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Journal Abstract Search

139 related items for PubMed ID: 14987917

  • 1.
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  • 2. Genetic characterization of patients with Bernard-Soulier syndrome and their relatives from Southern Iran.
    Afrasiabi A, Lecchi A, Artoni A, Karimi M, Ashouri E, Peyvandi F, Mannucci PM.
    Platelets; 2007 Sep; 18(6):409-13. PubMed ID: 17763149
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  • 3. [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
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  • 4. [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 26; 126(43):1834-41. PubMed ID: 9005523
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  • 6. First Turkish case of Bernard-Soulier syndrome associated with GPIX N45S.
    Dağistan N, Kunishima S.
    Acta Haematol; 2007 Oct 26; 118(3):146-8. PubMed ID: 17804902
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  • 7. Flow cytometry as a tool in the diagnosis of Bernard-Soulier syndrome in Brazilian patients.
    Beltrame MP, Malvezzi M, Zanis J, Pasquini R.
    Platelets; 2009 Jun 26; 20(4):229-34. PubMed ID: 19459130
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  • 11. Novel point mutation in a leucine-rich repeat of the GPIbalpha chain of the platelet von Willebrand factor receptor, GPIb/IX/V, resulting in an inherited dominant form of Bernard-Soulier syndrome affecting two unrelated families: the N41H variant.
    Vettore S, Scandellari R, Moro S, Lombardi AM, Scapin M, Randi ML, Fabris F.
    Haematologica; 2008 Nov 26; 93(11):1743-7. PubMed ID: 18815197
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  • 12. Decreased platelet reactivity identified by whole blood flow cytometry in Fanconi anaemia patients.
    Holzhauer S, Sitaru AG, Ebell W, Schindler D, Hanenberg H, Wirbelauer J, Walter U, Grossmann R.
    Thromb Haemost; 2007 Dec 26; 98(6):1291-7. PubMed ID: 18064327
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  • 13. Autosomal dominant macrothrombocytopenia in Italy is most frequently a type of heterozygous Bernard-Soulier syndrome.
    Savoia A, Balduini CL, Savino M, Noris P, Del Vecchio M, Perrotta S, Belletti S, Poggi, Iolascon A.
    Blood; 2001 Mar 01; 97(5):1330-5. PubMed ID: 11222377
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  • 14. Platelet surface glycoprotein changes in patients with cerebral ischemia.
    Legrand C, Woimant F, Haguenau M, Caen J.
    Nouv Rev Fr Hematol (1978); 1991 Mar 01; 33(6):497-9. PubMed ID: 1818306
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  • 17. Bernard-Soulier syndrome: quantitative characterization of megakaryocytes and platelets by flow cytometric and platelet kinetic measurements.
    Tomer A, Scharf RE, McMillan R, Ruggeri ZM, Harker LA.
    Eur J Haematol; 1994 Apr 01; 52(4):193-200. PubMed ID: 8005229
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  • 18. [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 01; 22(9):464-6. PubMed ID: 11758225
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  • 19. An inherited macrothrombocytopenic disorder with abnormal large granules.
    Wu S, Wang Z, Dai L, Huang R, Wang X, Li S, Bai X, Mao D, Ruan C.
    Platelets; 2006 Jun 01; 17(4):259-65. PubMed ID: 16769603
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