Výsledky vyhledávání - "Miki Nishitani"

Interprofessional Team-based Care of the Hematopoietic Cell Transplantation Patient With Hepatic Veno-occlusive Disease/Sinusoidal Obstruction Syndrome

Autor: Kristin L. Mangada, Jerelyn Moffet, Miki Nishitani, Stacey Albuquerque, Christine N. Duncan

Publikováno v: Journal of Pediatric Hematology/Oncology. 45:12-17

Hepatic veno-occlusive disease/sinusoidal obstruction syndrome (VOD/SOS) is a well-recognized complication of allogeneic and autologous hematopoietic cell transplantation (HCT). The diagnosis and treatment of VOD/SOS require the involvement of multip

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ef1090623512bd18360df1cc279e7f22
https://doi.org/10.1097/mph.0000000000002594

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Perceptions of the Stressful Job Search for Pediatric Hematology/Oncology Fellows

Autor: Miki Nishitani, Scott Moerdler, Jennifer Kesselheim

The PHO workforce landscape has been evolving over the past decades, with concern for waning interest in the subspecialty. In this study, we aimed to evaluate perceptions of the PHO workforce (both fellows and faculty), the experience of seeking an i

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6938209ee8f75d54fbf32216e7e8cde8
https://doi.org/10.22541/au.166184826.67626995/v1

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Hyperferritinemia: A Diagnostic Marker for Disseminated Neonatal Herpes Simplex Virus Infection?

Autor: Lily Tran, Joseph R. Hageman, Julia C. Rosebush, Grace Chong, Muayad Alali, Miki Nishitani, Reem Nubani, Aliya N Husain

Publikováno v: Pediatric Annals. 50

Although the prognosis of neonatal herpes simplex virus (HSV) infection has improved with intravenous acyclovir, the morbidity and mortality of disseminated disease remains high. Transaminitis and thrombocytopenia have been reported to be sensitive m

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2b715e10edbdaa35b0a4ee35e5327998
https://doi.org/10.3928/19382359-20210513-01

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37. NEEDS ASSESSMENT OF BOARD PREPARATION CURRICULA AND CERTIFICATION RATES AMONG U.S. PEDIATRIC RESIDENCY PROGRAMS

Autor: Miki Nishitani, Nicola M. Orlov

Publikováno v: Academic Pediatrics. 19:e18

Background The Accreditation Council for Graduate Medical Education (ACGME) requires pediatric residency programs to achieve an overall 70% pass rate on the American Board of Pediatrics Certification Exam. There is high variability in board preparati

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::42c742da2aa24c639029ad3add966cd2
https://doi.org/10.1016/j.acap.2019.05.051

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Clinical Characteristics of a Cohort of 244 Patients with Congenital Adrenal Hyperplasia

Autor: Miki Nishitani, Mimi S. Kim, Deborah P. Merke, Gabriela P. Finkielstain, James C. Reynolds, Ninet Sinaii, Reem M. Hanna, Carol Van Ryzin, Suvimol Hill

Publikováno v: The Journal of Clinical Endocrinology & Metabolism. 97:4429-4438

Patients with congenital adrenal hyperplasia (CAH) often suffer from long-term complications secondary to chronic glucocorticoid therapy and suboptimal treatment regimens.The aim of the study was to describe clinical characteristics of a large cohort

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c24685f6fc4780aa99199e21a08e090a
https://doi.org/10.1210/jc.2012-2102

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Extracellular histone induces plasma hyaluronan-binding protein (factor VII activating protease) activation in vivo

Autor: Tadashi Kikuchi, Miki Nishitani, Keiji Hasumi, Shingo Yamamichi, Yasuhiko Matsushita, Yukari Fujiwara

Publikováno v: Biochemical and Biophysical Research Communications. 409:483-488

Plasma hyaluronan-binding protein (PHBP), an activator of factor VII and prourokinase, is a serine protease circulating as a single-chain proenzyme (pro-PHBP). Pro-PHBP converts to the active two-chain form through autoproteolysis, and effectors that

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::babfcf59b0b4257bc2f06334833adde5
https://doi.org/10.1016/j.bbrc.2011.05.030

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Tenascin-X Haploinsufficiency Associated with Ehlers-Danlos Syndrome in Patients with Congenital Adrenal Hyperplasia

Autor: Ana T. Acevedo, Vandana Sachdev, Sujata M Shanbhag, Deborah P. Merke, Nazli B. McDonnell, Andrew E. Arai, Zhi Xu, Wuyan Chen, Carol Van Ryzin, Miki Nishitani, Rachel Morissette, Hwaida Hannoush

The gene for congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency, CYP21A2, is flanked by the gene encoding tenascin-X (TNXB), a connective tissue extracellular matrix protein that has been linked to both autosomal dominant and autos

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aa79fea5eb9df2d65b892c9d7cdde2e5
https://europepmc.org/articles/PMC3565116/

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