Results 81 to 90 of about 7,496 (162)

RECENT INSIGHTS INTO SECONDARY ERYTHROCYTOSIS: PART II. MANAGEMENT APPROACHES

Клінічна та профілактична медицина
Introduction. The etiological heterogeneity of secondary erythrocytosis (SE), together with the coexistence of several potential contributing factors in a single patient, complicates the standardization of therapeutic strategies and warrants an ...
Mariia A. Trypilka, Oksana M. Kostiukevych, Lesia K. Benkovska   +2 more
doaj   +1 more source

The need for dried plasma—Still a national issue: Where are we and recommendations

Transfusion, EarlyView.
Anthony E. Pusateri, Shibani Pati, Toby A. Silverman, Roman Dudaryk, Joseph F. Rappold, Lisa Buckley, Andrew P. Cap, Jose A. Cancelas, Laurence M. Corash, G. Michael Fitzpatrick, Michael Ganio, Adam Gerber, Richard Gonzales, Jennifer M. Gurney, Ernest E. Moore, Hunter B. Moore, Vijayan Nair, Michael Policastro, Travis M. Polk, Jeffrey W. Shupp, Jason L. Sperry, Ralph R. Vassallo, Therese A. West, John B. Holcomb, Lester Martinez‐Lopez   +24 more
wiley   +1 more source

Hemodynamic Changes in Blood Donors

Majallah-i Dānishgāh-i ’Ulūm-i Pizishkī-i Shahīd Ṣadūqī Yazd, 2004
Introduction: Everyday, millions of people around the world go through phlebotomy, either to donate blood or for therapeutic intention. The most important worrisome adverse effects are hemodynamic alterations. In this study, hemodynamic changes following
M Rafiei, M Moddares-Mosadegh, M Emami- Maibodi, M Sadr-Bafghi, MH Ahmadieh   +4 more
doaj  

The oral ferroportin inhibitor vamifeport prevents liver iron overload in a mouse model of hemochromatosis

HemaSphere
Hemochromatosis is an inherited iron overload condition caused by mutations that reduce the levels of the iron‐regulatory hormone hepcidin or its binding to ferroportin.
Naja Nyffenegger, Anna Flace, Ahmet Varol, Patrick Altermatt, Cédric Doucerain, Hanna Sundstrom, Franz Dürrenberger, Vania Manolova   +7 more
doaj   +1 more source

Erythropoiesis: insights into pathophysiology and treatments in 2017

Molecular Medicine, 2018
Erythropoiesis is a tightly-regulated and complex process originating in the bone marrow from a multipotent stem cell and terminating in a mature, enucleated erythrocyte.
Andrea Zivot, Jeffrey M. Lipton, Anupama Narla, Lionel Blanc   +3 more
doaj   +1 more source

Serum Ferritin in Women With HFE p.C282Y Homozygosity: Positive Associations With Age, Live Births, Menopause, and Transferrin Saturation

eJHaem
Background We sought to determine associations of serum ferritin (SF) with live birth numbers and other iron‐related variables in women with HFE p.C282Y (rs1800562) homozygosity. Methods We studied non‐pregnant, non‐Hispanic white women in post‐screening
James C. Barton, J. Clayborn Barton, Ronald T. Acton   +2 more
doaj   +1 more source

Blood letting as an ancient cure for an unusual manifestation of polycythemia

Annals of Vascular Surgery - Brief Reports and Innovations
A 52-year-old woman presented with acute digital ischemia and pain in all five digits of her right hand. Upper extremity arterial duplex demonstrated normal flow to the wrist, but upper extremity Computed Tomography Angiography (CTA) demonstrated an ...
Margarita I Pipinos, Elizabeth A Amato-Hanner, Aaron M Murray, Shalmali Mirajkar, Jennifer L Gamache, Safina Hafeez, Tanya M Wildes, Jason N MacTaggart   +7 more
doaj   +1 more source

Performance and safety of therapeutic erythrocytapheresis in polycythemia and hemochromatosis treatment: single centre experience

Hematology, Transfusion and Cell Therapy
Abstarct: Introduction: Therapeutic erythrocytapheresis has some advantages over therapeutic phlebotomy, the standard treatment for cytoreduction in polycythemia and hemochromatosis.
Iva Lucija Burnać, Ines Bojanić, Sanja Mazić, Marija Lukić, Branka Golubić Ćepulić   +4 more
doaj   +1 more source

From Cyanosis to Extensive Systemic‐to‐Pulmonary Collaterals Formation: A Case With an Iatrogenic Connection of the Inferior Vena Cava to the Left Atrium

Clinical Case Reports
Atrial septal defect (ASD) is a prevalent congenital heart abnormality that can be effectively repaired through either surgical or interventional procedures. We decide to describe a 50‐year‐old male with a history of dyspnea, cyanosis, and hypoxemia.
Akram Nakhaee, Roya Sattarzadeh Badkoubeh, Mehrzad Rahmanian, Maryam Roozitalab   +3 more
doaj   +1 more source

Pathogenesis Diagnostics and Treatment of Hereditary Haemochromatosis: A 150 Year-Long Understanding of an Iron Overload Disorder

European Medical Journal, 2017
Haemochromatosis is an iron overload disorder that can be inherited or acquired and when diagnosis is delayed, disease progression and death can occur.
Anastasia Asimakopoulou, Sabine Weiskirchen, Ralf Weiskirchen   +2 more
doaj