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 *

104 related articles for article (PubMed ID: 6377037)

  • 1. Hereditary nephritis, deafness and thrombocytopenia. Case report and review.
    Thomas HS; Bauer JH
    Mo Med; 1984 Jun; 81(6):305-7, 311. PubMed ID: 6377037
    [No Abstract]   [Full Text] [Related]  

  • 2. Hereditary macrothrombocytopenia, deafness, nephropathy.
    Catarini M
    Haematologica; 1988; 73(1):43-7. PubMed ID: 3131204
    [No Abstract]   [Full Text] [Related]  

  • 3. The case ∣ proteinuria and low platelet count.
    Piccoli GB; Vigotti FN; Balduini CL; Pecci A
    Kidney Int; 2012 May; 81(9):927-8. PubMed ID: 22499142
    [No Abstract]   [Full Text] [Related]  

  • 4. Fechtner syndrome: clinical and genetic aspects.
    Gershoni-Baruch R; Baruch Y; Viener A; Lichtig C
    Am J Med Genet; 1988 Oct; 31(2):357-67. PubMed ID: 3232700
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Hereditary nephritis with macrothrombocytopenia: phenotypic variety and the genotypic defect.
    Basile C; Schiavone P; Heidet L; Grünfeld JP
    J Nephrol; 2002; 15(3):320-3. PubMed ID: 12113606
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Hereditary nephritis and deafness. Report of a family.
    Shani M; Fine LG
    Isr J Med Sci; 1970; 6(4):544-8. PubMed ID: 5472337
    [No Abstract]   [Full Text] [Related]  

  • 7. [Hereditary nephritis with deafness in one family].
    Golev GD
    Klin Med (Mosk); 1989 Nov; 67(11):128-30. PubMed ID: 2625948
    [No Abstract]   [Full Text] [Related]  

  • 8. 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]  

  • 9. [Hereditary nephritis with hearing impairment].
    Stobaeus N
    Lakartidningen; 1973 Apr; 70(17):1773-4. PubMed ID: 4700526
    [No Abstract]   [Full Text] [Related]  

  • 10. [Clinical and molecular study on Fechtner syndrome--case report and literature review].
    Yang HY; Wang ZY; Su YH; Cao LJ; Bai X; Ruan CG
    Zhonghua Xue Ye Xue Za Zhi; 2007 Mar; 28(3):160-4. PubMed ID: 17649707
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Familial hereditary nephritis.
    Reiter JH
    Rocky Mt Med J; 1972 May; 69(5):72-4. PubMed ID: 5034952
    [No Abstract]   [Full Text] [Related]  

  • 12. Thrombocytopenia and proteinuria. Nonmuscle myosin heavy-chain-9-related disease ( MYH9 RD) or Epstein syndrome (ES).
    Bhatt A; Broxson E; Witte D; Omoloja A
    Pediatr Nephrol; 2009 Mar; 24(3):485-8. PubMed ID: 18781340
    [No Abstract]   [Full Text] [Related]  

  • 13. [Familial hereditary nephritis].
    Urbańczyk J
    Wiad Lek; 1969 Oct; 22(20):1881-4. PubMed ID: 5368500
    [No Abstract]   [Full Text] [Related]  

  • 14. Hereditary thrombocytopenia. Report of three families.
    Myllylä G; Pelkonen R; Ikkala E; Apajalahti J
    Scand J Haematol; 1967 Dec; 4(6):441-52. PubMed ID: 6082223
    [No Abstract]   [Full Text] [Related]  

  • 15. Association of familial nephritis without deafness and multiple sclerosis.
    Czeizel AE; Uri-Szabó K
    Clin Nephrol; 1994 Oct; 42(4):277-8. PubMed ID: 7834925
    [No Abstract]   [Full Text] [Related]  

  • 16. Hereditary nephritis.
    Barsoum RS; Milad M; Shaheen MH
    J Egypt Med Assoc; 1977; 60(7-8):567-9. PubMed ID: 752685
    [No Abstract]   [Full Text] [Related]  

  • 17. Autosomal dominant thrombocytopenia with microthrombocytes: a family study.
    Jackson N; Mohammad S; Zainal N; Jamaluddin N; Hishamuddin M
    Med J Malaysia; 1995 Dec; 50(4):421-4. PubMed ID: 8668069
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Hereditary macrothrombocytic thrombocytopenia. Description of a family carrying this anomaly].
    Patrone F; Armani U; Boy E; Boccaccio P
    Haematologica; 1972; 58(9):623-50. PubMed ID: 4206238
    [No Abstract]   [Full Text] [Related]  

  • 19. [Hereditary progressive sensorineural deafness--report of 30 cases in 12 families].
    Wang X
    Zhonghua Yi Xue Za Zhi; 1983 Nov; 63(11):694-8. PubMed ID: 6426737
    [No Abstract]   [Full Text] [Related]  

  • 20. Fechtner's syndrome.
    Velasco F; Espinosa M; Torres A
    Haematologica; 2000 Sep; 85(9):988. PubMed ID: 10980641
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 6.