about
PRES in Children Undergoing Hematopoietic Stem Cell or Solid Organ TransplantationEpilepsy in Mowat-Wilson syndrome: delineation of the electroclinical phenotypeLong-term effects of antepartum bed rest on offspring.Neuroimaging findings in Mowat-Wilson syndrome: a study of 54 patientsCentral Nervous System Complications in Children Receiving Chemotherapy or Hematopoietic Stem Cell TransplantationVNS in drug resistant epilepsy: preliminary report on a small group of patients.Sensorial saturation: an effective analgesic tool for heel-prick in preterm infants: a prospective randomized trial.Mutations in CTC1, encoding conserved telomere maintenance component 1, cause Coats plus.Conventional magnetic resonance imaging and diffusion tensor imaging studies in children with novel GPR56 mutations: further delineation of a cobblestone-like phenotype.Succinate-CoA ligase deficiency due to mutations in SUCLA2 and SUCLG1: phenotype and genotype correlations in 71 patients.Cytogenetic and molecular characterization of a recombinant X chromosome in a family with a severe neurologic phenotype and macular degeneration.Analgesic effect of watching TV during venipuncture.Symmetric polymicrogyria and pachygyria associated with TUBB2B gene mutations.Efficacy and safety of felbamate in children under 4 years of age: a retrospective chart review.Mutations in SNORD118 cause the cerebral microangiopathy leukoencephalopathy with calcifications and cysts.Acute diplopia in the pediatric Emergency Department. A cohort multicenter Italian study.Juvenile dermatomyositis: A report of three cases.Cerebral ischemic involvement in Vogt-Koyanagi-Harada disease.Fever as a seizure precipitant factor in Panayiotopoulos syndrome: a clinical and genetic study.A mutation in PAK3 with a dual molecular effect deregulates the RAS/MAPK pathway and drives an X-linked syndromic phenotype.Leukoencephalopathy with calcifications and cysts: a purely neurological disorder distinct from coats plus.Effect of multisensory stimulation on analgesia in term neonates: a randomized controlled trial.Post-ictal circulating levels of allopregnanolone in children with partial or generalized seizures.Prospective study on long-term treatment with oxcarbazepine in pediatric epilepsy.A comparative study of hydrocortisone versus deflazacort in drug-resistant epilepsy of childhood.Is an excessive number of prenatal echographies a risk for fetal growth?A new PLA2G6 mutation in a family with infantile neuroaxonal dystrophy.Intracranial pressure during procedural pain.Progressive cerebral white matter involvement in a patient with Congenital Cataracts Facial Dysmorphisms Neuropathy (CCFDN).Diagnosis of congenital myasthenic syndrome with mutation of the RAPSN gene after general anaesthesia.Psychotic episode during steroid therapy in hashimoto encephalopathy.Etiology, characteristics and outcome of seizures after pediatric hematopoietic stem cell transplantation.Status epilepticus as a main manifestation of posterior reversible encephalopathy syndrome after pediatric hematopoietic stem cell transplantation.Corrigendum to "A new PLA2G6 mutation in a family with infantile neuroaxonal dystrophy" [J. Neurol. Sci. 381C (2017) 209-212].Epilepsy in Mowat-Wilson syndrome: is it a matter of GABA?Use of sound-absorbing panel to reduce noisy incubator reverberating effects.Is the ABC pain scale reliable for premature babies?Life-threatening complications of posterior reversible encephalopathy syndrome in children.The "eye-of-the-tiger" sign may be absent in the early stages of classic pantothenate kinase associated neurodegeneration.Early onset absence epilepsy with onset in the first year of life: a multicenter cohort study.
P50
Q28081572-82B999D6-1602-43C5-AC07-6BAC5AD7000AQ28283452-BF2840E3-BE52-493B-AB32-2AA68B8D0226Q30540479-E93B6538-FACF-4AF3-82B2-DCBF3EA9505EQ31141777-B035E108-93C2-4D41-8588-0A4794576810Q33679931-8CD8A1B7-E097-4226-A7FB-F93743B771FDQ33809239-49753ADB-2F14-4153-A638-2FCFF96D8276Q34085165-F0B31800-0091-434F-B0E7-C45D3F2D181DQ34248892-8DC6879D-5715-413F-BB6F-AE485A9BF57DQ34320039-6A72DA79-37B3-47DA-950A-8B5093503FF2Q34498316-F4167C0C-BCE4-4C85-8DED-24026CAD8D47Q35908169-6D08060E-3E59-45B6-A6E1-EDA3DD31D083Q36153485-495214E4-6321-4FFA-92B6-DAAE60C0B776Q36170406-AB3A46CB-BC0F-475C-B01E-866A17B13B2BQ37219705-768E9B7E-12B6-4185-895E-5231D0BBC293Q37302596-BF698BA4-C0C5-40A6-B375-97B6D2B9BFA8Q38720615-0D9582FA-4CA1-4764-9BA8-11C237601F65Q39990391-220425FC-443E-4480-BFF1-866297E6E24AQ40191341-7265F9BD-3BFE-473D-98ED-00C6C8AFFFDEQ40308616-A48CB812-E74B-4199-B4C2-83FF64F480CDQ41930624-466DBD25-6575-4A9B-9171-3BF7F9B60EB7Q42452162-23E21F2E-3B4F-499C-B814-C304172DAFE9Q43937292-CBA1526B-30A8-4F8F-8D6E-5147E6EC815AQ45278288-E694C94F-2D08-42E1-B1AB-9B9753B033B5Q45929795-A194C9F0-B344-40BF-9469-9A91BC12D416Q46559202-6B30B0D3-B38F-4C38-900B-C91547C3C099Q46590900-55C58B56-5FED-4150-B915-0E7CD501DFF7Q48027620-846A42F7-CFCA-437A-AF1D-28F258322EC4Q48191563-36DEAA64-FFA3-40A8-9B33-D28456B012DCQ48255423-1435415D-A584-4FB1-92F1-B7A3EF5C450AQ48282137-3C760526-265C-4C26-A301-2EBD9D960677Q48596471-10121931-966D-49F9-B058-BA680392E621Q48837118-9EB46DCC-939B-441A-8A99-EEAB6A2D81B2Q48849293-0B346466-9AAF-4ECF-843B-DE5961CF7270Q49646309-2DEBCB16-69C1-4C6F-92EF-BE905C8C2F52Q50866521-A1DD5628-A99E-49AC-8D5A-226B5C677D1AQ51804125-2FC09602-D84A-44C3-AAB5-88477CDD2BB7Q53023799-77444DC9-9664-41EB-A66E-F6A2F12CB41BQ53066615-53A13BC9-3458-4140-86B3-357E4AE51F3BQ54564698-DFDC2DCA-CA28-4557-A4A4-23B3C74B25BCQ54721290-9C194767-503C-4C43-BE96-8AD3ED1D1225
P50
description
hulumtues
@sq
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Duccio M Cordelli
@es
Duccio M Cordelli
@nl
Duccio M Cordelli
@sl
Duccio M. Cordelli
@en
type
label
Duccio M Cordelli
@es
Duccio M Cordelli
@nl
Duccio M Cordelli
@sl
Duccio M. Cordelli
@en
altLabel
Duccio Maria Cordelli
@en
prefLabel
Duccio M Cordelli
@es
Duccio M Cordelli
@nl
Duccio M Cordelli
@sl
Duccio M. Cordelli
@en
P1053
Q-4983-2016
P106
P1153
6506814479
P21
P2798
P31
P3829
P496
0000-0002-1367-6419
P569
2000-01-01T00:00:00Z