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Hemoglobin S polymerization: primary determinant of the hemolytic and clinical severity of the sickling syndromes

Author
BRITTENHAM, G. M1 ; SCHECHTER, A. N; NOGUCHI, C. T
[1] Case westernm res. univ., school medicine, Cleveland OH 44109, United States
Source

Blood. 1985, Vol 65, Num 1, pp 183-189 ; ref : 55 ref

ISSN
0006-4971
Scientific domain
Medical oncology; Hematology
Publisher
The Americain Society of Hematology, Washington, DC
Publication country
United States
Document type
Article
Language
English
Keyword (fr)
Anémie hématie falciforme Etiopathogénie Hémoglobine S Hémolyse Hémopathie Polymérisation
Keyword (en)
Sickle cell anemia Etiopathogenesis Hemoglobin S Hemolysis Hemopathy Polymerization
Keyword (es)
Anemia hematies falciformes Etiopatogenia
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
9159075

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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