Publications by authors named "Simona Treidler"

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Less Common Mononeuropathies.
Simona Treidler

Semin Neurol· February 2025

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Neuropathy due to bi-allelic SH3TC2 variants: genotype-phenotype correlation and natural history.
Tyler Rehbein, Tong Tong Wu, Simona Treidler, Davide Pareyson, Richard Lewis

Brain· September 2023

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Newborn Screening for Spinal Muscular Atrophy in New York State: Clinical Outcomes From the First 3 Years.
Bo Hoon Lee, Stella Deng, Claudia A Chiriboga, Denise M Kay, Obehioya Irumudomon, Simona O Treidler

Neurology· October 2022

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Erythromelalgia: A Child With V400M Mutation in the Gene.
Chineze Nwebube, Sabrina Bulancea, Adrian Marchidann, Lourdes Bello-Espinosa, Simona Treidler

Neurol Genet· April 2021

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Implementation of population-based newborn screening reveals low incidence of spinal muscular atrophy.
Denise M Kay, Colleen F Stevens, April Parker, Carlos A Saavedra-Matiz, Virginia Sack, Simona Treidler

Genet Med· August 2020

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Variable penetrance of Andersen-Tawil syndrome in a family with a rare missense mutation.
Reem Deeb, Aravindhan Veerapandiyan, Rabi Tawil, Simona Treidler

Neurol Genet· December 2018

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