Diagnosis and management of paroxysmal nocturnal hemoglobinuria - Wikidata - thesis-toulmin - TriplyDB

Diagnosis and management of paroxysmal nocturnal hemoglobinuria

Diagnosis and management of paroxysmal nocturnal hemoglobinuria

http://www.wikidata.org/entity/Q24670119

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Eculizumab for treating patients with paroxysmal nocturnal hemoglobinuria Eculizumab for treating patients with paroxysmal nocturnal hemoglobinuria How I treat paroxysmal nocturnal hemoglobinuria Biosynthesis and deficiencies of glycosylphosphatidylinositol Pesg PNH diagnosis, follow-up and treatment guidelines Using functional signatures to identify repositioned drugs for breast, myelogenous leukemia and prostate cancer Review article: the aetiology of primary Budd-Chiari syndrome - differences between the West and China.Stochastic dynamics and the evolution of mutations in stem cells The management of Cesarean delivery in a parturient with paroxysmal nocturnal hemoglobinuria complicated by severe preeclampsia.A case of paroxysmal nocturnal hemoglobinuria presenting with intra-abdominal bleeding due to splenic rupture, developing renal infarct.Paroxysmal nocturnal hemoglobinuria and pregnancy before the eculizumab era: the French experience.Thrombolytic therapy is effective in paroxysmal nocturnal hemoglobinuria: a series of nine patients and a review of the literature.Paroxysmal nocturnal hemoglobinuria in pediatric patients.Predictors of hemoglobin response to eculizumab therapy in paroxysmal nocturnal hemoglobinuria.Increased plasma thrombopoietin levels in patients with myelodysplastic syndrome: a reliable marker for a benign subset of bone marrow failure.Paroxysmal nocturnal haemoglobinuria. Experience over a 10 years period.Clinical-Pathological Conference Series from the Medical University of Graz Case No 155: 26-year-old woman in third trimester of pregnancy with epigastric pain and thrombocytopenia.Flow cytometry screening for paroxysmal nocturnal hemoglobinuria: A single-center experience in Saudi Arabia.Long Standing Eculizumab Treatment without Anticoagulant Therapy in High-Risk Thrombogenic Paroxysmal Nocturnal Hemoglobinuria Hypomegakaryocytic thrombocytopenia (HMT): an immune-mediated bone marrow failure characterized by an increased number of PNH-phenotype cells and high plasma thrombopoietin levels.Paroxysmal Nocturnal Hemoglobinuria in the Differential Diagnosis of Thrombocytopenia.Baseline characteristics and disease burden in patients in the International Paroxysmal Nocturnal Hemoglobinuria Registry.A hypomorphic PIGA gene mutation causes severe defects in neuron development and susceptibility to complement-mediated toxicity in a human iPSC model Paroxysmal nocturnal hemoglobinuria with copy number-neutral 6pLOH in GPI (+) but not in GPI (-) granulocytes The challenging world of cytopenias: distinguishing myelodysplastic syndromes from other disorders of marrow failure Hematopoietic stem cell transplantation for paroxysmal nocturnal hemoglobinuria: long-term results of a retrospective study on behalf of the Gruppo Italiano Trapianto Midollo Osseo (GITMO).Long-term outcome of fludarabine-based reduced-intensity allogeneic hematopoietic cell transplantation for debilitating paroxysmal nocturnal hemoglobinuria.Provirus activation plus CD59 blockage triggers antibody-dependent complement-mediated lysis of latently HIV-1-infected cells.Automated analysis of GPI-deficient leukocyte flow cytometric data using GemStone™.Dose-dependent regulation of primitive erythroid maturation and identity by the transcription factor Eklf Deep sequencing reveals stepwise mutation acquisition in paroxysmal nocturnal hemoglobinuria.Paroxysmal nocturnal hemoglobinuria Simple monitoring of gene targeting efficiency in human somatic cell lines using the PIGA gene.Hemoglobinuria misidentified as hematuria: review of discolored urine and paroxysmal nocturnal hemoglobinuria.Clinical management of paroxysmal nocturnal haemoglobinuria in pregnancy: three case reports.The use of the complement inhibitor eculizumab (Soliris®) for treating Korean patients with paroxysmal nocturnal hemoglobinuria.Paroxysmal nocturnal hemoglobinuria: a single Spanish center's experience over the last 40 yr Molecular basis of clonal expansion of hematopoiesis in 2 patients with paroxysmal nocturnal hemoglobinuria (PNH).Complement blockade with a C1 esterase inhibitor in paroxysmal nocturnal hemoglobinuria Safety and efficacy of the terminal complement inhibitor eculizumab in Japanese patients with paroxysmal nocturnal hemoglobinuria: the AEGIS clinical trial.

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Diagnosis and management of paroxysmal nocturnal hemoglobinuria

http://www.wikidata.org/entity/Q24670119

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2005 nî lūn-bûn

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2005 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած

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2005 թվականի դեկտեմբերին հրատարակված գիտական հոդված

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2005年の論文

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2005年学术文章

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2005年学术文章

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2005年学术文章

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2005年学术文章

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2005年学术文章

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2005年學術文章

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Diagnosis and management of paroxysmal nocturnal hemoglobinuria

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Diagnosis and management of paroxysmal nocturnal hemoglobinuria

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Diagnosis and management of paroxysmal nocturnal hemoglobinuria

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Diagnosis and management of paroxysmal nocturnal hemoglobinuria

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Diagnosis and management of paroxysmal nocturnal hemoglobinuria

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Diagnosis and management of paroxysmal nocturnal hemoglobinuria

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Diagnosis and management of paroxysmal nocturnal hemoglobinuria

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Diagnosis and management of paroxysmal nocturnal hemoglobinuria

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Diagnosis and management of paroxysmal nocturnal hemoglobinuria

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Diagnosis and management of paroxysmal nocturnal hemoglobinuria

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Diagnosis and management of paroxysmal nocturnal hemoglobinuria

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Diagnosis and management of paroxysmal nocturnal hemoglobinuria

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Diagnosis and management of paroxysmal nocturnal hemoglobinuria

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Charles Parker

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Gerard Socié

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Jun-Ichi Nishimura

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Mitsuhiro Omine

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Monica Bessler

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Russell Ware

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Taroh Kinoshita

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Wendell Rosse

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P2860

Amplicon melting analysis with labeled primers: a closed-tube method for differentiating homozygotes and heterozygotes

Effect of sildenafil on oesophageal motor function in healthy subjects and patients with oesophageal motor disorders

Inherited complete deficiency of 20-kilodalton homologous restriction factor (CD59) as a cause of paroxysmal nocturnal hemoglobinuria

Deficiency of the GPI anchor caused by a somatic mutation of the PIG-A gene in paroxysmal nocturnal hemoglobinuria

Paroxysmal nocturnal hemoglobinuria and the risk of venous thrombosis: review and recommendations for management of the pregnant and nonpregnant patient.

Clinical significance of a minor population of paroxysmal nocturnal hemoglobinuria-type cells in bone marrow failure syndrome.

Prognostic features of paroxysmal nocturnal hemoglobinuria in Japan.

Paroxysmal nocturnal haemoglobinuria: long-term follow-up and prognostic factors. French Society of Haematology.

Application of flow cytometry to the diagnosis of paroxysmal nocturnal hemoglobinuria.

Improved detection and characterization of paroxysmal nocturnal hemoglobinuria using fluorescent aerolysin

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