Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Keppen MD"'
Autor:
Jessica A. Slostad, MD, Minetta C. Liu, MD, Jacob B. Allred, MS, Lori A. Erickson, MD, Kandelaria M. Rumilla, MD, Matthew S. Block, MD, PhD, Michael Keppen, MD, David King, MD, Svetomir N. Markovic, MD, PhD, Robert R. McWilliams, MD
Publikováno v:
Mayo Clinic Proceedings: Innovations, Quality & Outcomes, Vol 5, Iss 6, Pp 1012-1020 (2021)
Objective: To evaluate the prognostic significance of detectable circulating cell-free DNA (cfDNA) BRAF V600E/K mutations in patients with advanced melanoma enrolled in a clinical trial without BRAF-targeted therapy. Patients and Methods: BRAF V600E/
Externí odkaz:
https://doaj.org/article/eba5613feb94492ca5a70349231da792
Autor:
Jonathan S. Bleeker, MD, Christopher J. Sumey, MD, Steven F. Powell, MD, Preston D. Steen, MD, Michael D. Keppen, MD, Michele Lohr, MD, Thavam Thambi-Pillai, MD, Peter Kurniali, MD, Miroslaw Mazurczak, MD, Mark M. Gitau, MD, Miran J. Blanchard, MD, Ryan K. Nowak, MD, Steven McGraw, MD, Robert Sticca, MD, Daniel Tuvin, MD, Gary Timmerman, MD
Publikováno v:
Surgery Open Science, Vol 2, Iss 4, Pp 25-31 (2020)
Background: Treatment paradigms for borderline resectable pancreatic cancer are evolving with increasing use of neoadjuvant chemotherapy and neoadjuvant chemoradiation. Variations in the definition of borderline resectable pancreatic cancer and neoad
Externí odkaz:
https://doaj.org/article/5d764d46775f4490a0e8ad7e217a1857
Autor:
Harmatz P1, Hendriksz CJ2, Lampe C3, McGill JJ4, Parini R5, Leão Teles E6, Valayannopoulos V7, Cole TJ8, Matousek R9, Graham S9, Guffon N10, Quartel A9, he MPS VI Study Group co investigators were Yasmina Amraoui, Children's Hospital, Md, University of Mainz, Germany, Laila, Arash, Children's Hospital, University of Mainz, Germany, Javier Arroyo, Md, Hospital San Pedro de Alcantara, Hospital de día de Pediatría, Caceres, Spain, Ana, Cecliaíazevedo, Serviço de Genética Médica/HCPA, Md, Department of Genetics/UFRGS, Porto Alegre, Brazil, Barone, RITA MARIA ELISA, Department of Pediatrics, Md, University of Catania, Catania, Italy, Michael Beck, Md, D. N. Bennett Jones, Md, Consultant General Renal Physician, Whitehaven, Philippe Bernard, Md, Centre Hospitalier d'Arras, Arras, France, Thierry Billette de Villemeur, Hôpital Trousseau, Paris, France, Raquel, Boy, Hospital Universitário Pedro Ernesto, Md, Rio de Janeiro, Brazil, Susan, Conrad, Research Center Oakland, Oakland, Ca, Usa, Eduardo Coopman, Md, Hospital del Cobre D. e. Salvador, Calama, Chile, Agata Fiumara, Md, Department of Pediatrics, University of Catania, Catania, Italy, William, Frischman, The Townsville Hospital, Md, Townsville, Australia, Roberto, Giugliani, Phd, Md, Serviço de Genética Médica/HCPA, Department of Genetics/UFRGS, Porto Alegre, Brazil, Elio Gizzi, Md, Children's Hospital Research Center Oakland, Oakland, Usa, Ca, Paul, Harmatz, John J. Hopwood, Department of Genetic Medicine, Women'S, Children's Hospital Adelaide, North Adelaide, Australia, Simon Jones, Md, Royal Manchester Children's Hospital, Manchester, Paige Kaplan, Children's Hospital of Philadelphia, Philadelphia, Pa, Laura Keppen, Md, Department of Pediatrics, University of South Dakota School of Medicine, Sioux Falls, Sd, David Ketteridge, Department of Genetic Medicine, Prof Rudolf Korinthenberg, Universitätsklinikum Freiburg, Zentrum für Kinderheilkunde und Jugendmedizin, Klinik II Neuropädiatrie und Muskelerkrankungen, Freiburg, Germany, Michel, Kretz, Hôpital Civil de Colmar, Md, Le Parc Centre de la Mère et de l'Enfant, Colmar, Elisa Leão Teles, Md, Unidade de Doenças Metabólicas, Departamento Pediatria, Hospital de Sao João, Porto, Portugal, Claudia Lee, Mph, Shuan Pei Lin, MacKay Memorial Hospital, Md, Department of Genetics, Taipei, Taiwan, Lionel