syndrome 22
A mosaic pattern of INI1/SMARCB1 protein expression distinguishes Schwannomatosis and NF2-associated peripheral schwannomas from solitary peripheral schwannomas and NF2-associated vestibular schwannomas 22
Sindromi Neurocutanee 22
Phacomatosis Pigmentokeratotica 21
Actualities on molecular pathogenesis and repairing processes of cerebral damage in perinatal hypoxic-ischemic encephalopathy 21
Ketogenic diet for infants with epilepsy: A literature review 21
Encefalopatia acuta da probabile deficit cerebrale di acido folico in paziente con iperfenilalaninemia da deficit di DHPR 21
Blue Rubber Bleb Nevus Syndrome 21
Childhood neurofibromatosis type 2 (NF2) and related disorders: From bench to bedside and biologically targeted therapies [Neurofibromatosi tipo 2 (NF2) e sindromi correlate in età infantile: dalla biologia molecolare alla pratica clinica e nuove terapie con farmaci biologici] 21
Congenital/Primitive Hydrocephalus: Classification, Clinical Aspects, and Rehabilitation Approach 21
Rediagnosing one of Smith's patients (John McCann) with "neuromas tumours" (1849) 20
Speckled Lentiginous Nevus Syndrome 20
Neurofibromatosis type 1 and infantile spasms 20
TSC1 and TSC2: Tuberous Sclerosis Complex and Its Related Epilepsy Phenotype 20
Prognostic challenges of SCN1A genetic mutations: report of two children with mild features 20
Neurologia Pediatrica - Dalle cause biologiche alla pratica clinica 20
Type II Autoimmune Hepatitis and Small Duct Sclerosing Cholangitis in a Seven Years Old Child: An Overlap Syndrome? 20
Megalencephaly: Classification, Genetic Causes, and Related Syndromes 20
Foreword: A Special Issue on Central Nervous System Malformations 19
Biochemical Insights into Merlin/NF2 Pathophysiology and Biologically Targeted Therapies in Childhood NF2 and Related Forms 19
A mild phenotype associated with a de novo microdeletion 10q23.1-q23.2: A new patient with a novel feature 19
Primary Microcephaly with Novel Variant of MCPH1 Gene in Twins: Both Manifesting in Childhood at the Same Time with Hashimoto's Thyroiditis 19
Mutazione PRRT2 in un bambino con caratteristiche dismorfiche, microcefalia congenita e convulsioni epilettiche gravi 19
Megalencephaly: Classification, Genetic Causes, and Related Syndromes 19
Intramuscular vs intradermal route for hepatitis B booster vaccine in celiac children 19
A Probable Topiramate-induced Limbs Paraesthesia and Rigid Fingers Flexion 19
Early acute pancreatitis in a child with compound heterozygosis ∆F508/R1438W/Y1032C cystic fibrosis: a case report 19
A New Patient with Potocki-Lupski Syndrome: A Literature Review 19
Resuming the obsolete term "small head": when microcephaly occurs without cognitive impairment 19
Syntaxin binding protein 1 related epilepsies 18
ACQUIRED PERIPHERAL NEUROPATHY: A REPORT ON 20 CHILDREN 18
A girl with a 14.7 Mb 3q26.32-q28 duplication: a new report of 3q duplication syndrome and a literature review 18
Is benign familial neonatal KCNQ2-related epilepsy always familially benign? J pediatric neonatal individualized medicine 18
Anti-MOG Antibody Syndrome and Cerebral Sinovenous Thrombosis: A Cause-Effect Hypothesis 18
Disturbi del sonno: uno studio prospettico pilota basato sulla somministrazione di questionario online 18
Determinants of Rotavirus Vaccine Acceptance in an Area of Southern Italy with Low Vaccination Coverage: A Case-Control Study by the Health Belief Model Questionnaire 18
A sudden weight gain in a child as clinical presentation of Chiari Type I malformation: a case report 18
