Literature DB >> 5686316

The Pelger-Huët anomaly of leukocytes: description of a Quebec kindred.

E Rioux, G St-Arneault, C Brosseau.   

Abstract

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Year:  1968        PMID： 5686316      PMCID： PMC1945286     

Source DB:  PubMed          Journal:  Can Med Assoc J        ISSN： 0008-4409            Impact factor:   8.262


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  16 in total

1.  The Pelger-Huët anomaly in three families and its use in determining the disappearance of transfused neutrophils from the peripheral blood.

Authors:  W F ROSSE; C W GURNEY
Journal:  Blood       Date:  1959-02       Impact factor: 22.113

2.  [Human homozygote Pelger-Huët anomaly].

Authors:  A G CIPLEA
Journal:  Presse Med       Date:  1958-03-26       Impact factor: 1.228

3.  The Pelger-Huët anomaly: investigation of family A.

Authors:  W M DAVIDSON; S D LAWLER; A G ACKERLEY
Journal:  Ann Hum Genet       Date:  1954-07       Impact factor: 1.670

4.  [Association of Pelger's nuclear abnormality with blood dyscrasias].

Authors:  A ALDER; F SCHAUB
Journal:  Dtsch Med Wochenschr       Date:  1952-10-17       Impact factor: 0.628

5.  [The question of constitutional granulation anomalies of leukocytes in their relation to endochondral dysostosis].

Authors:  O ULLRICH; H R WIEDEMANN
Journal:  Klin Wochenschr       Date:  1953-02-01

6.  Homozygous form of Pelger-Huët's nuclear anomaly in man.

Authors:  N HAVERKAMP BEGEMANN; A VAN LOOKEREN CAMPAGNE
Journal:  Acta Haematol       Date:  1952-05       Impact factor: 2.195

7.  Reversible pseudo-Pelger anomaly related to sulfisoxazole therapy.

Authors:  J M Kaplan; O Barrett
Journal:  N Engl J Med       Date:  1967-08-24       Impact factor: 91.245

8.  Pelger-Huët anomaly of the granulocytes in a Cape colored family.

Authors:  P Lanzkowsky; P Colussi; D McKenzie
Journal:  J Pediatr       Date:  1965-11       Impact factor: 4.406

9.  [Findings in homozygous carriers of Pelger's anomaly].

Authors:  H Stobbe; D Jorke
Journal:  Schweiz Med Wochenschr       Date:  1965-10-30

10.  [Genetic, cytochemical, cytoenzymatic and molecular biochemical investigations in the Pelger-Huet anomaly].

Authors:  N Gingold; D Nicolae; A Caratzali; D Micu; E Mihăilescu; S Maximilian; P Teitel; V Bratu; I Marcu; A Xenachis
Journal:  Stud Cercet Med Interna       Date:  1965
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  1 in total

1.  Severe generalized muscular atrophia, nerve optic atrophia, ear problem and disability with Pelger-Huet anomaly.

Authors:  Hassan Mahmoodi Nesheli; Naimeh Nakhjavani; Tahere Galini Moghaddam
Journal:  Caspian J Intern Med       Date:  2011
  1 in total

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