標題: Titlebook: Diseases of the Liver and Biliary Tree; Annarosa Floreani Book 2021 Springer Nature Switzerland AG 2021 Cholangiopathies.Autoimmune cholan [打印本頁] 作者: Falter 時間: 2025-3-21 19:26
書目名稱Diseases of the Liver and Biliary Tree影響因子(影響力)
書目名稱Diseases of the Liver and Biliary Tree影響因子(影響力)學科排名
書目名稱Diseases of the Liver and Biliary Tree網(wǎng)絡公開度
書目名稱Diseases of the Liver and Biliary Tree網(wǎng)絡公開度學科排名
書目名稱Diseases of the Liver and Biliary Tree被引頻次
書目名稱Diseases of the Liver and Biliary Tree被引頻次學科排名
書目名稱Diseases of the Liver and Biliary Tree年度引用
書目名稱Diseases of the Liver and Biliary Tree年度引用學科排名
書目名稱Diseases of the Liver and Biliary Tree讀者反饋
書目名稱Diseases of the Liver and Biliary Tree讀者反饋學科排名
作者: Interferons 時間: 2025-3-21 23:29
Congenital Cystic Lesions of the Biliary Treeryogenesis of the primordial ductal plate caused by a genetically determined dysfunction of morphogenetic proteins expressed in the primary cilia of cholangiocytes (“ciliopathies”). Among this group, it is important to notice three different clusters of disease: polycystic liver diseases (PLDs), fib作者: 虛情假意 時間: 2025-3-22 04:10 作者: Charlatan 時間: 2025-3-22 05:26 作者: 單色 時間: 2025-3-22 11:21 作者: 拋媚眼 時間: 2025-3-22 15:05
Liver Disease in Cystic Fibrosishich encodes for the CFTR protein, a chloride channel located at the apical membrane of epithelial cells. CF is a multiorgan disease affecting mostly the lungs, the pancreas, liver, intestine and sweat glands. With advances in medical care, a remarkable increase in survival has occurred, from 16?yea作者: 拋媚眼 時間: 2025-3-22 18:30 作者: FLIRT 時間: 2025-3-22 22:02 作者: 眨眼 時間: 2025-3-23 05:00 作者: 慢跑鞋 時間: 2025-3-23 05:58 作者: 灰姑娘 時間: 2025-3-23 10:35
Overlap Syndromesforms of PBC, PSC, and AIH, which are characterized by the presence of features of two diseases, typically PBC and AIH or PSC and AIH in the same patient. The diagnosis of OS is based on the presence or sequential development of biochemical, serological, histologic, and cholangiographic features of 作者: 粘連 時間: 2025-3-23 13:53 作者: 圣人 時間: 2025-3-23 21:09
Drug-Induced Cholangiopathiesctive metabolites. Liver toxicity is a challenging issue and a frequent cause of failure during drug development. In particular, drug-induced bile duct injury is a side effect of several drugs and dietary supplements, that can be either easy to manage and characterized by a good outcome, or mostly u作者: champaign 時間: 2025-3-24 02:12
Cholangiocarcinoma biliary tree. Histologically, they usually are adenocarcinomas. It is a rare cancer accounting about 3% of all gastrointestinal malignancies. Based on its anatomical location, CCA is classified as intrahepatic (iCCA), perihilar (pCCA), and distal (dCCA). Currently, the three types of CCA are consid作者: linear 時間: 2025-3-24 04:18
Annarosa FloreaniBroadens our understanding of scientific advances in the field of biliary diseases.Provides information on the new treatments of autoimmune cholestatic liver diseases.Includes special topics like bili作者: 健談 時間: 2025-3-24 07:54
http://image.papertrans.cn/e/image/281315.jpg作者: arrhythmic 時間: 2025-3-24 12:38
https://doi.org/10.1007/978-3-030-65908-0Cholangiopathies; Autoimmune cholangiopathies; Genetic cholangiopathies; Congenital biliary abnormaliti作者: 進取心 時間: 2025-3-24 15:21 作者: hegemony 時間: 2025-3-24 19:43
Synthesis of Therapeutic Oligonucleotidesew weeks of life with pale stools and dark urine in otherwise healthy infants. It is the end result of a destructive inflammatory process of the bile ducts, with unclear origins. BA is a condition seemingly unique to the neonatal period, characterized by obliteration of both intra and extrahepatic b作者: addition 時間: 2025-3-24 23:38
