Results 11 to 20 of about 24,424 (206)

Association of subcutaneous testosterone pellet therapy with developing secondary polycythemia

open access: yesAsian Journal of Andrology, 2018
A variety of methods for testosterone replacement therapy (TRT) exist, and the major potential risks of TRT have been well established. The risk of developing polycythemia secondary to exogenous testosterone (T) has been reported to range from 0.4% to 40%
Katherine Lang Rotker   +6 more
doaj   +1 more source

Aberrant expression of microRNA in polycythemia vera

open access: yesHaematologica, 2008
Background Polycythemia vera is a clonal hematopoietic stem cell disorder in which the JAK2 V617F mutation is observed in >95% of patients, but an as yet unidentified process appears to initiate the clonal expansion of hematopoiesis.
Hana Bruchova   +2 more
doaj   +1 more source

Clinical features and outcome of dogs and cats with bidirectional and continuous right‐to‐left shunting patent ductus arteriosus

open access: yesJournal of Veterinary Internal Medicine, 2021
Background Studies describing the clinical progression of animals with reverse patent ductus arteriosus (PDA) are lacking. Objectives To describe the signalment, presenting signs, echocardiographic features, and survival in a group of dogs and cats with ...
Victoria Greet   +5 more
doaj   +1 more source

Polycythemia in chronic obstructive pulmonary disease in Minia Cardiothoracic University Hospital

open access: yesEgyptian Journal of Chest Disease and Tuberculosis, 2023
Background Secondary polycythemia is linked to cigarette smoking and chronic obstructive pulmonary disease (COPD). However, the prevalence of polycythemia and its possible risk factors in patients with COPD have not been widely studied.
Rasha A Abdelfattah   +4 more
doaj   +1 more source

Development and Validation of Prediction Models for Severe Obstructive Sleep Apnea Based on Periodic Health Examinations. [PDF]

open access: yesClin Respir J
This study developed and validated two prediction models for severe obstructive sleep apnea using data from periodic health examinations. These models enable early detection of high‐risk individuals and may facilitate timely referral and intervention in occupational and clinical settings.
Kanno K   +6 more
europepmc   +2 more sources

Extent of hematopoietic involvement by TET2 mutations in JAK2V617F polycythemia vera

open access: yesHaematologica, 2011
TET2 mutations are found in polycythemia vera and it was initially reported that there is a greater TET2 mutational burden than JAK2V617F in polycythemia vera stem cells and that TET2 mutations precede JAK2V617F.
Sabina I. Swierczek   +7 more
doaj   +1 more source

Polycythemia vera is a medical condition characterized by raised hematocrit. Owing to increased viscosity, the blood flow in the vessels become sluggish leading to the clinical features of polycythemia such as headache, blurring of vision, red skin, dizzi

open access: yesJournal of Bahria University Medical and Dental College, 2021
Polycythemia vera is a medical condition characterized by raised hematocrit. Owing to increased viscosity, the blood flow in the vessels become sluggish leading to the clinical features of polycythemia such as headache, blurring of vision, red skin ...
Nabeela Iqbal   +2 more
doaj   +1 more source

Frequent reduction or absence of detection of the JAK2-mutated clone in JAK2V617F-positive patients within the first years of hydroxyurea therapy

open access: yesHaematologica, 2008
We analyzed the effect of hydroxyurea on the JAK2V617F allelic ratio (%JAK2V617F), measured in purified blood granulocytes, of patients with polycythemia vera and essential thrombocythemia.
François Girodon   +8 more
doaj   +1 more source

Case Report: A novel EPAS1 mutation in a case of paraganglioma complicated with polycythemia and atrial septal defect

open access: yesFrontiers in Endocrinology, 2023
BackgroundParaganglioma is a rare neuroendocrine tumor and is highly associated with hereditary susceptibility genes, often occurring as part of a genetic syndrome. The genetic heterogeneity of paraganglioma poses challenges in diagnosis, counseling, and
Haiyan Yang   +5 more
doaj   +1 more source

Utility of Hounsfield Unit: Haematocrit Ratio in Diagnosing Acute Cerebral Venous Sinus Thrombosis on Unenhanced Computed Tomography [PDF]

open access: yesInternational Journal of Anatomy Radiology and Surgery, 2021
Introduction: The non-invasive imaging technique of choice in diagnosing Cerebral Venous Sinus Thrombosis (CVST) is Magnetic Resonance Imaging (MRI), but it has its own set of limitations like not being available universally in the acute setting ...
NARASIPURA LINGAIAH RAJENDRA KUMAR   +3 more
doaj   +1 more source

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