Zobrazeno 1 - 10
of 37
pro vyhledávání: '"Samuel B Reynolds"'
Autor:
Rahul Mhaskar, Bryan Kane, Jordan Davies, Angela Davis, Maria Karagias, Matthew Molnar, Robert Postlethwaite, Brittany Quinn, Samuel B. Reynolds, Monica Stewart, Nicholas Werbeckes, Robert Barraco
BACKGROUND The information-seeking behavior of physicians to cater to the patient's information needs is not comprehensively studied. OBJECTIVE Our cross-sectional study's key goals were to understand providers' information-seeking behavior regarding
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::22656c17fac9019a373bfc1696acddef
https://doi.org/10.2196/preprints.48180
https://doi.org/10.2196/preprints.48180
Autor:
Samuel B. Reynolds, Kristen Pettit
Publikováno v:
Hematology Am Soc Hematol Educ Program
Myelofibrosis (MF) is a clonal hematopoietic stem cell neoplasm characterized by constitutional symptoms, splenomegaly, and risks of marrow failure or leukemic transformation and is universally driven by Jak/STAT pathway activation. Despite sharing t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f494baf7cf3ee72ebc3e8424fb2442e5
https://pubmed.ncbi.nlm.nih.gov/36485113
https://pubmed.ncbi.nlm.nih.gov/36485113
Publikováno v:
Cancer Research. 83:4537-4537
Erdheim Chester Disease (ECD) is a rare, non-Langerhans cell histiocytic disease, characterized as a neoplastic disorder in 2016. MAP Kinase and PI3-AKT pathway somatic mutations and/or fusion genes have been shown to play a significant role in disea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::786bb93173a8291e2f6cae563b4f5280
https://doi.org/10.1158/1538-7445.am2023-4537
https://doi.org/10.1158/1538-7445.am2023-4537
Publikováno v:
Cancer Research. 83:4536-4536
Introduction: Rosai Dorfman Disease (RDD) is a non-Langerhans cell histiocytic disease whose pathologic features include sinus histiocytosis with variable emperipolesis. Traditional management consists of local therapies (resection, radiation) for li
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8fff99a442b6e51628b1d000ddf9a6df
https://doi.org/10.1158/1538-7445.am2023-4536
https://doi.org/10.1158/1538-7445.am2023-4536
Publikováno v:
Journal of Onco-Nephrology. 5:178-182
Hereditary leiomyomatosis is a genetic disorder that follows an autosomal dominant pattern of inheritance. Along with a variety of leiomyomas, affected individuals are predisposed to developing an aggressive form of type 2 papillary renal malignancy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cb70eb0e1404da3b204fd8fb0d5b1ec5
https://doi.org/10.1177/23993693211041370
https://doi.org/10.1177/23993693211041370
Publikováno v:
Cureus.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d03cd42d08f65dc13ff62cdee2890038
https://doi.org/10.7759/cureus.22816
https://doi.org/10.7759/cureus.22816
Publikováno v:
Annals of Clinical Psychiatry. 33:53-55
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1625468236061c2bb15a2635c979b97b
https://doi.org/10.12788/acp.0017
https://doi.org/10.12788/acp.0017
Publikováno v:
Cureus
Ignatzschineria is a recently identified genus of bacteria that has been isolated from the digestive tract of multiple flies associated with decomposing tissue. Species within this genus are rarely implicated in human disease, and less than 10 cases
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9757460ee4e1c17575d165367fe84e71
http://europepmc.org/articles/PMC8126268
http://europepmc.org/articles/PMC8126268
Publikováno v:
Cureus
The acute complications of multiple myeloma can be varied and devastating, including electrolyte derangements, renal failure, and infections amongst others. The varying pathological mechanisms behind these complications make the management of patient
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8bd014c8babb389a4534047566b2ff99
https://doi.org/10.7759/cureus.10463
https://doi.org/10.7759/cureus.10463