Zobrazeno 1 - 7
of 7
pro vyhledávání: '"A Salovin"'
Autor:
Rosenberg, Miriam I., Greenstein, Erez, Buchkovich, Martin, Peres, Ayelet, Santoni-Rugiu, Eric, Yang, Lei, Mikl, Martin, Vaksman, Zalman, Gibbs, David L., Reshef, Dan, Salovin, Amy, Irwin, Meredith S., Naranjo, Arlene, Ulitsky, Igor, de Alarcon, Pedro A., Matthay, Katherine K., Weigman, Victor, Yaari, Gur, Panzer, Jessica A., Friedman, Nir, Maris, John M.
Publikováno v:
In Cell Reports 29 August 2023 42(8)
Autor:
Miriam I. Rosenberg, Erez Greenstein, Martin Buchkovich, Ayelet Peres, Eric Santoni-Rugiu, Lei Yang, Martin Mikl, Zalman Vaksman, David L. Gibbs, Dan Reshef, Amy Salovin, Meredith S. Irwin, Arlene Naranjo, Igor Ulitsky, Pedro A. de Alarcon, Katherine K. Matthay, Victor Weigman, Gur Yaari, Jessica A. Panzer, Nir Friedman, John M. Maris
Publikováno v:
Cell Reports, Vol 42, Iss 8, Pp 112879- (2023)
Summary: Neuroblastoma is a lethal childhood solid tumor of developing peripheral nerves. Two percent of children with neuroblastoma develop opsoclonus myoclonus ataxia syndrome (OMAS), a paraneoplastic disease characterized by cerebellar and brainst
Externí odkaz:
https://doaj.org/article/506516905d124cd99326d2bc5f05f4f1
Autor:
MI Rosenberg, E Greenstein, M Buchkovich, M Mikl, A Peres, E Santoni-Rugiu, D Reshef, A Salovin, DL Gibbs, MS Irwin, A Naranjo, I Ulitsky, PA de Alarcon, V Weigman, G Yaari, JA Panzer, N Friedman, JM Maris
SummaryNeuroblastoma is a lethal childhood solid tumor of developing peripheral nerves. Two percent of children with neuroblastoma develop Opsoclonus Myoclonus Ataxia Syndrome (OMAS), a paraneoplastic disease characterized by cerebellar and brainstem
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c14aa2a979a20ce12a67a3c7a8280b8f
https://doi.org/10.1101/2021.12.14.471886
https://doi.org/10.1101/2021.12.14.471886
Autor:
Elisia M. Clark, Yi Na Dong, Elizabeth Mercado-Ayon, Mattieu Zhai, Emily E. McMillan, Nathan Warren, Joseph T. Johnson, Hong Lin, David A. Lynch, Amy Salovin
Publikováno v:
Neuronal Signaling
Friedreich ataxia (FRDA) is a progressive neurodegenerative disease with developmental features caused by a genetic deficiency of frataxin, a small, nuclear-encoded mitochondrial protein. Frataxin deficiency leads to impairment of iron–sulphur clus
Publikováno v:
NEUROLOGY-NEUROIMMUNOLOGY & NEUROINFLAMMATION
r-FSJD: Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
instname
r-FSJD. Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
r-FSJD: Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
instname
r-FSJD. Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
OBJECTIVE: To determine whether there is an association between nonencephalitic herpes simplex virus 1 (HSV-1) infection and anti-NMDA receptor encephalitis (anti-NMDARE). METHODS: Antibody testing was performed using samples from 2 cohorts in a case
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::6a0248201842dd0e0a8457ca1178d940
http://fundanet.fsjd.org/Publicaciones/ProdCientif/PublicacionFrw.aspx?id=14164
http://fundanet.fsjd.org/Publicaciones/ProdCientif/PublicacionFrw.aspx?id=14164
Publikováno v:
Neurology® Neuroimmunology & Neuroinflammation
ObjectiveTo determine whether there is an association between nonencephalitic herpes simplex virus 1 (HSV-1) infection and anti-NMDA receptor encephalitis (anti-NMDARE).MethodsAntibody testing was performed using samples from 2 cohorts in a case-cont
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