222 related articles for article (PubMed ID: 12745286)
1. Sebastian syndrome: report of the first case in a South American family.
Balderramo DC; Ricchi BN; Marun SG; Scaliter G; Alonso M
Haematologica; 2003 May; 88(5):ECR17. PubMed ID: 12745286
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. Sebastian syndrome: case report and review of the literature.
Young G; Luban NL; White JG
Am J Hematol; 1999 May; 61(1):62-5. PubMed ID: 10331513
[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. 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: 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]
7. 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]
8. 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]
9. 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]
10. What is the difference between May-Hegglin anomaly and Sebastian platelet syndrome?
Tsurusawa M; Mamiya S
Int J Hematol; 2000 Jun; 71(4):400-1. PubMed ID: 10905064
[No Abstract] [Full Text] [Related]
11. MYH9 related platelet disorders - often unknown and misdiagnosed.
Althaus K; Najm J; Greinacher A
Klin Padiatr; 2011 May; 223(3):120-5. PubMed ID: 21567368
[TBL] [Abstract][Full Text] [Related]
12. MYH9-related platelet disorders.
Althaus K; Greinacher A
Semin Thromb Hemost; 2009 Mar; 35(2):189-203. PubMed ID: 19408192
[TBL] [Abstract][Full Text] [Related]
13. [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]
14. Neutrophil secretory defect in the gray platelet syndrome: a new case.
Chedani H; Dupuy E; Massé JM; Cramer EM
Platelets; 2006 Feb; 17(1):14-9. PubMed ID: 16308182
[TBL] [Abstract][Full Text] [Related]
15. Haematological characteristics of MYH9 disorders due to MYH9 R702 mutations.
Kunishima S; Yoshinari M; Nishio H; Ida K; Miura T; Matsushita T; Hamaguchi M; Saito H
Eur J Haematol; 2007 Mar; 78(3):220-6. PubMed ID: 17241369
[TBL] [Abstract][Full Text] [Related]
16. [May-Hegglin's syndrome. Hereditary macrothrombocytopenia with inclusions in neutrophil granulocytes].
Stavem P; Hovig T; Brosstad F; Holm B
Tidsskr Nor Laegeforen; 1997 May; 117(14):2036-8. PubMed ID: 9235682
[TBL] [Abstract][Full Text] [Related]
17. Genetic thrombocytopenia with an autosomal dominant transmission: a study of 54 cases.
Najean Y; Lecompte T; Ardaillou N; Faille A; Dufour V
Nouv Rev Fr Hematol (1978); 1990; 32(1):67-70. PubMed ID: 2349084
[TBL] [Abstract][Full Text] [Related]
18. [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]
19. R1933X mutation in the MYH9 gene in May-Hegglin anomaly mimicking idiopathic thrombocytopenic purpura.
Sung CC; Lin SH; Chao TK; Chen YC
J Formos Med Assoc; 2014 Jan; 113(1):56-9. PubMed ID: 23759689
[TBL] [Abstract][Full Text] [Related]
20. Sebastian platelet syndrome: a hereditary macrothrombocytopenia.
Rodriguez V; Nichols WL; Charlesworth JE; White JG
Mayo Clin Proc; 2003 Nov; 78(11):1416-21. PubMed ID: 14601703
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]