Cognitive disabilities and bioethical implications in down syndrome 17
FOXG1 Gene and Its Related Phenotypes 17
SCN8A and Its Related Epileptic Phenotypes 17
Reconstructive Surgery in Children with Down's Syndrome: Bioethical Implications 17
Congenital familial myasthenic syndromes: disease and course in an affected dizygotic twin pair 17
Cervical neurenteric cyst and Klippel-Feil syndrome: An abrupt onset of myelopathic signs in a young patient 17
Rare Neurocutaneous Disorders: State of the Art and Update 17
Early history of the different forms of neurofibromatosis from ancient Egypt to the British Empire and beyond: First descriptions, medical curiosities, misconceptions, landmarks, and the persons behind the syndromes 17
COVID-19 Pandemic Outbreak and its Psychological Impact on Patients with Rare Lysosomal Diseases 17
Cerebellotrigeminal Dermal Dysplasia (Gómez-López-Hernández Syndrome) 17
Hydranencephaly: cerebral spinal fluid instead of cerebral mantles 17
CDKL5 gene: Beyond rett syndrome 17
Sindrome del vomito ciclico: analisi di una popolazione di 20 bambini e revisione della letteratura 17
Allergia agli insetti 17
ACCIDENTAL ETHYL ALCOHOL INTOXICATION IN A -DAY-OLD INFANT. CLINICAL FINDINGS AND NEUROLOGICAL FOLLOW-UP 17
Mosaic Neurocutaneous Disorders and Their Causes 16
Encefalite GluR3: fenotipo clinico e strumentale di quattro pazienti 16
Una febbre “strana” nel lattante 16
West syndrome treatment: new roads for an old syndrome 16
Mycoplasma pneumoniae: dalla polmonite atipica primaria alle complicanze extrapolmonari 16
Chromosome 15q BP3 to BP5 deletion is a likely locus for speech delay and language impairment: Report on a four-member family and an unrelated boy 16
Malformations of the Cerebral Commissures 16
Encefalite da Anticorpi anti-GluR3 in sei pazienti in età pediatrica 16
Autonomic Dysfunction Manifesting With Asymmetric Face Flushing and Paroxysmal Nonconvulsive Episodes 16
COVID-19 vaccination for children: may be necessary for the full eradication of the disease 16
Tetralogy of Fallot variant with pulmonary atresia (pseudotruncus arteriosus) in a case of maternal PKU syndrome 16
Mycoplasma Pneumoniae: non solo polmonite atipica primaria. Esperienza personale e revisione della letteratura 16
Propranolol: effectiveness and failure in infantile cutaneous haemangiomas 15
Sprengel deformity: a rare congenital anomaly of the scapula 15
SCN1A and its related epileptic phenotypes 15
At the Basis of Brain Malformations: Brain Plasticity, Developmental Neurobiology, and Considerations for Rehabilitation 15
Heterogeneity of resting-state EEG features in juvenile myoclonic epilepsy and controls 15
Early Immunotherapy and Longer Corticosteroid Treatment Are Associated With Lower Risk of Relapsing Disease Course in Pediatric MOGAD 15
E se non fossero solo incubi notturni? 15
Megalencephaly Capillary Malformation Syndrome 15
I farmaci orfani e i farmaci innovativi. Aspetti regolatori e accesso alle cure 15
Sindrome di Sturge Weber: presentazione atipica con malformazione capillare cerebrale 15
Hypomelanosis of Ito: a round on the frequency and type of epileptic complications 15
GRIN2A and GRIN2B and Their Related Phenotypes 15
Totale 2.003
Categoria #
all - tutte 22.764
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 22.764


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2023/20249 0 0 0 0 0 0 0 0 0 0 3 6
2024/20252.916 3 6 7 370 329 295 290 157 433 375 405 246
2025/2026234 234 0 0 0 0 0 0 0 0 0 0 0
Totale 3.159