Steven W Pipe
Laurence A Boxer M.D. Research Professor of Pediatrics
Professor of Pediatrics and Communicable Diseases
Professor of Pathology
[email protected]

Available to mentor

Steven W Pipe
Professor
  • Recent Publications
  • Recent Publications See All Publications
    • Journal Article
      Stable and durable factor IX levels in patients with hemophilia B over 3 years after etranacogene dezaparvovec gene therapy.
      von Drygalski A, Gomez E, Giermasz A, Castaman G, Key NS, Lattimore SU, Leebeek FWG, Miesbach WA, Recht M, Gut R, Dolmetsch R, Monahan PE, Le Quellec S, Pipe SW. Blood Adv, 2023 Oct 10; 7 (19): 5671 - 5679. DOI:10.1182/bloodadvances.2022008886
      PMID: 36490302
    • Journal Article
      Molecular evaluation and vector integration analysis of HCC complicating AAV gene therapy for hemophilia B.
      Schmidt M, Foster GR, Coppens M, Thomsen H, Dolmetsch R, Heijink L, Monahan PE, Pipe SW. Blood Adv, 2023 Sep 12; 7 (17): 4966 - 4969. DOI:10.1182/bloodadvances.2023009876
      PMID: 37352263
    • Journal Article
      Corrigendum to 'Efficacy of emicizumab is maintained throughout dosing intervals for bleed prophylaxis' [Research and Practice in Thrombosis and Haemostasis, Volume 7, Issue 2, February 2023, 100077].
      Pipe SW, Trzaskoma B, Minhas M, Lehle M, Ko RH, Gao L, Mahlangu J, Kempton CL, Kessler CM, Kruse-Jarres R. Res Pract Thromb Haemost, 2023 May; 7 (4): 100191 DOI:10.1016/j.rpth.2023.100191
      PMID: 37538504
    • Journal Article
      Fitusiran prophylaxis in people with severe haemophilia A or haemophilia B without inhibitors (ATLAS-A/B): a multicentre, open-label, randomised, phase 3 trial.
      Srivastava A, Rangarajan S, Kavakli K, Klamroth R, Kenet G, Khoo L, You C-W, Xu W, Malan N, Frenzel L, Bagot CN, Stasyshyn O, Chang C-Y, Poloskey S, Qiu Z, Andersson S, Mei B, Pipe SW. Lancet Haematol, 2023 May; 10 (5): e322 - e332. DOI:10.1016/S2352-3026(23)00037-6
      PMID: 37003278
    • Journal Article
      Heterogeneity in the half-life of factor VIII concentrate in patients with hemophilia A is due to variability in the clearance of endogenous von Willebrand factor.
      Elsheikh E, Lavin M, Heck LA, Larkin N, Mullaney B, Doherty D, Kennedy M, Keenan C, Guest T, O'Mahony B, Fazavana J, Fallon PG, Preston RJS, Gormley J, Ryan K, O'Connell NM, Singleton E, Byrne M, McGowan M, Roche S, Doyle M, Crowley MP, O'Shea SI, Reipert BM, Johnsen JM, Pipe SW, Di Paola J, Turecek PL, O'Donnell JS, iPATH study group . J Thromb Haemost, 2023 May; 21 (5): 1123 - 1134. DOI:10.1016/j.jtha.2023.01.013
      PMID: 36775768
    • Journal Article
      Characteristics of BAY 2599023 in the Current Treatment Landscape of Hemophilia A Gene Therapy.
      Pipe SW, Arruda VR, Lange C, Kitchen S, Eichler H, Wadsworth S. Curr Gene Ther, 2023 23 (2): 81 - 95. DOI:10.2174/1566523222666220914105729
      PMID: 36111754
    • Journal Article
      Macrophage Galactose Lectin Contributes to the Regulation of FVIII (Factor VIII) Clearance in Mice-Brief Report.
      Ward SE, Guest T, Byrne C, Lopes P, O'Sullivan JM, Doherty D, O'Connell D, Gutierrez Llaneza S, Chion A, Fazavana J, Fallon PG, Preston RJS, Johnsen JM, Pipe SW, Turecek PL, O'Donnell JS, iPATH Study Group . Arterioscler Thromb Vasc Biol, 2023 Apr; 43 (4): 540 - 546. DOI:10.1161/ATVBAHA.122.317807
      PMID: 36727518
    • Journal Article
      Efficacy of emicizumab is maintained throughout dosing intervals for bleed prophylaxis.
      Pipe SW, Trzaskoma B, Minhas M, Lehle M, Ko RH, Gao L, Mahlangu J, Kempton CL, Kessler CM, Kruse-Jarres R. Res Pract Thromb Haemost, 2023 Feb; 7 (2): 100077 DOI:10.1016/j.rpth.2023.100077
      PMID: 36908770