RNA Synthesis Using the CEM Groupryogenesis of the primordial ductal plate caused by a genetically determined dysfunction of morphogenetic proteins expressed in the primary cilia of cholangiocytes (“ciliopathies”). Among this group, it is important to notice three different clusters of disease: polycystic liver diseases (PLDs), fib作者: 夾克怕包裹 時間: 2025-3-25 05:59 作者: 整理 時間: 2025-3-25 07:47
https://doi.org/10.1007/978-3-030-02625-7 by multisystem anomalies resulting from the abnormal development of intrahepatic bile ducts, heart, kidneys, bones, eyes, and vessels. After 50?years from its first description in 1969, this chapter provides a comprehensive overview of Alagille syndrome with particular regard to the associated live作者: 廚房里面 時間: 2025-3-25 14:46
https://doi.org/10.1007/978-3-030-02625-7tities caused by an abnormal embryologic development of the ductal plate. CD is characterized by non-obstructive dilatations of the large intrahepatic bile ducts that communicate with the biliary system. It can be diffuse, segmental, or multifocal. “.” defines the presence of CD and hepatic fibrosis作者: 辭職 時間: 2025-3-25 16:27
https://doi.org/10.1007/978-3-030-02625-7hich encodes for the CFTR protein, a chloride channel located at the apical membrane of epithelial cells. CF is a multiorgan disease affecting mostly the lungs, the pancreas, liver, intestine and sweat glands. With advances in medical care, a remarkable increase in survival has occurred, from 16?yea作者: cumber 時間: 2025-3-25 21:44
Marcin Paduch,Anthony A. Kossiakoff of 40; (2) Recurrence of symptoms after cholecystectomy; (3) Intrahepatic cholelithiasis or intrahepatic hyperechogenic foci; (4) History of intrahepatic lithiasis in first-degree relatives. The genetic defect consists into a mutation of . gene which encodes for multidrug resistance protein 3. As c作者: 說笑 時間: 2025-3-26 02:28
https://doi.org/10.1007/978-1-62703-625-2ion of the small intrahepatic bile ducts. The disease develops due a combination of a genetic predisposition and environmental and possibly infectious triggers. The diagnosis is generally confirmed in case of cholestatic abnormalities, a positivity for antimitochondrial antibody or antinuclear-speci作者: 細節(jié) 時間: 2025-3-26 05:53 作者: Vulnerable 時間: 2025-3-26 08:27 作者: 抒情短詩 時間: 2025-3-26 15:49
Vandana Sharma,Yohei Yokobayashiforms of PBC, PSC, and AIH, which are characterized by the presence of features of two diseases, typically PBC and AIH or PSC and AIH in the same patient. The diagnosis of OS is based on the presence or sequential development of biochemical, serological, histologic, and cholangiographic features of 作者: 變形詞 時間: 2025-3-26 18:28
Guangyuan Wang,Yuhui Du,Tingjian Chen medical emergency characterized by the obstruction and subsequent infection of the biliary tree. Partial or complete obstruction of the bile duct and subsequent infection is generally the primary factor triggering the development of acute cholangitis. Choledocholithiasis, defined as the presence of作者: 斷斷續(xù)續(xù) 時間: 2025-3-26 21:44
Guangyuan Wang,Yuhui Du,Tingjian Chenctive metabolites. Liver toxicity is a challenging issue and a frequent cause of failure during drug development. In particular, drug-induced bile duct injury is a side effect of several drugs and dietary supplements, that can be either easy to manage and characterized by a good outcome, or mostly u作者: larder 時間: 2025-3-27 03:30 作者: 消音器 時間: 2025-3-27 08:48
https://doi.org/10.1007/978-3-030-02625-7hepatic manifestations of ALGS, illustrates the modalities and the criteria needed for diagnosis, describes the cornerstones of disease management, and discusses unresolved questions and clinical challenges.作者: Mendicant 時間: 2025-3-27 09:28 作者: 臭名昭著 時間: 2025-3-27 13:53 作者: Gudgeon 時間: 2025-3-27 20:58 作者: tenuous 時間: 2025-3-27 23:20
