Gaucher disease (GD), the most common inherited lysosomal storage disorder, is a multiorgan disease due to an autosomal recessive defect of the gene encoding glucocerebrosidase enzyme. Our aim in this study is to spot light on the clinical and laboratory characteristics of children with Gaucher disease and to evaluate the outcome of enzyme replacement therapy in Iraq, As most of cases in the developing countries still under diagnosed.
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Gaucher disease (GD), the most common inherited lysosomal storage disorder, is a multiorgan disease due to an autosomal recessive defect of the gene encoding glucocerebrosidase enzyme. Our aim in this study is to spot light on the clinical and laboratory characteristics of children with Gaucher disease and to evaluate the outcome of enzyme replacement therapy in Iraq, As most of cases in the developing countries still under diagnosed.
Assistant Prof. Dr. Rabab Farhan graduated from collage of medicine/ Baghdad university 1983, Candidate of Arab board in Pediatrics 1993.Assistant Professor of Pediatric Gastroenterology and liver disease/ Medical collage/ University of Baghdad. Consultant Pediatric gastroenterology in Children Welfare Teaching Hospital, Medical city, Baghdad.
Les informations fournies dans la section « A propos du livre » peuvent faire référence à une autre édition de ce titre.
Vendeur : BuchWeltWeit Ludwig Meier e.K., Bergisch Gladbach, Allemagne
Taschenbuch. Etat : Neu. This item is printed on demand - it takes 3-4 days longer - Neuware -Gaucher disease (GD), the most common inherited lysosomal storage disorder, is a multiorgan disease due to an autosomal recessive defect of the gene encoding glucocerebrosidase enzyme. Our aim in this study is to spot light on the clinical and laboratory characteristics of children with Gaucher disease and to evaluate the outcome of enzyme replacement therapy in Iraq, As most of cases in the developing countries still under diagnosed. 64 pp. Englisch. N° de réf. du vendeur 9783330043398
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Vendeur : AHA-BUCH GmbH, Einbeck, Allemagne
Taschenbuch. Etat : Neu. nach der Bestellung gedruckt Neuware - Printed after ordering - Gaucher disease (GD), the most common inherited lysosomal storage disorder, is a multiorgan disease due to an autosomal recessive defect of the gene encoding glucocerebrosidase enzyme. Our aim in this study is to spot light on the clinical and laboratory characteristics of children with Gaucher disease and to evaluate the outcome of enzyme replacement therapy in Iraq, As most of cases in the developing countries still under diagnosed. N° de réf. du vendeur 9783330043398
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Vendeur : Revaluation Books, Exeter, Royaume-Uni
Paperback. Etat : Brand New. 64 pages. 8.66x5.91x0.15 inches. In Stock. N° de réf. du vendeur 3330043393
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Vendeur : moluna, Greven, Allemagne
Etat : New. Dieser Artikel ist ein Print on Demand Artikel und wird nach Ihrer Bestellung fuer Sie gedruckt. Autor/Autorin: Farhan RababAssistant Prof. Dr. Rabab Farhan graduated from collage of medicine/ Baghdad university 1983, Candidate of Arab board in Pediatrics 1993.Assistant Professor of Pediatric Gastroenterology and liver disease/ Medical collage. N° de réf. du vendeur 151234212
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Vendeur : buchversandmimpf2000, Emtmannsberg, BAYE, Allemagne
Taschenbuch. Etat : Neu. This item is printed on demand - Print on Demand Titel. Neuware -Gaucher disease (GD), the most common inherited lysosomal storage disorder, is a multiorgan disease due to an autosomal recessive defect of the gene encoding glucocerebrosidase enzyme. Our aim in this study is to spot light on the clinical and laboratory characteristics of children with Gaucher disease and to evaluate the outcome of enzyme replacement therapy in Iraq, As most of cases in the developing countries still under diagnosed.VDM Verlag, Dudweiler Landstraße 99, 66123 Saarbrücken 64 pp. Englisch. N° de réf. du vendeur 9783330043398
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