IRIS
PRATICO', ANDREA DOMENICO
 Distribuzione geografica
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Continente #
AS - Asia 1.191
NA - Nord America 633
EU - Europa 459
SA - Sud America 340
AF - Africa 22
OC - Oceania 1
Totale 2.646
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Nazione #
US - Stati Uniti d'America 607
SG - Singapore 557
HK - Hong Kong 518
BR - Brasile 316
IE - Irlanda 173
IT - Italia 77
DE - Germania 63
TR - Turchia 50
FR - Francia 47
GB - Regno Unito 24
AT - Austria 15
CA - Canada 12
FI - Finlandia 10
AR - Argentina 9
IN - India 9
MX - Messico 8
PL - Polonia 8
RU - Federazione Russa 8
BD - Bangladesh 7
NL - Olanda 7
UZ - Uzbekistan 7
ES - Italia 6
IQ - Iraq 5
UA - Ucraina 5
ZA - Sudafrica 5
AE - Emirati Arabi Uniti 4
CO - Colombia 4
MA - Marocco 4
TN - Tunisia 4
JM - Giamaica 3
JP - Giappone 3
KE - Kenya 3
LA - Repubblica Popolare Democratica del Laos 3
LT - Lituania 3
RO - Romania 3
VE - Venezuela 3
AM - Armenia 2
AZ - Azerbaigian 2
BO - Bolivia 2
BW - Botswana 2
CL - Cile 2
EG - Egitto 2
JO - Giordania 2
KW - Kuwait 2
KZ - Kazakistan 2
LV - Lettonia 2
PE - Perù 2
PH - Filippine 2
PK - Pakistan 2
SA - Arabia Saudita 2
SE - Svezia 2
AL - Albania 1
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
NP - Nepal 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
VN - Vietnam 1
Totale 2.646
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Città #
Hong Kong 518
Singapore 258
Santa Clara 196
Dublin 173
The Dalles 158
Istanbul 46
São Paulo 27
Los Angeles 23
Munich 16
Düsseldorf 14
Frankfurt am Main 12
Assago 10
Rome 10
Catania 9
Rio de Janeiro 9
Chicago 8
San Francisco 8
Turku 8
Ashburn 7
Curitiba 7
Tashkent 7
Artena 6
Boston 6
Brasília 6
Brooklyn 6
Lauterbourg 6
Portsmouth 6
Seattle 6
Atlanta 5
Bari 5
Belo Horizonte 5
Caxias do Sul 5
Duque de Caxias 5
Falkenstein 5
Mexico City 5
Milan 5
New York 5
Palermo 5
Roubaix 5
Vienna 5
Bexley 4
Chennai 4
Porto Alegre 4
Praia Grande 4
Ribeirão Preto 4
São José dos Campos 4
Uberlândia 4
Warsaw 4
Wroclaw 4
Amsterdam 3
Ankara 3
Boardman 3
Charlotte 3
Dubai 3
Juiz de Fora 3
Medellín 3
Minneapolis 3
Nairobi 3
Naples 3
New Delhi 3
Newark 3
Niterói 3
Phoenix 3
Ribeirão das Neves 3
Santa Luzia 3
São Bernardo do Campo 3
São Sebastião do Paraíso 3
Tokyo 3
Tramandaí 3
Vientiane 3
Amman 2
Aparecida de Goiânia 2
Araranguá 2
Athens 2
Barquisimeto 2
Bauru 2
Belém 2
Bologna 2
Brumadinho 2
Buenos Aires 2
Calgary 2
Capivari 2
Cariacica 2
Contagem 2
Curvelo 2
Dallas 2
Denver 2
Dhaka 2
Dourados 2
Feira de Santana 2
Gaborone 2
Goiânia 2
Helsinki 2
Hortolândia 2
Joinville 2
João Monlevade 2
Juazeiro 2
Juazeiro do Norte 2
Jundiaí 2
Kingston 2
Totale 1.785
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Nome #
An 11-year follow-up of neonatal onset bath-induced alternating hemiplegia of childhood in monozygotic twins 38
KCNT1-Related Epilepsy: A Review 35
Neonatal seizures as onset of Inborn Errors of Metabolism (IEMs): from diagnosis to treatment. A systematic review 33
A neurocutaneous phenotype with paired hypo- and hyperpigmented macules, microcephaly and stunted growth as prominent features 32
Congenital generalized hypertrichosis: the skin as a clue to complex malformation syndromes 27
A child with rhombencephalosynapsis, agenesis of the trigeminal ganglion and optic coloboma (without alopecia): A variant of the cerebellotrigeminal dermal dysplasia? 27
Focal Cortical Dysplasia: Diagnosis, Classification, and Treatment Options 27
Anomalies of the Craniocervical Junction (Chiari Malformations) 25
HyperCKemia as a biomarker for muscular diseases 24
Cutis Tricolor 24
Manuale di Pediatria, quinta edizione. Capitolo 2 "Anamnesi ed esame obiettivo". Capitolo 29 "Malattie Neurologiche" 23
