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 *

95 related articles for article (PubMed ID: 8043458)

  • 1. Fechtner syndrome variant: a new family with mild Alport's manifestations.
    Pujol-Moix N; Muñiz-Diaz E; Hernandez A; Romero MA; Puig J
    Br J Haematol; 1994 Mar; 86(3):686-7. PubMed ID: 8043458
    [No Abstract]   [Full Text] [Related]  

  • 2. Sebastian platelet syndrome: a new variant of hereditary macrothrombocytopenia with leukocyte inclusions.
    Greinacher A; Nieuwenhuis HK; White JG
    Blut; 1990 Nov; 61(5):282-8. PubMed ID: 2176899
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Fechtner syndrome. A rare differential Alport syndrome diagnosis].
    Delb W; Schenk J; Iro H
    HNO; 2000 Aug; 48(8):616-20. PubMed ID: 10994174
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [The Sebastian platelet syndrome. A new form of hereditary thrombocytopenia with giant thrombocytes and inclusion bodies in granulocytes].
    Greinacher A; Nieuwenhuis HK; White JG
    Beitr Infusionsther; 1990; 26():383-5. PubMed ID: 1703879
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Fechtner syndrome--a variant of Alport's syndrome with leukocyte inclusions and macrothrombocytopenia.
    Peterson LC; Rao KV; Crosson JT; White JG
    Blood; 1985 Feb; 65(2):397-406. PubMed ID: 2981587
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The first Japanese family with Sebastian platelet syndrome.
    Tsurusawa M; Kawakami N; Sawada K; Kunishima S; Agata H; Fujimoto T
    Int J Hematol; 1999 Apr; 69(3):206-10. PubMed ID: 10222662
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A variant of the Sebastian platelet syndrome with unique neutrophil inclusions.
    White JG; Mattson JC; Nichols WL; Luban NL; Greinacher A
    Platelets; 2002 Mar; 13(2):121-7. PubMed ID: 11897048
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Fechtner syndrome, a nonmuscle myosin heavy chain 9 gene mutation related disease: a case report and literature review].
    Hu R; Hao JH; Yang HL; Zhu Y; Li SY; Zhao J; Lin FR; Niu ZY
    Zhonghua Xue Ye Xue Za Zhi; 2011 Feb; 32(2):103-6. PubMed ID: 21429376
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Fechtner syndrome: report of two families and review of the literature on the related disorders].
    Takai K; Sanada M; Hattori A; Koike T; Shibata A
    Nihon Ketsueki Gakkai Zasshi; 1989 May; 52(3):644-54. PubMed ID: 2559568
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Pathologic quiz case: twin neonates with thrombocytopenia. May-Hegglin anomaly.
    Scurlock D; Nguyen A; Wahed A
    Arch Pathol Lab Med; 2005 Apr; 129(4):e111-2. PubMed ID: 15794695
    [No Abstract]   [Full Text] [Related]  

  • 11. [Clinical features and MYH9 gene variant in two Chinese siblings with Fechtner syndrome].
    Zhao SL; Zhao F; Zhang AH; Huang SM
    Zhonghua Er Ke Za Zhi; 2019 Apr; 57(4):286-290. PubMed ID: 30934202
    [No Abstract]   [Full Text] [Related]  

  • 12. Fechtner syndrome: report of a third family and literature review.
    Rocca B; Laghi F; Zini G; Maggiano N; Landolfi R
    Br J Haematol; 1993 Oct; 85(2):423-6. PubMed ID: 8280620
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Perioperative management of a patient with Fechtner syndrome.
    Matzdorff AC; White JG; Malzahn K; Greinacher A
    Ann Hematol; 2001 Jul; 80(7):436-9. PubMed ID: 11529472
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Macrothrombopenia, nephritis and hearing loss--a new case of Epstein syndrome].
    Kóbor J; Túri S; Erdös A; Bodrogi T; Virág I
    Orv Hetil; 1991 Aug; 132(34):1875-7. PubMed ID: 1881666
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Successful immunostaining demonstrates abnormal intracytoplasmic MYH9 protein (NMMHC-IIA) in neutrophils of a dog with May-Hegglin anomaly.
    Flatland B; Kunishima S
    Vet Clin Pathol; 2011 Dec; 40(4):409-410. PubMed ID: 22136472
    [No Abstract]   [Full Text] [Related]  

  • 16. 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]  

  • 17. A 69-year-old man with long-standing thrombocytopenia.
    Ehrenschwender M; Koessler J
    Clin Chem; 2012 May; 58(5):953-4. PubMed ID: 22544859
    [No Abstract]   [Full Text] [Related]  

  • 18. Fechtner syndrome: physiologic analysis of macrothrombocytopenia.
    McBane RD; Elliott MA; White JG; Charlesworth JE; Costopoulos MG; Owen WG; Nichols WL
    Blood Coagul Fibrinolysis; 2000 Apr; 11(3):243-7. PubMed ID: 10870804
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Pay attention to neutrophil inclusions in pediatric patients with thrombocytopenia.
    Iqbal NT; Li W
    Blood; 2019 Sep; 134(11):907. PubMed ID: 31515229
    [No Abstract]   [Full Text] [Related]  

  • 20. [Autosomal dominant macrothrombocytopenia with leukocyte inclusion bodies and MYH9 disorders].
    Kunishima S
    Rinsho Byori; 2009 Apr; 57(4):365-70. PubMed ID: 19489439
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.