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Fast Facts: Pyruvate Kinase Deficiency - Softcover

 
9783318072556: Fast Facts: Pyruvate Kinase Deficiency
  • PublisherKarger Verlag
  • Publication date2025
  • ISBN 10 3318072559
  • ISBN 13 9783318072556
  • BindingPaperback
  • LanguageEnglish
  • Number of pages118

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Glader, Bertil; Barcellini, Wilma; Grace, Rachael
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Taschenbuch. Condition: Neu. Neuware - Pyruvate kinase (PK) deficiency is an inherited disease that affects red blood cells and manifests as hemolytic anemia. It is a lifelong condition, with symptoms that range from mild to severe. Despite an ever-growing understanding of its pathophysiology, etiology, and epidemiology, and an active research program, PK deficiency remains unfamiliar to many medical practitioners. PK deficiency is clinically heterogeneous, so healthcare professionals need to consider the possibility of this disorder in all patients with a congenital hemolytic anemia. Seller Inventory # 9783318072556

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Taschenbuch. Condition: Neu. Neuware -Pyruvate kinase (PK) deficiency is an inherited disease that affects red blood cells and manifests as hemolytic anemia. It is a lifelong condition, with symptoms that range from mild to severe. Despite an ever-growing understanding of its pathophysiology, etiology, and epidemiology, and an active research program, PK deficiency remains unfamiliar to many medical practitioners. PK deficiency is clinically heterogeneous, so healthcare professionals need to consider the possibility of this disorder in all patients with a congenital hemolytic anemia. Seller Inventory # 9783318072556

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Glader, Bertil (Author)/ Barcellini, Wilma (Author)/ Grace, Rachael (Author)
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Taschenbuch. Condition: Neu. Neuware -Pyruvate kinase (PK) deficiency is an inherited disease that affects red blood cells and manifests as hemolytic anemia. It is a lifelong condition, with symptoms that range from mild to severe. Despite an ever-growing understanding of its pathophysiology, etiology, and epidemiology, and an active research program, PK deficiency remains unfamiliar to many medical practitioners. PK deficiency is clinically heterogeneous, so healthcare professionals need to consider the possibility of this disorder in all patients with a congenital hemolytic anemia. 118 pp. Englisch. Seller Inventory # 9783318072556

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Taschenbuch. Condition: Neu. Neuware -Pyruvate kinase (PK) deficiency is an inherited disease that affects red blood cells and manifests as hemolytic anemia. It is a lifelong condition, with symptoms that range from mild to severe. Despite an ever-growing understanding of its pathophysiology, etiology, and epidemiology, and an active research program, PK deficiency remains unfamiliar to many medical practitioners. PK deficiency is clinically heterogeneous, so healthcare professionals need to consider the possibility of this disorder in all patients with a congenital hemolytic anemia. 118 pp. Englisch. Seller Inventory # 9783318072556

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