Zobrazeno 1 - 10
of 31
pro vyhledávání: '"Bridget Sinnott"'
Autor:
Bridget Sinnott, Cara Ray, Frances Weaver, Beverly Gonzalez, Elizabeth Chu, Sarah Premji, Mattie Raiford, Rachel Elam, Scott Miskevics, Stephen Parada, Laura Carbone
Publikováno v:
JBMR Plus, Vol 6, Iss 3, Pp n/a-n/a (2022)
ABSTRACT We used Veterans Health Administration (VHA) national administrative data files to identify a cohort (fiscal years 2005–2014) of veterans with spinal cord injuries and disorders (SCID) to determine risk factors for and consequences of lowe
Externí odkaz:
https://doaj.org/article/697a5ceaaef74b30bd980cd6da366cbf
Autor:
Anvay Shah, MBBS, Bridget Sinnott, MD
Publikováno v:
AACE Clinical Case Reports, Vol 8, Iss 4, Pp 181-182 (2022)
Externí odkaz:
https://doaj.org/article/154472b56faa4836990059f642f1f40b
Autor:
Seth Kay, MD, Mara Piltin, DO, Vicoria Loseva, MD, Bridget Sinnott, MD, J.Robert Brennan, MD, Swati Mehrotra, MD, David Terris, MD, FACE, FACS
Publikováno v:
AACE Clinical Case Reports, Vol 4, Iss 5, Pp e362-e366 (2018)
ABSTRACT: Objective: Describe the presentation, work-up, and management of a rare co-occurrence of familial hypocalciuric hypercalcemia (FHH) and primary hyperparathyroidism (PHPT) in a single patient. Additionally, to explore the challenges in diagn
Externí odkaz:
https://doaj.org/article/cccb9089d8f440ebb6f5aa6540b131fc
Autor:
Brian Le, Beverly Gonzalez, Frances Weaver, Bridget Sinnott, Cara Ray, Elizabeth Chu, Sara Premji, Mattie Raiford, Omkar Mayur, Laura Carbone
Publikováno v:
The Journal of Spinal Cord Medicine. :1-7
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bcff3b7767b4fb5e1c457cdc9b6389a4
https://doi.org/10.1080/10790268.2023.2188391
https://doi.org/10.1080/10790268.2023.2188391
Autor:
Anvay Shah, Bridget Sinnott
Publikováno v:
Journal of the Endocrine Society. 6:A219-A220
Introduction Diamond Blackfan anemia (DBA) is a form of pure red cell aplasia characterized by erythroid hypoplasia, congenital deformities, and increased risk of malignancy. It is typically diagnosed in first year of life. Treatments include chronic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2e288bf1304e8c1ae5b5bed4dbbc1922
https://doi.org/10.1210/jendso/bvac150.451
https://doi.org/10.1210/jendso/bvac150.451
Autor:
David Cromer, Bridget Sinnott
Publikováno v:
Journal of the Endocrine Society. 6:A211-A212
Background Autoimmune polyglandular syndrome type 1 (APS-1) is a rare disorder, with an estimated worldwide prevalence of 1 in 80-100,000, resulting from a mutation in the autoimmune regulator (AIRE) gene responsible for immune tolerance. It is chara
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3ead01ab46b0d62ae4dcf2b626db98cc
https://doi.org/10.1210/jendso/bvac150.434
https://doi.org/10.1210/jendso/bvac150.434
Publikováno v:
Journal of the Endocrine Society
We describe a case of a biochemically silent pheochromocytoma, which raises the question about the appropriate pre-operative approach in cases of biochemically “silent” adrenal tumors. A 37-year-old white female was referred to our endocrinology
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cbd6a30aded34bdecce91ffe345feb1c
https://doi.org/10.1210/js.2019-mon-396
https://doi.org/10.1210/js.2019-mon-396
Autor:
Vicoria Loseva, Swati Mehrotra, David J. Terris, Seth Kay, Bridget Sinnott, Mara A. Piltin, J.Robert Brennan
Publikováno v:
AACE Clinical Case Reports, Vol 4, Iss 5, Pp e362-e366 (2018)
Objective: Describe the presentation, work-up, and management of a rare co-occurrence of familial hypocalciuric hypercalcemia (FHH) and primary hyperparathyroidism (PHPT) in a single patient. Additionally, to explore the challenges in diagnosing in s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e92bcf7ad6815715941f6b352a2328d9
http://www.sciencedirect.com/science/article/pii/S2376060520301553
http://www.sciencedirect.com/science/article/pii/S2376060520301553
Autor:
Maya Patel, Bridget Sinnott
Publikováno v:
BMJ Case Rep
This is a case of a 20-year-old woman who presented with a left jaw mass which was resected and found to be a giant cell granuloma of the mandible. Her history and physical examination were suggestive for Noonan syndrome which was confirmed with gene
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::78c0218e457ce35bc9855919ffaec715
https://pubmed.ncbi.nlm.nih.gov/29848529
https://pubmed.ncbi.nlm.nih.gov/29848529
Publikováno v:
Oxford Medicine
Conditions associated with nephrocalcinosis and nephrolithiasis are described. Some (cystinuria, urate) have specific therapies, and there are some general measure, particular for calcium-containing stones (urine volume, dietary salt, urinary citrate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::07519ba6b770279397da15a60a4eece4
https://doi.org/10.1093/med/9780199592548.003.0205_update_001
https://doi.org/10.1093/med/9780199592548.003.0205_update_001
