Zobrazeno 1 - 8 of 8 pro vyhledávání: '"Backman Johansson, Carolina"'
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Measurement of lactate in pleural fluid rapidly identify infection and guide therapy
Autor: Johansson, Niclas, Ydsten, Karin Andersson, Backman-Johansson, Carolina, Vondracek, Martin, Hedlund, Jonas
Publikováno v: Infectious Diseases. 55:396-404
Measurements of pleural fluid biomarkers for rapid identification of complicated parapneumonic effusion (CPPE) are crucial for optimal management. Previous studies for biomarker evaluation were however based on pleura culture, not modern DNA techniqu
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::05e8496e731b539c5a24a430f258d02a
https://doi.org/10.1080/23744235.2023.2192278
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2
Akademický článek
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Akademický článek
Expanded Screening of One Million Swedish Babies with R4S and CLIR for Post-Analytical Evaluation of Data.
Autor: Sörensen L; Centre for Inherited Metabolic Diseases, Karolinska University Hospital Solna, SE-171 76 Stockholm, Sweden; ulrika.vondobeln@sll.se (U.v.D.); henrik.ahlman@sll.se (H.Å.); annika.ohlsson@eskilstuna.se (A.O.); martin.engvall@sll.se (M.E.); karin.naess@ki.se (K.N.); carolina.backman-johansson@sll.se (C.B.-J.); yvonne.m.nordqvist@sll.se (Y.N.); anna.wedell@ki.se (A.W.); rolf.zetterstrom@sll.se (R.H.Z.).; Department of Molecular Medicine and Surgery, Karolinska Institutet, SE-171 76 Stockholm, Sweden., von Döbeln U; Centre for Inherited Metabolic Diseases, Karolinska University Hospital Solna, SE-171 76 Stockholm, Sweden; ulrika.vondobeln@sll.se (U.v.D.); henrik.ahlman@sll.se (H.Å.); annika.ohlsson@eskilstuna.se (A.O.); martin.engvall@sll.se (M.E.); karin.naess@ki.se (K.N.); carolina.backman-johansson@sll.se (C.B.-J.); yvonne.m.nordqvist@sll.se (Y.N.); anna.wedell@ki.se (A.W.); rolf.zetterstrom@sll.se (R.H.Z.).; Department of Medical Biochemistry and Biophysics, Division of Molecular Metabolism, Karolinska Institutet, SE-171 77 Stockholm, Sweden., Åhlman H; Centre for Inherited Metabolic Diseases, Karolinska University Hospital Solna, SE-171 76 Stockholm, Sweden; ulrika.vondobeln@sll.se (U.v.D.); henrik.ahlman@sll.se (H.Å.); annika.ohlsson@eskilstuna.se (A.O.); martin.engvall@sll.se (M.E.); karin.naess@ki.se (K.N.); carolina.backman-johansson@sll.se (C.B.-J.); yvonne.m.nordqvist@sll.se (Y.N.); anna.wedell@ki.se (A.W.); rolf.zetterstrom@sll.se (R.H.Z.)., Ohlsson A; Centre for Inherited Metabolic Diseases, Karolinska University Hospital Solna, SE-171 76 Stockholm, Sweden; ulrika.vondobeln@sll.se (U.v.D.); henrik.ahlman@sll.se (H.Å.); annika.ohlsson@eskilstuna.se (A.O.); martin.engvall@sll.se (M.E.); karin.naess@ki.se (K.N.); carolina.backman-johansson@sll.se (C.B.-J.); yvonne.m.nordqvist@sll.se (Y.N.); anna.wedell@ki.se (A.W.); rolf.zetterstrom@sll.se (R.H.Z.).; Department of Medical Biochemistry and Biophysics, Division of Molecular Metabolism, Karolinska Institutet, SE-171 77 Stockholm, Sweden., Engvall M; Centre for Inherited Metabolic Diseases, Karolinska University Hospital Solna, SE-171 76 Stockholm, Sweden; ulrika.vondobeln@sll.se (U.v.D.); henrik.ahlman@sll.se (H.