Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Ashley E Rawls"'
Autor:
Svitlana Garbuzova-Davis, Michael K Louis, Edward M Haller, Hiranya M Derasari, Ashley E Rawls, Paul R Sanberg
Publikováno v:
PLoS ONE, Vol 6, Iss 3, p e16601 (2011)
BACKGROUND: Sanfilippo syndrome type B (MPS III B) is caused by a deficiency of α-N-acetylglucosaminidase enzyme, leading to accumulation of heparan sulfate within lysosomes and eventual progressive cerebral and systemic multiple organ abnormalities
Externí odkaz:
https://doaj.org/article/b8e2ad51f3854081aeb2432485035a77
Autor:
Ashley E. Rawls
Publikováno v:
CONTINUUM: Lifelong Learning in Neurology. 28:1301-1313
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::402fe43206e10b38b9ffd378ff068c9c
https://doi.org/10.1212/con.0000000000001160
https://doi.org/10.1212/con.0000000000001160
Autor:
Hiranya M. Derasari, Nicole Kuzmin-Nichols, Olga Zayko, Paul R. Sanberg, Ron F Mervis, Chris R James, Ashley E. Rawls, Svitlana Garbuzova-Davis, Cyndy D. Sanberg, Alison E. Willing
Publikováno v:
Cell Transplantation, Vol 23 (2014)
Sanfilippo syndrome type III B (MPS III B) is an inherited disorder characterized by a deficiency of α- N-acetylglucosaminidase (Naglu) enzyme leading to accumulation of heparan sulfate in lysosomes and severe neurological deficits. We have previous
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::084509aedab4920faa587784228bdbf6
https://doaj.org/article/3a1dbfc86def4d23b29dd76e7210db45
https://doaj.org/article/3a1dbfc86def4d23b29dd76e7210db45
Autor:
Svitlana Garbuzova-Davis, Hiranya M. Derasari, Edward M Haller, Michael K. Louis, Ashley E. Rawls, Paul R. Sanberg
Publikováno v:
PLoS ONE
PLoS ONE, Vol 6, Iss 3, p e16601 (2011)
PLoS ONE, Vol 6, Iss 3, p e16601 (2011)
BACKGROUND: Sanfilippo syndrome type B (MPS III B) is caused by a deficiency of α-N-acetylglucosaminidase enzyme, leading to accumulation of heparan sulfate within lysosomes and eventual progressive cerebral and systemic multiple organ abnormalities
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a2c098416ff141723e14df3686c51a52
https://pubmed.ncbi.nlm.nih.gov/21408219
https://pubmed.ncbi.nlm.nih.gov/21408219
Autor:
Alison E. Willing Ph.D., Svitlana N. Garbuzova-Davis, Olga Zayko, Hiranya M. Derasari, Ashley E. Rawls, Chris R. James, Ron F. Mervis, Cyndy D. Sanberg, Nicole Kuzmin-Nichols, Paul R. Sanberg
Publikováno v:
Cell Transplantation, Vol 23 (2014)
Sanfilippo syndrome type III B (MPS III B) is an inherited disorder characterized by a deficiency of α- N -acetylglucosaminidase (Naglu) enzyme leading to accumulation of heparan sulfate in lysosomes and severe neurological deficits. We have previou
Externí odkaz:
https://doaj.org/article/3a1dbfc86def4d23b29dd76e7210db45