Skip to search form
Skip to main content
Skip to account menu
Semantic Scholar
Semantic Scholar's Logo
Search 225,649,470 papers from all fields of science
Search
Sign In
Create Free Account
Primary amyloidosis
Known as:
AMYLOIDOSIS, SYSTEMIC
, AMYLOIDOSIS, IDIOPATHIC
, amyloidosis primary
Expand
A plasma cell neoplasm that secretes an abnormal immunoglobulin, which deposits in tissues and forms a beta-pleated sheet structure that binds Congo…
Expand
National Institutes of Health
Create Alert
Alert
Related topics
Related topics
23 relations
Broader (2)
Amyloidosis
Immunoglobulin deposition disease
Atypical lymphocyte
B lymphoblast
B-Lymphocytes
Congestive heart failure
Expand
Narrower (1)
Primary Systemic Amyloidosis
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2013
2013
Potent in vitro and in vivo activity of sorafenib in multiple myeloma: induction of cell death, CD138‐downregulation and inhibition of migration through actin depolymerization
J. Udi
,
J. Schüler
,
+7 authors
M. Engelhardt
British Journal of Haematology
2013
Corpus ID: 23298768
Despite considerable advances, multiple myeloma (MM) remains incurable and the development of novel therapies targeting the…
Expand
Review
2008
Review
2008
The pathologist's perspective on vitreous opacities
S. E. Coupland
Eye
2008
Corpus ID: 28973688
BackgroundVitreous opacities are diverse in nature. Many underlying diseases are sight-threatening and several are also lethal…
Expand
2004
2004
Two familial cases with tumor necrosis factor receptor-associated periodic syndrome caused by a non-cysteine mutation (T50M) in the TNFRSF1A gene associated with severe multiorganic amyloidosis.
T. Kallinich
,
Sonia Briese
,
+6 authors
D. Haffner
Journal of Rheumatology
2004
Corpus ID: 7452389
An adolescent boy had had recurrent episodes of fever, abdominal pain, and arthralgias since the age of 7 years. Progressive…
Expand
Highly Cited
2001
Highly Cited
2001
Brain Aβ amyloidosis in APPsw mice induces accumulation of presenilin‐1 and tau
Y. Tomidokoro
,
Y. Harigaya
,
+7 authors
M. Shoji
Journal of Pathology
2001
Corpus ID: 9609520
APPsw transgenic mice (Tg2576) overproducing mutant amyloid β protein precursor (βAPP) show substantial brain Aβ amyloidosis and…
Expand
1998
1998
A simple screening test for variant transthyretins associated with familial transthyretin amyloidosis using isoelectric focusing.
L. Connors
,
Thomas Ericsson
,
+4 authors
Martha Skinner
Biochimica et Biophysica Acta
1998
Corpus ID: 30384898
Review
1994
Review
1994
Role of bioincompatibility in dialysis morbidity and mortality.
J. Lazarus
,
William F. Owen
American Journal of Kidney Diseases
1994
Corpus ID: 22935153
1988
1988
Immunoglobulin synthesis in primary and myeloma amyloidosis.
Jean-Louis Preud'homme
,
D. Ganeval
,
Jean-Pierre Grünfeld
,
L. Striker
,
J. Brouet
Clinical and Experimental Immunology
1988
Corpus ID: 21448420
Bone marrow cells from 14 patients with primary amyloidosis and two patients with myeloma amyloidosis were studied by…
Expand
Highly Cited
1972
Highly Cited
1972
Immunoglobulins and amyloidosis. An immunologic study of sixty-two patients with biopsy-proved disease.
E. Cathcart
,
R. Ritchie
,
A. Cohen
,
K. Brandt
American Journal of Medicine
1972
Corpus ID: 32805712
Review
1961
Review
1961
Joint Symptoms in Myelomatosis and Similar Conditions *
E. Hamilton
,
E. Bywaters
Annals of the Rheumatic Diseases
1961
Corpus ID: 27397
The commonest presenting symptom in myelo- matosis is pain in the back, which is frequently associated with vertebral collapse…
Expand
Highly Cited
1953
Highly Cited
1953
Familial Primary Amyloidosis with Nervous System Involvement
A. Kantarjian
,
R. Dejong
Neurology
1953
Corpus ID: 40702406
PRIMARY AMYLOIDOSIS is a rare systemic disease; a total of about 80 cases have been reported in the 1iterature.l In the majority…
Expand
By clicking accept or continuing to use the site, you agree to the terms outlined in our
Privacy Policy
(opens in a new tab)
,
Terms of Service
(opens in a new tab)
, and
Dataset License
(opens in a new tab)
ACCEPT & CONTINUE