Zobrazeno 1 - 10
of 482
pro vyhledávání: '"PRIMARY AMYLOIDOSIS"'
Autor:
Nitin J. Burkule
Publikováno v:
Journal of the Indian Academy of Echocardiography & Cardiovascular Imaging, Vol 8, Iss 1, Pp 17-32 (2024)
Cardiac amyloid cardiomyopathy (CM) is a rapidly progressive disease that is frequently underrecognized and frequently diagnosed late in a significant number of individuals suffering from heart failure. Cardiac amyloid infiltration resulting in myoca
Externí odkaz:
https://doaj.org/article/0a83ffc3a6c24e12bf48e1754cc814f2
Autor:
Irina G. Rekhtina, Victoria A. Khyshova, Nadezhda I. Zozulya, Valentina N. Dvirnyk, Larisa P. Mendeleyeva
Publikováno v:
Терапевтический архив, Vol 95, Iss 9, Pp 746-750 (2023)
Aim. To analyze the frequency and nature of hemorrhagic and thrombotic complications in patients with systemic AL-amyloidosis and compare with laboratory changes in the hemostasis system. Materials and methods. The prospective study included 40 pa
Externí odkaz:
https://doaj.org/article/26adafdf0ba8425b9a2a4b45f43ce5e5
Publikováno v:
Patient Related Outcome Measures, Vol Volume 14, Pp 297-304 (2023)
Avery A Rizio,1 Kristen L McCausland,1 Michelle K Carty,1 Ansgar Conrad,2 Tiffany P Quock2 1QualityMetric Incorporated, LLC, Johnston, RI, USA; 2Prothena Biosciences Inc, South San Francisco, CA, USACorrespondence: Avery A Rizio, QualityMetric Incorp
Externí odkaz:
https://doaj.org/article/ef980462f4f7429e85ab137a8dd7a6d1
Publikováno v:
Journal of Nepal Medical Association, Vol 61, Iss 266 (2023)
Primary systemic amyloidosis is a systemic disease characterised by the deposition of misfolded proteins extracellularly in different organs without any known cause in the background, eventually leading to multiorgan dysfunction and death. The incide
Externí odkaz:
https://doaj.org/article/10f76d1dc03a4136aa7d2d4be375bf77
Akademický článek
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Autor:
Kehui Liu, Yezhou Ding, Yumin Xu, Weiliang Tang, Mingyang Feng, Yunye Liu, Shisan Bao, Hui Wang
Publikováno v:
BMC Gastroenterology, Vol 22, Iss 1, Pp 1-6 (2022)
Abstract Background Immunoglobulin light chain (AL) amyloidosis commonly affects the kidney or heart, but may also involve the liver at a histopathological level. Early diagnosis of AL amyloidosis is important for proper management with desirable out
Externí odkaz:
https://doaj.org/article/01608ea6f06544d994fda30444ca6eb3
Publikováno v:
Онкогематология, Vol 16, Iss 3, Pp 74-82 (2021)
Objective of the study: analysis of AL-amyloidosis (AL-A) diagnostics in real clinical practice and to determine the main approaches for the earlier detection of this disease.Materials and methods. A retrospective analysis of medical records of 34 pa
Externí odkaz:
https://doaj.org/article/96f5f7a1f70d4719a864d17f6036b3d6
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-13 (2020)
Abstract Background Immunoglobulin light chain (AL) amyloidosis is a rare, multi-systemic disorder characterized by two disease processes: an underlying plasma cell dyscrasia that provides the source of pathologic light chains, and the resulting orga
Externí odkaz:
https://doaj.org/article/7fc8ddae801d40c48734706dc8c79a42
Publikováno v:
Urology Case Reports, Vol 41, Iss , Pp 101967- (2022)
Primary amyloidosis of the ureter is a rare disease that is difficult to distinguish from urothelial carcinoma. Only 50 cases of primary ureter amyloidosis have been reported since it was first described in 1937. Of these, only five cases of ureter a
Externí odkaz:
https://doaj.org/article/02f6fabc334046a4b70852d154978872
Publikováno v:
Iberoamerican Journal of Medicine, Vol 3, Iss 2, Pp 173-175 (2021)
Retinitis pigmentosa (RP) or hereditary retinal dystrophy is a rare disease that can be isolated (non-syndromic RP) or associated with other systemic signs (syndromic RP). Kidney damage is exceptionally reported in patients with RP, particularly in s
Externí odkaz:
https://doaj.org/article/8e83e686ba134940979a1a0f5beff8d0