IRIS
PRATICO', ANDREA DOMENICO
 Distribuzione geografica
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Continente #
AS - Asia 244
NA - Nord America 220
EU - Europa 138
AF - Africa 2
OC - Oceania 1
SA - Sud America 1
Totale 606
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Nazione #
SG - Singapore 224
US - Stati Uniti d'America 219
IE - Irlanda 81
DE - Germania 20
IT - Italia 20
HK - Hong Kong 10
AT - Austria 6
LA - Repubblica Popolare Democratica del Laos 3
RO - Romania 3
GB - Regno Unito 2
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
TR - Turchia 1
UZ - Uzbekistan 1
ZA - Sudafrica 1
Totale 606
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Città #
Santa Clara 188
Singapore 153
Dublin 81
Munich 13
Hong Kong 10
Artena 6
Los Angeles 6
Falkenstein 5
Palermo 5
Boardman 3
Vientiane 3
Bologna 2
Rome 2
Sassari 2
Târgovişte 2
Vienna 2
Ambrolauri 1
Ashburn 1
Brussels 1
Bucharest 1
Catania 1
Doha 1
Eskişehir 1
Helsinki 1
Jerusalem 1
La Paz 1
Lisbon 1
Newark 1
Oslo 1
Riga 1
Riyadh 1
Seattle 1
Stezzano 1
Tashkent 1
Tirana 1
Yerevan 1
Totale 503
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Nome #
Pediatric Lemierre's Syndrome: A Comprehensive Literature Review 16
A child with rhombencephalosynapsis, agenesis of the trigeminal ganglion and optic coloboma (without alopecia): A variant of the cerebellotrigeminal dermal dysplasia? 11
Cutis Tricolor 11
Congenital generalized hypertrichosis: the skin as a clue to complex malformation syndromes 10
An 11-year follow-up of neonatal onset bath-induced alternating hemiplegia of childhood in monozygotic twins 10
Sindromi Neurocutanee 10
HyperCKemia as a biomarker for muscular diseases 9
Mycoplasma pneumoniae: dalla polmonite atipica primaria alle complicanze extrapolmonari 9
Focal Cortical Dysplasia: Diagnosis, Classification, and Treatment Options 9
Neurocutaneous syndromes in art and antiquities 8
Infantile spasms in the setting of Sturge-Weber syndrome 8
A clinical review on megalencephaly: A large brain as a possible sign of cerebral impairment 8
Is benign familial neonatal KCNQ2-related epilepsy always familially benign? J pediatric neonatal individualized medicine 8
Manuale di Pediatria, quinta edizione. Capitolo 2 "Anamnesi ed esame obiettivo". Capitolo 29 "Malattie Neurologiche" 7
Cognitive disabilities and bioethical implications in down syndrome 7
ACQUIRED PERIPHERAL NEUROPATHY: A REPORT ON 20 CHILDREN 7
A child with congenital heart disease and situs viscerum inversus 7
Anomalies of the Craniocervical Junction (Chiari Malformations) 7
Phacomatosis Pigmentokeratotica 6
Biochemical Insights into Merlin/NF2 Pathophysiology and Biologically Targeted Therapies in Childhood NF2 and Related Forms 6
Wyburn-Mason Syndrome 6
Encefalopatia acuta da probabile deficit cerebrale di acido folico in paziente con iperfenilalaninemia da deficit di DHPR 6
E se non fossero solo incubi notturni? 6
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 6
A girl with a 14.7 Mb 3q26.32-q28 duplication: a new report of 3q duplication syndrome and a literature review 6
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 6
Neurologia Pediatrica - Dalle cause biologiche alla pratica clinica 6
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] 6
A Probable Topiramate-induced Limbs Paraesthesia and Rigid Fingers Flexion 6
Allergia agli insetti 6
Aicardi-Goutières Syndrome Type 2: A Report on Two Cases with Different Phenotypes Caused by RNASEH2B Gene Mutations 6
A mosaic pattern of INI1/SMARCB1 protein expression distinguishes Schwannomatosis and NF2-associated peripheral schwannomas from solitary peripheral schwannomas and NF2-associated vestibular schwannomas 6
Rediagnosing one of Smith's patients (John McCann) with "neuromas tumours" (1849) 5
Ataxia in children: early recognition and clinical evaluation 5
Sprengel deformity: a rare congenital anomaly of the scapula 5
SCN1A and its related epileptic phenotypes 5
Mosaic Neurocutaneous Disorders and Their Causes 5
Chromosome 2p15-p16.1 microduplication in a boy with congenital anomalies: Is it a distinctive syndrome? 5
WDR45 gene and its role in pediatric epilepsies 5
Previously Unreported COL7A1 Mutation in a Somali Patient with Dystrophic Epidermolysis Bullosa 5
TSC1 and TSC2: Tuberous Sclerosis Complex and Its Related Epilepsy Phenotype 5
At the Basis of Brain Malformations: Brain Plasticity, Developmental Neurobiology, and Considerations for Rehabilitation 5
Lissencephaly, Pachygyrias, Band Heterotopias, RELN Pathway, and ARX Mutations (Incomplete Neuron Migration) 5
La Tosse 5
Paternally inherited 17q12 microduplication: similar pattern of neurological signs and features in the father and his children 5