Pediatric Lemierre's Syndrome: A Comprehensive Literature Review 23
Lissencephaly, Pachygyrias, Band Heterotopias, RELN Pathway, and ARX Mutations (Incomplete Neuron Migration) 22
Sindromi Neurocutanee 22
Neurocutaneous syndromes in art and antiquities 21
Infantile spasms in the setting of Sturge-Weber syndrome 21
Schizencephaly: Etiopathogenesis, Classification, Therapeutic, and Rehabilitative Approach 21
Wyburn-Mason Syndrome 21
Nevus Sebaceous Syndrome 21
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 21
Aicardi-Goutières Syndrome Type 2: A Report on Two Cases with Different Phenotypes Caused by RNASEH2B Gene Mutations 21
A child with congenital heart disease and situs viscerum inversus 21
A clinical review on megalencephaly: A large brain as a possible sign of cerebral impairment 20
WDR45 gene and its role in pediatric epilepsies 20
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 20
Becker's Nevus Syndrome 20
Congenital/Primitive Hydrocephalus: Classification, Clinical Aspects, and Rehabilitation Approach 20
Megalencephaly: Classification, Genetic Causes, and Related Syndromes 20
Phacomatosis Pigmentokeratotica 19
Actualities on molecular pathogenesis and repairing processes of cerebral damage in perinatal hypoxic-ischemic encephalopathy 19
Speckled Lentiginous Nevus Syndrome 19
Neurofibromatosis type 1 and infantile spasms 19
Ketogenic diet for infants with epilepsy: A literature review 19
Encefalopatia acuta da probabile deficit cerebrale di acido folico in paziente con iperfenilalaninemia da deficit di DHPR 19
TSC1 and TSC2: Tuberous Sclerosis Complex and Its Related Epilepsy Phenotype 19
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] 19
Type II Autoimmune Hepatitis and Small Duct Sclerosing Cholangitis in a Seven Years Old Child: An Overlap Syndrome? 19
A mosaic pattern of INI1/SMARCB1 protein expression distinguishes Schwannomatosis and NF2-associated peripheral schwannomas from solitary peripheral schwannomas and NF2-associated vestibular schwannomas 19
Biochemical Insights into Merlin/NF2 Pathophysiology and Biologically Targeted Therapies in Childhood NF2 and Related Forms 18
Prognostic challenges of SCN1A genetic mutations: report of two children with mild features 18
Primary Microcephaly with Novel Variant of MCPH1 Gene in Twins: Both Manifesting in Childhood at the Same Time with Hashimoto's Thyroiditis 18
Megalencephaly: Classification, Genetic Causes, and Related Syndromes 18
Neurologia Pediatrica - Dalle cause biologiche alla pratica clinica 18
Intramuscular vs intradermal route for hepatitis B booster vaccine in celiac children 18
Resuming the obsolete term "small head": when microcephaly occurs without cognitive impairment 18
Rediagnosing one of Smith's patients (John McCann) with "neuromas tumours" (1849) 17
Foreword: A Special Issue on Central Nervous System Malformations 17
Blue Rubber Bleb Nevus Syndrome 17
A mild phenotype associated with a de novo microdeletion 10q23.1-q23.2: A new patient with a novel feature 17
Disturbi del sonno: uno studio prospettico pilota basato sulla somministrazione di questionario online 17
Early acute pancreatitis in a child with compound heterozygosis ∆F508/R1438W/Y1032C cystic fibrosis: a case report 17
A New Patient with Potocki-Lupski Syndrome: A Literature Review 17
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 17
FOXG1 Gene and Its Related Phenotypes 16
SCN8A and Its Related Epileptic Phenotypes 16
Reconstructive Surgery in Children with Down's Syndrome: Bioethical Implications 16
Syntaxin binding protein 1 related epilepsies 16
