Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Olga Neyman"'
Autor:
Amjad Samara, Rachel Rahn, Olga Neyman, Ki Yun Park, Ahmad Samara, Bess Marshall, Joseph Dougherty, Tamara Hershey
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 14, Iss 1, Pp 1-14 (2019)
Abstract Wolfram syndrome is a rare multisystem disorder caused by mutations in WFS1 or CISD2 genes leading to brain structural abnormalities and neurological symptoms. These abnormalities appear in early stages of the disease. The pathogenesis of Wo
Externí odkaz:
https://doaj.org/article/d1a0ded280414884a78b89ab597cc6ed
Autor:
Heather M. Lugar, Jonathan M. Koller, Jerrel Rutlin, Sarah A. Eisenstein, Olga Neyman, Anagha Narayanan, Ling Chen, Joshua S. Shimony, Tamara Hershey
Publikováno v:
Scientific Reports, Vol 9, Iss 1, Pp 1-11 (2019)
Abstract Wolfram syndrome is a rare disease caused by mutations in the WFS1 gene leading to symptoms in early to mid-childhood. Brain structural abnormalities are present even in young children, but it is not known when these abnormalities arise. Suc
Externí odkaz:
https://doaj.org/article/41b133a9020c497c8b1dc5bf0c1d1452
Autor:
Amjad Samara, Tatianna Murphy, Jeremy Strain, Jerrel Rutlin, Peng Sun, Olga Neyman, Nitya Sreevalsan, Joshua S. Shimony, Beau M. Ances, Sheng-Kwei Song, Tamara Hershey, Sarah A. Eisenstein
Publikováno v:
Frontiers in Human Neuroscience, Vol 13 (2020)
Human obesity is associated with low-grade chronic systemic inflammation, alterations in brain structure and function, and cognitive impairment. Rodent models of obesity show that high-calorie diets cause brain inflammation (neuroinflammation) in mul
Externí odkaz:
https://doaj.org/article/af9489b989a94c56b361b757fe9fa3ef
Autor:
Olga Neyman, Ahmad M. Samara, Amjad Samara, Ki Yun Park, Bess A. Marshall, Joseph D. Dougherty, Rachel M. Rahn, Tamara Hershey
Publikováno v:
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases, Vol 14, Iss 1, Pp 1-14 (2019)
Orphanet Journal of Rare Diseases, Vol 14, Iss 1, Pp 1-14 (2019)
Wolfram syndrome is a rare multisystem disorder caused by mutations in WFS1 or CISD2 genes leading to brain structural abnormalities and neurological symptoms. These abnormalities appear in early stages of the disease. The pathogenesis of Wolfram syn
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d7c38265ebcffeb9d2518fac57c30ede
https://pubmed.ncbi.nlm.nih.gov/31796109
https://pubmed.ncbi.nlm.nih.gov/31796109
Autor:
Olga Neyman, Tamara Hershey
This chapter focuses on the neurocognitive effects of diabetes mellitus, particularly type 1 and type 2 diabetes. Although many of the side effects of diabetes—such as retinopathy, nephropathy, and peripheral neuropathy—are well known, the conseq
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::86fe935f1487f5d8f8e2c4a089e51646
https://doi.org/10.1093/oxfordhb/9780190664121.013.6
https://doi.org/10.1093/oxfordhb/9780190664121.013.6
Autor:
Olga Neyman, Ling Chen, Tamara Hershey, Heather M. Lugar, Anagha Narayanan, Jonathan M. Koller, Joshua S. Shimony, Sarah A. Eisenstein, Jerrel Rutlin
Publikováno v:
Scientific Reports
Scientific Reports, Vol 9, Iss 1, Pp 1-11 (2019)
Scientific Reports, Vol 9, Iss 1, Pp 1-11 (2019)
Wolfram syndrome is a rare disease caused by mutations in the WFS1 gene leading to symptoms in early to mid-childhood. Brain structural abnormalities are present even in young children, but it is not known when these abnormalities arise. Such informa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::79813b444f38c957fb497418fa39c934
https://doi.org/10.1038/s41598-019-42447-9
https://doi.org/10.1038/s41598-019-42447-9