Results 181 to 190 of about 159,323 (346)
Sa1897 AMYLOIDOSIS-DIAGNOSIS BY ENDOSCOPIC FULL-THICKNESS RESEKTION (EFTR) [PDF]
, 2018 Alexander Braun
openalex +1 more source
P1723CLINICAL AND LABORATORY CHARACTERISTICS OF RENAL TRANSPLANT PATIENTS WITH AA AMYLOIDOSIS IN A TERTIARY CENTER IN TURKEY [PDF]
, 2020 Ece Bilgic +6 more
openalex +1 more source
Canadian Medical Association Journal, 2013 Barry, Ladizinski, Kachiu Cecilia, Lee
openaire +2 more sources
DEN Open, Volume 7, Issue 1, April 2027.ABSTRACT Amyloidosis, characterized by the deposition of abnormal protein fibrils in organs, is classified as systemic or localized. Amyloid light chain (AL)‐type localized amyloidosis is uncommon, particularly when confined to the gastrointestinal tract.
Shunsuke Kojimahara +7 more
wiley +1 more source
Rheumatological Manifestations of Systemic Amyloidosis: A Retrospective Single-Centre Study From a Tertiary Care Hospital in India. [PDF]
CureusGopal M +5 more
europepmc +1 more source
P374Cardiac amyloidosis - the importance of mapping sequences [PDF]
, 2019 Alina Ioana Nicula +4 more
openalex +1 more source
Nerve Ultrasound Detects Peripheral Nerve Enlargement in Cerebrotendinous Xanthomatosis
Muscle &Nerve, Volume 73, Issue 6, Page 1082-1088, June 2026.ABSTRACT Introduction/Aims Cerebrotendinous xanthomatosis (CTX) is a rare autosomal recessive disorder caused by variants in the CYP27A1 gene, resulting in cholestanol accumulation in various tissues, including peripheral nerves. Polyneuropathy is common but often under‐recognized in CTX.
Antonio Edvan Camelo‐Filho +8 more
wiley +1 more source
Exploring the MicroRNA Landscape in Cardiac Amyloidosis: Molecular Insights and Clinical Applications. [PDF]
Genes (Basel)Kontaraki JE +11 more
europepmc +1 more source