Mutazione PRRT2 in un bambino con caratteristiche dismorfiche, microcefalia congenita e convulsioni epilettiche gravi 16
Is benign familial neonatal KCNQ2-related epilepsy always familially benign? J pediatric neonatal individualized medicine 16
Rare Neurocutaneous Disorders: State of the Art and Update 16
Anti-MOG Antibody Syndrome and Cerebral Sinovenous Thrombosis: A Cause-Effect Hypothesis 16
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 16
A Probable Topiramate-induced Limbs Paraesthesia and Rigid Fingers Flexion 16
COVID-19 Pandemic Outbreak and its Psychological Impact on Patients with Rare Lysosomal Diseases 16
Hydranencephaly: cerebral spinal fluid instead of cerebral mantles 16
CDKL5 gene: Beyond rett syndrome 16
Sindrome del vomito ciclico: analisi di una popolazione di 20 bambini e revisione della letteratura 16
Mycoplasma Pneumoniae: non solo polmonite atipica primaria. Esperienza personale e revisione della letteratura 16
A sudden weight gain in a child as clinical presentation of Chiari Type I malformation: a case report 16
Cognitive disabilities and bioethical implications in down syndrome 15
Mosaic Neurocutaneous Disorders and Their Causes 15
ACQUIRED PERIPHERAL NEUROPATHY: A REPORT ON 20 CHILDREN 15
West syndrome treatment: new roads for an old syndrome 15
Mycoplasma pneumoniae: dalla polmonite atipica primaria alle complicanze extrapolmonari 15
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 15
A girl with a 14.7 Mb 3q26.32-q28 duplication: a new report of 3q duplication syndrome and a literature review 15
Congenital familial myasthenic syndromes: disease and course in an affected dizygotic twin pair 15
Cervical neurenteric cyst and Klippel-Feil syndrome: An abrupt onset of myelopathic signs in a young patient 15
Encefalite da Anticorpi anti-GluR3 in sei pazienti in età pediatrica 15
COVID-19 vaccination for children: may be necessary for the full eradication of the disease 15
Tetralogy of Fallot variant with pulmonary atresia (pseudotruncus arteriosus) in a case of maternal PKU syndrome 15
Cerebellotrigeminal Dermal Dysplasia (Gómez-López-Hernández Syndrome) 15
Allergia agli insetti 15
Wide spectrum of congenital anomalies including choanal atresia, malformed extremities, and brain and spinal malformations in a girl with a de novo 5.6-Mb deletion of 13q12.11-13q12.13 15
ACCIDENTAL ETHYL ALCOHOL INTOXICATION IN A -DAY-OLD INFANT. CLINICAL FINDINGS AND NEUROLOGICAL FOLLOW-UP 15
Hypomelanosis of Ito 15
Propranolol: effectiveness and failure in infantile cutaneous haemangiomas 14
SCN1A and its related epileptic phenotypes 14
At the Basis of Brain Malformations: Brain Plasticity, Developmental Neurobiology, and Considerations for Rehabilitation 14
E se non fossero solo incubi notturni? 14
Megalencephaly Capillary Malformation Syndrome 14
Encefalite GluR3: fenotipo clinico e strumentale di quattro pazienti 14
I farmaci orfani e i farmaci innovativi. Aspetti regolatori e accesso alle cure 14
Una febbre “strana” nel lattante 14
GRIN2A and GRIN2B and Their Related Phenotypes 14
Holoprosencephaly and Recurrent Episodes of Severe Neurogenic Hypernatremia 14
Mixed Vascular Nevus Syndrome 14
Malformations of the Cerebral Commissures 14
Autonomic Dysfunction Manifesting With Asymmetric Face Flushing and Paroxysmal Nonconvulsive Episodes 14
Neuroaspergillosis as the Presenting Sign of a Chronic Granulomatous Disease 14
Totale 1.829
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Categoria #
all - tutte 20.905
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 20.905
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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
2024/20252.834 3 6 7 370 329 295 290 157 433 376 406 162
Totale 2.843