Sharon Aharoni
Petah Tiqwa, M, Israel
Last Updated: 09/26/2026
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Found 38 publications
Recreational nitrous oxide-related myeloneuropathy in adolescents: a multicenter retrospective case series and systematic literature review.
Journal: European journal of pediatrics
Published: January 04, 2026
The Clinical, Histological, and Genetic Spectrum of RYR1 Variants-A Multi-Center Israeli Cohort Study.
Journal: Journal of clinical medicine
Published: December 09, 2025
Assessment of Fine Motor Abilities Among Children with Spinal Muscular Atrophy Treated with Nusinersen Using a New Touchscreen Application: A Pilot Study.
Journal: Children (Basel, Switzerland)
Published: July 31, 2025
N-terminal truncating variants in CACNB1 cause a new congenital muscular disorder.
Journal: European journal of human genetics : EJHG
Published: June 19, 2025
The impact of a pandemic as an example of a stressful event, on anxiety and related emotional disorders of NF1 patients compared to healthy children.
Journal: Frontiers in psychiatry
Published: February 22, 2025
A rare homozygous CAPN3 variant with distinct clinical features in unrelated families of Iraqi Jewish descent.
Journal: Journal of neuromuscular diseases
Published: February 20, 2025
Fluoroscopic guidance for intrathecal delivery of nusinersen in pediatric patients with spinal muscular atrophy and complex spines.
Journal: Neuromuscular disorders : NMD
Published: October 22, 2024
Respiratory outcomes of onasemnogene abeparvovec treatment for spinal muscular atrophy: national real-world cohort study.
Journal: European journal of pediatrics
Published: August 08, 2024
Outcomes for patients in the RESTORE registry with spinal muscular atrophy and four or more SMN2 gene copies treated with onasemnogene abeparvovec.
Journal: European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society
Published: April 25, 2024
Neurologic complications of thiamine (B1) deficiency following bariatric surgery in adolescents.
Journal: European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society
Published: November 01, 2023
Pulmonary function tests for evaluating the severity of Duchenne muscular dystrophy disease.
Journal: Acta paediatrica (Oslo, Norway : 1992)
Published: September 16, 2022
Real-Life Outcome After Gene Replacement Therapy for Spinal Muscular Atrophy: A Multicenter Experience.
Journal: Pediatric neurology
Published: August 01, 2022
Last Updated: 09/26/2026