diagnosisendoscopic therapyevidence-based guidelinesmanagementpancreatic replacement therapytropical pancreatitisCurrent knowledge about chronic pancreatitis (CP) is limited and there is a particular dearth of information about the entity known as tropical pancreatitis. A consensus working party was convened by ...
美[ˌheməˌkroʊmə'toʊsɪs] 英[ˌheməˌkrəʊmə'təʊsɪs] n.血色素沉着病 网络血色病;血色素沉着症;血色沉着病 英汉 英英 网络释义 n. 1. 血色素沉着病,血色沉着病 释义: 全部,血色素沉着病,血色病,血色素沉着症,血色沉着病...
Diagnosis of hemochromatosis. Focuses on the diagnosis of hemochromatosis. Information about hemochromatosis; Pathogenesis and progression of the disease throughout the lifespan; Clinic... Powell,Lawrie,W.,... - 《Annals of Internal Medicine》 被引量: 185发表: 1998年 Diagnosis of hemochromatosis in...
When liver failure is diagnosed in the first 1-2 days of life, neonatal hemochromatosis is by far the most common diagnosis. Afterward, many other conditions can manifest and must be excluded. They include all other causes of hepatic failure, including infective, metabolic, and hemorrhagic causes...
Diagnosis of Hemochromatosis Genetic testing is required to confirm the presence of hereditary hemochromatosis. It is relatively easy to test for hemochromatosis when it is suspected. Hemochromatosis test include: Serum Ferritin Level. Ferritin is good reflection of the amount of iron that is available...
Diagnosis of celiac sprue Leptin, obesity, and liver disease Lawrence K. Gates, Dawn V. Holladay Gastroenterology Alan L. Buchman, James Scolapio, Jon Fryer Gastroenterology Volume 122, Issue 1, Pages (January 2002) Systematic review of the comorbidity of irritable bowel syndrome with other disord...
代谢性疾病,如威尔逊氏病, 血色沉着, α -1 型胰岛素缺乏症均可导致肝损伤. 互联网 FERRITIN - Iron - containing serum protein measured by laboratory to help establish a diagnosis ofhemochromatosis. 铁蛋白 —— 含铁的血清蛋白,由实验室血液检测帮助诊断血色沉着病. ...
7 ⅐ No. 1 A 6-year survey of HFE gene test for hemochromatosis diagnosis Catherine Mura, PhD, Odile Ragu´enes, BSc, Virginie Scotet, BSc, Sandrine Jacolot, BSc, Anne-Yvonne Mercier, MD, and Claude F´erec, MD, PhD Purpose: A 6-year survey of HFE gene test was conducted to...
Diagnosis: Diagnosis is mainly based on laboratory exploration. Paraclinical exploration which are used for the diagnosis of primary hemochromatosis are addressed to iron metabolism: Increased transferrin saturation coefficient, over 45%; Increased serum ferritinover 200 ng / ml in men and 250 ng / ...
Diagnosis of hemochromatosis in family members of probands: A comparison of phenotyping and James C. Barton, MD', Barry E. Rothenberg, P h P , Luigi F. Bertoli, MD1,and Ronald I:Acton, P h p Purpose: We wanted to compare phenotyping and HFE genotyping for diagnosis of hemochromatosis ...