Rabbolini DJ - Search Results

1

Prevalence and natural history of variants in the ANKRD26 gene: a short review and update of reported cases.

Vyas H, Alcheikh A, Lowe G, Stevenson WS, Morgan NV, Rabbolini DJ. Vyas H, et al. Among authors: rabbolini dj. Platelets. 2022 Nov 17;33(8):1107-1112. doi: 10.1080/09537104.2022.2071853. Epub 2022 May 19. Platelets. 2022. PMID: 35587581 Free PMC article. Review.

2

Inherited macrothrombocytopenias.

Rabbolini DJ, Morel-Kopp MC, Stevenson W, Ward CM. Rabbolini DJ, et al. Semin Thromb Hemost. 2014 Oct;40(7):774-84. doi: 10.1055/s-0034-1387922. Epub 2014 Aug 31. Semin Thromb Hemost. 2014. PMID: 25173502

3

Paris-Trousseau thrombocytopenia is phenocopied by the autosomal recessive inheritance of a DNA-binding domain mutation in FLI1.

Stevenson WS, Rabbolini DJ, Beutler L, Chen Q, Gabrielli S, Mackay JP, Brighton TA, Ward CM, Morel-Kopp MC. Stevenson WS, et al. Among authors: rabbolini dj. Blood. 2015 Oct 22;126(17):2027-30. doi: 10.1182/blood-2015-06-650887. Epub 2015 Aug 27. Blood. 2015. PMID: 26316623 Free article.

4

GFI1B variants associated with thrombocytopenia.

Rabbolini DJ, Morel-Kopp MC, Ward CM, Stevenson WS. Rabbolini DJ, et al. Platelets. 2017 Jul;28(5):525-527. doi: 10.1080/09537104.2017.1317734. Epub 2017 Jun 5. Platelets. 2017. PMID: 28580815 Free article. No abstract available.

5

Thrombocytopenia and CD34 expression is decoupled from α-granule deficiency with mutation of the first growth factor-independent 1B zinc finger.

Rabbolini DJ, Morel-Kopp MC, Chen Q, Gabrielli S, Dunlop LC, Chew LP, Blair N, Brighton TA, Singh N, Ng AP, Ward CM, Stevenson WS. Rabbolini DJ, et al. J Thromb Haemost. 2017 Nov;15(11):2245-2258. doi: 10.1111/jth.13843. Epub 2017 Oct 13. J Thromb Haemost. 2017. PMID: 28880435 Free article.

6

Diagnosis and treatment of MYH9-RD in an Australasian cohort with thrombocytopenia.

Rabbolini DJ, Chun Y, Latimer M, Kunishima S, Fixter K, Valecha B, Tan P, Chew LP, Kile BT, Burt R, Radhakrishnan K, Bird R, Ockelford P, Gabrielli S, Chen Q, Stevenson WS, Ward CM, Morel-Kopp MC. Rabbolini DJ, et al. Platelets. 2018 Dec;29(8):793-800. doi: 10.1080/09537104.2017.1356920. Epub 2017 Nov 1. Platelets. 2018. PMID: 29090586 Free article.

7

Receptor homodimerization plays a critical role in a novel dominant negative P2RY12 variant identified in a family with severe bleeding.

Mundell SJ, Rabbolini D, Gabrielli S, Chen Q, Aungraheeta R, Hutchinson JL, Kilo T, Mackay J, Ward CM, Stevenson W, Morel-Kopp MC. Mundell SJ, et al. J Thromb Haemost. 2018 Jan;16(1):44-53. doi: 10.1111/jth.13900. Epub 2017 Dec 2. J Thromb Haemost. 2018. PMID: 29117459 Free article.

8

Mean platelet diameter measurements to classify inherited thrombocytopenias.

Fixter K, Rabbolini DJ, Valecha B, Morel-Kopp MC, Gabrielli S, Chen Q, Stevenson WS, Ward CM. Fixter K, et al. Among authors: rabbolini dj. Int J Lab Hematol. 2018 Apr;40(2):187-195. doi: 10.1111/ijlh.12763. Epub 2017 Nov 16. Int J Lab Hematol. 2018. PMID: 29143464

9

Anti-glycoprotein VI mediated immune thrombocytopenia: An under-recognized and significant entity?

Rabbolini DJ, Gardiner EE, Morel-Kopp MC, Dunkley S, Jahangiri A, Lee CS, Stevenson WS, Ward CM. Rabbolini DJ, et al. Res Pract Thromb Haemost. 2017 Aug 24;1(2):291-295. doi: 10.1002/rth2.12033. eCollection 2017 Oct. Res Pract Thromb Haemost. 2017. PMID: 30046699 Free PMC article.

10

An integrated approach to inherited platelet disorders: results from a research collaborative, the Sydney Platelet Group.

Rabbolini D, Connor D, Morel-Kopp MC, Donikian D, Kondo M, Chen W, Alessi MC, Stevenson W, Chen V, Joseph J, Brighton T, Ward C; Sydney Platelet Group. Rabbolini D, et al. Pathology. 2020 Feb;52(2):243-255. doi: 10.1016/j.pathol.2019.10.005. Epub 2020 Jan 10. Pathology. 2020. PMID: 31932033

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