Lubitz, Md, Royal Children's Hospital, Melbourne, Ana Maria Martins, Md, Unifesp, Instituto de Oncologia Pediátrica, Graacc/unifesp, Departamento de Pediatria, São Paulo, Brazil, Clara Sá Miranda, M., Unidade de Biologia do Lisossoma e. Peroxisoma, Md, Instituto de Biologia Molecular e. Celular, Porto, Stephanie Oates, RN Department of Genetic Medicine, Anne O'Meara, Md, Our Lady's Hospital for Sick Children, Dublin, Ireland, Ans van der Ploeg, Md, Erasmus MC University Medical Center, Rotterdam, The, Netherlands, Isabel Cristina Neves de Souza, Md, Universidade Federal do Pará, Centro de Ciências Biológicas, Hospital Universitário João de Barros Barreto, Belém, Ray Pais, Md, Pediatric Hematology/Oncology, East Tennessee Children's Hospital, Knoxville, Tn, Gregory Pastores, Md, Phd, NYU Medical Center, Rusk Institute, New York, Usa, Ny, Lorenzo, Pavone, Barbara Plecko, U. n. i. v. Klinik fur Kinder und Jugendheilkunde, Graz, Austria, Silvio, Pozzi, Ospedale Vito Fazzi, Md, UO Pediatria, Lecce, Uwe Preiss, Md, Universitaetsklinik und Poliklinik fuer Kinder, Halle, Emerson Santana Santos, Md, Fundação Universidade de Ciências da Saúde de Alagoas Governador, Departamento de Pediatria, Maceió, Brazil, Maurizio, Scarpa, Department of Pediatrics, University of Padova, Padova, Italy, Schwartz, Ida Vanessa D., David, Sillence, Westmead, Australia, Luiz Carlos Santana da Silva, Phd, Universidade Federal do Pará, Centro de Ciências Biológicas, Hospital Universitário João de Barros Barreto, Belém, Brazil, Julie, Simon, Children's Hospital, Rn, Prof Giovanni Sorge, Department of Pediatrics, Robert Steiner, Departments of Pediatrics, Molecular, Medical, Genetics, Oregon Health Science University, Portland, Usa, Or, Valadares, Eugênia R., Hospital das Clínicas, Faculdade de Medicina da Universidade Federal de Minas Gerais UFMG, Avenida Professor Alfredo Balena, Belo Horizonte Minas Gerais, Bonito Victor, Md, Lewis Waber, Md, Phd, Pediatric Genetics, Metabolism, University of Texas Southwest Medical Center, Dallas, Usa, Tx, John, Waterson, Whitley, Chester B., University of Minnesota Medical School, Minneapolis, Usa, Mn, Edmond Wraith, J., Royal Manchester Children's Hospital, Md, Manchester, U. k.
Publikováno v:
Molecular genetics and metabolism. 122(1-2)
Mucopolysaccharidosis (MPS) VI is an autosomal recessive lysosomal storage disorder arising from deficient activity of N-acetylgalactosamine-4-sulfatase (arylsulfatase B) and subsequent intracellular accumulation of the glycosaminoglycans (GAGs) derm
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a0f77c6e102bd23c0c21993def3378be
https://pubmed.ncbi.nlm.nih.gov/28457718
https://pubmed.ncbi.nlm.nih.gov/28457718
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Autor:
Bleeker JS; Sanford USD Medical Center, Sioux Falls, SD., Sumey CJ; Sanford USD Medical Center, Sioux Falls, SD., Powell SF; Sanford USD Medical Center, Sioux Falls, SD., Steen PD; Sanford Roger Maris Cancer Center, Fargo, ND., Keppen MD; Sanford USD Medical Center, Sioux Falls, SD., Lohr M; Sanford USD Medical Center, Sioux Falls, SD., Thambi-Pillai T; Sanford USD Medical Center, Sioux Falls, SD., Kurniali P; Sanford Cancer Center, Bismarck, ND., Mazurczak M; Sanford USD Medical Center, Sioux Falls, SD., Gitau MM; Sanford Roger Maris Cancer Center, Fargo, ND., Blanchard MJ; Sanford Roger Maris Cancer Center, Fargo, ND., Nowak RK; Sanford USD Medical Center, Sioux Falls, SD., McGraw S; Sanford USD Medical Center, Sioux Falls, SD., Sticca R; Sanford Roger Maris Cancer Center, Fargo, ND., Tuvin D; Sanford Roger Maris Cancer Center, Fargo, ND., Timmerman G; Sanford USD Medical Center, Sioux Falls, SD.
Publikováno v:
Surgery open science [Surg Open Sci] 2020 Jul 29; Vol. 2 (4), pp. 25-31. Date of Electronic Publication: 2020 Jul 29 (Print Publication: 2020).