Roberto Micheli
Brescia, Italy
Last Updated: 09/26/2026
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Found 15 publications
Progressive Depletion of B and T Lymphocytes in Patients with Ataxia Telangiectasia: Results of the Italian Primary Immunodeficiency Network.
Journal: Journal of clinical immunology
Published: September 27, 2021
Risk of Optic Pathway Glioma in Neurofibromatosis Type 1: No Evidence of Genotype-Phenotype Correlations in A Large Independent Cohort.
Journal: Cancers
Published: September 28, 2019
Visuoperceptual Impairment in Children with NF1: From Early Visual Processing to Procedural Strategies.
Journal: Behavioural neurology
Published: June 22, 2018
Human parechovirus type 6 and Guillain-Barré syndrome: a case report.
Journal: Journal of neurovirology
Published: February 09, 2018
Minimum effective betamethasone dosage on the neurological phenotype in patients with ataxia-telangiectasia: a multicenter observer-blind study.
Journal: European journal of neurology
Published: October 27, 2017
Neurovisual Assessment in Children with Ataxia Telangiectasia.
Journal: Neuropediatrics
Published: October 10, 2017
ATM splicing variants as biomarkers for low dose dexamethasone treatment of A-T.
Journal: Orphanet journal of rare diseases
Published: March 16, 2017
The Key Search Subtest of the Behavioural Assessment of the Dysexecutive Syndrome in Children (BADS-C) Instrument Reveals Impaired Planning Without External Constraints in Children With Neurofibromatosis Type 1.
Journal: Journal of child neurology
Published: February 15, 2017
Novel compound heterozygous mutations in a child with Ataxia-Telangiectasia showing unrelated cerebellar disorders.
Journal: Journal of the neurological sciences
Published: October 06, 2015
Occlusal traits in children with neurofibromatosis type 1.
Journal: Orthodontics & craniofacial research
Published: September 04, 2015
Development of global rating instruments for pediatric patients with ataxia telangiectasia.
Journal: European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society
Published: July 12, 2015
ClC-1 mutations in myotonia congenita patients: insights into molecular gating mechanisms and genotype-phenotype correlation.
Journal: The Journal of physiology
Published: February 13, 2015
Last Updated: 09/26/2026