Results 51 to 60 of about 11,801 (249)

Spurious laboratory results associated with immunoglobulin M gammopathy in a dog with multiple myeloma

open access: yesJournal of Veterinary Internal Medicine, 2022
An 11 year old female‐neutered Labrador presented for facial swelling. Clinicopathological abnormalities included hyperglobulinemia, azotemia, hypercalcemia, nonregenerative anemia, thrombocytopenia, and spurious hypoglycemia.
Samantha C. Loane   +4 more
doaj   +1 more source

Waldenström’s Macroglobulinemia in a Normoproteinemic Dog with Atypical Bimorphic Plasmacytoid Differentiation and Monoclonal Gammopathy

open access: yesVeterinary Sciences, 2023
A 2-year-old neutered female Small Munsterlander dog was presented for an insect bite. Physical examination revealed a poor body condition, a peripheral lymphadenomegaly, and suspected splenomegaly.
Maud Guerlin   +6 more
doaj   +1 more source

Identification of epidermal Pdx1 expression discloses different roles of Notch1 and Notch2 in murine KrasG12D-induced skin carcinogenesis in vivo [PDF]

open access: yes, 2010
Background The Ras and Notch signaling pathways are frequently activated during development to control many diverse cellular processes and are often dysregulated during tumorigenesis.
Barbara M. Grüner   +9 more
core   +4 more sources

Brown Tumors Mimicking Skeletal Metastases: A Diagnostic Pitfall in Primary Hyperparathyroidism

open access: yesClinical Case Reports, Volume 13, Issue 12, December 2025.
ABSTRACT Brown tumors are rare but important manifestations of primary hyperparathyroidism (PHPT). These benign, fibrotic, and erosive bony lesions result from localized rapid osteoclastic activity driven by excessive parathyroid hormone levels. Although brown tumors are considered one of the most pathognomonic signs of PHPT, they are infrequently ...
Uzma Akbar   +7 more
wiley   +1 more source

Clinical profile of the spectrum of multiple myeloma in a teaching hospital

open access: yesMedical Journal of Dr. D.Y. Patil University, 2014
Aim: To analyze the clinical and laboratory features of multiple myeloma (MM). Settings and Design: A cross-sectional study of 20 newly diagnosed patients with MM over a period of 1 year in a tertiary health-care center.
Arundhati G Diwan   +3 more
doaj   +1 more source

Primary amyloidosis with initial gastrointestinal manifestation. A case report [PDF]

open access: yesArchives of the Balkan Medical Union, 2018
Introduction. Amyloidosis is a rare disease associated with extracellular accumulation of abnormal protein – amyloid in various organs and systems. This disease can be either acquired or hereditary, systemic or localized.
Tatyana M. BETOVA   +4 more
doaj   +1 more source

ENZYMATICALLY PRODUCED SUBUNITS OF PROTEINS FORMED BY PLASMA CELLS IN MICE : II. β2A-MYELOMA PROTEIN AND BENCE JONES PROTEIN [PDF]

open access: yes, 1962
The relationship of Bence Jones protein (mol wt = 45,000) to a β2A-myeloma protein (mol wt = 160,000) formed by the same mouse plasma cell tumor (MPC-2) was investigated.
Askonas, Brigitte A., Fahey, J. L.
core   +1 more source

Primary hyperparathyroidism associated with multiple myeloma: a case report

open access: yesPAMJ Clinical Medicine, 2020
Primary hyperparathyroidism and malignant diseases are the most frequent causes of hypercalcemia. Cases in which hypercalcemia is due to both these diseases have been included in a few reports.
Meryam Elbahi   +3 more
doaj   +1 more source

An Examination Of The Lambda-Type Bence-Jones Protein In Relation To The Role It Plays As A Model Light Chain Immunoglobulin With A Blocked N-Terminal [PDF]

open access: yes, 1974
The simplest subunit by which the immune systems of higher animals function is the immunoglobulin. Immunoglobulins are proteins endowed with antibody activity, that is, the ability to bind and inactivate those foreign substances capable of illiciting an ...
Brayko, Craig
core   +1 more source

POEMS neuropathy: optimising diagnosis and management [PDF]

open access: yes, 2018
POEMS syndrome is a rare and disabling autoinflammatory condition characterised by a typical peripheral neuropathy and the presence of a monoclonal plasma cell disorder.
Carr, AS   +5 more
core   +1 more source

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