These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

117 related articles for article (PubMed ID: 835044)

  • 1. [Pelger-huët anomaly. A study of thirteen families (author's transl)].
    Aznar J; Fernandez MA; Vaya A
    Sangre (Barc); 1977; 22(1):23-9. PubMed ID: 835044
    [No Abstract]   [Full Text] [Related]  

  • 2. [The Pelger-Huët leukocyte nuclear anomaly: a morphologic, cytochemical, cytogenetic and ultrastructural study of 39 cases (authors' transl)].
    Milanesi B
    Quad Sclavo Diagn; 1980 Dec; 15(4):1097-115. PubMed ID: 7454963
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Prevalence of Pelger-Huët anomaly of leucocytes in Adivasi population of western Madhya Pradesh.
    Gehlot GS; Monga JN
    Indian J Med Res; 1973 May; 61(5):653-62. PubMed ID: 4763945
    [No Abstract]   [Full Text] [Related]  

  • 4. [Pelger-Hüet's congenital anomaly: morphologic and functional study on 140 cases in Abruzzo (author's transl)].
    Riario Sforza G; Salvati F; Troia C
    Haematologica; 1981 Feb; 66(1):46-56. PubMed ID: 6785167
    [No Abstract]   [Full Text] [Related]  

  • 5. [Genetic and hematologic study of a family presenting the Pelger-Huet anomaly associated, in one case, with epilepsy and, in another case, with polythelia].
    Boreux G; Bourquin P; Bourquin L
    J Genet Hum; 1968 Jan; 16(3):57-70. PubMed ID: 5710713
    [No Abstract]   [Full Text] [Related]  

  • 6. Pelger-Huet anomaly in Chinese family in Singapore.
    Boon WH
    J Singapore Paediatr Soc; 1978; 20(3):148-53. PubMed ID: 750755
    [No Abstract]   [Full Text] [Related]  

  • 7. [Pelger-Huët anomaly. Cases in a Mexican family].
    Muñoz-Quiles I; Saldaña-García EA
    Bol Med Hosp Infant Mex; 1987 Jan; 44(1):21-5. PubMed ID: 3814331
    [No Abstract]   [Full Text] [Related]  

  • 8. [Pelger-Huët nuclear anomaly in childhood and its genetic relations].
    Kálmán E; Bors J; Osztovics M
    Acta Paediatr Acad Sci Hung; 1969; 10(1):65-72. PubMed ID: 5793290
    [No Abstract]   [Full Text] [Related]  

  • 9. [Pelger-Huet anomaly observed in a Warsaw family].
    Wrõblewska-Cieliszak K
    Pediatr Pol; 1971 Sep; 46(9):1157-61. PubMed ID: 5122481
    [No Abstract]   [Full Text] [Related]  

  • 10. [Case of Pelger-Huet anomaly in its exceptional homozygotic variant].
    Ciatto A; Ferretti GF
    Minerva Med; 1978 Mar; 69(11):697-700. PubMed ID: 643213
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Biologic study of a case of Pelger-Huet anomaly and another of Chediak-Higashi disease].
    Salazar-Mallén M; Mitrani-Levy D; Amezcua E
    Gac Med Mex; 1969 Sep; 99(9):828-35. PubMed ID: 5345021
    [No Abstract]   [Full Text] [Related]  

  • 12. [The occurrence of Pelger-Huet anomaly in Slovakia].
    Kallo J
    Bratisl Lek Listy; 1985 Nov; 84(5):606-13. PubMed ID: 4063864
    [No Abstract]   [Full Text] [Related]  

  • 13. Tuberculosis and Pelger-Huët anomaly. Case report.
    Cicchitto G; Parravicini M; De Lorenzo S; Di Pisa G; Malacrida A
    Panminerva Med; 1999 Dec; 41(4):367-9. PubMed ID: 10705722
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [The most extensive pedigree of Pelger-Huët anomaly so far was found recently in Czechoslovakia].
    Kallo J
    Schweiz Rundsch Med Prax; 1986 Jul; 75(28):853-6. PubMed ID: 3738331
    [No Abstract]   [Full Text] [Related]  

  • 15. [Pelger-Huet familial anomaly of nuclei in 2 siblings].
    Stoińska-Zimpel G
    Pediatr Pol; 1967 Jul; 42(7):841-5. PubMed ID: 6052293
    [No Abstract]   [Full Text] [Related]  

  • 16. [The Pelger-Huet granulocytic anomaly: first report of 2 homozygous subjects in the same family].
    Riario-Sforza G; Salvati F; Troya C
    Arch Sci Med (Torino); 1981; 138(4):511-5. PubMed ID: 7340736
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Nuclear abnormalities in Pelger-Huet anomaly; progress in blood cell morphology].
    Tomonaga M
    Rinsho Byori; 2005 Jan; 53(1):54-60. PubMed ID: 15724491
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Studies on four hereditary blood disorders in Iceland.
    Jensson O
    Acta Med Scand Suppl; 1978; 618():1-28. PubMed ID: 308294
    [No Abstract]   [Full Text] [Related]  

  • 19. Pelger-Huët anomaly in a child with 1q42.3-44 deletion.
    Kalfa TA; Zimmerman SA; Goodman BK; McDonald MT; Ware RE
    Pediatr Blood Cancer; 2006 May; 46(5):645-8. PubMed ID: 16007606
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Occurrence of Pelger-Huet familial nuclear anomaly].
    Schmidt P; Petr B; Madĕrová H; Korínková A
    Cas Lek Cesk; 1967 Sep; 106(40):1058-60. PubMed ID: 6062299
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 6.