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Congenital 6-phosphogluconate dehydrogenase (6PGD) deficiency associated with chronic hemolytic anemia in a Spanish family

Author
VIVES CORRONS, J. L1 ; COLOMER, D1 ; PUJADES, A1 ; ROVIRA, A1 ; AYMERICH, M1 ; MERINO, A1 ; AGUILAR I BASCOMPTE, J. L1
[1] Haematology Laboratory Department, Postgraduates School of Hematology Farreras Valenti, Hospital Clinic i Provincial, University of Barcelona, Barcelona, Spain
Source

American journal of hematology. 1996, Vol 53, Num 4, pp 221-227 ; ref : 34 ref

CODEN
AJHEDD
ISSN
0361-8609
Scientific domain
Hematology
Publisher
Wiley-Liss, New York, NY
Publication country
United States
Document type
Article
Language
English
Keyword (fr)
Anémie hémolytique Déficit Etiologie Etude familiale Glucose-6-phosphate 1-dehydrogenase Homme Espagne Enzyme Enzymopathie Hémopathie Maladie héréditaire Métabolisme pathologie Oxidoreductases Europe
Keyword (en)
Hemolytic anemia Deficiency Etiology Family study Glucose-6-phosphate 1-dehydrogenase Human Spain Enzyme Enzymopathy Hemopathy Genetic disease Metabolic diseases Oxidoreductases Europe
Keyword (es)
Anemia hemolítica Déficiencia Etiología Estudio familiar Glucose-6-phosphate 1-dehydrogenase Hombre España Enzima Enzimopatía Hemopatía Enfermedad hereditaria Metabolismo patología Oxidoreductases Europa
Classification
Pascal
002 Biological and medical sciences / 002B Medical sciences / 002B19 Hematologic and hematopoietic diseases / 002B19A Diseases of red blood cells / 002B19A01 Anemias. Hemoglobinopathies

Discipline
Blood diseases
Origin
Inist-CNRS
Database
PASCAL
INIST identifier
2504437

Sauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS / Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS / A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRS

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