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Ajouter au panierPAP. Etat : New. New Book. Shipped from UK. Established seller since 2000.
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Ajouter au panierPAP. Etat : New. New Book. Shipped from UK. Established seller since 2000.
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Ajouter au panierTaschenbuch. Etat : 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.
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Ajouter au panierTaschenbuch. Etat : 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.
Vendeur : BuchWeltWeit Ludwig Meier e.K., Bergisch Gladbach, Allemagne
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Ajouter au panierTaschenbuch. Etat : 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.
Edité par S. Karger Publishers Ltd, 2018
ISBN 10 : 191079788X ISBN 13 : 9781910797884
Langue: anglais
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Ajouter au panierEtat : New. This is a Brand-new US Edition. This Item may be shipped from US or any other country as we have multiple locations worldwide.
Vendeur : Rheinberg-Buch Andreas Meier eK, Bergisch Gladbach, Allemagne
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Ajouter au panierTaschenbuch. Etat : 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.
Edité par S. Karger Publishers Ltd, 2018
ISBN 10 : 191079788X ISBN 13 : 9781910797884
Langue: anglais
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Ajouter au panierEtat : Used. pp. 64.
Edité par S. Karger Publishers Ltd, 2018
ISBN 10 : 191079788X ISBN 13 : 9781910797884
Langue: anglais
Vendeur : Biblios, Frankfurt am main, HESSE, Allemagne
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Ajouter au panierEtat : Used. pp. 64.
Edité par S. Karger Publishers Ltd, 2018
ISBN 10 : 191079788X ISBN 13 : 9781910797884
Langue: anglais
Vendeur : Majestic Books, Hounslow, Royaume-Uni
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Ajouter au panierPaperback. Etat : Brand New. 118 pages. 5.71x0.43x8.03 inches. In Stock.
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