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Elsevier电子期刊(53)

在“Elsevier电子期刊”中，命中：53条，耗时：0.041945 秒

在所有数据库中总计命中：96条

1.The Longitudinal Study of Liver Cysts in Patients With Autosomal Dominant Polycystic Kidney Disease and Polycystic Liver Disease

作者：Ryo Matsuura¹ ; Kenjiro Honda¹ ; ^{khonda-tky@umin.ac.jp} ; Yoshifumi Hamasaki² ; Kent Doi³ ; Eisei Noiri¹ ; Masaomi Nangaku¹ ; ²

关键词：autosomal dominant polycystic kidney disease ; polycystic liver disease

刊名：Kidney International Reports

出版年：2017

2.Gastrointestinal Manifestations of Autosomal-Dominant Polycystic Kidney Disease

作者：Adam E. Mikolajczyk^&lowast ; ; ^{aemikolaj@gmail.com} ; Helen S. Te^&lowast ; ; Arlene B. Chapman^&Dagger ;

关键词：ADPKD ; Cysts ; Diverticulosis ; Hernia

刊名：Clinical Gastroenterology and Hepatology

出版年：2017

3.Outcomes and Durability of Hepatic Reduction after Combined Partial Hepatectomy and Cyst Fenestration for Massive Polycystic Liver Disease

作者：Fouad T. Chebib ; MD^a ; Amber Harmon^a ; Maria V. Irazabal Mira ; MD^a ; Yeon Soon Jung ; MD ; PhD^a ; Marie E. Edwards^a ; Marie C. Hogan ; MBChB ; MD ; PhD^a ; Patrick S. Kamath ; MD^b ; Vicente E. Torres ; MD ; PhD^a ; David M. Nagorney ; MD ; FACS^c ; ^{nagorney.david@mayo.edu" class="auth_mail" title="E-mail the corresponding author}

关键词：ADPKD ; autosomal dominant polycystic kidney disease ; IQR ; interquartile range ; LV ; liver volume ; LV1 ; preoperative liver volume ; LV2 ; postoperative liver volume ; LV3 ; liver volume at follow-up ; MELD ; Model for End-Stage Liver Disease ; PHCF ; partial hepatectomy and cyst fenestration ; PLD ; polycystic liver disease

刊名：Journal of the American College of Surgeons

出版年：2016

4.Ursodeoxycholic acid in advanced polycystic liver disease: A phase 2 multicenter randomized controlled trial

作者：Hedwig M.A. D&rsquo ; Agnolo¹ ; Wietske Kievit² ; R. Bart Takkenberg³ ; Ioana Riañ ; o⁴ ; Luis Bujanda⁴ ; Myrte K. Neijenhuis¹ ; Ellen J.L. Brunenberg⁵ ; Ulrich Beuers³ ; Jesus M. Banales⁴ ; Joost P.H. Drenth¹ ; ^{joostphdrenth@cs.com" class="auth_mail" title="E-mail the corresponding author}

关键词：ADPKD ; autosomal dominant polycystic kidney disease ; ADPLD ; autosomal dominant polycystic liver disease ; AP ; alkaline phosphatase ; ALT ; alanine aminotransaminase ; AST ; aspartate aminotransaminase ; Ca2+i ; intracellular calcium ; cAMP ; cyclic adenosine monophosphate ; CT ; computed tomography ; EORTC ; European organization for research and treatment for cancer quality of life questionnaire ; ECOG ; Eastern cooperative oncology group &ndash ; performance status ; GGT ; gamma-glutamyltransferase ; HRQL ; healt

刊名：Journal of Hepatology

出版年：2016

5.Fatal liver cyst rupture in polycystic liver disease complicated with autosomal dominant polycystic kidney disease: A case report

作者：Fang Tong^a ; ^{fytongfang@gmail.com" class="auth_mail" title="E-mail the corresponding author} ; Yue Liang^a ; ^{yueyueashin@gmail.com" class="auth_mail" title="E-mail the corresponding author} ; Lin Zhang^a ; ^{lyre2008@126.com" class="auth_mail" title="E-mail the corresponding author} ; Wenhe Li^a ; ^{18707165089@163.com" class="auth_mail" title="E-mail the corresponding author} ; Peng Chen^b ; ^{276538406@qq.com" class="auth_mail" title="E-mail the corresponding author} ; Yijie Duan^a ; ^{gerichtsarzt@hotmail.com" class="auth_mail" title="E-mail the corresponding author} ; Yiwu Zhou^a ; ^{zhouyiwu@outlook.com" class="auth_mail" title="E-mail the corresponding author}

关键词：Forensic pathology ; Autosomal dominant polycystic kidney disease ; Polycystic liver disease ; Genetic analysis

刊名：Forensic Science International

出版年：2016

6.Mutations in DCDC2 (doublecortin domain containing protein 2) in neonatal sclerosing cholangitis

