Results 131 to 140 of about 16,704,778 (257)

Spontaneous rupture of the spleen in AL amyloidosis [PDF]

, 2003
Betül Oran, Daniel G. Wright, David C. Seldin, David McAneny, M Skinner, Vaishali Sanchorawala   +5 more
openalex   +1 more source

Nodular immunocyte-derived (AL) amyloidosis in the trachea of a dog [PDF]

, 2004
M. Faulkner Besancon, Brian A. Stacy, Andrew E. Kyles, Peter F. Moore, William Vernau, Sean D. Smarick, Liberty A. Rasor   +6 more
openalex   +1 more source

Sharpening therapeutic strategy in AL amyloidosis [PDF]

, 2004
Giampaolo Merlini
openalex   +1 more source

AL-amyloidosis and light-chain deposition disease light chains induce divergent phenotypic transformations of human mesangial cells [PDF]

, 2004
John Keeling, Jiamin Teng, Guillermo A. Herrera   +2 more
openalex   +1 more source

AL-amyloidosis is underdiagnosed in renal biopsies [PDF]

, 2004
Lea Novak, W.J. Cook, Guillermo A. Herrera, Paul W. Sanders   +3 more
openalex   +1 more source

Endomyocardial biopsy-proven light chain amyloidosis (AL) without echocardiographic features of infiltrative cardiomyopathy

, 1997
Morie A. Gertz, Martha Grogan, Robert A. Kyle, A. Jamil Tajik   +3 more
openalex   +1 more source

Ascites revealing peritoneal amyloidosis and IgG kappa multiple myeloma: A case report

Radiology Case Reports
AL amyloidosis is a rare systemic disease characterized by the deposition of amyloid protein in various organs, including the kidneys, heart, peripheral nervous system, digestive tract, skin, and muscles.
Samia Sabri, Houda Bachir, Siham Hamaz, Habiba Alaoui Bennesser, Khalid Serraj   +4 more
doaj  

PRIMARY AMYLOIDOSIS (AL) AS A CAUSE OF NEPHROTIC SYNDROME [PDF]

, 2005
Yoann Bataille, Christophe Bovy, Patrizio Lancellotti, V. Melchior, Katty Delbecque, Yves Béguin, Krzesinski Jm   +6 more
openalex   +1 more source

Clinical clues for suspecting wild-type transthyretin cardiac amyloidosis in patients with monoclonal gammopathy of undetermined significance: a case report

The Egyptian Heart Journal
Background Myeloproliferative disorders, including monoclonal gammopathy of undetermined significance (MGUS), are often associated with amyloid light-chain (AL)-type cardiac amyloidosis (CA) but occasionally with wild-type transthyretin (ATTR) CA.
Tomoaki Haga, Takahiro Okumura, Yasuhiko Harada, Hiroaki Hiraiwa, Ryota Morimoto, Shinji Kaneko, Nagaaki Kato, Masanori Shinoda, Toyoaki Murohara   +8 more
doaj   +1 more source

Quantitative diagnosis of amyloid without Congo red staining using polarized light microscopy [PDF]

arXiv
Amyloidosis is a protein misfolding disease caused by the deposition of large, insoluble aggregates (amyloid fibrils) of protein in a tissue, which has been associated with various conditions, such as lymphoid disorders, Alzheimer's disease, diabetes mellitus type 2, chronic inflammatory processes, and cancers. Amyloid fibrils are commonly diagnosed by
arxiv