Chiara Gelmini

Reggio Nell'emilia, 42123, Italy

Last Updated: 09/26/2026

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Found 16 publications

ACT-ON-DIP: Study Protocol of a Randomized Controlled Trial of a Home-Based ACTion Observation Tele-RehabilitatioN for Upper Limb in Children with DIPlegic Cerebral Palsy.

ACT-ON-DIP: Study Protocol of a Randomized Controlled Trial of a Home-Based ACTion Observation Tele-RehabilitatioN for Upper Limb in Children with DIPlegic Cerebral Palsy.

Journal: Children (Basel, Switzerland)

Published: July 22, 2025

Mathematical skills in heritage bilingual children with and without developmental dyscalculia: A comparative study.

Mathematical skills in heritage bilingual children with and without developmental dyscalculia: A comparative study.

Journal: Research in developmental disabilities

Published: June 19, 2025

Split Hand-Foot and Deafness in a Patient with 7q21.13-q21.3 Deletion Not Including the DLX5/6 Genes.

Split Hand-Foot and Deafness in a Patient with 7q21.13-q21.3 Deletion Not Including the DLX5/6 Genes.

Journal: Genes

Published: June 30, 2023

Improving the phenotype description of Basel-Vanagaite-Smirin-Yosef syndrome, MED25-related: polymicrogyria as a distinctive neuroradiological finding.

Improving the phenotype description of Basel-Vanagaite-Smirin-Yosef syndrome, MED25-related: polymicrogyria as a distinctive neuroradiological finding.

Journal: Neurogenetics

Published: June 15, 2020

A Novel CCND2 Mutation in a Previously Reported Case of Megalencephaly and Perisylvian Polymicrogyria with Postaxial Polydactyly and Hydrocephalus.

A Novel CCND2 Mutation in a Previously Reported Case of Megalencephaly and Perisylvian Polymicrogyria with Postaxial Polydactyly and Hydrocephalus.

Journal: Neuropediatrics

Published: April 12, 2018

Complex cranio-vertebral malformation: disruption sequence or iniencephaly?

Complex cranio-vertebral malformation: disruption sequence or iniencephaly?

Journal: Clinical dysmorphology

Published: March 02, 2018

Prematurity, ventricular septal defect and dysmorphisms are independent predictors of pathogenic copy number variants: a retrospective study on array-CGH results and phenotypical features of 293 children with neurodevelopmental disorders and/or multiple congenital anomalies.

Prematurity, ventricular septal defect and dysmorphisms are independent predictors of pathogenic copy number variants: a retrospective study on array-CGH results and phenotypical features of 293 children with neurodevelopmental disorders and/or multiple congenital anomalies.

Journal: Italian journal of pediatrics

Published: August 21, 2017

Van Maldergem syndrome and Hennekam syndrome: Further delineation of allelic phenotypes.

Van Maldergem syndrome and Hennekam syndrome: Further delineation of allelic phenotypes.

Journal: American journal of medical genetics. Part A

Published: March 08, 2017

Cognitive-behavioural phenotype in a group of girls from 1.2 to 12 years old with the Incontinentia Pigmenti syndrome: Recommendations for clinical management.

Cognitive-behavioural phenotype in a group of girls from 1.2 to 12 years old with the Incontinentia Pigmenti syndrome: Recommendations for clinical management.

Journal: Applied neuropsychology. Child

Published: June 09, 2016

Multiple sulfatase deficiency with neonatal manifestation.

Multiple sulfatase deficiency with neonatal manifestation.

Journal: Italian journal of pediatrics

Published: August 11, 2014

Incontinentia pigmenti: learning disabilities are a fundamental hallmark of the disease.

Incontinentia pigmenti: learning disabilities are a fundamental hallmark of the disease.

Journal: PloS one

Published: July 26, 2013

Multiple tumor types including leiomyoma and Wilms tumor in a patient with Gorlin syndrome due to 9q22.3 microdeletion encompassing the PTCH1 and FANC-C loci.

Multiple tumor types including leiomyoma and Wilms tumor in a patient with Gorlin syndrome due to 9q22.3 microdeletion encompassing the PTCH1 and FANC-C loci.

Journal: American journal of medical genetics. Part A

Published: July 25, 2013

Showing 1-12 of 16

Last Updated: 09/26/2026