Jayadev S - Search Results

1

Novel Report of Phosphoserine Phosphatase Deficiency in an Adult with Myeloneuropathy and Limb Contractures.

Byers HM, Bennett RL, Malouf EA, Weiss MD, Feng J, Scott CR, Jayadev S. Byers HM, et al. Among authors: jayadev s. JIMD Rep. 2016;30:103-108. doi: 10.1007/8904_2015_510. Epub 2015 Nov 21. JIMD Rep. 2016. PMID: 26589312 Free PMC article.

2

Erratum to: Novel Report of Phosphoserine Phosphatase Deficiency in an Adult with Myeloneuropathy and Limb Contractures.

Byers HM, Bennett RL, Malouf EA, Weiss MD, Feng J, Scott CR, Jayadev S. Byers HM, et al. Among authors: jayadev s. JIMD Rep. 2016;30:109. doi: 10.1007/8904_2016_540. Epub 2016 Feb 19. JIMD Rep. 2016. PMID: 26888760 Free PMC article. No abstract available.

3

Depletion of the AD Risk Gene SORL1 Selectively Impairs Neuronal Endosomal Traffic Independent of Amyloidogenic APP Processing.

Knupp A, Mishra S, Martinez R, Braggin JE, Szabo M, Kinoshita C, Hailey DW, Small SA, Jayadev S, Young JE. Knupp A, et al. Among authors: jayadev s. Cell Rep. 2020 Jun 2;31(9):107719. doi: 10.1016/j.celrep.2020.107719. Cell Rep. 2020. PMID: 32492427 Free PMC article.

4

Transcription factor p53 influences microglial activation phenotype.

Jayadev S, Nesser NK, Hopkins S, Myers SJ, Case A, Lee RJ, Seaburg LA, Uo T, Murphy SP, Morrison RS, Garden GA. Jayadev S, et al. Glia. 2011 Oct;59(10):1402-13. doi: 10.1002/glia.21178. Epub 2011 May 19. Glia. 2011. PMID: 21598312 Free PMC article.

5

Hereditary ataxias: overview.

Jayadev S, Bird TD. Jayadev S, et al. Genet Med. 2013 Sep;15(9):673-83. doi: 10.1038/gim.2013.28. Epub 2013 Mar 28. Genet Med. 2013. PMID: 23538602 Free article. Review.

6

Presenilin 2 influences miR146 level and activity in microglia.

Jayadev S, Case A, Alajajian B, Eastman AJ, Möller T, Garden GA. Jayadev S, et al. J Neurochem. 2013 Dec;127(5):592-9. doi: 10.1111/jnc.12400. Epub 2013 Sep 30. J Neurochem. 2013. PMID: 23952003 Free PMC article.

7

Novel pregnancy-triggered episodes of CAPOS syndrome.

Chang IJ, Adam MP, Jayadev S, Bird TD, Natarajan N, Glass IA. Chang IJ, et al. Among authors: jayadev s. Am J Med Genet A. 2018 Jan;176(1):235-240. doi: 10.1002/ajmg.a.38502. Epub 2017 Nov 1. Am J Med Genet A. 2018. PMID: 29090527 Free PMC article. Review.

8

Novel compound heterozygous FBXO7 mutations in a family with early onset Parkinson's disease.

Lorenzo-Betancor O, Lin YH, Samii A, Jayadev S, Kim HM, Longfellow K, Distad BJ, Yearout D, Mata IF, Zabetian CP. Lorenzo-Betancor O, et al. Among authors: jayadev s. Parkinsonism Relat Disord. 2020 Nov;80:142-147. doi: 10.1016/j.parkreldis.2020.09.035. Epub 2020 Sep 22. Parkinsonism Relat Disord. 2020. PMID: 33002721 Free PMC article.

9

Conjugal Alzheimer disease: risk in children when both parents have Alzheimer disease.

Jayadev S, Steinbart EJ, Chi YY, Kukull WA, Schellenberg GD, Bird TD. Jayadev S, et al. Arch Neurol. 2008 Mar;65(3):373-8. doi: 10.1001/archneurol.2007.61. Arch Neurol. 2008. PMID: 18332250

10

Neuropathological Comparison of Adult Onset and Juvenile Huntington's Disease with Cerebellar Atrophy: A Report of a Father and Son.

Latimer CS, Flanagan ME, Cimino PJ, Jayadev S, Davis M, Hoffer ZS, Montine TJ, Gonzalez-Cuyar LF, Bird TD, Keene CD. Latimer CS, et al. Among authors: jayadev s. J Huntingtons Dis. 2017;6(4):337-348. doi: 10.3233/JHD-170261. J Huntingtons Dis. 2017. PMID: 29036832 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

187 results

Search Page