Fast Facts: Pyruvate Kinase Deficiency
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ISBN 10: 3318072559 ISBN 13: 9783318072556
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Title: Fast Facts: Pyruvate Kinase Deficiency
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Fast Facts: Pyruvate Kinase Deficiency
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Fast Facts: Pyruvate Kinase Deficiency
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Fast Facts: Pyruvate Kinase Deficiency
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Taschenbuch. Condition: Neu. Fast Facts: Pyruvate Kinase Deficiency | Bertil Glader (u. a.) | Taschenbuch | Englisch | 2025 | Karger Verlag | EAN 9783318072556 | Verantwortliche Person für die EU: Karger Freiburg, Wilhelmstr. 20a, 79098 Freiburg, orders[at]karger[dot]com | Anbieter: preigu. Seller Inventory # 132569660
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Fast Facts: Pyruvate Kinase Deficiency
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Fast Facts: Pyruvate Kinase Deficiency
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Karger Verlag Apr 2025, 2025
ISBN 10: 3318072559
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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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Fast Facts: Pyruvate Kinase Deficiency
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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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Fast Facts: Pyruvate Kinase Deficiency
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Karger Verlag Apr 2025, 2025
ISBN 10: 3318072559
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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.Karger Verlag, Schnewlinstraße 12, 79098 Freiburg 118 pp. Englisch. Seller Inventory # 9783318072556
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Fast Facts: Pyruvate Kinase Deficiency
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Karger Verlag Apr 2025, 2025
ISBN 10: 3318072559
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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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Fast Facts: Pyruvate Kinase Deficiency
Published by
Karger Verlag Apr 2025, 2025
ISBN 10: 3318072559
ISBN 13: 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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