AmyCo: the amyloidoses collection
نویسندگان
چکیده
منابع مشابه
The hereditary amyloidoses.
Hereditary amyloidosis is, in general, a systemic condition related to multiple organ system involvement by beta-structured protein deposits. As such, it often mimics the more common forms of systemic amyloidosis: immunoglobulin light chain (AL, primary) and reactive (AA, secondary). The challenge diagnostically is to recognize hereditary amyloidosis as a distinct entity and then to determine t...
متن کاملنقد و بررسی کتاب the collection of the quran
جان برتن استاد بازنشسته دانشگاه سنتاندروز، مولف کتاب جمعآوری قرآن است. این اثر در سال 1977 توسط انتشارات دانشگاه کمبریج به چاپ رسید. در نگاه اول، اثر مذکور مشتمل بر دو بخش و هر بخش دارای پنج فصل است. مولف در بخش اول به مسأله نسخ میپردازد و در مورد این که آیا قرآن سنت را نسخ کرده و یا بالعکس، به تفصیل سخن میگوید. نظرات شافعی و مخالفانش را در اینباره به طور مشروح بیان میکند. وی سه شکل ن...
15 صفحه اولEmerging treatment approaches for the systemic amyloidoses.
A 57-year-old man was diagnosed with AL amyloidosis after presenting with nephrotic syndrome. He had been well until 6 months earlier, when he noticed intermittent ankle swelling. He sought medical attention approximately 2 months later because of increased swelling of his legs and progressive fatigue. At that time, his urinary protein excretion was 7.4 g/day. Serum creatinine was 0.9 mg/dL and...
متن کاملDiagnosis and management of the cardiac amyloidoses.
Cardiac amyloidosis is a manifestation of one of several systemic diseases known as the amyloidoses.1,2 This uncommon disease is probably underdiagnosed, and even when a diagnosis of amyloidosis of the heart is made, the fact that there are several types of amyloid, each with its unique features and treatment, is often unrecognized. This can lead to errors in management and in the information c...
متن کاملEchocardiographic assessment of the cardiac amyloidoses.
Cardiac amyloidosis is a cardiomyopathy characterized by increased left ventricular (LV) wall thickness and normal or decreased LV cavity size. Congestive heart failure in cardiac amyloidosis is generally considered a predominantly diastolic phenomenon, with systolic dysfunction only occurring in late-stage disease. Echocardiography is a noninvasive, reproducible method of assessing cardiac fea...
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ژورنال
عنوان ژورنال: Amyloid
سال: 2019
ISSN: 1350-6129,1744-2818
DOI: 10.1080/13506129.2019.1603143