Low Phospholipid-Associated Cholelithiasis (LPAC)n. . mutations have been described in up to 50% of cases. Ursodeoxycholic acid is the long-term treatment; cholecystectomy is indicated in the case of symptomatic gallstones. Hepato-biliary malignancy is a very rare event. Patients with end-stage liver disease may be candidates for liver transplantation.作者: GLOOM 時間: 2025-3-28 03:25
Inflammatory Cholangitistis has evolved radically over the past century, moving from a purely surgical approach to an endoscopic one. Endoscopic retrograde cholangiopancreatography (ERCP) is currently the treatment of choice to establish biliary drainage and often to remove gallstones.作者: Exuberance 時間: 2025-3-28 06:20 作者: 思考而得 時間: 2025-3-28 12:32
cholestatic liver diseases.Includes special topics like bili.This book provides a comprehensive overview of the diagnosis and management of diseases of the biliary tree. Topics covered include: congenital biliary abnormalities, genetic cholangiopathies, autoimmune cholangiopathies, inflammatory and 作者: MIRE 時間: 2025-3-28 16:19 作者: CREST 時間: 2025-3-28 21:37
Biliary Hamartomas complexes, and typically are small cystic lesions (less than 1.5 cm), encountered as an incidental finding on imaging exams. The gold standard for the diagnosis is magnetic resonance, which demonstrates the cystic lesions in the intrahepatic biliary tree. Usually, they are benign lesions, and the risk of malignancy is extremely rare.作者: 夸張 時間: 2025-3-28 23:36
Synthesis of Therapeutic Oligonucleotidesile ducts and amenable to surgical treatment by Kasai portoenterostomy, in the attempt to restore bile flow. In the most experienced centers, approximately half of children who underwent Kasai portoenterostomy achieve jaundice clearance, avoiding a rapid referral to liver transplantation, required in those in whom this approach is unsuccessful.作者: Hemiparesis 時間: 2025-3-29 05:15
https://doi.org/10.1007/978-3-030-02625-7. The diagnosis is based upon Magnetic Resonance (MR) findings. Typical symptoms include right upper quadrant abdominal pain and jaundice, related to recurrent bile stasis, with consequent stone formations and cholangitis episodes.作者: 轎車 時間: 2025-3-29 09:31
https://doi.org/10.1007/978-3-030-02625-7rs in 1970 to 47.7?years in 2016. Further improvements are predicted in the near future due to the recent availability of an increasing number of innovative drugs targeting the CF basic defect (CFTR modulators) [1].作者: 微生物 時間: 2025-3-29 12:26
Biliary Atresiaile ducts and amenable to surgical treatment by Kasai portoenterostomy, in the attempt to restore bile flow. In the most experienced centers, approximately half of children who underwent Kasai portoenterostomy achieve jaundice clearance, avoiding a rapid referral to liver transplantation, required in those in whom this approach is unsuccessful.作者: Exonerate 時間: 2025-3-29 18:12 作者: Antarctic 時間: 2025-3-29 21:18
Liver Disease in Cystic Fibrosisrs in 1970 to 47.7?years in 2016. Further improvements are predicted in the near future due to the recent availability of an increasing number of innovative drugs targeting the CF basic defect (CFTR modulators) [1].作者: 認為 時間: 2025-3-30 03:52 作者: 染色體 時間: 2025-3-30 07:29 作者: Facet-Joints 時間: 2025-3-30 12:08
Primary Sclerosing Cholangitisnt fluctuant clinical symptoms and serum cholestasis marker, makes the prognostic assessment of these patients challenging. To date, no effective medical therapy has been registered, and liver transplantation is the only therapeutic option in patients developing end-stage liver disease..In this chap
