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Current Treatment Options in Oncology, 2006
Amyloidosis is a disease in which abnormal proteins form fibrillar tissue deposits that can compromise key viscera and lead to early death. In order to treat amyloidosis, the type of abnormal protein must be identified. The most common type is monoclonal immunoglobulin light chain or AL amyloidosis; the other important type is hereditary, caused by ...
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Amyloidosis is a disease in which abnormal proteins form fibrillar tissue deposits that can compromise key viscera and lead to early death. In order to treat amyloidosis, the type of abnormal protein must be identified. The most common type is monoclonal immunoglobulin light chain or AL amyloidosis; the other important type is hereditary, caused by ...
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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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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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International Journal of Dermatology, 1988
ABSTRACT: Three patients developed a peculiar pigmentation arising from prolonged mechanical friction with the skin due to the use of rough nylon towel or back scratcher for many years. Histochemical stains could not show the existence of amyloid in one of the cases, but amyloid deposition was identified in successive electron microscopic ...
C K, Wong, C S, Lin
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ABSTRACT: Three patients developed a peculiar pigmentation arising from prolonged mechanical friction with the skin due to the use of rough nylon towel or back scratcher for many years. Histochemical stains could not show the existence of amyloid in one of the cases, but amyloid deposition was identified in successive electron microscopic ...
C K, Wong, C S, Lin
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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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Surgical Pathology Clinics, 2014
Amyloidosis is an uncommon group of diseases in which soluble proteins aggregate and deposit extracellularly in tissue as insoluble fibrils, leading to tissue destruction and progressive organ dysfunction. More than 25 proteins have been identified as amyloid precursor proteins.
Nasreen, Mohamed, Samih H, Nasr
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Amyloidosis is an uncommon group of diseases in which soluble proteins aggregate and deposit extracellularly in tissue as insoluble fibrils, leading to tissue destruction and progressive organ dysfunction. More than 25 proteins have been identified as amyloid precursor proteins.
Nasreen, Mohamed, Samih H, Nasr
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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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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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Serum amyloidosis: a cardiac amyloidosis
European Heart Journal - Cardiovascular Imaging, 2023Jeremy A Slivnick +3 more
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CRISPR-Cas9 In Vivo Gene Editing for Transthyretin Amyloidosis
New England Journal of Medicine, 2021Julian D Gillmore +2 more
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