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Items: 47


Impaired human hematopoiesis due to a cryptic intronic GATA1 splicing mutation.

Abdulhay NJ, Fiorini C, Verboon JM, Ludwig LS, Ulirsch JC, Zieger B, Lareau CA, Mi X, Roy A, Obeng EA, Erlacher M, Gupta N, Gabriel SB, Ebert BL, Niemeyer CM, Khoriaty RN, Ancliff P, Gazda HT, Wlodarski MW, Sankaran VG.

J Exp Med. 2019 May 6;216(5):1050-1060. doi: 10.1084/jem.20181625. Epub 2019 Mar 26.


The incidence of invasive fungal infections in children, adolescents and young adults with acute lymphoblastic leukaemia/lymphoma treated with the UKALL2011 protocol: a multicentre retrospective study.

O'Reilly MA, Govender D, Kirkwood AA, Vora A, Samarasinghe S, Khwaja A, Grandage V, Rao A, Ancliff P, Pavasovic V, Cheng D, Carpenter B, Daw S, Hough R, O'Connor D.

Br J Haematol. 2019 Feb 15. doi: 10.1111/bjh.15798. [Epub ahead of print] No abstract available.


Durable remissions in TCF3-HLF positive acute lymphoblastic leukemia with blinatumomab and stem cell transplantation.

Mouttet B, Vinti L, Ancliff P, Bodmer N, Brethon B, Cario G, Chen-Santel C, Elitzur S, Hazar V, Kunz J, Möricke A, Stein J, Vora A, Yaman Y, Schrappe M, Anak S, Baruche A, Locatelli F, von Stackelberg A, Stanulla M, Bourquin JP.

Haematologica. 2019 Jun;104(6):e244-e247. doi: 10.3324/haematol.2018.210104. Epub 2019 Feb 14. No abstract available.


MECOM-associated syndrome: a heterogeneous inherited bone marrow failure syndrome with amegakaryocytic thrombocytopenia.

Germeshausen M, Ancliff P, Estrada J, Metzler M, Ponstingl E, Rütschle H, Schwabe D, Scott RH, Unal S, Wawer A, Zeller B, Ballmaier M.

Blood Adv. 2018 Mar 27;2(6):586-596. doi: 10.1182/bloodadvances.2018016501.


Targeting acute myeloid leukemia by drug-induced c-MYB degradation.

Walf-Vorderwülbecke V, Pearce K, Brooks T, Hubank M, van den Heuvel-Eibrink MM, Zwaan CM, Adams S, Edwards D, Bartram J, Samarasinghe S, Ancliff P, Khwaja A, Goulden N, Williams G, de Boer J, Williams O.

Leukemia. 2018 Apr;32(4):882-889. doi: 10.1038/leu.2017.317. Epub 2017 Nov 1.


Myelodysplasia and liver disease extend the spectrum of RTEL1 related telomeropathies.

Cardoso SR, Ellison ACM, Walne AJ, Cassiman D, Raghavan M, Kishore B, Ancliff P, Rodríguez-Vigil C, Dobbels B, Rio-Machin A, Al Seraihi AFH, Pontikos N, Tummala H, Vulliamy T, Dokal I.

Haematologica. 2017 Aug;102(8):e293-e296. doi: 10.3324/haematol.2017.167056. Epub 2017 May 11. No abstract available.


Sirolimus therapy for children with problematic kaposiform haemangioendothelioma and tufted angioma.

Tasani M, Ancliff P, Glover M.

Br J Dermatol. 2017 Dec;177(6):e344-e346. doi: 10.1111/bjd.15640. Epub 2017 Nov 22. No abstract available.


Stem cell transplantation in severe congenital neutropenia: an analysis from the European Society for Blood and Marrow Transplantation.

Fioredda F, Iacobelli S, van Biezen A, Gaspar B, Ancliff P, Donadieu J, Aljurf M, Peters C, Calvillo M, Matthes-Martin S, Morreale G, van 't Veer-Tazelaar N, de Wreede L, Al Seraihy A, Yesilipek A, Fischer A, Bierings M, Ozturk G, Smith O, Veys P, Ljungman P, Peffault de Latour R, Sánchez de Toledo Codina J, Or R, Ganser A, Afanasyev B, Wynn R, Kalwak K, Marsh J, Dufour C; Severe Aplastic Anemia the Inborn Error, and the Pediatric Disease Working Parties of the European Society for Blood and Bone Marrow Transplantation (EBMT) and Stem Cell Transplant for Immunodeficiencies in Europe (SCETIDE).

