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Items: 1 to 20 of 26

1.

Newborn screening for sickle cell disease in Europe: recommendations from a Pan-European Consensus Conference.

Lobitz S, Telfer P, Cela E, Allaf B, Angastiniotis M, Backman Johansson C, Badens C, Bento C, Bouva MJ, Canatan D, Charlton M, Coppinger C, Daniel Y, de Montalembert M, Ducoroy P, Dulin E, Fingerhut R, Frömmel C, García-Morin M, Gulbis B, Holtkamp U, Inusa B, James J, Kleanthous M, Klein J, Kunz JB, Langabeer L, Lapouméroulie C, Marcao A, Marín Soria JL, McMahon C, Ohene-Frempong K, Périni JM, Piel FB, Russo G, Sainati L, Schmugge M, Streetly A, Tshilolo L, Turner C, Venturelli D, Vilarinho L, Yahyaoui R, Elion J, Colombatti R; with the endorsement of EuroBloodNet, the European Reference Network in Rare Haematological Diseases.

Br J Haematol. 2018 Nov;183(4):648-660. doi: 10.1111/bjh.15600. Epub 2018 Oct 18.

PMID:
30334577
2.

Prevalence of left ventricular hypertrabeculation/noncompaction among children with sickle cell disease.

Morrison ML, McMahon C, Tully R, Enright N, Pignatelli R, Towbin JA, McMahon CJ.

Congenit Heart Dis. 2018 May;13(3):440-443. doi: 10.1111/chd.12592. Epub 2018 Feb 21.

PMID:
29468808
3.

Distinct driver mutation profiles of childhood and adolescent essential thrombocythemia.

Langabeer SE, Haslam K, McMahon C.

Pediatr Blood Cancer. 2015 Jan;62(1):175-6. doi: 10.1002/pbc.25190. Epub 2014 Aug 17. No abstract available.

PMID:
25132652
4.

The molecular landscape of childhood myeloproliferative neoplasms.

Langabeer SE, Haslam K, McMahon C.

Leuk Res. 2014 Aug;38(8):997-8. doi: 10.1016/j.leukres.2014.06.003. Epub 2014 Jun 12.

PMID:
24986380
5.

A case of parvovirus B19-induced pure red cell aplasia in a child following heart transplant.

Kelleher E, McMahon C, McMahon CJ.

Cardiol Young. 2015 Feb;25(2):373-5. doi: 10.1017/S1047951114000225. Epub 2014 Feb 21.

PMID:
24555951
6.

CALR mutations are rare in childhood essential thrombocythemia.

Langabeer SE, Haslam K, McMahon C.

Pediatr Blood Cancer. 2014 Aug;61(8):1523. doi: 10.1002/pbc.24984. Epub 2014 Feb 13. No abstract available.

PMID:
24523226
7.

The JAK2 V617F mutation in pediatric myeloproliferative neoplasms: how and when?

Langabeer SE, Smith OP, McMahon C.

Pediatr Hematol Oncol. 2014 Mar;31(2):138-9. doi: 10.3109/08880018.2013.869288. Epub 2014 Jan 2. No abstract available.

PMID:
24383477
8.

A prenatal origin of childhood essential thrombocythaemia.

Langabeer SE, Haslam K, McMahon C.

Br J Haematol. 2013 Dec;163(5):676-8. doi: 10.1111/bjh.12533. Epub 2013 Aug 16. No abstract available.

PMID:
23952300
9.

Allogeneic stem cell transplantation as immunotherapy for X-linked lymphoproliferative disease-associated cerebral T-cell lymphoma.

Goodyer M, Sargent J, Bond J, McMahon C, Dunne B, Smith O.

Br J Haematol. 2013 Oct;163(1):133-5. doi: 10.1111/bjh.12454. Epub 2013 Jul 6. No abstract available.

PMID:
23829589
10.

Treatment of Epstein Barr virus-induced haemophagocytic lymphohistiocytosis with rituximab-containing chemo-immunotherapeutic regimens.

