Amyloidosis (AL). Clinical and laboratory features in 229 cases.
about
Intraventricular dyssynchrony in light chain amyloidosis: a new mechanism of systolic dysfunction assessed by 3-dimensional echocardiography.Syncope in cardiac amyloidosis and chronic ischemic heart disease: A case reportGerm line origin and somatic mutations determine the target tissues in systemic AL-amyloidosis.Remission of nephrotic syndrome in a patient with renal amyloidosis associated with Takayasu's arteritis after treatment with dimethylsulphoxide.Familial (ATTR) amyloidosis misdiagnosed as the primary (AL) variant: a case reportBiochemical and clinical aspects of amyloidosis.Treatment of peripheral neuropathiesProximal weakness of the extremities as main feature of amyloid myopathySmall intestinal amyloidosis: a rare cause of diverticular disease.Intestinal pseudo-obstruction in patients with amyloidosis: clinicopathologic differences between chemical types of amyloid protein.Primary amyloidosis and severe intrahepatic cholestatic jaundice.Aberrant immunoglobulin synthesis in light chain amyloidosis. Free light chain and light chain fragment production by human bone marrow cells in short-term tissue culture.Amyloidosis of the renal pelvis: a harbinger of mammary carcinoma?Perforation of the sigmoid colon secondary to localised amyloidosisA reappraisal of immunoglobulin variable gene primers and its impact on assessing clonal relationships between PB B cells and BM plasma cells in AL amyloidosis.Amyloid in the cardiovascular system: a reviewPulmonary diffuse alveolar septal amyloidosis--diagnosed by transbronchial lung biopsy.Subacute liver failure secondary to amyloid light-chain amyloidosis.The treatment of nephrotic syndrome caused by primary (light chain) amyloid with vincristine, doxorubicin and dexamethasone.Chronic Renal Failure: Determining the causeOrthotopic heart transplant facilitated autologous hematopoietic stem cell transplantation in light-chain amyloidosis.Clinical challenges of an oligosecretory plasma cell dyscrasia.Destructive bone lesions in primary amyloidosis.Amyloid myopathy and myeloma: response to treatmentAmyloid (AL) in an octogenarian diagnosed by abdominal wall fat biopsySystemic amyloidosis--three illustrative casesRapidly progressive obstructive jaundice due to Congo red negative amyloidosis.KTP Laser in Laryngeal Amyloidosis: Five Cases with Review of LiteratureHepatic response after high-dose melphalan and stem cell transplantation in patients with AL amyloidosis associated liver disease.Incidence, diagnosis and prognosis of cardiac amyloidosis.Light chain amyloidosis: a case presentation and review.Renal replacement therapy in multiple myeloma and systemic amyloidosisSurgical complications of amyloid disease.Massive macroglossia, amyloidosis and myeloma.Behçet's disease associated with amyloidosis in Turkey and in the world.Transthyretin amyloid neuropathy has earlier neural involvement but better prognosis than primary amyloid counterpart: an answer to the paradox?Haemarthrosis due to fracture through amyloid deposits in bone in Portuguese familial amyloidosis.Systemic amyloidosis AL with temporal artery involvement revealing lymphoplasmacytic malignancy in a man presenting as polymyalgia rheumatica.Vertebra collapse due to primary amyloidosis causing neurological compromise.Cardiac transplantation for AL amyloidosis
P2860
Q30483215-6DB8F311-10EC-468B-A4CD-2D3A241F67A4Q33160234-8898C9DF-A3FA-4DAF-A2B2-FE8FE572D0DDQ33301336-43E61F09-495E-4DF9-B0D5-A1A4F22FAA5BQ33566892-AE2B990F-A1BD-4BD3-8710-225C5E354114Q33580469-58A18768-69E5-44D1-A9EB-48480696F1D0Q33614731-ADF9D293-CF62-4650-B47E-6F1DA37A9CC3Q33621708-5DD28531-0A4D-4B80-AA6F-1A964B249591Q33629613-5225FE53-D8E8-40C4-8897-A88FCB67A126Q33796675-4F791DF1-454F-4331-B632-D8D9FB2FFC13Q34378133-26A407BE-9C6E-418D-97D7-BDBA102D21BEQ34382142-31C647E0-B63E-46BB-83E0-BC63376D1D11Q34539341-BDB32B6A-FBF9-4B3F-A20A-D4D913A77325Q35015764-3438724D-90C6-4299-AADD-3A121BA1FA65Q35039070-9B44B730-075D-4789-817D-5A62DA156A0BQ35573416-A78491BA-B0FC-46AF-98CD-74DEE8A8F57EQ35588349-52F31666-31F2-43B3-8FEF-35DA4FDDD551Q35948606-DFBC7525-260D-41AC-B66D-1B105349756DQ36002205-50BF3114-F0E0-4441-A36F-1E1888FA12ACQ36115009-023B18A3-21DA-4858-B836-42EFC84FFE37Q36283907-D322875C-1B84-4E00-9AC1-A2578E3AD4BDQ36367009-6F50CC20-4062-44E2-A185-5A32F5B0E7A7Q36704936-63E6ED94-CCAA-4CC3-9035-9096FCFFAB01Q36707567-0C857AFD-4D9A-4AA8-B89B-1F1527CE980BQ36721257-A9B2209D-0256-4E04-9D5A-79CC6B9CCA16Q36721311-DC0D9AAF-ADCD-4CEA-A441-F75677B05A4DQ36750220-2D6CCF3C-3C25-4B51-9444-D81CB668CDE7Q36939276-9200A42B-01B5-46AA-BC04-64E7AE048B92Q37034209-7C273A40-3DB6-4558-A1AF-12F00CD63444Q37246780-C258DBF0-3A14-48BC-9B15-6C80994E47A7Q37399628-7CEF58A3-FC40-4EFF-B772-8F6337B5B0CBQ37829345-D517CEF0-31DA-4C3F-91AF-CB0B0ADEC4B5Q38661322-6E434DF9-43AE-4474-8584-AA62015AD118Q39164510-F805407E-E59F-45DF-B297-4EC3FF22F74CQ39187346-D39771E4-EF20-4E7A-BD91-3B3A71E98A1CQ39635455-D01D7A24-1E2A-4CBE-8F9A-1F6848A7277DQ41046690-9D2135E9-9C3B-4D2A-8494-81757F6AB4ADQ41241833-8F9DC13F-0AD3-46B3-A274-EA6B442D1B32Q41259964-F805F863-FBA4-4B79-BE12-242E8BC69CD7Q41822878-97502701-7EBF-4F9C-953C-EDF266F8ECEAQ42129011-46C310FB-6B0E-4448-90C8-37999276BB21
P2860
Amyloidosis (AL). Clinical and laboratory features in 229 cases.
description
1983 nî lūn-bûn
@nan
1983年の論文
@ja
1983年論文
@yue
1983年論文
@zh-hant
1983年論文
@zh-hk
1983年論文
@zh-mo
1983年論文
@zh-tw
1983年论文
@wuu
1983年论文
@zh
1983年论文
@zh-cn
name
Amyloidosis (AL). Clinical and laboratory features in 229 cases.
@en
type
label
Amyloidosis (AL). Clinical and laboratory features in 229 cases.
@en
prefLabel
Amyloidosis (AL). Clinical and laboratory features in 229 cases.
@en
P1476
Amyloidosis (AL). Clinical and laboratory features in 229 cases
@en
P2093
P304
P407
P577
1983-10-01T00:00:00Z