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Mostrati risultati da 1 a 20 di 62
Titolo Data di pubblicazione Autori Tipo File Abstract
Negative atopy patch test and negative skin prick test reduce the need for oral food challenge in children with atopic dermatitis 2011 Peron A.Tenconi R. + Article (author) -
Electroclinical findings in DUPXQ28 syndrome 2011 A. PeronA. VignoliF. La BriolaM.P. Canevini + Article (author) -
Electroclinical pattern in MECP2 duplication syndrome : eight new reported cases and review of literature 2012 A. VignoliA. PeronC. BonagliaBELLINI, MELISSAF. La BriolaM. P. Canevini + Article (author) -
Medical care of adolescents and women with Rett syndrome : an Italian study 2012 A. VignoliF. La BriolaA. PeronK. TurnerM. SaviniM.P. Canevini + Article (author) -
Electroclinical pattern in MECP2 duplication syndrome : eight new reported cases and review of literature 2012 A. VignoliA. PeronF. La BriolaM.P. Canevini + Article (author) -
Snyder-Robinson syndrome : a novel nonsense mutation in spermine synthase and expansion of the phenotype 2013 A. Peron + Article (author) -
Neonatal suppression-burst without epileptic seizures : Expanding the electroclinical phenotype of STXBP1-related, early-onset encephalopathy 2013 A. PeronRAVIGLIONE, FEDERICO + Article (author) -
Interstitial 6q microdeletion syndrome and epilepsy : a new patient and review of the literature 2013 A. VignoliA. PeronF. La BriolaM.P. Canevini + Article (author) -
Prenatal and postnatal findings in five cases of Fryns syndrome 2014 A. PeronG.M. BafferoR. FoglianiF. MoscaE. Leva + Article (author) -
Hot water epilepsy : a video case of European boy with positive family history and subsequent non-reflex epilepsy 2014 A. VignoliM.N. SaviniF. La BriolaV. ChiesaA. PeronM.P. Canevini + Article (author) -
Corrigendum to "Snyder-Robinson syndrome: A novel nonsense mutation in spermine synthase and expansion of the phenotype. Am J Med Genet 2013, 161A: 2316-2320" 2014 Peron A. + Article (author) -
Molecular cytogenetic characterization of a 2q35-q37 duplication and a 4q35.1-q35.2 deletion in two cousins : a genotype-phenotype analysis 2015 L. RonzoniA. PeronM. BaccarinR. Silipigni + Article (author) -
Glioblastoma multiforme in a child with tuberous sclerosis complex 2015 A. VignoliE. LesmaA. PeronE. SchiavelloS. AnconaG. BulfamanteA. GorioM.P. Canevini + Article (author) -
7p22.1 microduplication syndrome : clinical and molecular characterization of an adult case and review of the literature 2015 A. VignoliA. PeronM.P. RecalcatiI. CatusiL. Larizza + Article (author) -
Autism spectrum disorder in tuberous sclerosis complex : searching for risk markers 2015 A. VignoliF. La BriolaA. PeronK. TurnerE. MagnaghiM.P. Canevini + Article (author) -
Women with TSC : Relationship between Clinical, Lung Function and Radiological Features in a Genotyped Population Investigated for Lymphangioleiomyomatosis 2016 F. Di MarcoS. TerraneoG. ImeriG. PalumboF. La BriolaS. TresoldiL. GualandriF. GhelmaE. MontanariA. GorioE. LesmaA. PeronM.P. CaneviniS. Centanni + Article (author) -
Do patients with tuberous sclerosis complex have an increased risk for malignancies? 2016 A. PeronA. VignoliF. La BriolaE. MontanariE. MorenghiF. GhelmaG. BulfamanteG. CefaloM.P. Canevini + Article (author) -
Long-term outcome of epilepsy with onset in the first three years of life: findings from a large cohort of patients 2016 A. VignoliA. PeronK. TurnerF. La BriolaV. ChiesaM.P. Canevini + Article (author) -
Epilepsy in ring chromosome 20 syndrome 2016 A. VignoliA. PeronM.P. Canevini + Article (author) -
Effectiveness and tolerability of antiepileptic drugs in 104 girls with Rett syndrome 2017 A. VignoliA. PeronM.P. Canevini + Article (author) -
Mostrati risultati da 1 a 20 di 62
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