Chellapandian D, Das R, Zelley K, Wiener SJ, Zhao H, Teachey DT, Nichols KE; EBV-HLH Rituximab Study Group.

Br J Haematol. 2013 Aug;162(3):376-82. doi: 10.1111/bjh.12386. Epub 2013 May 21.

11.

The correlation of ultrasonographic placental architecture with placental histology in the low-risk primigravid population.

Cooley SM, Donnelly JC, Walsh T, McMahon C, Gillan J, Geary MP.

J Perinat Med. 2013 Sep 1;41(5):505-9. doi: 10.1515/jpm-2013-0015.

PMID:
23515100
12.

Intranasal fentanyl versus intravenous morphine in the emergency department treatment of severe painful sickle cell crises in children: study protocol for a randomised controlled trial.

Barrett MJ, Cronin J, Murphy A, McCoy S, Hayden J, an Fhailí S, Grant T, Wakai A, McMahon C, Walsh S, O'Sullivan R.

Trials. 2012 May 30;13:74. doi: 10.1186/1745-6215-13-74.

13.

Protein C and free protein S in children with sickle cell anemia.

Piccin A, Murphy C, Eakins E, Kinsella A, McMahon C, Smith OP, Murphy WG.

Ann Hematol. 2012 Oct;91(10):1669-71. doi: 10.1007/s00277-012-1447-9. Epub 2012 Mar 21. No abstract available.

PMID:
22434279
14.

Composition and significance of splenic Gamna-Gandy bodies in sickle cell anemia.

Piccin A, Rizkalla H, Smith O, McMahon C, Furlan C, Murphy C, Negri G, Mc Dermott M.

Hum Pathol. 2012 Jul;43(7):1028-36. doi: 10.1016/j.humpath.2011.08.011. Epub 2011 Nov 12.

PMID:
22079355
15.

The impact of positive acquired thrombophilia serology on ultrasound, obstetric outcome and the placenta in a low-risk primigravid population.

Cooley SM, Donnelly JC, Walsh T, Collins C, McMahon C, Gillan J, Geary MP.

Obstet Med. 2011 Mar;4(1):15-9. doi: 10.1258/om.2010.100057. Epub 2011 Mar 1.

16.

South-east Asian ovalocytosis and the cryohydrocytosis form of hereditary stomatocytosis show virtually indistinguishable cation permeability defects.

Guizouarn H, Borgese F, Gabillat N, Harrison P, Goede JS, McMahon C, Stewart GW, Bruce LJ.

Br J Haematol. 2011 Mar;152(5):655-64. doi: 10.1111/j.1365-2141.2010.08454.x. Epub 2011 Jan 23.

PMID:
21255002
17.

The impact of ultrasonographic placental architecture on antenatal course, labor and delivery in a low-risk primigravid population.

Cooley SM, Donnelly JC, Walsh T, McMahon C, Gillan J, Geary MP.

J Matern Fetal Neonatal Med. 2011 Mar;24(3):493-7. doi: 10.3109/14767058.2010.497877. Epub 2010 Jul 7.

PMID:
20608801
18.

Esophageal strictures during treatment for acute lymphoblastic leukemia.

Kelly K, Storey L, O' Sullivan M, Butler K, McDermott M, Corbally M, McMahon C, Smith OP, O' Marcaigh A.

J Pediatr Hematol Oncol. 2010 Mar;32(2):124-7. doi: 10.1097/MPH.0b013e3181ced25c.

PMID:
20168244
19.

Congenital JAK2V617F polycythemia vera: where does the genotype-phenotype diversity end?

Kelly K, McMahon C, Langabeer S, Eliwan H, O'Marcaigh A, Smith OP.

Blood. 2008 Nov 15;112(10):4356-7. doi: 10.1182/blood-2008-08-175620. No abstract available.

20.

Sickle cell disease and dental treatment.

Piccin A, Fleming P, Eakins E, McGovern E, Smith OP, McMahon C.

J Ir Dent Assoc. 2008 Apr-May;54(2):75-9. Review.

PMID:
18578383

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