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2. 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]
3. [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]
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. 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]
6. [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]
7. [Platelet shape in various clinical conditions. Its relation to the disease and significance (author's transl)]. Hattori A; Sanada M; Kojima T; Ihzumi T; Shibata A Nihon Ketsueki Gakkai Zasshi; 1979 Jun; 42(3):558-9. PubMed ID: 495020 [No Abstract] [Full Text] [Related]
8. [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]
9. 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]
11. [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]
12. 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]
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16. 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]
17. 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]