IRIS
CAMA, ARMANDO
 Distribuzione geografica
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Continente #
EU - Europa 4.679
Totale 4.679
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Nazione #
IT - Italia 4.679
Totale 4.679
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Città #
Genova 2.991
Rapallo 647
Vado Ligure 534
Genoa 498
Bordighera 9
Totale 4.679
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Nome #
Molecular fingerprinting reflects different histotypes and brain region in low grade gliomas 167
Near-miss events are really missed! Reflections on incident reporting in a department of pediatric surgery. 166
Idiopathic Cervical Hematomyelia in an Infant: Spinal Cord Injury without Radiographic Abnormality Caused by a Trivial Trauma? Case Report and Review of the Literature 157
A 3-year-old boy with drug-resistant complex partial seizures 156
Treatment and outcome of children with cerebral cavernomas: a survey on 32 patients. 145
AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disorders 145
Specific gene expression signatures of low-grade gliomas (LGG) 144
Interferon-related transcriptome alterations in the cerebrospinal fluid cells of Aicardi-Goutières patients 138
Epilepsy associated with supratentorial brain tumors under 3 years of life. 129
Brain damage as detected by cDNA-microarray in the spinal fluid of patients with Aicardi-Goutieres syndrome 126
A rare case of osteoblastoma associated to aneurysmal bone cyst of the spine. Case report 125
Erratum to: Treatment and outcome of children with cerebral cavernomas: a survey on 32 patients. 123
Medulloblastoma variants: age-dependent occurrence and relation to Gorlin syndrome--a new clinical perspective. 109
Dermoid and Epidermoid Cysts of Scalp: Case Series of 234 Consecutive Patients 107
Chiari malformation type I: what information from the genetics? 105
A Distinct Gene-Expression Profile in Pediatric Ganglioglioma 102
Genetic Screening of Pediatric Cavernous Malformations 102
Currarino syndrome: Proposal of a diagnostic and therapeutic protocol 97
Pineal Germinoma in a Child with Interferon-γ Receptor 1 Deficiency. Case Report and Literature Review 94
Exclusion of the Sonic Hedgeog gene as responsible for Currarino syndrome and anorectal malformations with sacral hypodevelopment 92
Final results of the second prospective AIEOP protocol for pediatric intracranial ependymoma 90
Pure Bilateral Lambdoid and Posterior Sagittal Synostosis (Mercedes−Benz Syndrome): Case Report and Literature Review 89
FOCAL PHARMACORESISTANT EPILEPSY IN A CHILD WITH NEUROCUTANEOUS MELANOSIS 88
Tonsillar herniation spectrum: more than just Chiari I. Update and controversies on classification and management 88
Exome sequencing of two Italian pedigrees with non-isolated Chiari malformation type i reveals candidate genes for cranio-facial development 84
Endocrine and growth features in childhood craniopharyngioma: a mono-institutional study. 79
NO MAJOR ROLE FOR THE EMX2 GENE IN SCHIZENCEPHALY. 78
A Novel Skin and Fascia Opening for Subfascial Inserting of Intrathecal Baclofen Pump 78
Incidental findings on routine brain MRI scans in preterm infants 78
Radiation-Induced Moyamoya Syndrome in Children with Brain Tumors: Case Series and Literature Review 76
Intraspinal Inclusion Tumor After Myelomeningocele Repair: A Long-Term Single-Center Experience 75
Whole exome sequencing identifies novel predisposing genes in neural tube defects 75
Glioneuronal tumors and epilepsy in children: seizure outcome related to lesionectomy. 73
Craniosinostosi 70
Targeted re-sequencing in pediatric and perinatal stroke 69
Distinctive Genetic Profile With IDH1, TP53, and MLH1 Mutations in a Radiation-Induced Anaplastic Astrocytoma 67
Brain damage as detected by cDNA-microarray in the spinal fluid of patients with aicardi-goutières syndrome 66
Interferon-related transcriptome alterations in the cerebrospinal fluid cells of aicardi-goutières patients 65
Focal unilateral polymicrogyria and epilepsy surgery 65
Management: opinions from different centers—the Istituto Giannina Gaslini experience 65
Pediatric pituitary adenoma with mixed FSH and TSH immunostaining and FSH hypersecretion in a 6 year-old girl with precocious puberty: case report and multidisciplinary management 64
Burr Holes Revascularization in Three Pediatric Cases of Moyamoya Syndrome: Easy Choice or Insidious Trap? Case Series and Review 62
Grisel Syndrome in Pediatric Age: A Single-Center Italian Experience and Review of the Literature 60
Analysis of NADP+-dependent isocitrate dehydrogenase-1/2 gene mutations in pediatric brain tumors: Report of a secondary anaplastic astrocytoma carrying the IDH1 mutation 54
Spontaneous rupture of middle fossa arachnoid cysts: surgical series from a single center pediatric hospital and literature review 50
Potential biomarkers of childhood brain tumor identified by proteomics of cerebrospinal fluid from extraventricular drainage (EVD) 48
Importance of early diagnosis of spinal dysraphia. Dermoid cyst of the cauda equina associated with a pilonidal sinus: case report 43
Limits and pitfalls of indirect revascularization in moyamoya disease and syndrome 43
Consensus statement from the international consensus meeting on post-traumatic cranioplasty 40
Hemispheric surgery for severe epilepsy in early childhood: a case series 38
FZD6 is a novel gene for human neural tube defects 34
Non-robotized frameless stereotactic magnetic resonance guided laser interstitial thermal therapy for hypothalamic hamartoma: preliminary results of 2 cases and review of the literature 30
Natural history of cavernous malformations in children with brain tumors treated with radiotherapy and chemotherapy 26
Value of 18F-3,4-dihydroxyphenylalanine pet/mr image fusion in pediatric supratentorial infiltrative astrocytomas: A prospective pilot study 25
External ventricular drainage for posthemorrhagic ventricular dilatation in preterm infants: insights on efficacy and failure 23
Technical description of a novel device for external ventricular drainage in neonatal and pediatric patients: Results from a single referral center experience 20
Exclusion of the Sonic Hedgehog gene as responsible for Currarino syndrome and anorectal malformations with sacral hypodevelopment 13
Risk factors for renal function impairment in a series of 502 patients born with spinal dysraphisms 12
Long-term urologic outcome in patients with caudal regression syndrome, compared with meningomyelocele and spinal cord lipoma 10
Caudal regression syndrome: An online multicentre survey. Urological long-term results 10
Totale 4.752
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Categoria #
all - tutte 17.632
article - articoli 16.697
book - libri 0
conference - conferenze 716
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 219
Totale 35.264
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020984 0 0 0 0 0 130 207 112 159 191 135 50
2020/2021548 37 23 82 80 42 54 34 44 33 59 32 28
2021/2022627 31 27 50 61 36 28 33 134 68 64 18 77
2022/2023743 60 74 11 60 99 118 7 78 128 8 89 11
2023/2024380 19 39 12 49 30 55 11 26 27 11 27 74
2024/2025578 61 80 28 98 174 137 0 0 0 0 0 0
Totale 4.752