Literature DB >> 5923604

Hemoglobin H disease. A family study.

T F Necheles, M Cates, R G Sheehan, H J Meyer.   

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Year:  1966        PMID： 5923604

Source DB:  PubMed          Journal:  Blood        ISSN： 0006-4971            Impact factor:   22.113


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  6 in total

1.  An unusual hemoglobin anomaly and its relation to alpha-thalassemia and hemoglobin-H disease.

Authors:  G D Efremov; R N Wrightstone; T H Huisman; W A Schroeder; C Hyman; J Ortega; K Williams
Journal:  J Clin Invest       Date:  1971-08       Impact factor: 14.808

2.  Alpha thalassemia: five cases of hemoglobin H disease in three Oriental-Canadian families.

Authors:  R Y Ing; J H Crookston
Journal:  Can Med Assoc J       Date:  1968-07-13       Impact factor: 8.262

3.  [Alpha-thalassemia with HbH and Hb Bart's in a German family].

Authors:  P Rönisch; E Kleihauer
Journal:  Klin Wochenschr       Date:  1967-12-01

4.  Hematologic improvement following splenectomy for hemoglobin-H disease.

Authors:  G M Wagner; S A Liebhaber; H O Cutting; S H Embury
Journal:  West J Med       Date:  1982-10

5.  Globin chain synthesis in the alpha thalassemia syndromes.

Authors:  Y W Kan; E Schwartz; D G Nathan
Journal:  J Clin Invest       Date:  1969-11       Impact factor: 14.808

6.  Thalassemia and G-6-PD deficiency in Chinese-Canadians: admission screening of a hospital population.

Authors:  G R Gray; R B Marion
Journal:  Can Med Assoc J       Date:  1971-08-07       Impact factor: 8.262
  6 in total

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