Blood. 2015 Oct 15;126(16):1885-92; quiz 1970. doi: 10.1182/blood-2015-02-628859. Epub 2015 Jul 16.


Disease evolution and outcomes in familial AML with germline CEBPA mutations.

Tawana K, Wang J, Renneville A, Bödör C, Hills R, Loveday C, Savic A, Van Delft FW, Treleaven J, Georgiades P, Uglow E, Asou N, Uike N, Debeljak M, Jazbec J, Ancliff P, Gale R, Thomas X, Mialou V, Döhner K, Bullinger L, Mueller B, Pabst T, Stelljes M, Schlegelberger B, Wozniak E, Iqbal S, Okosun J, Araf S, Frank AK, Lauridsen FB, Porse B, Nerlov C, Owen C, Dokal I, Gribben J, Smith M, Preudhomme C, Chelala C, Cavenagh J, Fitzgibbon J.

Blood. 2015 Sep 3;126(10):1214-23. doi: 10.1182/blood-2015-05-647172. Epub 2015 Jul 10.


Congenital acute megakaryoblastic leukemia.

Bain BJ, Chakravorty S, Ancliff P.

Am J Hematol. 2015 Oct;90(10):963. doi: 10.1002/ajh.24109. Epub 2015 Sep 1. No abstract available.


PAX5 alterations in genetically unclassified childhood Precursor B-cell acute lymphoblastic leukaemia.

Stasevich I, Inglott S, Austin N, Chatters S, Chalker J, Addy D, Dryden C, Ancliff P, Ford A, Williams O, Kempski H.

Br J Haematol. 2015 Oct;171(2):263-272. doi: 10.1111/bjh.13543. Epub 2015 Jun 26.


Nutritional status in children with Shwachman-diamond syndrome.

Pichler J, Meyer R, Köglmeier J, Ancliff P, Shah N.

Pancreas. 2015 May;44(4):590-5. doi: 10.1097/MPA.0000000000000291.


Rare Association of Myeloid leukaemia of Down Syndrome with Granulocytic Sarcoma.

Obaid MA, Bourusly M, Ancliff P, Al Matter E.

Gulf J Oncolog. 2014 Jul;1(16):101-4.


Outcome of central nervous system relapses in childhood acute lymphoblastic leukaemia--prospective open cohort analyses of the ALLR3 trial.

Masurekar AN, Parker CA, Shanyinde M, Moorman AV, Hancock JP, Sutton R, Ancliff PJ, Morgan M, Goulden NJ, Fraser C, Hoogerbrugge PM, Revesz T, Darbyshire PJ, Krishnan S, Love SB, Saha V.

PLoS One. 2014 Oct 3;9(10):e108107. doi: 10.1371/journal.pone.0108107. eCollection 2014.


GATA2 mutations in sporadic and familial acute myeloid leukaemia patients with CEBPA mutations.

Green CL, Tawana K, Hills RK, Bödör C, Fitzgibbon J, Inglott S, Ancliff P, Burnett AK, Linch DC, Gale RE.

Br J Haematol. 2013 Jun;161(5):701-5. doi: 10.1111/bjh.12317. Epub 2013 Apr 5.


Squamous cell carcinoma in a child with Clericuzio-type poikiloderma with neutropenia.

Rodgers W, Ancliff P, Ponting CP, Sanchez-Pulido L, Burns S, Hayman M, Kimonis V, Sebire N, Bulstrode N, Harper JI.

Br J Dermatol. 2013 Mar;168(3):665-7. doi: 10.1111/bjd.12016. Epub 2012 Nov 2. No abstract available.


Phenotypic heterogeneity and evidence of a founder effect associated with G6PC3 mutations in patients with severe congenital neutropenia.

Smith BN, Evans C, Ali A, Ancliff PJ, Hayee B, Segal AW, Hall G, Kaya Z, Shakoori AR, Linch DC, Gale RE.

Br J Haematol. 2012 Jul;158(1):146-9. doi: 10.1111/j.1365-2141.2012.09110.x. Epub 2012 Apr 2. No abstract available.


Dysregulation of the HIF pathway due to VHL mutation causing severe erythrocytosis and pulmonary arterial hypertension.

Bond J, Gale DP, Connor T, Adams S, de Boer J, Gascoyne DM, Williams O, Maxwell PH, Ancliff PJ.

Blood. 2011 Mar 31;117(13):3699-701. doi: 10.1182/blood-2010-12-327569. No abstract available.


Prevalence and predictors of anthracycline cardiotoxicity in children treated for acute myeloid leukaemia: retrospective cohort study in a single centre in the United Kingdom.

