Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Satabdi Chakrabarti"'
Publikováno v:
Case Reports in Neurology, Vol 11, Iss 3, Pp 290-294 (2019)
Hypertrophic pachymeningitis (HP) is characterized by inflammation of the dura mater. It has been described in the setting of numerous systemic inflammatory diseases including immunoglobulin G4 (IgG4)-related disease as well as granulomatosis with po
Externí odkaz:
https://doaj.org/article/5f3254370a4e4e7192307081cd7b58db
Publikováno v:
Sunday, April 23.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5b20b0c4bf315ac0447437ab5c9da833
https://doi.org/10.1212/wnl.0000000000202463
https://doi.org/10.1212/wnl.0000000000202463
Akademický článek
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Publikováno v:
Case Reports in Neurology, Vol 11, Iss 3, Pp 290-294 (2019)
Case Reports in Neurology
Case Reports in Neurology
Hypertrophic pachymeningitis (HP) is characterized by inflammation of the dura mater. It has been described in the setting of numerous systemic inflammatory diseases including immunoglobulin G4 (IgG4)-related disease as well as granulomatosis with po
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::874764f5411e3b220ede12ed96aeb1c3
https://doi.org/10.1159/000502569
https://doi.org/10.1159/000502569
Autor:
Kelly J. Baldwin, Carolina Vivar, Anthony Noto, Satabdi Chakrabarti, Lisa Beckett, Christopher L Cummings
Publikováno v:
Stroke. 50
Neurohospitalist programs have been hypothesized to improve the cost and quality of care. Since data supporting the cost-effectiveness of neurohospitalist programs is lacking, this study aims to compare the LOS of patients discharged with a diagnosis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5993c0af5750d0698546ded0a7898456
https://doi.org/10.1161/str.50.suppl_1.wp410
https://doi.org/10.1161/str.50.suppl_1.wp410
Autor:
Akiko Shimamura, Joan Moore, Peter E. Newburger, Stella M. Davies, Satabdi Chakrabarti, Blanche P. Alter, Audrey Anna Bolyard, David C. Dale, Theresa Cole, Jordan M. Bond, Richard E. Harris, Laurence A. Boxer
Publikováno v:
Blood. 118:4367-4367
Abstract 4367 Shwachman-Diamond syndrome (SDS) is an autosomal recessively inherited disorder defined clinically by marrow failure and exocrine pancreatic dysfunction. Previous research estimates that 90% of patients harbor biallelic mutations in the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6989f2811dea8df7d73d501dece1c6a1
https://doi.org/10.1182/blood.v118.21.4367.4367
https://doi.org/10.1182/blood.v118.21.4367.4367