Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

Search Results

51 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Results By Year timeline is not available.
Page 1
Author Response.
Schrier Vergano SA. Schrier Vergano SA. Pediatrics. 2022 Aug 1;150(2):e2022057888. doi: 10.1542/peds.2022-057888B. Pediatrics. 2022. PMID: 35896833 No abstract available.
Making Decisions About Krabbe Disease Newborn Screening.
Schrier Vergano SA, Kanungo S, Arnold G. Schrier Vergano SA, et al. Pediatrics. 2022 Apr 1;149(4):e2021053175. doi: 10.1542/peds.2021-053175. Pediatrics. 2022. PMID: 35229104 No abstract available.
Case 3: The Hypothermic Newborn.
Erickson J, Schrier Vergano SA. Erickson J, et al. Among authors: schrier vergano sa. Neoreviews. 2019 Feb;20(2):e93-e95. doi: 10.1542/neo.20-2-e93. Neoreviews. 2019. PMID: 31261091 No abstract available.
Rare Cause of Arrhythmia and Seizures in a Late-Preterm Newborn.
Tiwari P, Dwyer K, Siegfried B, Schrier Vergano SA. Tiwari P, et al. Among authors: schrier vergano sa. Neoreviews. 2022 Oct 1;23(10):e696-e698. doi: 10.1542/neo.23-10-e696. Neoreviews. 2022. PMID: 36180729 No abstract available.
Language Impairments in Individuals With Coffin-Siris Syndrome.
Vasko A, Schrier Vergano SA. Vasko A, et al. Among authors: schrier vergano sa. Front Neurosci. 2022 Jan 20;15:802583. doi: 10.3389/fnins.2021.802583. eCollection 2021. Front Neurosci. 2022. PMID: 35126043 Free PMC article.
Heterozygous variants in PRPF8 are associated with neurodevelopmental disorders.
O'Grady L, Schrier Vergano SA, Hoffman TL, Sarco D, Cherny S, Bryant E, Schultz-Rogers L, Chung WK, Sacharow S, Immken LL, Holder S, Blackwell RR, Buchanan C, Yusupov R, Lecoquierre F, Guerrot AM, Rodan L, de Vries BBA, Kamsteeg EJ, Santos Simarro F, Palomares-Bralo M, Brown N, Pais L, Ferrer A, Klee EW, Babovic-Vuksanovic D, Rhodes L, Person R, Begtrup A, Keller-Ramey J, Santiago-Sim T, Schnur RE, Sweetser DA, Gold NB. O'Grady L, et al. Among authors: schrier vergano sa. Am J Med Genet A. 2022 Sep;188(9):2750-2759. doi: 10.1002/ajmg.a.62772. Epub 2022 May 11. Am J Med Genet A. 2022. PMID: 35543142
Association of the missense variant p.Arg203Trp in PACS1 as a cause of intellectual disability and seizures.
Stern D, Cho MT, Chikarmane R, Willaert R, Retterer K, Kendall F, Deardorff M, Hopkins S, Bedoukian E, Slavotinek A, Schrier Vergano S, Spangler B, McDonald M, McConkie-Rosell A, Burton BK, Kim KH, Oundjian N, Kronn D, Chandy N, Baskin B, Guillen Sacoto MJ, Wentzensen IM, McLaughlin HM, McKnight D, Chung WK. Stern D, et al. Clin Genet. 2017 Aug;92(2):221-223. doi: 10.1111/cge.12956. Epub 2017 Jan 23. Clin Genet. 2017. PMID: 28111752 Free PMC article.
51 results