Simona O Treidler, MD

Dr. Simona Treidler is trained to treat all neurological disorders.  She is board certified in Neurology, Clinical Neurophysiology and Neuromuscular Medicine.  She has special clinical interest in Neuromuscular disorders such as ALS and Duchene Muscular Dystrophy.  

Erythromelalgia: A Child With V400M Mutation in the SCN9A Gene.

Nwebube C, Bulancea S, Marchidann A, Bello-Espinosa L, Treidler S. Neurol Genet. 2021 Mar 1;7(2):e570. doi: 10.1212/NXG.0000000000000570. eCollection 2021 Apr. PMID: 33688580 Free PMC article. No abstract available.

Newborn Screening for Spinal Muscular Atrophy in New York State: Clinical Outcomes From the First 3 Years.

Lee BH, Deng S, Chiriboga CA, Kay DM, Irumudomon O, Laureta E, Delfiner L, Treidler SO, Anziska Y, Sakonju A, Kois C, Farooq O, Engelstad K, Laurenzano A, Hogan K, Caggana M, Saavedra-Matiz CA, Stevens CF, Ciafaloni E. Neurology. 2022 Jul 14;99(14):e1527-37. doi: 10.1212/WNL.0000000000200986. Online ahead of print. PMID: 35835557 Free PMC article.

Implementation of population-based newborn screening reveals low incidence of spinal muscular atrophy.

Kay DM, Stevens CF, Parker A, Saavedra-Matiz CA, Sack V, Chung WK, Chiriboga CA, Engelstad K, Laureta E, Farooq O, Ciafaloni E, Lee BH, Malek S, Treidler S, Anziska Y, Delfiner L, Sakonju A, Caggana M. Genet Med. 2020 Aug;22(8):1296-1302. doi: 10.1038/s41436-020-0824-3. Epub 2020 May 18. PMID: 32418989 Free article.

Variable penetrance of Andersen-Tawil syndrome in a family with a rare missense KCNJ2 mutation.

Deeb R, Veerapandiyan A, Tawil R, Treidler S. Neurol Genet. 2018 Oct 25;4(6):e284. doi: 10.1212/NXG.0000000000000284. eCollection 2018 Dec. PMID: 30533530