Primary Microcephaly with Novel Variant of MCPH1 Gene in Twins: Both Manifesting in Childhood at the Same Time with Hashimoto's Thyroiditis 5
Ganglioneuroblastoma-associated vitamin D deficiency rickets 5
Megalencephaly: Classification, Genetic Causes, and Related Syndromes 5
SCN1B gene: A close relative to SCN1A 5
Anti-MOG Antibody Syndrome and Cerebral Sinovenous Thrombosis: A Cause-Effect Hypothesis 5
KCNT1-Related Epilepsy: A Review 5
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 5
Becker's Nevus Syndrome 5
Anti-mog associated encephalitis: when steroid therapy is not enough 5
Early acute pancreatitis in a child with compound heterozygosis ∆F508/R1438W/Y1032C cystic fibrosis: a case report 5
A New Patient with Potocki-Lupski Syndrome: A Literature Review 5
Pediatria dalla A alla Z - Guida Pratica alla diagnosi e al trattamento. Neurologia, disturbi psichiatrici e comportamentali 5
Microcephaly-Capillary Malformation Syndrome 5
Actualities on molecular pathogenesis and repairing processes of cerebral damage in perinatal hypoxic-ischemic encephalopathy 4
Speckled Lentiginous Nevus Syndrome 4
Schizencephaly: Etiopathogenesis, Classification, Therapeutic, and Rehabilitative Approach 4
Ketogenic diet for infants with epilepsy: A literature review 4
A neurocutaneous phenotype with paired hypo- and hyperpigmented macules, microcephaly and stunted growth as prominent features 4
Syntaxin binding protein 1 related epilepsies 4
Congenital muscular dystrophy: from muscle to brain 4
Diagnosis, Management, and New Therapeutic Options in Childhood Neurofibromatosis Type 2 and Related Forms 4
Telangiectasia Macularis Eruptive Perstans (TMEP) in childhood: a case report and literature review" 4
Megalencephaly Capillary Malformation Syndrome 4
Encefalite GluR3: fenotipo clinico e strumentale di quattro pazienti 4
Nevus Sebaceous Syndrome 4
I farmaci orfani e i farmaci innovativi. Aspetti regolatori e accesso alle cure 4
Blue Rubber Bleb Nevus Syndrome 4
A mild phenotype associated with a de novo microdeletion 10q23.1-q23.2: A new patient with a novel feature 4
Microcephaly and Its Related Syndromes: Classification, Genetic, Clinical, and Rehabilitative Considerations 4
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 4
Two siblings with a homozygous MTHFR C677T (G80A-RFC1) mutation and stroke 4
GRIN2A and GRIN2B and Their Related Phenotypes 4
Mutazione PRRT2 in un bambino con caratteristiche dismorfiche, microcefalia congenita e convulsioni epilettiche gravi 4
Mixed Vascular Nevus Syndrome 4
Cervical neurenteric cyst and Klippel-Feil syndrome: An abrupt onset of myelopathic signs in a young patient 4
Encefalite da Anticorpi anti-GluR3 in sei pazienti in età pediatrica 4
Encephalocraniocutaneous Lipomatosis (Haberland Syndrome or Fishman Syndrome) 4
Neonatal seizures as onset of Inborn Errors of Metabolism (IEMs): from diagnosis to treatment. A systematic review 4
COVID-19 Pandemic Outbreak and its Psychological Impact on Patients with Rare Lysosomal Diseases 4
Spine and brain malformations in a patient obligate carrier of MTHFR with autism and mental retardation 4
Cerebellotrigeminal Dermal Dysplasia (Gómez-López-Hernández Syndrome) 4
Sindrome del vomito ciclico: analisi di una popolazione di 20 bambini e revisione della letteratura 4
Brain ultrasound features in multiple births due to spontaneous conception compared with assisted reproductive techniques: a cross-sectional, population-based study 4
Did Cro-Magnon 1 have neurofibromatosis type 2? 4
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 4
In vitro efficacy of ARQ 092, an allosteric AKT inhibitor, on primary fibroblast cells derived from patients with PIK3CA-related overgrowth spectrum (PROS) 4
ACCIDENTAL ETHYL ALCOHOL INTOXICATION IN A -DAY-OLD INFANT. CLINICAL FINDINGS AND NEUROLOGICAL FOLLOW-UP 4
Hypomelanosis of Ito 4
Multiseptate Gallbladder in a Child: A Possible Cause of Poor Growth? 4
Correlazione genotipo/fenotipo nella Sclerosi Tuberosa (TSC1 vs. TSC2) in 81 pazienti siciliani 4
The spectrum of KCNQ2- And KCNQ3-related epilepsy 4
A sudden weight gain in a child as clinical presentation of Chiari Type I malformation: a case report 4
Megalencephaly: Classification, Genetic Causes, and Related Syndromes 4
Phacomatosis Pigmentovascularis 4
Hemihydranencephaly: living with half brain dysfunction 3
Totale 543
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Categoria #
all - tutte 6.594
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 6.594
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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
2024/2025786 3 6 7 370 329 71 0 0 0 0 0 0
Totale 795