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 *

194 related articles for article (PubMed ID: 7811433)

  • 1. A patient with pituitary growth hormone deficiency and May-Hegglin anomaly: a distinct entity?
    Gerver WJ; Neucker AV; Schrander-Stumpel CT
    Genet Couns; 1994; 5(3):307-10. PubMed ID: 7811433
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [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]  

  • 3. 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]  

  • 4. [Anesthetic management of a patient with May-Hegglin anomaly].
    Suzuki H; Fukuda H; Hirabayashi Y; Saitoh K; Igarashi T; Shimizu R
    Masui; 2000 Aug; 49(8):899-900. PubMed ID: 10998887
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Usefulness of immunofluorescence analysis of neutrophil nonmuscle myosin heavy chain-A for diagnosing in two sisters with May-Hegglin anomaly].
    Kimura N; Matsumoto M; Matsumoto K; Asai N; Kunishima S
    Rinsho Ketsueki; 2008 Dec; 49(12):1614-8. PubMed ID: 19110523
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [The May-Hegglin anomaly in a family].
    Javier G; Millá F; Prats Viñas J; Feliu E
    Sangre (Barc); 1989 Feb; 34(1):71-3. PubMed ID: 2540536
    [No Abstract]   [Full Text] [Related]  

  • 7. Sebastian platelet syndrome: two Japanese families originally diagnosed with May-Hegglin anomaly.
    Tsuda H; Yamasaki H; Miyayama H
    Int J Hematol; 1999 Dec; 70(4):290-3. PubMed ID: 10643156
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Identification of six novel MYH9 mutations and genotype-phenotype relationships in autosomal dominant macrothrombocytopenia with leukocyte inclusions.
    Kunishima S; Matsushita T; Kojima T; Amemiya N; Choi YM; Hosaka N; Inoue M; Jung Y; Mamiya S; Matsumoto K; Miyajima Y; Zhang G; Ruan C; Saito K; Song KS; Yoon HJ; Kamiya T; Saito H
    J Hum Genet; 2001; 46(12):722-9. PubMed ID: 11776386
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [May-hegglin anomaly].
    Lesesve J; Latger-Cannard V; Briquel M; André E; Maistre ED; Lecompte T
    Ann Biol Clin (Paris); 2000; 58(2):204-7. PubMed ID: 10760708
    [No Abstract]   [Full Text] [Related]  

  • 10. A study of platelet function and morphology in a new family with May-Hegglin anomaly.
    Girolami A; Randi M; Casonato A; Pasini L; Boccato C; Fabris F
    Folia Haematol Int Mag Klin Morphol Blutforsch; 1980; 107(2):256-68. PubMed ID: 6159266
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Identification of a novel MYH9 mutation in a patient with May-Hegglin anomaly.
    Otsubo K; Kanegane H; Nomura K; Ogawa J; Miyawaki T; Kunishima S
    Pediatr Blood Cancer; 2006 Dec; 47(7):968-9. PubMed ID: 16642488
    [No Abstract]   [Full Text] [Related]  

  • 12. First description of somatic mosaicism in MYH9 disorders.
    Kunishima S; Matsushita T; Yoshihara T; Nakase Y; Yokoi K; Hamaguchi M; Saito H
    Br J Haematol; 2005 Feb; 128(3):360-5. PubMed ID: 15667538
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [May-Hegglin anomaly--from genome research to clinical laboratory].
    Kunishima S
    Rinsho Byori; 2003 Sep; 51(9):898-904. PubMed ID: 14560660
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Coronary bypass surgery in May-Hegglin anomaly].
    Everlien M; Knoch K; Farah I; Greve H
    Dtsch Med Wochenschr; 2001 Jan; 126(3):47-9. PubMed ID: 11205478
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Hereditary thrombocytopenia. Differential diagnosis of a case].
    Doubek M; Smejkal P; Dostálová V; Trnavská I; Buliková A; Brychtová Y; Mayer J
    Cas Lek Cesk; 2003; 142(11):683-6. PubMed ID: 14689830
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Platelet studies in the pathogenesis of thrombocytopenia in May-Hegglin anomaly.
    Burns ER
    Am J Pediatr Hematol Oncol; 1991; 13(4):431-6. PubMed ID: 1664660
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Two cases of May-Hegglin anomaly (author's transl)].
    Onodera S; Sasaki Y; Sasaki T; Murata T
    Nihon Ketsueki Gakkai Zasshi; 1975 Dec; 38(6):782-5. PubMed ID: 178140
    [No Abstract]   [Full Text] [Related]  

  • 18. Hematological abnormalities in a patient with a 22q11.2 deletion.
    Saito M; Ishikawa T; Ito Y; Shimizu H
    Brain Dev; 2004 Aug; 26(5):342-4. PubMed ID: 15165677
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Anesthetic management for cesarean delivery in a patient with May-Hegglin anomaly].
    Takabayashi R; Nishikido O; Nagano K; Doi A; Nishisako R; Tateda T
    Masui; 2007 Oct; 56(10):1198-9. PubMed ID: 17966627
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Twenty-one cases of Sebastian platelet syndrome].
    Yamazaki E; Harano H; Fujisawa S; Kobayashi S; Ogawa K; Ishigatsubo Y
    Rinsho Ketsueki; 2001 Nov; 42(11):1139-41. PubMed ID: 11808085
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.