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 *

69 related articles for article (PubMed ID: 4766778)

  • 1. [Congenital type 2 dyserythropoiesis. 2 familial cases revealed by neonatal hemolytic anemia].
    Bachelot C; Rambaud P; Déchelette E; Dieterlen M; Mouriquand C; Beaudoing A
    Pediatrie; 1973; 28(5):495-503. PubMed ID: 4766778
    [No Abstract]   [Full Text] [Related]  

  • 2. [Diagnosis and gene analysis of congenital hemolytic anemia].
    Ideguchi H
    Rinsho Byori; 2006 Jun; 54(6):593-600. PubMed ID: 16872009
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Congenital dyserythropoiesis with erythroblastic polyploidy. Report of a variety found in Argentinian Mesopotamia (author's transl)].
    Accame EA; de Tezanos Pinto M
    Sangre (Barc); 1981; 26(5-A):545-55. PubMed ID: 7323912
    [No Abstract]   [Full Text] [Related]  

  • 4. [A family of congenital dyserythropoietic anemia type II (HEMPAS)].
    Kuwabara T; Sakamoto F; Horikoshi H; Dan K; Kuriya S; Nomura T
    Rinsho Ketsueki; 1982 Dec; 23(12):1924-9. PubMed ID: 7166822
    [No Abstract]   [Full Text] [Related]  

  • 5. [Familial erythrocyte ATP: pyruvate phosphotransferase deficiency].
    Torliński L; Karoń H; Czech A; Michalewska D; Duczmal B
    Acta Haematol Pol; 1982; 13(3-4):157-63. PubMed ID: 7184297
    [No Abstract]   [Full Text] [Related]  

  • 6. [On a familial strain of hemoglobin H].
    De Luca S; Floris F
    Minerva Ginecol; 1968 Nov; 20(22):1795-6. PubMed ID: 5711251
    [No Abstract]   [Full Text] [Related]  

  • 7. [Hereditary hemolytic anemias].
    Busch D
    Med Klin; 1970 Mar; 65(10):432-6. PubMed ID: 5419577
    [No Abstract]   [Full Text] [Related]  

  • 8. [Case of congenital ovalocytic hemolytic anemia].
    Dygin VP; Siubaeva NI
    Probl Gematol Pereliv Krovi; 1970 Mar; 15(3):58-9. PubMed ID: 5449829
    [No Abstract]   [Full Text] [Related]  

  • 9. [Anemia caused by congenital dyserythropoiesis: type II (Hempas). Value of splenectomy].
    Sondag D; Weill JP; Oberling F
    Nouv Presse Med; 1982 Jul 10-17; 11(32):2419. PubMed ID: 7111012
    [No Abstract]   [Full Text] [Related]  

  • 10. [Report on a family with congenital hemolytic anemia with an unusual spleen condition].
    Bombara R; Cassi E; Visca U
    Haematologica; 1968; 53(11):885-90. PubMed ID: 4977186
    [No Abstract]   [Full Text] [Related]  

  • 11. [Metabolic studies in a family with 3 cases of congenital non-spherocytic hemolytic anemia with a pyruvate kinase deficiency].
    Busch D
    Folia Haematol (Frankf); 1964; 9(3):375-83. PubMed ID: 5888811
    [No Abstract]   [Full Text] [Related]  

  • 12. [Efficacy of splenectomy in 2 cases of hemolytic anemia caused by pyruvate kinase deficiency].
    Savanelli A; Di Maio S; Cigliano B; Di Martino L; Albini F; Dente L
    Pediatria (Napoli); 1983; 91(4):419-27. PubMed ID: 6545405
    [No Abstract]   [Full Text] [Related]  

  • 13. [Minkowski-Chauffard disease. Apropos of a triple familial case].
    Giard P; Routier G; Lamoril JL
    J Sci Med Lille; 1969 Dec; 87(12):735-43. PubMed ID: 5403370
    [No Abstract]   [Full Text] [Related]  

  • 14. [A case of familial pyruvate kinase deficiency associated with acute myelomonocytic leukemia].
    Ohta C; Katayama N; Uno N; Minami N; Karitani Y; Shirakawa S
    Rinsho Ketsueki; 1984 Jan; 25(1):75-81. PubMed ID: 6589417
    [No Abstract]   [Full Text] [Related]  

  • 15. [Two cases of pyruvate kinase variants (author's transl)].
    Takeda A; Ito T; Mori H; Suzuki H; Ninomiya N; Miyako M; Fujii H; Miwa S
    Rinsho Ketsueki; 1982 Feb; 23(2):206-14. PubMed ID: 7098012
    [No Abstract]   [Full Text] [Related]  

  • 16. VPS4A mutation in syndromic congenital hemolytic anemia without obvious signs of dyserythropoiesis.
    Lunati A; Petit A; Lapillonne H; Gameiro C; Saillour V; Garel C; Doummar D; Qebibo L; Aissat A; Fanen P; Bartolucci P; Galactéros F; Funalot B; Burglen L; Mansour-Hendili L
    Am J Hematol; 2021 Apr; 96(4):E121-E123. PubMed ID: 33460484
    [No Abstract]   [Full Text] [Related]  

  • 17. [Minkowski-Chauffard disease in 1 family].
    Atanasov K; Tashev V; Vakrilov V
    Vutr Boles; 1984; 23(6):106-8. PubMed ID: 6531863
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Haemolytic anaemia due to hereditary defect of erythrocyte pyruvate kinase. Clinical, familial, and biological study of ten cases (author's transl)].
    Vives-Corrons JL; Pujades MA; Aguilar JL; Feliú E; Jou JM
    Sangre (Barc); 1980; 25(1):51-62. PubMed ID: 7384966
    [No Abstract]   [Full Text] [Related]  

  • 19. Hereditary hemolytic disorders.
    Jaffé ER
    Bull N Y Acad Med; 1970 Jun; 46(6):397-410. PubMed ID: 5267233
    [No Abstract]   [Full Text] [Related]  

  • 20. Hereditary pyropoikilocytosis: report of two cases from Saudi Arabia.
    Mallouh A; Sa'di AR; Ahmad MS; Salamah M
    Am J Med Genet; 1984 Jul; 18(3):413-7. PubMed ID: 6476002
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 4.