Literature DB >> 13509426

[Congenital cardiac defect with cyanosis caused by pathological blood pigment (hemoglobin M)].

W HECK, H WOLF.   

Abstract

Entities:  

Keywords:  METHEMOGLOBINEMIA/case reports

Mesh：

Substances：

Year:  1958        PMID： 13509426

Source DB:  PubMed          Journal:  Ann Paediatr        ISSN： 0365-4966


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  7 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.  A critical review of human haemoglobin variants. II. Individual haemoglobins.

Authors:  G H BEAVEN; W B GRATZER
Journal:  J Clin Pathol       Date:  1959-03       Impact factor: 3.411

3.  [Hemoglobin anomalies].

Authors:  K BETKE
Journal:  Blut       Date:  1961

4.  A human hemoglobin with lowered oxygen affinity and impaired heme-heme interactions.

Authors:  K R REISSMANN; W E RUTH; T NOMURA
Journal:  J Clin Invest       Date:  1961-10       Impact factor: 14.808

5.  [Occureence and heterogeneity of abnormal haemoglobins and thalassemia syndromes in the German population (author's transl)].

Authors:  E Kohne; E Kleihauer
Journal:  Klin Wochenschr       Date:  1974-11-01

6.  [Hemoglobin Köln disease: familial hypochromic hemolytic anemia with hemoglobin anomaly].

Authors:  W Pribilla; P Klesse; K Betke; H Lehmann; D Beale
Journal:  Klin Wochenschr       Date:  1965-10-01

7.  [HbM Hamburg, a beta chain anomaly: alpha-2-beta-2-63Tyr (equals HbM Saskatoon)].

Authors:  K Betke; E Kleihauer; R Gehring-Müller; G Braunitzer; J Jacobi; I Schmidt
Journal:  Klin Wochenschr       Date:  1966-08-15
  7 in total

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