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

93 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Results By Year timeline is not available.
Page 1
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. Lee BH, et al. Among authors: engelstad k. Neurology. 2022 Oct 3;99(14):e1527-e1537. doi: 10.1212/WNL.0000000000200986. Neurology. 2022. PMID: 35835557 Free PMC article.
Weakness and fatigue in diverse neuromuscular diseases.
Montes J, Blumenschine M, Dunaway S, Alter AS, Engelstad K, Rao AK, Chiriboga CA, Sproule DM, De Vivo DC. Montes J, et al. Among authors: engelstad k. J Child Neurol. 2013 Oct;28(10):1277-83. doi: 10.1177/0883073813493663. Epub 2013 Jul 11. J Child Neurol. 2013. PMID: 23847297
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. Kay DM, et al. Among authors: engelstad k. Genet Med. 2020 Aug;22(8):1296-1302. doi: 10.1038/s41436-020-0824-3. Epub 2020 May 18. Genet Med. 2020. PMID: 32418989 Free article.
Protean phenotypic features of the A3243G mitochondrial DNA mutation.
Kaufmann P, Engelstad K, Wei Y, Kulikova R, Oskoui M, Battista V, Koenigsberger DY, Pascual JM, Sano M, Hirano M, DiMauro S, Shungu DC, Mao X, De Vivo DC. Kaufmann P, et al. Among authors: engelstad k. Arch Neurol. 2009 Jan;66(1):85-91. doi: 10.1001/archneurol.2008.526. Arch Neurol. 2009. PMID: 19139304 Free PMC article.
Autonomic symptoms in carriers of the m.3243A>G mitochondrial DNA mutation.
Parsons T, Weimer L, Engelstad K, Linker A, Battista V, Wei Y, Hirano M, Dimauro S, De Vivo DC, Kaufmann P. Parsons T, et al. Among authors: engelstad k. Arch Neurol. 2010 Aug;67(8):976-9. doi: 10.1001/archneurol.2010.174. Arch Neurol. 2010. PMID: 20697048 Free PMC article.
Long-term clinical course of Glut1 deficiency syndrome.
Alter AS, Engelstad K, Hinton VJ, Montes J, Pearson TS, Akman CI, De Vivo DC. Alter AS, et al. Among authors: engelstad k. J Child Neurol. 2015 Feb;30(2):160-9. doi: 10.1177/0883073814531822. Epub 2014 Apr 30. J Child Neurol. 2015. PMID: 24789115
Analysis of Gait Disturbance in Glut 1 Deficiency Syndrome.
Blumenschine M, Montes J, Rao AK, Engelstad K, De Vivo DC. Blumenschine M, et al. Among authors: engelstad k. J Child Neurol. 2016 Nov;31(13):1483-1488. doi: 10.1177/0883073816661662. Epub 2016 Aug 10. J Child Neurol. 2016. PMID: 27511993
Paroxysmal eye-head movements in Glut1 deficiency syndrome.
Pearson TS, Pons R, Engelstad K, Kane SA, Goldberg ME, De Vivo DC. Pearson TS, et al. Among authors: engelstad k. Neurology. 2017 Apr 25;88(17):1666-1673. doi: 10.1212/WNL.0000000000003867. Epub 2017 Mar 24. Neurology. 2017. PMID: 28341645 Free PMC article.
93 results