Results 271 to 280 of about 98,806 (295)
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Orvosi Hetilap, 2010
Az amyloidosis különböző eredetű fibrilláris jellegű anyag extracelluláris felhalmozódása. Különböző szervekben lerakódva azok működését károsítja. A funkciókárosodásból adódnak a klinikai tünetek, az agyon kívül minden szerv érintett lehet, leggyakrabban a vese, a máj, a lép, a gastrointestinalis rendszer, az endokrin szervek, a bőr, a szív, a tüdő és
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Az amyloidosis különböző eredetű fibrilláris jellegű anyag extracelluláris felhalmozódása. Különböző szervekben lerakódva azok működését károsítja. A funkciókárosodásból adódnak a klinikai tünetek, az agyon kívül minden szerv érintett lehet, leggyakrabban a vese, a máj, a lép, a gastrointestinalis rendszer, az endokrin szervek, a bőr, a szív, a tüdő és
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Otorinolaringologia, 2020
Laryngeal amyloidosis is a rare and idiopathic disease that represents about 1% of all benign laryngeal lesions. It is characterized by the extracellular deposition of an abnormal amount of non-soluble fibrillar proteins in larynx. This disease presents unspecific symptoms and laringoscopic findings that make difficult to diagnose it.
Verro B., Ferrara S., Gargano R.
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Laryngeal amyloidosis is a rare and idiopathic disease that represents about 1% of all benign laryngeal lesions. It is characterized by the extracellular deposition of an abnormal amount of non-soluble fibrillar proteins in larynx. This disease presents unspecific symptoms and laringoscopic findings that make difficult to diagnose it.
Verro B., Ferrara S., Gargano R.
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Current Opinion in Rheumatology, 1993
Major advances of the past year in the amyloidoses include a better understanding of the polymorphism of the acute-phase reactant serum amyloid A protein and the appearance of a new mouse model for primary amyloidosis. The list of single point mutations in transthyretin in different families with slightly varied clinical manifestations of the disease ...
A S, Cohen, L A, Jones
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Major advances of the past year in the amyloidoses include a better understanding of the polymorphism of the acute-phase reactant serum amyloid A protein and the appearance of a new mouse model for primary amyloidosis. The list of single point mutations in transthyretin in different families with slightly varied clinical manifestations of the disease ...
A S, Cohen, L A, Jones
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Fortschritte der Medizin, 1976
Recent studies have clearly indicated that amyloid is a generic term which includes a number of different substances, all of which have a beta-pleated sheet structure and a characteristic fibrillar appearance in the electron microscope. The most common types are made of immunoglobulin light chain (AL) fragments in the primary and myeloma-associated ...
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Recent studies have clearly indicated that amyloid is a generic term which includes a number of different substances, all of which have a beta-pleated sheet structure and a characteristic fibrillar appearance in the electron microscope. The most common types are made of immunoglobulin light chain (AL) fragments in the primary and myeloma-associated ...
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[Amyloidosis and hepatic amyloidosis].
Nihon rinsho. Japanese journal of clinical medicine, 1993The classification of amyloid and amyloidosis has undergone several revisions. The 1990 revision of the nomenclature at the 6th Internal Symposium on Amyloidosis in Oslo has been widely accepted and the basis for nomenclature and classification is the fibril protein making up the amyloid deposits.
T, Murakami, S, Yi
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Journal of the American Academy of Dermatology, 1988
Cutaneous lesions are present in up to 40% of patients with primary and myeloma-associated systemic amyloidosis and occur as a result of tissue deposition of immunoglobulin light chain material derived from a circulating paraprotein. The occurrence of waxy, purpuric mucocutaneous lesions provides a crucial early pointer to underlying occult plasma cell
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Cutaneous lesions are present in up to 40% of patients with primary and myeloma-associated systemic amyloidosis and occur as a result of tissue deposition of immunoglobulin light chain material derived from a circulating paraprotein. The occurrence of waxy, purpuric mucocutaneous lesions provides a crucial early pointer to underlying occult plasma cell
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Scandinavian Journal of Rheumatology, 1995
Diagnosis of amyloidosis still relies on tissue biopsy for microscopic examination. Biopsy from a symptom-giving organ may be used but more often an easily available tissue which is affected in most forms of systemic amyloidosis is utilized. Rectal biopsy has its place but a fine needle aspiration biopsy of subcutaneous adipose tissue offers a safe and
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Diagnosis of amyloidosis still relies on tissue biopsy for microscopic examination. Biopsy from a symptom-giving organ may be used but more often an easily available tissue which is affected in most forms of systemic amyloidosis is utilized. Rectal biopsy has its place but a fine needle aspiration biopsy of subcutaneous adipose tissue offers a safe and
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Serum amyloidosis: a cardiac amyloidosis
European Heart Journal - Cardiovascular Imaging, 2023Jeremy A Slivnick +3 more
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The Journal of Laryngology & Otology, 1990
AbstractLaryngeal amyloidosis is a rare disease. Surgery has been the mainstay of treatment either endoscopically or by an external neck approach. In more recent years, surgery with the carbon dioxide laser has been advocated for this condition. Four cases of laryngeal amyloidosis are presented.
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AbstractLaryngeal amyloidosis is a rare disease. Surgery has been the mainstay of treatment either endoscopically or by an external neck approach. In more recent years, surgery with the carbon dioxide laser has been advocated for this condition. Four cases of laryngeal amyloidosis are presented.
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