Contents
  1. Clinical course of non-severe aplastic anemia in adults.
  2. Aplastic Anemia
  3. Aplastic anemia - Wikipedia
  4. Revista da Faculdade de Ciências Médicas de Sorocaba

Acquired aplastic anemia (aAA) is a severe and rare disease, characterized by hematopoietic bone marrow failure and peripheral cytopenia. Int J Hematol. Jun;91(5) doi: /s Epub Jun 5. Clinical course of non-severe aplastic anemia in adults. Kwon JH(1) . Tratamento atual da anemia aplástica adquirida grave A sobrevida em pacientes com grave anemia aplástica melhorou muito nas .. Epub ahead of print.

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Anemia Aplasica Epub

Acquired aplastic anemia and Fanconi anemia - Brazilian Guidelines in Hematopoietic Stem Cell Transplantation. Rev. Bras. Hematol. Epub June 11, Year/Month, Html, Pdf, Epub, Total. , 0, 45, 0, April, 0, 40, 0, 40 . March, 1, 12, 0, February, 0, 4, 0, 4. January, 0, 1, 0, 1. Year/Month, Html, Pdf, Epub, Total. April, 0, 0, 0, 0. March, 0, 0, 0, 0. February, 0, 0, 0, 0. January, 0, 0, 0, 0. December, 0, 0, 0, 0.

Int J Hematol. Epub Jun 5. Clinical course of non-severe aplastic anemia in adults. The clinical course of non-severe aplastic anemia is variable, and risk factors related to disease progression are not well known. We reviewed clinical and laboratory data of the patients who were diagnosed with non-severe aplastic anemia from to at Seoul National University Hospital and analyzed the clinical course and outcomes in these patients.

Causes[ edit ] Aplastic anemia can be caused by exposure to certain chemicals, drugs, radiation, infection, immune disease; in about half the cases, a definitive cause is unknown. It is not a familial line hereditary condition, nor is it contagious.

It can be acquired due to exposure to other conditions but if a person develops the condition, their offspring would not develop it by virtue of their genetic relationship. Many drugs are associated with aplasia mainly according to case reports, but at a very low probability. As an example, chloramphenicol treatment associated with aplasia in less than one in 40, treatment courses, and carbamazepine aplasia is even rarer. Marie Curie , famous for her pioneering work in the field of radioactivity , died of aplastic anemia after working unprotected with radioactive materials for a long period of time; the damaging effects of ionizing radiation were not then known.

Bone marrow findings in systemic lupus erythematosus patients with peripheral cytopenias.

Clinical course of non-severe aplastic anemia in adults.

Clin Rheumatol. Arthritis Rheum. Clinical features of systemic lupus erythematosus. Philadelphia: Mosby Elsevier; Management of immune cytopenias in patients with systemic lupus erythematosus: old and new.

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Haematological presentation of systemic lupus erythematosus. J Assoc Physicians India. A case of systemic lupus erythematosus with aplastic anaemia.

Aplastic Anemia

J Pak Med Assoc. Levine AB, Erkan D. Clinical assessment and management of cytopenias in lupus patients.

Curr Rheumatol Rep. Hochberg MC. Updating the American College of Rheumatology revised criteria for the classification of systemic lupus erythematosus. Derivation and validation of the Systemic Lupus International Collaborating Clinics classification criteria of systemic lupus erythematosus. Young NS. Medicina interna de Harrison.

Two types of autoantibody-mediated thrombocytopenia in patients with systemic lupus erythematosus. Rheumatology Oxford.

Epub Jan The significance of thrombocytopenia in systemic lupus erythematosus. Thrombotic thrombocytopenic purpura in two patients with systemic lupus erythematosus: clinical significance of anti-platelet antibodies.

Aplastic anemia - Wikipedia

Clin Immunol Immunopathol. Paroxysmal nocturnal hemoglobinuria and the complement system: recent insights and novel anticomplement strategies.

Adv Exp Med Biol ; Sangre Barc ; Relation between the hemolytic system and cell variants in paroxysmal nocturnal hemoglobinuria. Paroxysmal nocturnal hemoglobinuria: current concepts and controversies.

Rev Clin Esp ; Nocturnal paroxysmal hemoglobinuria: analysis of 36 cases. Figure 1. Overall survival of the 31 patients with paroxymal nocturnal hemoglobinuria. Rev Biomed ; 1: Chromosomic findings in patients with paroxysmal nocturnal hemoglobinuria.

Int J Hematol ; Rev Invest Clin ; Clinical spectrum and prognostic factors in paroxysmal nocturnal hemoglobinuria in Mexico.

Revista da Faculdade de Ciências Médicas de Sorocaba

Rev Invest Clin ; 46 Supl. Natural history of paroxysmal nocturnal hemoglobinuria in adolescents, adults, and children: the Mexican experience.

Rev Biomed ; Flow cytometric analysis of glycosylphosphatidyl-inositol-anchored proteins to assess paroxysmal nocturnal hemoglobinuria clone size.

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