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 *

128 related articles for article (PubMed ID: 13289137)

  • 1. [New data on the identification and genetics of the constitutional hemoglobinopathies].
    VECCHIO F; DI FRANCESCO L
    Pediatria (Napoli); 1955; 63(4):603-14. PubMed ID: 13289137
    [No Abstract]   [Full Text] [Related]  

  • 2. [Hemolytic anemia caused by hereditary hemoglobin anomalies].
    GATTO I
    Acta Genet Med Gemellol (Roma); 1956 Sep; 5(3):327-61. PubMed ID: 13372174
    [No Abstract]   [Full Text] [Related]  

  • 3. [Association of hemoglobinosis and spherocytoanemia in a family with constitutional hemolytic anemia].
    GIGUENS WT; PACHECO-OLIVERA M; TEMESIO N; DRETS ME
    Arch Pediatr Urug; 1959 Aug; 30():477-86. PubMed ID: 13849966
    [No Abstract]   [Full Text] [Related]  

  • 4. Hereditary hemoglobinopathies.
    SACKS MS
    Ann Intern Med; 1954 Oct; 41(4):849-54. PubMed ID: 13198033
    [No Abstract]   [Full Text] [Related]  

  • 5. [Clinical aspects, diagnosis and treatment of hereditary hemolytic anemia caused by carrier state of unstable hemoglobin].
    Idel'son LI; Didkovskiĭ NA
    Ter Arkh; 1976; 48(8):120-7. PubMed ID: 1024290
    [No Abstract]   [Full Text] [Related]  

  • 6. Pulse oximetry and genetic hemoglobinopathies.
    Mariette S; Leteurtre S; Lambilliotte A; Leclerc F
    Intensive Care Med; 2005 Nov; 31(11):1597; author reply 1598. PubMed ID: 16132883
    [No Abstract]   [Full Text] [Related]  

  • 7. Chronic familial nonspherocytic hemolytic anemia.
    LIPTON EL; GROSSMAN HJ; RICHMOND JB
    Pediatrics; 1953 Oct; 12(4):384-94. PubMed ID: 13099909
    [No Abstract]   [Full Text] [Related]  

  • 8. Hemolytic anemia presumably due to coexistence of the genes for thalassemia and sickling.
    LAWRENCE JS; NEEL JV; ITANO HA
    Trans Assoc Am Physicians; 1952; 65():203-13. PubMed ID: 13005662
    [No Abstract]   [Full Text] [Related]  

  • 9. Chronic hemolytic anemia in a white child due to thalassemia and sicklemia; with a genealogic survey.
    WASSERMAN CF; PHELPS VR; HERTZOG AJ
    Pediatrics; 1952 Mar; 9(3):286-9. PubMed ID: 14911293
    [No Abstract]   [Full Text] [Related]  

  • 10. Postsplenectomy erythrocytosis in hemoglobin Köln disease.
    Egan EL; Fairbanks VF
    N Engl J Med; 1973 May; 288(18):929-31. PubMed ID: 4693245
    [No Abstract]   [Full Text] [Related]  

  • 11. Familial non-spherocytic haemolytic anemia.
    HOLLIDAY TD
    J Clin Pathol; 1953 Aug; 6(3):219-23. PubMed ID: 13084768
    [No Abstract]   [Full Text] [Related]  

  • 12. Hemoglobinopathies in childhood (a study of 51 cases).
    Giri DD; Patra SB; Patel RZ
    Indian J Pathol Microbiol; 1984 Apr; 27(2):81-9. PubMed ID: 6511037
    [No Abstract]   [Full Text] [Related]  

  • 13. [Hemolytic anemias in hemoglobinopathies].
    Marti HR
    Ther Umsch; 1968 Aug; 25(8):416-9. PubMed ID: 5729304
    [No Abstract]   [Full Text] [Related]  

  • 14. Familial haemolytic anaemia: concurrent crises in three members of a family.
    MOORHOUSE JA; MATHEWSON FA
    Can Med Assoc J; 1956 Jul; 75(2):133-5. PubMed ID: 13343068
    [No Abstract]   [Full Text] [Related]  

  • 15. [Genetics and pathology. II. Study of diseases at the molecular level].
    Lisker R
    Gac Med Mex; 1967 Dec; 97(12):1577-82. PubMed ID: 5611799
    [No Abstract]   [Full Text] [Related]  

  • 16. [Anomalous unstable hemoglobins, a special group of hereditary hemolytic anemias (survey of the literature and the authors' own data].
    Didkovskiĭ NA; Filippova AV; Idel'son LI
    Probl Gematol Pereliv Krovi; 1972 Nov; 17(11):38-46. PubMed ID: 4356586
    [No Abstract]   [Full Text] [Related]  

  • 17. Diseases of disordered hemoglobin degradation.
    Martelo OJ
    Adv Intern Med; 1975; 20():345-62. PubMed ID: 1090123
    [No Abstract]   [Full Text] [Related]  

  • 18. The life span of the elliptocyte; hereditary elliptocytosis and its relationship to other familial hemolytic diseases.
    MOTULSKY AG; SINGER K; CROSBY WH; SMITH V
    Blood; 1954 Jan; 9(1):57-72. PubMed ID: 13115472
    [No Abstract]   [Full Text] [Related]  

  • 19. Haemoglobin G St. José in an Italian family.
    Ricco G; Gallo E; Pich PG; Rossi G; Miniero R; Mazza U
    Acta Haematol; 1974; 52(3):180-8. PubMed ID: 4214182
    [No Abstract]   [Full Text] [Related]  

  • 20. Symposium: Hemoglobinopathies in Japan. 4. Molecular basis of the clinical signs in hemoglobin M disease.
    Hayashi A
    Nihon Ketsueki Gakkai Zasshi; 1968 Oct; 31(5):891-900. PubMed ID: 5753627
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 7.