Å.); annika.ohlsson@eskilstuna.se (A.O.); martin.engvall@sll.se (M.E.); karin.naess@ki.se (K.N.); carolina.backman-johansson@sll.se (C.B.-J.); yvonne.m.nordqvist@sll.se (Y.N.); anna.wedell@ki.se (A.W.); rolf.zetterstrom@sll.se (R.H.Z.).; Department of Molecular Medicine and Surgery, Karolinska Institutet, SE-171 76 Stockholm, Sweden., Naess K; Centre for Inherited Metabolic Diseases, Karolinska University Hospital Solna, SE-171 76 Stockholm, Sweden; ulrika.vondobeln@sll.se (U.v.D.); henrik.ahlman@sll.se (H.Å.); annika.ohlsson@eskilstuna.se (A.O.); martin.engvall@sll.se (M.E.); karin.naess@ki.se (K.N.); carolina.backman-johansson@sll.se (C.B.-J.); yvonne.m.nordqvist@sll.se (Y.N.); anna.wedell@ki.se (A.W.); rolf.zetterstrom@sll.se (R.H.Z.).; Department of Medical Biochemistry and Biophysics, Division of Molecular Metabolism, Karolinska Institutet, SE-171 77 Stockholm, Sweden., Backman-Johansson C; Centre for Inherited Metabolic Diseases, Karolinska University Hospital Solna, SE-171 76 Stockholm, Sweden; ulrika.vondobeln@sll.se (U.v.D.); henrik.ahlman@sll.se (H.Å.); annika.ohlsson@eskilstuna.se (A.O.); martin.engvall@sll.se (M.E.); karin.naess@ki.se (K.N.); carolina.backman-johansson@sll.se (C.B.-J.); yvonne.m.nordqvist@sll.se (Y.N.); anna.wedell@ki.se (A.W.); rolf.zetterstrom@sll.se (R.H.Z.)., Nordqvist Y; Centre for Inherited Metabolic Diseases, Karolinska University Hospital Solna, SE-171 76 Stockholm, Sweden; ulrika.vondobeln@sll.se (U.v.D.); henrik.ahlman@sll.se (H.Å.); annika.ohlsson@eskilstuna.se (A.O.); martin.engvall@sll.se (M.E.); karin.naess@ki.se (K.N.); carolina.backman-johansson@sll.se (C.B.-J.); yvonne.m.nordqvist@sll.se (Y.N.); anna.wedell@ki.se (A.W.); rolf.zetterstrom@sll.se (R.H.Z.).; Department of Medical Biochemistry and Biophysics, Division of Molecular Metabolism, Karolinska Institutet, SE-171 77 Stockholm, Sweden., Wedell A; Centre for Inherited Metabolic Diseases, Karolinska University Hospital Solna, SE-171 76 Stockholm, Sweden; ulrika.vondobeln@sll.se (U.v.D.); henrik.ahlman@sll.se (H.Å.); annika.ohlsson@eskilstuna.se (A.O.); martin.engvall@sll.se (M.E.); karin.naess@ki.se (K.N.); carolina.backman-johansson@sll.se (C.B.-J.); yvonne.m.nordqvist@sll.se (Y.N.); anna.wedell@ki.se (A.W.); rolf.zetterstrom@sll.se (R.H.Z.).; Department of Molecular Medicine and Surgery, Karolinska Institutet, SE-171 76 Stockholm, Sweden., Zetterström RH; Centre for Inherited Metabolic Diseases, Karolinska University Hospital Solna, SE-171 76 Stockholm, Sweden; ulrika.vondobeln@sll.se (U.v.D.); henrik.ahlman@sll.se (H.Å.); annika.ohlsson@eskilstuna.se (A.O.); martin.engvall@sll.se (M.E.); karin.naess@ki.se (K.N.); carolina.backman-johansson@sll.se (C.B.-J.); yvonne.m.nordqvist@sll.se (Y.N.); anna.wedell@ki.se (A.W.); rolf.zetterstrom@sll.se (R.H.Z.).; Department of Molecular Medicine and Surgery, Karolinska Institutet, SE-171 76 Stockholm, Sweden.
Publikováno v: International journal of neonatal screening [Int J Neonatal Screen] 2020 May 27; Vol. 6 (2), pp. 42. Date of Electronic Publication: 2020 May 27 (Print Publication: 2020).
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8
Akademický článek
Newborn screening for sickle cell disease in Europe: recommendations from a Pan-European Consensus Conference.