Temming P, Qureshi A, Hardt J, Leiper AD, Levitt G, Ancliff PJ, Webb DK.

Pediatr Blood Cancer. 2011 Apr;56(4):625-30. doi: 10.1002/pbc.22908.


Effect of mitoxantrone on outcome of children with first relapse of acute lymphoblastic leukaemia (ALL R3): an open-label randomised trial.

Parker C, Waters R, Leighton C, Hancock J, Sutton R, Moorman AV, Ancliff P, Morgan M, Masurekar A, Goulden N, Green N, Révész T, Darbyshire P, Love S, Saha V.

Lancet. 2010 Dec 11;376(9757):2009-17. doi: 10.1016/S0140-6736(10)62002-8. Epub 2010 Dec 3.


Recent advances in the understanding of genetic defects of neutrophil number and function.

Bouma G, Ancliff PJ, Thrasher AJ, Burns SO.

Br J Haematol. 2010 Nov;151(4):312-26. doi: 10.1111/j.1365-2141.2010.08361.x. Epub 2010 Aug 31. Review.


Enteropathic histopathological features may be associated with Shwachman-Diamond syndrome.

Shah N, Cambrook H, Koglmeier J, Mason C, Ancliff P, Lindley K, Smith VV, Bajaj-Elliott M, Sebire NJ.

J Clin Pathol. 2010 Jul;63(7):592-4. doi: 10.1136/jcp.2010.077677. Epub 2010 May 24.


Acquisition of genome-wide copy number alterations in monozygotic twins with acute lymphoblastic leukemia.

Bateman CM, Colman SM, Chaplin T, Young BD, Eden TO, Bhakta M, Gratias EJ, van Wering ER, Cazzaniga G, Harrison CJ, Hain R, Ancliff P, Ford AM, Kearney L, Greaves M.

Blood. 2010 Apr 29;115(17):3553-8. doi: 10.1182/blood-2009-10-251413. Epub 2010 Jan 8.


Two patients with Hermansky Pudlak syndrome type 2 and novel mutations in AP3B1.

Wenham M, Grieve S, Cummins M, Jones ML, Booth S, Kilner R, Ancliff PJ, Griffiths GM, Mumford AD.

Haematologica. 2010 Feb;95(2):333-7. doi: 10.3324/haematol.2009.012286. Epub 2009 Aug 13.


Type II Gaucher disease manifesting as haemophagocytic lymphohistiocytosis.

Sharpe LR, Ancliff P, Amrolia P, Gilmour KC, Vellodi A.

J Inherit Metab Dis. 2009 Dec;32 Suppl 1:S107-10. doi: 10.1007/s10545-009-1091-2. Epub 2009 Mar 11.


Homozygous HAX1 mutations in severe congenital neutropenia patients with sporadic disease: a novel mutation in two unrelated British kindreds.

Smith BN, Ancliff PJ, Pizzey A, Khwaja A, Linch DC, Gale RE.

Br J Haematol. 2009 Mar;144(5):762-70. doi: 10.1111/j.1365-2141.2008.07493.x. Epub 2008 Nov 22.


Insertional mutagenesis combined with acquired somatic mutations causes leukemogenesis following gene therapy of SCID-X1 patients.

Howe SJ, Mansour MR, Schwarzwaelder K, Bartholomae C, Hubank M, Kempski H, Brugman MH, Pike-Overzet K, Chatters SJ, de Ridder D, Gilmour KC, Adams S, Thornhill SI, Parsley KL, Staal FJ, Gale RE, Linch DC, Bayford J, Brown L, Quaye M, Kinnon C, Ancliff P, Webb DK, Schmidt M, von Kalle C, Gaspar HB, Thrasher AJ.

J Clin Invest. 2008 Sep;118(9):3143-50. doi: 10.1172/JCI35798.


Successful outcome of allo-SCT in high-risk pediatric AML using chemotherapy-only conditioning and post transplant immunotherapy.

Bonanomi S, Connor P, Webb D, Ancliff P, Amrolia P, Rao K, McCloskey D, Hemmatpour S, Goulden N, Veys P.

Bone Marrow Transplant. 2008 Aug;42(4):253-7. doi: 10.1038/bmt.2008.160. Epub 2008 Jun 16. Erratum in: Bone Marrow Transplant. 2008 Nov;42(9):635. Bonnanomi, S [corrected to Bonanomi, S].


Stem cell transplantation for children with Glanzmann thrombasthenia.

Connor P, Khair K, Liesner R, Amrolia P, Veys P, Ancliff P, Mathias M.

Br J Haematol. 2008 Mar;140(5):568-71. doi: 10.1111/j.1365-2141.2007.06890.x. Epub 2008 Jan 16.


