353 related articles for article (PubMed ID: 18812282)
1. Sebastian syndrome with abnormal platelet response to ristocetin.
Redman R; Shunkwiler SM; Harris NS; Kedar A; Clapp WL
Lab Hematol; 2008; 14(3):19-23. PubMed ID: 18812282
[TBL] [Abstract][Full Text] [Related]
2. [Bernard-Soulier syndrome. An important differential diagnosis in chronic thrombocytopenia with bleeding complications].
Greinacher A; Zellner A; Brangenberg R; Kiefel V; Mueller-Eckhardt C
Monatsschr Kinderheilkd; 1993 Jun; 141(6):483-6. PubMed ID: 8336744
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Platelet function tests using platelet aggregometry: need for repetition of the test for diagnosis of defective platelet function.
Ghosh K; Nair S; Kulkarni B; Khare A; Shetty S; Mohanty D
Platelets; 2003 Sep; 14(6):351-4. PubMed ID: 14602548
[TBL] [Abstract][Full Text] [Related]
5. 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]
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. Spontaneous platelet aggregation in a hereditary giant platelet syndrome (MPS).
Milton JG; Frojmovic MM; Tang SS; White JG
Am J Pathol; 1984 Feb; 114(2):336-45. PubMed ID: 6696046
[TBL] [Abstract][Full Text] [Related]
8. [A novel point mutation in the transmembrane domain of platelet glycoprotein IX gene identified in a Bernard-Soulier syndrome patient].
Wang Z; Shi J; Han Y
Zhonghua Xue Ye Xue Za Zhi; 2001 Sep; 22(9):464-6. PubMed ID: 11758225
[TBL] [Abstract][Full Text] [Related]
9. Bernard-Soulier syndrome: a case report.
Pansatiankul BJ; Opartkiattikul N; Sangtawesin W
Southeast Asian J Trop Med Public Health; 1993; 24 Suppl 1():219-21. PubMed ID: 7886580
[TBL] [Abstract][Full Text] [Related]
10. Bernard-Soulier-like functional platelet defect in myelodysplastic syndrome and in acute myeloblastic leukemia associated with trilineage myelodysplasia.
Hiçsönmez G; Gümrük F; Cetin M; Ozbek N; Tuncer M; Gürsel T
Turk J Pediatr; 1995; 37(4):425-9. PubMed ID: 8560614
[TBL] [Abstract][Full Text] [Related]
11. Bernard-Soulier syndrome: a flow cytometric analysis of membrane GP-Ib expression.
Yeşilipek MA; Karadoğan I; Undar L
Turk J Pediatr; 1996; 38(3):375-9. PubMed ID: 8827910
[TBL] [Abstract][Full Text] [Related]
12. Platelet size and shape in hereditary giant platelet syndromes on blood smear and in suspension: evidence for two types of abnormalities.
Milton JG; Hutton RA; Tuddenham EG; Frojmovic MM
J Lab Clin Med; 1985 Sep; 106(3):326-35. PubMed ID: 4031633
[TBL] [Abstract][Full Text] [Related]
13. [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]
14. Giant platelet disorder in the Cavalier King Charles Spaniel.
Cowan SM; Bartges JW; Gompf RE; Hayes JR; Moyers TD; Snider CC; Gerard DA; Craft RM; Muenchen RA; Carroll RC
Exp Hematol; 2004 Apr; 32(4):344-50. PubMed ID: 15050744
[TBL] [Abstract][Full Text] [Related]
15. [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]
16. 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]
17. [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]
18. Platelet pathology in carriers of the X-linked GATA-1 macrothrombocytopenia.
White JG
Platelets; 2007 Dec; 18(8):620-7. PubMed ID: 18041654
[TBL] [Abstract][Full Text] [Related]
19. [Bernard-Soulier thrombocytopenia: clinical significance of a rare disorder].
Gengenbacher D; Tsakiris DA; Tichelli A; Marbet GA; Gratwohl A; Speck B
Schweiz Med Wochenschr; 1996 Oct; 126(43):1834-41. PubMed ID: 9005523
[TBL] [Abstract][Full Text] [Related]
20. Macrothrombocytopenia With Döhle Body-Like Granulocyte Inclusions: A Case Report of May-Hegglin Anomaly in a 33-Year-Old White Woman With an Update on the Molecular Findings of MYH9-Related Disease.
Ruhoy SM; Yates A
Lab Med; 2016 Aug; 47(3):246-50. PubMed ID: 27353381
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
