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 *

175 related articles for article (PubMed ID: 5011389)

  • 1. Hereditary macrothrombocytopathia, nephritis and deafness.
    Epstein CJ; Sahud MA; Piel CF; Goodman JR; Bernfield MR; Kushner JH; Ablin AR
    Am J Med; 1972 Mar; 52(3):299-310. PubMed ID: 5011389
    [No Abstract]   [Full Text] [Related]  

  • 2. Thrombocytopenia, macrothrombocytopathia, nephritis and deafness.
    Bernheim J; Dechavanne M; Bryon PA; Lagarde M; Colon S; Pozet N; Traeger J
    Am J Med; 1976 Jul; 61(1):145-50. PubMed ID: 945691
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [A new family displaying ophthalmic changes overlapping Epstein's triad (macrothrombocytopathia, nephritis and deafness) (author's transl)].
    Kuroda M; Kametani T; Morise T; Kita T; Sakato S; Miyazaki R; Tofuku Y; Takeda R
    Nihon Naika Gakkai Zasshi; 1982 Apr; 71(4):485-96. PubMed ID: 7202033
    [No Abstract]   [Full Text] [Related]  

  • 4. Hereditary macrothrombocytopathia, deafness and nephritis (Epstein's triad).
    Ozşahinoğlu C; Kümi M; Kilinç Y; Mete R
    Int J Pediatr Otorhinolaryngol; 1985 Aug; 9(3):257-61. PubMed ID: 4055260
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Hereditary nephritis with deafness.
    Hobday JD; Jones GD
    Med J Aust; 1969 Dec; 2(23):1140-3. PubMed ID: 5374052
    [No Abstract]   [Full Text] [Related]  

  • 6. A familial defect in platelet function associated with impaired release of adenosine diphosphate.
    Weiss HJ; Chervenick PA; Zalusky R; Factor A
    N Engl J Med; 1969 Dec; 281(23):1264-70. PubMed ID: 5349805
    [No Abstract]   [Full Text] [Related]  

  • 7. Bisalbuminaemia and defective platelets.
    Clancy R; Firkin B
    Aust N Z J Med; 1974 Apr; 4(2):182-6. PubMed ID: 4528448
    [No Abstract]   [Full Text] [Related]  

  • 8. Bleeding tendency with platelet dysfunction and albinism. A case report.
    Murakami M; Odake K; Matsuda T; Manmi S; Takase M
    Thromb Diath Haemorrh; 1972 Jul; 27(3):461-71. PubMed ID: 4662611
    [No Abstract]   [Full Text] [Related]  

  • 9. Hereditary thrombocytopathic thrombocytopenia. Observations on platelet function, size, lipid composition, metabolism and membrane function.
    Haanen C; Wessels H; Baadenhuysen H
    Nouv Rev Fr Hematol; 1973; 13(4):580-95. PubMed ID: 4271108
    [No Abstract]   [Full Text] [Related]  

  • 10. Hereditary nephritis with a characteristic renal lesion.
    Sherman RL; Churg J; Yudis M
    Am J Med; 1974 Jan; 56(1):44-51. PubMed ID: 4129269
    [No Abstract]   [Full Text] [Related]  

  • 11. Hereditary thrombocytopenia, deafness, and renal disease.
    Eckstein JD; Filip DJ; Watts JC
    Ann Intern Med; 1975 May; 82(5):639-45. PubMed ID: 1137259
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Gray platelet syndrome. A variety of qualitative platelet disorder.
    Raccuglia G
    Am J Med; 1971 Dec; 51(6):818-28. PubMed ID: 5129551
    [No Abstract]   [Full Text] [Related]  

  • 13. Essential athrombia: a family study.
    Goldman BA; Aledort LA
    Ann Intern Med; 1972 Feb; 76(2):269-73. PubMed ID: 5009593
    [No Abstract]   [Full Text] [Related]  

  • 14. Familial thrombopathic thrombocytopenia.
    Kurstjens R; Bolt C; Vossen M; Haanen C
    Br J Haematol; 1968 Sep; 15(3):305-17. PubMed ID: 5681484
    [No Abstract]   [Full Text] [Related]  

  • 15. Hereditary nephritis, deafness and abnormal thrombopoiesis. Study of a new kindred.
    Parsa KP; Lee DB; Zamboni L; Glassock RJ
    Am J Med; 1976 May; 60(5):665-72. PubMed ID: 1020755
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Platelet functional abnormalities: a report of two familial defects in interaction between collagen and platelets and ADP release.
    Papayannis AG; Watson-Williams EJ; Israëls MC
    Blood; 1971 Dec; 38(6):745-58. PubMed ID: 5126163
    [No Abstract]   [Full Text] [Related]  

  • 17. "Impotent" platelets in albinos with prolonged bleeding times.
    Maurer HM; Wolff JA; Buckingham S; Spielvogel AR
    Blood; 1972 Apr; 39(4):490-9. PubMed ID: 5011977
    [No Abstract]   [Full Text] [Related]  

  • 18. Hereditary thrombocytopathy: a familial bleeding disorder due to impaired platelet coagulant activity.
    Ardlie NG; Coupland WW; Schoefl GI
    Aust N Z J Med; 1976 Feb; 6(1):37-45. PubMed ID: 1065298
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Clinically mild thrombasthenia with normal platelet coagulant activities.
    Walsh PN; Rizza CR; McLennan R
    Thromb Diath Haemorrh; 1972 Dec; 28(3):440-6. PubMed ID: 4649278
    [No Abstract]   [Full Text] [Related]  

  • 20. Platelet-function studies in the Bernard-Soulier syndrome.
    Bithell TC; Parekh SJ; Strong RR
    Ann N Y Acad Sci; 1972 Oct; 201():145-60. PubMed ID: 4509679
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 9.