Autor: Lobitz S; Department of Paediatric Oncology/Haematology, Kinderkrankenhaus Amsterdamer Straße, Cologne, Germany.; Department of Paediatric Oncology/Haematology/BMT, Charité - Universitätsmedizin Berlin, Berlin, Germany., Telfer P; Department of Haematology, Bart's Health National Health Service Trust, Royal London Hospital, London, United Kingdom., Cela E; Department of Paediatric Oncology/Haematology, Hospital Universitario General Gregorio Marañón, Facultad de Medicina, Universidad Complutense Madrid, Madrid, Spain., Allaf B; NBS Laboratory for haemoglobinopathies, Hôpital universitaire Robert-Debré, Paris, France., Angastiniotis M; Thalassaemia International Federation, Nicosia, Cyprus., Backman Johansson C; Centre for Inherited Metabolic Diseases - PKU Laboratory, Karolinska University Hospital, Stockholm, Sweden., Badens C; Département de génétique médicale, Aix-Marseille Université, Hôpital de la Timone, Marseille, France., Bento C; Department of Haematology, Centro Hospitalar e Universitário de Coimbra, Coimbra, Portugal., Bouva MJ; Centre for Infectious Disease Research, Diagnostics and Screening, National Institute for Public Health and the Environment, Bilthoven, The Netherlands., Canatan D; Haemoglobinopathy Diagnosis Centre, Mediterranean Blood Diseases Foundation, Antalya, Turkey., Charlton M; Public Health England, NHS Sickle Cell and Thalassaemia Screening Programme, London, United Kingdom., Coppinger C; Public Health England, NHS Sickle Cell and Thalassaemia Screening Programme, London, United Kingdom., Daniel Y; Public Health England, NHS Sickle Cell and Thalassaemia Screening Programme, London, United Kingdom., de Montalembert M; Department of Paediatrics, Reference Centre for Sickle Cell Disease, AP-HP Hôpital Universitaire Necker-Enfants Malades, Paris, France., Ducoroy P; BIOMANEO, Dijon, France., Dulin E; Department of Paediatric Oncology/Haematology, Hospital Universitario General Gregorio Marañón, Facultad de Medicina, Universidad Complutense Madrid, Madrid, Spain., Fingerhut R; NBS Laboratory, Universitätskinderspital Zürich- Eleonorenstiftung, Zurich, Switzerland., Frömmel C; Labor Berlin - Charité Vivantes GmbH, Berlin, Germany., García-Morin M; Department of Paediatric Oncology/Haematology, Hospital Universitario General Gregorio Marañón, Facultad de Medicina, Universidad Complutense Madrid, Madrid, Spain., Gulbis B; Department of Clinical Chemistry, Cliniques universitaires de Bruxelles, Hôpital Erasme - ULB, Bruxelles, Belgium., Holtkamp U; Screening-Labor Hannover, Ronnenberg, Germany., Inusa B; Evelina London Children's Hospital, Guy's and St Thomas' NHS Trust, London, United Kingdom., James J; Sickle Cell Society UK, London, United Kingdom., Kleanthous M; Molecular Genetics Thalassaemia Department, The Cyprus School of Molecular Medicine, The Cyprus Institute of Neurology and Genetics, Nicosia, Cyprus., Klein J; NBS Laboratory, Charité - Universitätsmedizin Berlin, Berlin, Germany., Kunz JB; Department of Paediatric Oncology, Haematology and Immunology, University of Heidelberg, Heidelberg, Germany., Langabeer L; Our Lady's Children's Hospital, Crumlin, Dublin, Ireland., Lapouméroulie C; Laboratoire d'Excellence GR-Ex, UMR_S1134, Inserm, Université Paris Diderot, Sorbonne Paris Cité, Institut National de la Transfusion Sanguine, Paris, France., Marcao A; Department of Human Genetics - Newborn Screening, Metabolism and Genetics Unit, Instituto Nacional de Saúde Dr. Ricardo Jorge, Porto, Portugal., Marín Soria JL; Programa de Cribado Neonatal, Sección Errores Congénitos del Metabolismo, Servicio de Bioquímica y Genética Molecular, Hospital Clínic, Barcelona, Spain., McMahon C; Our Lady's Children's Hospital, Crumlin, Dublin, Ireland., Ohene-Frempong K; Sickle Cell Foundation of Ghana, Kumasi, Ghana., Périni JM; NBS Laboratory, University Hospital of Lille, Lille, France., Piel FB; Department of Epidemiology & Biostatistics, School of Public Health, Imperial College London, London, United Kingdom., Russo G; Department of Clinical and Experimental Medicine, Paediatric Haemato-Oncology Unit, University of Catania, Catania, Italy., Sainati L; Department of Child and Maternal Health, Clinic of Paediatric Haematology/Oncology, Azienda Ospedaliera-Università di Padova, Padova, Italy., Schmugge M; Department of Paediatric Haematology, Universitätskinderspital Zürich - Eleonorenstiftung, Zurich, Switzerland., Streetly A; School of Population Health and Environmental Sciences, Faculty of Life Sciences & Medicine, King's College London, London, United Kingdom.; Division of Healthcare Public Health, Health Protection and Medical Directorate, Public Health England, London, United Kingdom., Tshilolo L; Centre Hospitalier Monkole, Kinshasa, Democratic Republic of Congo., Turner C; WellChild Laboratory, Evelina London Children's Hospital, London, United Kingdom., Venturelli D; Department of Transfusion Medicine, University Hospital of Modena, Modena, Italy., Vilarinho L; Department of Human Genetics - Newborn Screening, Metabolism and Genetics Unit, Instituto Nacional de Saúde Dr. Ricardo Jorge, Porto, Portugal., Yahyaoui R; Instituto de Investigación Biomédica de Málaga, Málaga Regional University Hospital, Málaga, Spain., Elion J; Laboratoire d'Excellence GR-Ex, UMR_S1134, Inserm, Université Paris Diderot, Sorbonne Paris Cité, Institut National de la Transfusion Sanguine, Paris, France., Colombatti R; Department of Child and Maternal Health, Clinic of Paediatric Haematology/Oncology, Azienda Ospedaliera-Università di Padova, Padova, Italy.
Publikováno v: British journal of haematology [Br J Haematol] 2018 Nov; Vol. 183 (4), pp. 648-660. Date of Electronic Publication: 2018 Oct 18.
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