作者：Tassos Grammatikopoulos¹ ; ² ; ^{t.grammatikopoulos@nhs.net" class="auth_mail" title="E-mail the corresponding author} ; Melissa Sambrotta² ; Sandra Strautnieks³ ; Pierre Foskett³ ; A.S. Knisely³ ; ^&dagger ; ; Bart Wagner⁴ ; Maesha Deheragoda³ ; Chris Starling³ ; Giorgina Mieli-Vergani¹ ; ² ; Joshua Smith⁵ ; University of Washington Center for Mendelian Genomics⁵

关键词：ADPKD ; autosomal dominant polycystic kidney disease ; ARPKD ; autosomal recessive polycystic kidney disease ; ACALT ; acetylated alpha-tubulin ; BA ; biliary atresia ; Ca2+ ; calcium ; CHF ; congenital hepatic fibrosis ; DCDC2 ; doublecortin domain containing protein 2 ; DCX ; doublecortin gene family ; ERCP ; endoscopic retrograde cholangiopancreatography ; ERK ; extracellular signal-regulated kinase ; GGT ; γ-glutamyltransferase ; IFT ; intraflagellary transport system ; KCH ; King&rsquo ; s College Hospital ; LT ; liver

刊名：Journal of Hepatology

出版年：2016

7.MicroRNAs in cholangiopathies: Potential diagnostic and therapeutic tools

作者：Aitor Esparza-Baquer^a ; ¹ ; Ibone Labiano^a ; ¹ ; Luis Bujanda^a ; ^b ; Marí ; a J. Perugorria^a ; ^b ; ^c ; Jesú ; s M. Banales^a ; ^b ; ^c ; ^{jesus.banales@biodonostia.org" class="auth_mail" title="E-mail the corresponding author}

关键词：ADPKD ; autosomal dominant polycystic kidney disease ; ADPLD ; autosomal dominant polycystic liver disease ; AE2 ; Na+-independent Cl&minus ; /HCO3&minus ; exchanger 2 ; Akt ; protein kinase B ; ALP ; alkaline phosphatase ; AMAs ; anti-mitochondrial antibodies ; ANAs ; anti-nuclear antibodies ; ARPKD ; autosomal recessive polycystic kidney disease ; BA ; biliary atresia ; CA19-9 ; carbohydrate antigen 19-9 ; CCA ; cholangiocarcinoma ; Cdc25A ; cell division cycle 25 homolog A ; CEA ; carcinoembryonic antigen ; c-Myc ; Myc pr

刊名：Clinics and Research in Hepatology and Gastroenterology

出版年：2016

8.Stroke after cyst fenestration in a patient with autosomal dominant polycystic kidney disease and polycystic liver disease: Not necessarily aneurysm-related

作者：Chia-Ter Chao^a ; ^b ; John Huang^c ; Tze-Wah Kao^b ; ^{twkao2@ntuh.gov.tw" class="auth_mail" title="E-mail the corresponding author}

刊名：Journal of the Formosan Medical Association

出版年：2016

9.Daughter and mother with orofaciodigital syndrome type 1 and glomerulocystic kidney disease

作者：Takashi Iijima ; MD^a ; Junichi Hoshino ; MD ; MPH^a ; ^{hoshino@toranomon.gr.jp" class="auth_mail" title="E-mail the corresponding author} ; Koki Mise ; MD^a ; Keiichi Sumida ; MD^a ; Tatsuya Suwabe ; MD ; PhD^a ; Noriko Hayami ; MD^a ; Toshiharu Ueno ; MD ; PhD^a ; Kenmei Takaichi ; MD ; PhD^a ; ^b ; Takeshi Fujii ; MD ; PhD^c ; Kenichi Ohashi ; MD ; PhD^c ; ^e ; Naoya Morisada ; MD ; PhD^d ; Kazumoto Iijima ; MD ; PhD^d ; Yoshifumi Ubara ; MD ; PhD^a ; ^b

关键词：Orofaciodigital syndrome type 1 ; Glomerulocystic kidney disease ; X-linked dominant inheritance ; Polycystic kidney disease ; Canine defect ; Brachydactyly

刊名：Human Pathology

出版年：2016

10.Pheochromocytoma as a rare cause of arterial hypertension in a patient with autosomal dominant polycystic kidney disease: A diagnostic and therapeutic dilemma

作者：Amelia J. Hessheimer ; ^{ajhesshe@clinic.ub.es" class="auth_mail" title="E-mail the corresponding author} ; Oscar Vidal ; Mauro Valentini ; Juan Carlos Garcí ; a-Valdecasas

关键词：ACTH ; adrenocorticotropic hormone ; ADPKD ; autosomal dominant polycystic kidney disease ; PCC ; pheochromocytoma ; VHL ; von Hippel Lindau

刊名：International Journal of Surgery Case Reports

出版年：2015

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