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A role for intravenous immunoglobulin in the treatment of Acquired Von Willebrand Syndrome associated with IgM gammopathy
Author(s) -
Lavin M.,
Ryan K.,
White B.,
Byrne M.,
O'Connell N. M.,
O’Donnell J. S.
Publication year - 2018
Publication title -
haemophilia
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.213
H-Index - 92
eISSN - 1365-2516
pISSN - 1351-8216
DOI - 10.1111/hae.13374
Subject(s) - irish , medicine , philosophy , linguistics
1. Li R, Emsley J. The organizing principle of the platelet glycoprotein IbIXV complex. J Thromb Haemost. 2013;11:605-614. 2. Noris P, Perrotta S, Bottega R, et al. Clinical and laboratory features of 103 patients from 42 Italian families with inherited thrombocytopenia derived from the monoallelic Ala156Val mutation of GPIbalpha (Bolzano mutation). Haematologica. 2012;97:82-88. 3. Borhany M, Boijout H, Pellequer JL, et al. Genotype and phenotype relationships in 10 Pakistani unrelated patients with inherited factor VII deficiency. Haemophilia. 2013;19:893-897. 4. Zieger B, Jenny A, Tsakiris DA, et al. A large Swiss family with BernardSoulier syndrome Correlation phenotype and genotype. Hamostaseologie. 2009;29:161-167. 5. Savoia A, Kunishima S, De RD, et al. Spectrum of the mutations in BernardSoulier syndrome. Hum Mutat. 2014;35:1033-1045. 6. Gohda F, Uchiumi H, Handa H, et al. Identification of inherited macrothrombocytopenias based on mean platelet volume among patients diagnosed with idiopathic thrombocytopenia. Thromb Res. 2007;119:741-746. 7. Ali S, Ghosh K, Shetty S. Molecular pathology of BernardSoulier syndrome in Indian patients. Platelets. 2013;24:571-573. 8. Gonzalez-Manchon C, Larrucea S, Pastor AL, et al. Compound heterozygosity of the GPIbalpha gene associated with BernardSoulier syndrome. Thromb Haemost. 2001;86:1385-1391. 9. Kanaji T, Okamura T, Kurolwa M, et al. Molecular and genetic analysis of two patients with BernardSoulier syndrome–identification of new mutations in glycoprotein Ib alpha gene. Thromb Haemost. 1997;77:1055-1061. 10. Rivera CE, Villagra J, Riordan M, Williams S, Lindstrom KJ, Rick ME. Identification of a new mutation in platelet glycoprotein IX (GPIX) in a patient with BernardSoulier syndrome. Br J Haematol. 2001;112:105-108. 11. Kulkarni BP, Nair SB, Vijapurkar M, et al. Molecular pathology of rare bleeding disorders (RBDs) in India: a systematic review. PLoS ONE. 2014;9:e108683. 12. Boeckelmann D, Hengartner H, Greinacher A, et al. Patients with BernardSoulier syndrome and different severity of the bleeding phenotype. Blood Cells Mol Dis. 2017;pii:S1079-9796:30281-30289. 13. Ul Haq MI, Sohaib M, Khan S, Nazir M. BernardSoulier syndrome: a challenge for anesthetist in an emergency surgery. J Anaesthesiol Clin Pharmacol. 2015;31:416-417. 14. Zaffar N, Saleem M, Ahmed SA. Functional platelet defects: a clinicopathological study of 10 cases. J Pak Med Assoc. 1987;37:223-228. 15. Zafar S, Sultana S, Iqbal W, et al. Pregnancy outcome in BernardSoulier syndrome complicated by preeclampsia. J TurkishGerman Gynecol Assoc. 2007;8:324-326.