Results 261 to 270 of about 10,911,887 (292)
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Primary amyloidosis (AL) in families

American Journal of Hematology, 1986
AbstractWe report the occurrence of immunoglobulin‐related amyloidosis (AL) in three separate families, each family having two members affected. None of the six patients had evidence to suggest the presence of familial amyloidosis (AF). Previously, immunoglobulin‐related amyloidosis (AL) was considered to be a sporadic disease process.
M A, Gertz, J P, Garton, R A, Kyle
openaire   +2 more sources

[AL amyloidosis].

Revue medicale de Bruxelles, 2001
AL amyloidosis is a systemic disease caused by the deposition of fibrillar proteins in organs and tissues. These deposits are responsible for organic dysfunctions and may be rapidly lethal. Current therapy is unsatisfactory. We describe three clinical cases of multisystemic AL amyloidosis but with different initial presentation: nephrotic syndrome ...
A R, Hedeshi   +6 more
openaire   +1 more source

Impact of Earlier Diagnosis in Cardiac ATTR Amyloidosis Over the Course of 20 Years

Circulation, 2022
Adam Ioannou   +2 more
exaly  

AL amyloidosis

Medicine, 2021
Samir Asher, Majid Kazmi
openaire   +1 more source

[AL amyloidosis].

Nihon rinsho. Japanese journal of clinical medicine, 1995
AL amyloidosis is one type of systemic amyloidosis. AL represents Amyloid of Light chains (of Ig's) type. Diagnosis of amyloid must be carried out by patho-histological Congo-red stains of the biopsied materials under suspicion of amyloid deposits from patients with various clinical manifestations, including macroglossia, cardiac abnormalities, ECG ...
openaire   +1 more source

AL amyloidosis.

The Journal of the Association of Physicians of India, 2013
Susanta Kr, Das   +5 more
openaire   +3 more sources

Pathophysiology and Therapeutic Approaches to Cardiac Amyloidosis

Circulation Research, 2021
Mathew Maurer   +2 more
exaly  

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