Literature DB >> 14072052

ELUTION PROCEDURE FOR THE DEMONSTRATION OF METHAEMOGLOBIN IN RED CELLS OF HUMAN BLOOD SMEARS.

E KLEIHAUER, K BETKE.   

Abstract

Entities:  

Keywords:  ERYTHROCYTES; METHEMOGLOBIN; STAINS AND STAINING

Mesh：

Substances：

Year:  1963        PMID： 14072052     DOI： 10.1038/1991196b0

Source DB:  PubMed          Journal:  Nature        ISSN： 0028-0836            Impact factor:   49.962


× No keyword cloud information.
  13 in total

1.  HEREDITARY METHEMOGLOBINEMIC CYANOSIS IN A MAN WITH ATRIAL SEPTAL DEFECT.

Authors:  J C SPEARS; J L NAIMAN; J R EVANS; J H CROOKSTON
Journal:  Can Med Assoc J       Date:  1965-02-27       Impact factor: 8.262

2.  [CONGENITAL NONSPHEROCYTIC HEMOLYTIC ANEMIA IN FAMILIAL DPNH AND TPNH-DEPENDENT GLUTATHIONE REDUCTASE DEFICIENCY OF THE ERYTHROCYTES. I].

Authors:  G BRITTINGER; G LOEFFLER; E KOENIG
Journal:  Klin Wochenschr       Date:  1965-04-15

3.  Hemoglobinopathies are on the increase.

Authors:  Andreas E Kulozik
Journal:  Dtsch Arztebl Int       Date:  2010-02-05       Impact factor: 5.594

4.  [Congenital nonspherocytic hemolytic anemias caused by glucose-6-phosphate dehydrogenase deficiency of the erythrocytes in a Japanese family].

Authors:  T Abe; H Takafuji; M Yamamoto; S Daimon; K Nakajima
Journal:  Blut       Date:  1968-06

5.  59Fe study of red blood cells life span in glucose-6-phosphate dehydrogenase deficiency heterozygote.

Authors:  A Pawlak
Journal:  Humangenetik       Date:  1968

6.  [On 2 new cases of hereditary nonspherocytic hemolytic anemia associated with glucose-6-phosphate-dehydrogenase deficiency in a North-German family. I].

Authors:  J Weinreich; D Busch; U Gottstein; J Schaefer; J Rohr
Journal:  Klin Wochenschr       Date:  1968-02-01

7.  [Glutathione reduction in erythrocytes of healthy persons and enzyme defect carriers. Use of the azoester test by Kosower et al. in glucose-6-P-dehydrogenase and glutathione reductase deficiency].

Authors:  H D Waller; H C Benöhr; B Heuer; O Nerke
Journal:  Klin Wochenschr       Date:  1970-01-15

8.  [Glucose-6-phosphate dehydrogenase deficiency of erythrocytes in 3 German children. Determination of a new mutation].

Authors:  V Weidtman; O Tönz
Journal:  Klin Wochenschr       Date:  1966-04-15

9.  [On the cellular distribution of catalase in the blood of homozygous and heterozygous defect-carriers (acatalasia)].

Authors:  H Aebi; M Cantz
Journal:  Humangenetik       Date:  1966

Review 10.  Diagnosis of red blood cell enzymopathies in infants, children and adolescents.

Authors:  S P Samuel; T D Miale
Journal:  Indian J Pediatr       Date:  1987 May-Jun       Impact factor: 1.967
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.