Results 191 to 200 of about 17,175,483 (375)

Comparison of Two Strategies of Analysis of Urinary Protein Composition for the Diagnosis and Follow‐Up of Renal Diseases

ELECTROPHORESIS, EarlyView.
ABSTRACT Proteinuria analysis is necessary to detect the early stages of kidney disease before the estimated glomerular filtration rate deteriorates and to monitor the progression of treated kidney disease. Electrophoresis is often the first orientation test, although this test is time‐consuming and its interpretation may be subjective.
Joris Guyon, Jeanne Malaubier, Hong‐Van Pham, Lila Rami Arab, Laurence Pieroni, Marie‐Laure Curutchet‐Burtin, Rémi Segues, Sylvie Caspar‐Bauguil, Annie M. Bérard   +8 more
wiley   +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

A functional role for spontaneously occurring natural anti‐transthyretin antibodies from patients with transthyretin cardiac amyloidosis

European Journal of Heart Failure, EarlyView.
Ortal Tuvali, Michael Fassler, Sorel Goland, Clara Benaim, Sara Shimoni, Jacob George   +5 more
wiley   +1 more source

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

Classic features of primary systemic amyloidosis (AL amyloidosis) leading to diagnosis of plasma cell myeloma [PDF]

, 2019
The diagnosis of primary systemic amyloidosis, also known as AL (amyloid light-chain) amyloidosis, is often delayed owing to its nonspecific manifestations as well as its rarity.
Behrens, Emily, Tan, Kendra W, Tarbox, Michelle B, Zhu, Brian   +3 more
core  

Longitudinal strain is an independent predictor of survival and response to therapy in patients with systemic AL amyloidosis.

European Heart Journal, 2021
O. Cohen, A. Ismael, B. Pawarova, R. Manwani, S. Ravichandran, S. Law, Darren Foard, A. Petrie, Sevda Ward, Brooke Douglas, A. Martinez-Naharro, L. Chacko, C. Quarta, S. Mahmood, S. Sachchithanantham, H. Lachmann, P. Hawkins, J. Gillmore, M. Fontana, R. Falk, C. Whelan, A. Wechalekar   +21 more
semanticscholar   +1 more source

The mechanisms in glucose metabolism of aging hippocampus

Ibrain, EarlyView.
Cognitive decline in elders stems from the irreversible loss and functional decline of neurons, with the hippocampus being particularly susceptible to age‐related neuronal deterioration. Glucose acts as the primary fuel for the brain, and a constant provision of glucose to the hippocampus is essential for memory and cognitive functions.
Rui He, Fuxing Zhao, Zhiyu Yang, Tingting Wang, Yaohui Zhang, Jinglan Quan, Gaohong Zhu   +6 more
wiley   +1 more source

Living Donor Kidney and Autologous Stem Cell Transplantation for Primary Systemic Amyloidosis (AL) with Predominant Renal Involvement [PDF]

, 2005
Nelson Leung, Matthew D. Griffin, Angela Dispenzieri, Eric Haugen, James M. Gloor, Thomas R. Schwab, Stephen C. Textor, Martha Q. Lacy, Mark R. Litzow, Fernando G. Cosio, Timothy S. Larson, Morie A. Gertz, Mark D. Stegall   +12 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

‘Valvular’ AL amyloidosis

European Heart Journal, 2019
Csilla Jozsa, Guy Lloyd, Sanjeev Bhattacharyya   +2 more
openaire   +3 more sources