Author/Creator: Lordkipanidzé, M. - British Library Electronic Legal Deposit Catalogue-Journal Issues and Articles Search Results

Author/Creator Lordkipanidzé, M.

1. A novel mutation in the P2Y12 receptor and a function‐reducing polymorphism in protease‐activated receptor 1 in a patient with chronic bleeding. (May 2014)

Authors:: Patel, Y. M.; Lordkipanidzé, M.; Lowe, G. C.; Nisar, S. P.; Garner, K.; Stockley, J.; Daly, M. E.; Mitchell, M.; Watson, S. P.; Austin, S. K.; Mundell, S. J.
Journal:: Journal of thrombosis and haemostasis
Issue:: Volume 12:Number 5(2014:May)
Page Start:: 716
Record Type:: Journal Article
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2. Evaluation of a whole blood remote platelet function test for the diagnosis of mild bleeding disorders. (May 2014)

Authors:: Dovlatova, N.; Lordkipanidzé, M.; Lowe, G. C.; Dawood, B.; May, J.; Heptinstall, S.; Watson, S. P.; Fox, S. C.; for the UK GAPP Study Group
Journal:: Journal of thrombosis and haemostasis
Issue:: Volume 12:Number 5(2014:May)
Page Start:: 660
Record Type:: Journal Article
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3. Genotyping and phenotyping of platelet function disorders. (30th June 2013)

Authors:: Watson, S. P.; Lowe, G. C.; Lordkipanidzé, M.; Morgan, N. V.
Journal:: Journal of thrombosis and haemostasis
Issue:: Volume 11(2013)Supplement 1
Page Start:: 351
Record Type:: Journal Article
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4. Pharmacogenomics in cardiovascular disease: focus on aspirin and ADP receptor antagonists. (12th September 2013)

Authors:: Würtz, M.; Lordkipanidzé, M.; Grove, E. L.
Journal:: Journal of thrombosis and haemostasis
Issue:: Volume 11:Number 9(2013:Sep.)
Page Start:: 1627
Record Type:: Journal Article
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5. Study of the bioaccumulation of tinzaparin in renally impaired patients when given at prophylactic doses - The STRIP study. Issue 174 (February 2019)

Authors:: Projean, D.; Lalonde, S.; Morin, J.; Nogues, E.; Séguin, A.; Vincent, A.; Lafrance, J.P.; Masson, V.; Kassis, J.; Fafard, J.; Lordkipanidzé, M.
Journal:: Thrombosis research
Issue:: Issue 174(2019)
Page Start:: 48
Record Type:: Journal Article
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6. Use of next‐generation sequencing and candidate gene analysis to identify underlying defects in patients with inherited platelet function disorders. (27th January 2015)

Authors:: Leo, V. C.; Morgan, N. V.; Bem, D.; Jones, M. L.; Lowe, G. C.; Lordkipanidzé, M.; Drake, S.; Simpson, M. A.; Gissen, P.; Mumford, A.; Watson, S. P.; Daly, M. E.; the UK GAPP Study Group
Journal:: Journal of thrombosis and haemostasis
Issue:: Volume 13:Number 4(2015:Apr.)
Page Start:: 643
Record Type:: Journal Article
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7. Utility of the ISTH bleeding assessment tool in predicting platelet defects in participants with suspected inherited platelet function disorders. (12th September 2013)

Authors:: Lowe, G. C.; Lordkipanidzé, M.; Watson, S. P.
Journal:: Journal of thrombosis and haemostasis
Issue:: Volume 11:Number 9(2013:Sep.)
Page Start:: 1663
Record Type:: Journal Article
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