Initiating and cancer-propagating cells in TEL-AML1-associated childhood leukemia.

Hong D, Gupta R, Ancliff P, Atzberger A, Brown J, Soneji S, Green J, Colman S, Piacibello W, Buckle V, Tsuzuki S, Greaves M, Enver T.

Science. 2008 Jan 18;319(5861):336-9. doi: 10.1126/science.1150648.


Notch-1 mutations are secondary events in some patients with T-cell acute lymphoblastic leukemia.

Mansour MR, Duke V, Foroni L, Patel B, Allen CG, Ancliff PJ, Gale RE, Linch DC.

Clin Cancer Res. 2007 Dec 1;13(23):6964-9.


Unregulated actin polymerization by WASp causes defects of mitosis and cytokinesis in X-linked neutropenia.

Moulding DA, Blundell MP, Spiller DG, White MR, Cory GO, Calle Y, Kempski H, Sinclair J, Ancliff PJ, Kinnon C, Jones GE, Thrasher AJ.

J Exp Med. 2007 Sep 3;204(9):2213-24. Epub 2007 Aug 27.


Mutations in the SBDS gene in acquired aplastic anemia.

Calado RT, Graf SA, Wilkerson KL, Kajigaya S, Ancliff PJ, Dror Y, Chanock SJ, Lansdorp PM, Young NS.

Blood. 2007 Aug 15;110(4):1141-6. Epub 2007 May 3.


The Shwachman-Bodian-Diamond syndrome protein mediates translational activation of ribosomes in yeast.

Menne TF, Goyenechea B, Sánchez-Puig N, Wong CC, Tonkin LM, Ancliff PJ, Brost RL, Costanzo M, Boone C, Warren AJ.

Nat Genet. 2007 Apr;39(4):486-95. Epub 2007 Mar 11.


Two novel activating mutations in the Wiskott-Aldrich syndrome protein result in congenital neutropenia.

Ancliff PJ, Blundell MP, Cory GO, Calle Y, Worth A, Kempski H, Burns S, Jones GE, Sinclair J, Kinnon C, Hann IM, Gale RE, Linch DC, Thrasher AJ.

Blood. 2006 Oct 1;108(7):2182-9. Epub 2006 Jun 27.


Slide session, British Society for Haematology, 45th Annual Scientific Meeting, Manchester, 2005.

Bain BJ, Murray JA, Patterson KG, Chakravorty S, Ancliff P, Wong CC, Hann I, Wong C, Philpott N, Bolam S, Thomas W.

Clin Lab Haematol. 2005 Dec;27(6):363-9.


Ectopic thymus presenting as a subglottic mass: diagnostic and management dilemmas.

Pai I, Hegde V, Wilson PO, Ancliff P, Ramsay AD, Daya H.

Int J Pediatr Otorhinolaryngol. 2005 Apr;69(4):573-6. Epub 2005 Jan 20.


Non-Hodgkin's lymphoma presenting with uterine and renal enlargement in a young girl.

Moon LD, Brenner C, Ancliff P, McHugh K, DeBruyn R.

Pediatr Radiol. 2004 Mar;34(3):277-9. Epub 2003 Nov 4.


Congenital neutropenia.

Ancliff PJ.

Blood Rev. 2003 Dec;17(4):209-16. Review.


Neutrophil elastase mutations in congenital neutropenia.

Ancliff PJ, Gale RE, Linch DC.

Hematology. 2003 Jun;8(3):165-71. Review.


Thrombocytopenia-absent radius syndrome: a clinical genetic study.

Greenhalgh KL, Howell RT, Bottani A, Ancliff PJ, Brunner HG, Verschuuren-Bemelmans CC, Vernon E, Brown KW, Newbury-Ecob RA.

J Med Genet. 2002 Dec;39(12):876-81.


Paternal mosaicism proves the pathogenic nature of mutations in neutrophil elastase in severe congenital neutropenia.

Ancliff PJ, Gale RE, Watts MJ, Liesner R, Hann IM, Strobel S, Linch DC.

Blood. 2002 Jul 15;100(2):707-9.


The use of recombinant factor VIIa in a patient with severe Glanzmann's thrombasthenia to facilitate insertion of a Port-a-Cath.

Ancliff P, Liesner R, Khair K, Hann I.

Blood Coagul Fibrinolysis. 1999 Oct;10(7):447-8. No abstract available.


Trigger factors for prophylactic platelet transfusion.

Ancliff PJ, Machin SJ.

Blood Rev. 1998 Dec;12(4):234-8. Review.


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