Zobrazeno 1 - 10
of 72
pro vyhledávání: '"H J, Wolfe"'
Autor:
Amy H. J. Wolfe, MD, MEd, Pamela S. Hinds, PhD, Adre J. du Plessis, MD, Heather Gordish-Dressman, PhD, Robert M. Arnold, MD, Lamia Soghier, MD, MEd
Publikováno v:
Critical Care Explorations, Vol 4, Iss 7, p e0721 (2022)
OBJECTIVES:. This study had three aims: 1) quantify the difference in stress levels between low and high stress roles during simulated critical communication encounters using objective physiologic data (heart rate variability [HRV]) and subjective me
Externí odkaz:
https://doaj.org/article/a044f062b9414e38a3fa9e3704b25137
Publikováno v:
Pediatric Critical Care Medicine. 24:34-40
Discussion of prognosis is an essential component of decision-making family conferences in critical care. We do not know how clinicians convey prognosis to families of critically ill children. We, therefore, aimed to evaluate the frequency of prognos
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f07b699eeff850fe135bce060f2a559a
https://doi.org/10.1097/pcc.0000000000003116
https://doi.org/10.1097/pcc.0000000000003116
We evaluated 71 muscle-invasive transitional cell carcinomas (TCCs) of the bladder by tumor compartments. Kinetic parameters included mitotic figure counting, Ki-67 index, proliferation rate (DNA slide cytometry), and apoptotic index (in situ end lab
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::55b0346515776806e7ba3958fbd82e1e
Aggressive fibromatosis (also called deep fibromatosis or desmoid tumor) is a proliferation of cytologically benign-appearing fibrocytes, often resulting in significant functional loss. The nature of the lesion is controversial: some evidence suggest
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2ec42c82f20b7773283948c4c1037424
Atypical lymphocytic infiltrates that mimic cutaneous lymphoma (ie, pseudolymphoma) are often observed in skin biopsy specimens from patients with altered immune function. The latter may reflect systemic immune dysregulatory states such as collagen v
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::403e13e9db923564e7fef066d2c153c2
C-cell hyperplasias are normally multifocal in multiple endocrine neoplasia type 2A. We compared clonality, microsatellite pattern of tumor suppressor genes, and cellular kinetics of C-cell hyperplasia foci in each thyroid lobe. We selected 11 female
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3445866737dcad0b2966956843e07006
Autor:
Diaz-Cano, Salvador J., H J Wolfe
Conceptually, a clone is a group of genetically identical cells derived from a single common ancestor Most somatic tissues arc polyclonal, unless there is a significant growth advantage within a subset of cells which proliferate at the expense of sur
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::360d8ebf2f6c0eb5e56411b5e2630297
Superficial transitional cell carcinomas (TCC) of the urinary bladder have been shown to be monoclonal. However, no combined study of clonality and tumor suppressor genes (TSG) is available to date for muscle-invasive TCC. Forty-four muscle-invasive
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d6ddb5bd9b1ba86b80b20bac812e15f6
Autor:
Diaz-Cano, Salvador J., H J Wolfe
The paper addresses the topic of the clonal origin of neoplasms that frequently present as multiple lesions, such as Kaposi's sarcoma in patients with human immunodeficiency virus infection. The authors used a statistical analysis that showed the low
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ce152839e86a39b87415350cac490507
Autor:
Klaus Kruse, Qian Huang, Gernot H. G. Sinnecker, Olaf Hiort, H. J. Wolfe, D. W. Yandell, A. Sadeghi-Nejad
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 77:262-266
Recent studies indicate that mutations in the androgen receptor gene are associated with androgen insensitivity syndromes, a heterogeneous group of related disorders involving defective sexual differentiation in karyotypic males. In this report, we a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4f0993d187dda990cef2b456bcab2360
https://doi.org/10.1210/jcem.77.1.8325950
https://doi.org/10.1210/jcem.77.1.8325950