IRIS
PRATICO', ANDREA DOMENICO
 Distribuzione geografica
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Continente #
AS - Asia 207
EU - Europa 89
NA - Nord America 30
AF - Africa 2
OC - Oceania 1
SA - Sud America 1
Totale 330
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Nazione #
SG - Singapore 194
IE - Irlanda 43
US - Stati Uniti d'America 29
DE - Germania 19
IT - Italia 13
AT - Austria 5
HK - Hong Kong 4
LA - Repubblica Popolare Democratica del Laos 3
RO - Romania 3
AL - Albania 1
AM - Armenia 1
AU - Australia 1
BE - Belgio 1
BO - Bolivia 1
FI - Finlandia 1
GE - Georgia 1
IL - Israele 1
JM - Giamaica 1
LV - Lettonia 1
NO - Norvegia 1
PT - Portogallo 1
QA - Qatar 1
SA - Arabia Saudita 1
SC - Seychelles 1
UZ - Uzbekistan 1
ZA - Sudafrica 1
Totale 330
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Città #
Singapore 124
Dublin 43
Munich 13
Los Angeles 6
Falkenstein 5
Palermo 5
Hong Kong 4
Boardman 3
Vientiane 3
Bologna 2
Rome 2
Sassari 2
Târgovişte 2
Vienna 2
Ambrolauri 1
Brussels 1
Bucharest 1
Catania 1
Doha 1
Helsinki 1
Jerusalem 1
La Paz 1
Lisbon 1
Newark 1
Oslo 1
Riga 1
Riyadh 1
Tashkent 1
Tirana 1
Yerevan 1
Totale 232
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Nome #
Pediatric Lemierre's Syndrome: A Comprehensive Literature Review 15
Cutis Tricolor 9
Congenital generalized hypertrichosis: the skin as a clue to complex malformation syndromes 8
A child with rhombencephalosynapsis, agenesis of the trigeminal ganglion and optic coloboma (without alopecia): A variant of the cerebellotrigeminal dermal dysplasia? 8
Focal Cortical Dysplasia: Diagnosis, Classification, and Treatment Options 8
An 11-year follow-up of neonatal onset bath-induced alternating hemiplegia of childhood in monozygotic twins 7
Mycoplasma pneumoniae: dalla polmonite atipica primaria alle complicanze extrapolmonari 7
Is benign familial neonatal KCNQ2-related epilepsy always familially benign? J pediatric neonatal individualized medicine 7
Neurocutaneous syndromes in art and antiquities 6
HyperCKemia as a biomarker for muscular diseases 6
Infantile spasms in the setting of Sturge-Weber syndrome 6
A clinical review on megalencephaly: A large brain as a possible sign of cerebral impairment 6
Anomalies of the Craniocervical Junction (Chiari Malformations) 6
Cognitive disabilities and bioethical implications in down syndrome 5
ACQUIRED PERIPHERAL NEUROPATHY: A REPORT ON 20 CHILDREN 5
Allergia agli insetti 5
Manuale di Pediatria, quinta edizione. Capitolo 2 "Anamnesi ed esame obiettivo". Capitolo 29 "Malattie Neurologiche" 4
Phacomatosis Pigmentokeratotica 4
Biochemical Insights into Merlin/NF2 Pathophysiology and Biologically Targeted Therapies in Childhood NF2 and Related Forms 4
Wyburn-Mason Syndrome 4
Encefalopatia acuta da probabile deficit cerebrale di acido folico in paziente con iperfenilalaninemia da deficit di DHPR 4
TSC1 and TSC2: Tuberous Sclerosis Complex and Its Related Epilepsy Phenotype 4
At the Basis of Brain Malformations: Brain Plasticity, Developmental Neurobiology, and Considerations for Rehabilitation 4
E se non fossero solo incubi notturni? 4
Megalencephaly: Classification, Genetic Causes, and Related Syndromes 4
SCN1B gene: A close relative to SCN1A 4
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 4
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] 4
A Probable Topiramate-induced Limbs Paraesthesia and Rigid Fingers Flexion 4
Becker's Nevus Syndrome 4
Pediatria dalla A alla Z - Guida Pratica alla diagnosi e al trattamento. Neurologia, disturbi psichiatrici e comportamentali 4
Aicardi-Goutières Syndrome Type 2: A Report on Two Cases with Different Phenotypes Caused by RNASEH2B Gene Mutations 4
A child with congenital heart disease and situs viscerum inversus 4
Microcephaly-Capillary Malformation Syndrome 4
A mosaic pattern of INI1/SMARCB1 protein expression distinguishes Schwannomatosis and NF2-associated peripheral schwannomas from solitary peripheral schwannomas and NF2-associated vestibular schwannomas 4
Rediagnosing one of Smith's patients (John McCann) with "neuromas tumours" (1849) 3
Schizencephaly: Etiopathogenesis, Classification, Therapeutic, and Rehabilitative Approach 3
Ataxia in children: early recognition and clinical evaluation 3
Sprengel deformity: a rare congenital anomaly of the scapula 3
SCN1A and its related epileptic phenotypes 3
Mosaic Neurocutaneous Disorders and Their Causes 3
Chromosome 2p15-p16.1 microduplication in a boy with congenital anomalies: Is it a distinctive syndrome? 3
WDR45 gene and its role in pediatric epilepsies 3
Previously Unreported COL7A1 Mutation in a Somali Patient with Dystrophic Epidermolysis Bullosa 3
Congenital muscular dystrophy: from muscle to brain 3
