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5篇 您的检索式：作者名="Clancy AD"

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		题名	作者	年代	出处	被引量
	1	Transdifferentiation of cardiac fibroblasts, a fetal factor in anti-SSA/Ro-SSB/La antibody-mediated congenital heart block显示文摘	Clancy RM Askanase AD Kapur RP Chiopelas E Azar N Miranda-Carus ME	2002	J Immunol2002，169，4：	1
	2	Incident vertebral fractures during an 18 month observation period following discontinuation of LY333334 use in postmenopausal women with osteoporosis显示文摘	Lindsay R Scheele WH Clancy AD	2001	Journal of Bone Mineral Research2001，16，1：	1
	3	Anti-SSA/ Ro and anti-SSB/La autoantibodms bind the surface of apoptot- ic fetal cardiocytes ancpromote secretion of TNF-alpha by mac- rophages 显示文摘	Miranda-Cams ME Askanase AD Clancy RM	2000	J Immunol2000，165，：	1
	4	Immunohistologic evidence supports apoptosis, IgG deposition, and novel macrophage/fibroblast crosstalk in the pathologic cascade leading to congenital heart block 显示文摘	Clancy RM Kapur RP Molad Y Askanase AD Buyon JP	2004	Arthritis Rheum2004，50，：	1
	5	Identification of patients with pancreatic adenocarcinoma due to inheritable mutation:Challenges of daily clinical practice显示文摘BACKGROUND Identification of germ-line mutations in pancreatic ductal adenocarcinoma(PDAC) could impact on patient/family.AIM To assess the referral pathways for genetic consultations in PDAC.METHODS Electronic records of PDAC patients were reviewed retrospectively. Patients eligible for genetic consultation referral were identified following the European Registry of Hereditary Pancreatitis and Familial Pancreatic Cancer(EUROPAC)criteria.RESULTS Four-hundred patients were eligible. Of 113 patients(28.3%) meeting EUROPAC criteria, 8.8% were referred for genetic opinion. Germ-line mutations were identified in 0.75% of the whole population.CONCLUSIONEarlier referrals and increased awareness may be able to overcome the low rate of successful genetic appointments.	Alexander JP Fulton Angela Lamarca Christina Nuttall Lynne McCallum Rille Pihlak Derek O'Reilly Fiona Lalloo Mairéad G McNamara Richard A Hubner Tara Clancy Juan W Valle	2019	World Journal of Gastrointestinal Oncology2019，11，2：	0

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