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SHAREHOLDER ALERT: Brower Piven Notifies Investors of Class Action Lawsuit And Encourages Those Who Have ...


GlobeNewswire (press release) - Nov 27, 2016
... practices with respect to Soloris, a monoclonal antibody for the treatment of paroxysmal nocturnal hemoglobinuria (“PNH”) and atypical hemolytic uremic syndrome (“aHUS”), and the Company's revenues from Soloris sales were unlikely to be sustainable.
 

EU grants orphan drug status to Ra Pharma's RA101495 to treat paroxysmal nocturnal hemoglobinuria


pharmabiz.com - Nov 19, 2016
Ra Pharmaceuticals, a clinical stage biopharmaceutical company focusing on the development of next-generation therapeutics for diseases of complement dysregulation, announced that the European Commission has designated RA101495 as an orphan ...
 

Eculizumab in the management of paroxysmal nocturnal hemoglobinuria: patient selection and special considerations


Dove Medical Press - Aug 1, 2016
Abstract: Paroxysmal nocturnal hemoglobinuria (PNH) is a nonmalignant clonal disorder resulting from somatic mutation in the PIG-A gene leading to a deficiency of the membrane-anchoring molecule glycosylphosphatidylinositol. The lack of expression of ...
 

Hemoglobinuria - premium items on eBay

NEW Paraoxysmal Nocturnal Hemoglobinuria and Related Disorders


 

NEW Paroxysmal Nocturnal Hemoglobinuria and Related Disorders: Molecular Aspects


 

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Hemoglobinuria books

Hemoglobinuria: Webster's Timeline History, 1878 - 2007


by: Icon Group International
Webster's bibliographic and event-based timelines are comprehensive in scope, covering virtually all topics, geographic locations and people. They do so from a linguistic point of view, and in the case of this book, the focus is on "Hemoglobinuria," including when used in literature (e.g. all authors that might have Hemoglobinuria in their name). As such, this book represents the largest compilation of timeline events associated with Hemoglobinuria when it is used in proper noun form. Webster's timelines cover bibliographic citations, patented inventions, as well as non-conventional and alternative meanings which capture ambiguities in usage.
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Paraoxysmal Nocturnal Hemoglobinuria and Related Disorders


Few publications focus on the mysterious, genetically acquired disease paroxysmal nocturnal hemoglobinuria (PNH) and the related "intractable" disorders―aplastic anemia and myelodysplastic syndromes. Now, however, the latest understanding of the clinical and molecular genetic aspects of PNH is summarized here in the proceedings of the International Symposium held in Tokyo in 2001. Major topics reviewed include the molecular mechanisms of the PIG-A gene mutation; complement activation and inhibitors; experimental animal models; pathogenesis; the history of PNH research; the natural history of the disease; the mechanism of PNH clone expansion; the emergence of PNH clones under bone marrow failure syndromes; and treatment of the disease by immunosuppressive agents and stem cell transplantation.
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Paroxysmal Nocturnal Hemoglobinuria and Related Disorders: Molecular Aspects of Pathogenesis


Few publications focus on the mysterious, genetically acquired disease paroxysmal nocturnal hemoglobinuria (PNH) and the related "intractable" disorders―aplastic anemia and myelodysplastic syndromes. Now, however, the latest understanding of the clinical and molecular genetic aspects of PNH is summarized here in the proceedings of the International Symposium held in Tokyo in 2001. Major topics reviewed include the molecular mechanisms of the PIG-A gene mutation; complement activation and inhibitors; experimental animal models; pathogenesis; the history of PNH research; the natural history of the disease; the mechanism of PNH clone expansion; the emergence of PNH clones under bone marrow failure syndromes; and treatment of the disease by immunosuppressive agents and stem cell transplantation.
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Paroxysmal Nocturnal Hemoglobinuria: From Bench to Bedside


This volume reviews the fundamental understanding of this potentially life-threatening disease and the advances in treatment that have been achieved with the use of the monoclonal antibody eculizumab. Although the PIGA gene has been known for many years, the mechanism of clonal dominance in paroxysmal nocturnal hemoglobinuria is still largely unknown. This book, Paroxysmal Nocturnal Hemoglobinuria, discusses the direction of continuing research in this area, as well as the potential for the development of management guidelines.
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HEMOGLOBINURIA


POR: HERNANDO CORAL ROSERO M.H.
 

The Pathophysiology of Paroxysmal Nocturnal Hemoglobinuria - USMLE


http://www.usmlesuccess.net An in-depth look at the genetics and pathophysiology of PNH; for the USMLE Step 1 exam. Grab a FREE copy of the Step 1 BIBLE ...
 

Paroxysmal Nocturnal Hemoglobinuria: Most Important Points


Please visit www.doctorpaul.org for more videos.
 

Paroxysmal Nocturnal Hemoglobinuria


http://usmlefasttrack.com/?p=5629 Paroxysmal, Nocturnal, Hemoglobinuria, Findings, symptoms, findings, causes, mnemonics, review, what is, video, study, ...
 

Hemoglobinuria paroxística Nocturna


4to Curso -Formación temprana de profesores de Inmunología-