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Autor:
Lontok E; Barth Syndrome Foundation, Larchmont, New York, USA., Milligan E; Barth Syndrome Foundation, Larchmont, New York, USA., Bowen VM; Barth Syndrome Foundation, Larchmont, New York, USA., McCurdy KR; Barth Syndrome Foundation, Larchmont, New York, USA.
Publikováno v:
Journal of inherited metabolic disease [J Inherit Metab Dis] 2022 Jan; Vol. 45 (1), pp. 3-6. Date of Electronic Publication: 2021 Sep 16.
Autor:
Li Y; Department of Pediatrics, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania., Godown J; Division of Pediatric Cardiology, Monroe Carell Jr. Children's Hospital at Vanderbilt, Nashville, Tennessee., Taylor CL; Division of Cardiology, Department of Pediatrics, Medical University of South Carolina, Charleston, South Carolina., Dipchand AI; Division of Cardiology, Department of Pediatrics, Hospital for Sick Children, University of Toronto, Toronto, Ontario, Canada., Bowen VM; Barth Syndrome Foundation, Larchmont, New York., Feingold B; Departments of Pediatrics and Clinical and Translational Science, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania. Electronic address: brian.feingold@chp.edu.
Publikováno v:
The Journal of heart and lung transplantation : the official publication of the International Society for Heart Transplantation [J Heart Lung Transplant] 2021 Oct; Vol. 40 (10), pp. 1191-1198. Date of Electronic Publication: 2021 Jul 10.
Autor:
Steward CG; NHS Specialised Services Barth Syndrome Service, Royal Hospital for Children.; School of Cellular and Molecular Medicine, University of Bristol, Bristol, UK., Groves SJ; School of Cellular and Molecular Medicine, University of Bristol, Bristol, UK., Taylor CT; Department of Pediatrics, Division of Cardiology, Children's Hospital, Medical University of South Carolina, Charleston, South Carolina., Maisenbacher MK; Natera, San Carlos, California, USA., Versluys B; Department of Immunology/Hematology and BMT, University Medical Center Utrecht, Utrecht, The Netherlands., Newbury-Ecob RA; Department of Clinical Genetics, St Michael's Hospital, Bristol, UK., Ozsahin H; Former: University Children's Hospital, Geneva., Damin MK; Barth Syndrome Trust, Romsey, UK., Bowen VM; Barth Syndrome Foundation, Inc., Larchmont, New York, USA., McCurdy KR; Barth Syndrome Foundation, Inc., Larchmont, New York, USA., Mackey MC; Departments of Physiology, Physics, and Mathematics, Centre for Applied Mathematics in Bioscience and Medicine, McGill University, Montreal, Québec, Canada., Bolyard AA; Severe Chronic Neutropenia International Registry., Dale DC; Department of Medicine, University of Washington, Seattle, Washington, USA.
Publikováno v:
Current opinion in hematology [Curr Opin Hematol] 2019 Jan; Vol. 26 (1), pp. 6-15.
Autor:
Clarke SL; NHS Specialised Services Barth Syndrome Service, Royal Hospital for Children, Upper Maudlin St, Bristol, BS2 8BJ, UK. colin.steward@uhbristol.nhs.uk, Bowron A, Gonzalez IL, Groves SJ, Newbury-Ecob R, Clayton N, Martin RP, Tsai-Goodman B, Garratt V, Ashworth M, Bowen VM, McCurdy KR, Damin MK, Spencer CT, Toth MJ, Kelley RI, Steward CG
Publikováno v:
Orphanet journal of rare diseases [Orphanet J Rare Dis] 2013 Feb 12; Vol. 8, pp. 23. Date of Electronic Publication: 2013 Feb 12.