Diagnosis, Management, and New Therapeutic Options in Childhood Neurofibromatosis Type 2 and Related Forms 3
Telangiectasia Macularis Eruptive Perstans (TMEP) in childhood: a case report and literature review" 3
Megalencephaly Capillary Malformation Syndrome 3
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 3
Encefalite GluR3: fenotipo clinico e strumentale di quattro pazienti 3
Nevus Sebaceous Syndrome 3
I farmaci orfani e i farmaci innovativi. Aspetti regolatori e accesso alle cure 3
Blue Rubber Bleb Nevus Syndrome 3
Lissencephaly, Pachygyrias, Band Heterotopias, RELN Pathway, and ARX Mutations (Incomplete Neuron Migration) 3
A girl with a 14.7 Mb 3q26.32-q28 duplication: a new report of 3q duplication syndrome and a literature review 3
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 3
La Tosse 3
Paternally inherited 17q12 microduplication: similar pattern of neurological signs and features in the father and his children 3
Primary Microcephaly with Novel Variant of MCPH1 Gene in Twins: Both Manifesting in Childhood at the Same Time with Hashimoto's Thyroiditis 3
Mutazione PRRT2 in un bambino con caratteristiche dismorfiche, microcefalia congenita e convulsioni epilettiche gravi 3
Mixed Vascular Nevus Syndrome 3
Cervical neurenteric cyst and Klippel-Feil syndrome: An abrupt onset of myelopathic signs in a young patient 3
Encefalite da Anticorpi anti-GluR3 in sei pazienti in età pediatrica 3
Anti-MOG Antibody Syndrome and Cerebral Sinovenous Thrombosis: A Cause-Effect Hypothesis 3
Neurologia Pediatrica - Dalle cause biologiche alla pratica clinica 3
Encephalocraniocutaneous Lipomatosis (Haberland Syndrome or Fishman Syndrome) 3
KCNT1-Related Epilepsy: A Review 3
Anti-mog associated encephalitis: when steroid therapy is not enough 3
Neonatal seizures as onset of Inborn Errors of Metabolism (IEMs): from diagnosis to treatment. A systematic review 3
COVID-19 Pandemic Outbreak and its Psychological Impact on Patients with Rare Lysosomal Diseases 3
Spine and brain malformations in a patient obligate carrier of MTHFR with autism and mental retardation 3
Cerebellotrigeminal Dermal Dysplasia (Gómez-López-Hernández Syndrome) 3
Early acute pancreatitis in a child with compound heterozygosis ∆F508/R1438W/Y1032C cystic fibrosis: a case report 3
Sindrome del vomito ciclico: analisi di una popolazione di 20 bambini e revisione della letteratura 3
A New Patient with Potocki-Lupski Syndrome: A Literature Review 3
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 3
In vitro efficacy of ARQ 092, an allosteric AKT inhibitor, on primary fibroblast cells derived from patients with PIK3CA-related overgrowth spectrum (PROS) 3
Hypomelanosis of Ito 3
Multiseptate Gallbladder in a Child: A Possible Cause of Poor Growth? 3
Correlazione genotipo/fenotipo nella Sclerosi Tuberosa (TSC1 vs. TSC2) in 81 pazienti siciliani 3
Megalencephaly: Classification, Genetic Causes, and Related Syndromes 3
Phacomatosis Pigmentovascularis 3
Hemihydranencephaly: living with half brain dysfunction 2
Actualities on molecular pathogenesis and repairing processes of cerebral damage in perinatal hypoxic-ischemic encephalopathy 2
Speckled Lentiginous Nevus Syndrome 2
Reconstructive Surgery in Children with Down's Syndrome: Bioethical Implications 2
Ketogenic diet for infants with epilepsy: A literature review 2
A neurocutaneous phenotype with paired hypo- and hyperpigmented macules, microcephaly and stunted growth as prominent features 2
Heterogeneity of resting-state EEG features in juvenile myoclonic epilepsy and controls 2
Early Immunotherapy and Longer Corticosteroid Treatment Are Associated With Lower Risk of Relapsing Disease Course in Pediatric MOGAD 2
L’Atassia di Friedreich: nuove strategie terapeutiche 2
Epatite Autoimmune: esperienza personale e revisione della letteratura 2
Sindrome di Sturge Weber: presentazione atipica con malformazione capillare cerebrale 2
COVID-19 pandemic for Pediatric Health Care: disadvantages and opportunities 2
Prognostic challenges of SCN1A genetic mutations: report of two children with mild features 2
Graph theory in paediatric epilepsy: A systematic review 2
Symptomatic hypocalcemia in an epileptic child treated with valproic acid plus lamotrigine: a case report 2
The multiple faces of artwork diagnoses 2
Una febbre “strana” nel lattante 2
West syndrome treatment: new roads for an old syndrome 2
Totale 367
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Categoria #
all - tutte 4.838
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 4.838
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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
2024/2025510 3 6 7 370 124 0 0 0 0 0 0 0
Totale 519