Literature DB >> 14200251

CHROMOSOME-21 AND PAROXYSMAL NOCTURNAL HEMOGLOBINURIA.

E BEUTLER, E W GOLDENBURG, S OHNO, M YETTRA.   

Abstract

Entities:  

Keywords:  ACETYLCHOLINESTERASE; ADOLESCENCE; BLOOD ALKALINE PHOSPHATASE; BUSULFAN; CHILD; CHROMOSOME ABNORMALITIES; ERYTHROCYTES; HEMOGLOBINURIA, PAROXYSMAL; LEUKOCYTES; MERCAPTOPURINE; PHARMACOLOGY

Mesh：

Substances：

Year:  1964        PMID： 14200251

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


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  5 in total

1.  [Acute erythremia].

Authors:  H Lutz; J van Zyl; G Hartwich
Journal:  Blut       Date:  1972-11

2.  Red cell enzymes in trisomy 21.

Authors:  S N Pantelakis; A G Karaklis; D Alexiou; E Vardas; T Valaes
Journal:  Am J Hum Genet       Date:  1970-03       Impact factor: 11.025

3.  A platelet and granulocyte membrane defect in paroxysmal nocturnal hemoglobinuria: usefulness for the detection of platelet antibodies.

Authors:  R H Aster; S E Enright
Journal:  J Clin Invest       Date:  1969-07       Impact factor: 14.808

4.  [On endocrine influence on alkaline leukocyte phosphatase].

Authors:  D Müller
Journal:  Blut       Date:  1967-02

5.  Paroxysmal nocturnal hemoglobinuria in an identical twin.

Authors:  H Freeman; J R Hill; A M Edwards; M W Wolowyk
Journal:  Can Med Assoc J       Date:  1973-11-17       Impact factor: 8.262
  5 in total

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