المؤلفون: Degeling, K, Grazziotin Lago, L, Hayeems, RZ, Boycott, KM, Bernier, FP, Mendoza-Londono, R, Seeger, TA, Marshall, D

المصدر: In Value in Health July 2022 25(7) Supplement:S344-S344

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المؤلفون: Lee W; Program in Child Health Evaluative Sciences, The Hospital for Sick Children, Toronto, ON, Canada; Institute of Health Policy, Management and Evaluation, University of Toronto, Toronto, ON, Canada., Hirjikaka D; Genomics Health Services Research Program, Li Ka Shing Knowledge Institute, St. Michael's Hospital, Unity Health Toronto, Toronto, ON, Canada., Grewal S; Genomics Health Services Research Program, Li Ka Shing Knowledge Institute, St. Michael's Hospital, Unity Health Toronto, Toronto, ON, Canada., Shaw A; Genomics Health Services Research Program, Li Ka Shing Knowledge Institute, St. Michael's Hospital, Unity Health Toronto, Toronto, ON, Canada., Luca S; Program in Child Health Evaluative Sciences, The Hospital for Sick Children, Toronto, ON, Canada., Clausen M; Genomics Health Services Research Program, Li Ka Shing Knowledge Institute, St. Michael's Hospital, Unity Health Toronto, Toronto, ON, Canada., Bombard Y; Institute of Health Policy, Management and Evaluation, University of Toronto, Toronto, ON, Canada; Genomics Health Services Research Program, Li Ka Shing Knowledge Institute, St. Michael's Hospital, Unity Health Toronto, Toronto, ON, Canada., Hayeems RZ; Program in Child Health Evaluative Sciences, The Hospital for Sick Children, Toronto, ON, Canada; Institute of Health Policy, Management and Evaluation, University of Toronto, Toronto, ON, Canada. Electronic address: robin.hayeems@sickkids.ca.

مؤلفون مشاركون: Genetics Navigator Study Team

المصدر: Genetics in medicine : official journal of the American College of Medical Genetics [Genet Med] 2024 Jun; Vol. 26 (6), pp. 101122. Date of Electronic Publication: 2024 Mar 14.

نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: Elsevier Country of Publication: United States NLM ID: 9815831 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1530-0366 (Electronic) Linking ISSN: 10983600 NLM ISO Abbreviation: Genet Med Subsets: MEDLINE

مواضيع طبية MeSH: Genetic Testing*/methods, Humans ; Canada ; Attitude of Health Personnel ; Health Personnel ; Female ; Male ; Genetics, Medical ; Adult

المؤلفون: Xiao B; Child Health Evaluative Sciences, Peter Gilgan Centre for Research and Learning, The Hospital for Sick Children, Toronto, Ontario, Canada, penny.xiao@sickkids.ca., Yan J; Child Health Evaluative Sciences, Peter Gilgan Centre for Research and Learning, The Hospital for Sick Children, Toronto, Ontario, Canada., Hayeems RZ; Child Health Evaluative Sciences, Peter Gilgan Centre for Research and Learning, The Hospital for Sick Children, Toronto, Ontario, Canada.; Institute of Health Policy Management and Evaluation, University of Toronto, Toronto, Ontario, Canada.

المصدر: Public health genomics [Public Health Genomics] 2024; Vol. 27 (1), pp. 45-56. Date of Electronic Publication: 2024 Feb 21.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: S. Karger Country of Publication: Switzerland NLM ID: 101474167 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1662-8063 (Electronic) Linking ISSN: 16624246 NLM ISO Abbreviation: Public Health Genomics Subsets: MEDLINE

مواضيع طبية MeSH: Public Opinion* , Social Media* , Noninvasive Prenatal Testing*/methods, Humans ; Female ; Pregnancy ; Emotions

المؤلفون: Hartley T; Children's Hospital of Eastern Ontario Research Institute, Ottawa, Ontario, Canada; University of Ottawa, Ottawa, Ontario, Canada. Electronic address: thartley@cheo.on.ca., Gillespie MK; Children's Hospital of Eastern Ontario Research Institute, Ottawa, Ontario, Canada., Graham ID; University of Ottawa, Ottawa, Ontario, Canada; The Ottawa Hospital Research Institute, Ottawa, Ontario, Canada., Hayeems RZ; Hospital for Sick Children, Toronto, Ontario, Canada; University of Toronto, Toronto, Ontario, Canada., Li S; Children's Hospital of Eastern Ontario Research Institute, Ottawa, Ontario, Canada., Sampson M; Children's Hospital of Eastern Ontario Research Institute, Ottawa, Ontario, Canada., Boycott KM; Children's Hospital of Eastern Ontario Research Institute, Ottawa, Ontario, Canada; University of Ottawa, Ottawa, Ontario, Canada; Children's Hospital of Eastern Ontario, Ottawa, Ontario, Canada., Potter BK; University of Ottawa, Ottawa, Ontario, Canada. Electronic address: beth.potter@uottawa.ca.

المصدر: Genetics in medicine : official journal of the American College of Medical Genetics [Genet Med] 2023 Nov; Vol. 25 (11), pp. 100948. Date of Electronic Publication: 2023 Aug 05.

نوع المنشور: Journal Article; Review; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: Elsevier Country of Publication: United States NLM ID: 9815831 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1530-0366 (Electronic) Linking ISSN: 10983600 NLM ISO Abbreviation: Genet Med Subsets: MEDLINE

مواضيع طبية MeSH: Exome*/genetics , Societies*, Humans ; Chromosome Mapping

المؤلفون: D'Gama AM; Epilepsy Genetics Program, Division of Epilepsy and Neurophysiology, Department of Neurology, Boston Children's Hospital, Boston, MA, USA; Division of Newborn Medicine, Department of Pediatrics, Boston Children's Hospital, Boston, MA, USA; Department of Pediatrics, Harvard Medical School, Boston, MA, USA., Mulhern S; Victorian Clinical Genetics Service, Melbourne, VIC, Australia; Murdoch Children's Research Institute, Melbourne, VIC, Australia., Sheidley BR; Epilepsy Genetics Program, Division of Epilepsy and Neurophysiology, Department of Neurology, Boston Children's Hospital, Boston, MA, USA., Boodhoo F; Department of Neurology, Great Ormond Street Hospital, London, UK., Buts S; Department of Paediatric Neurology, Aachen University Hospital, Germany., Chandler NJ; North Thames Genomic Laboratory Hub, Great Ormond Street NHS Foundation Trust, London, UK., Cobb J; Murdoch Children's Research Institute, Melbourne, VIC, Australia., Curtis M; Division of Genome Diagnostics, Hospital for Sick Children, Toronto, ON, Canada., Higginbotham EJ; Division of Genome Diagnostics, Hospital for Sick Children, Toronto, ON, Canada., Holland J; Department of Neurology, Great Ormond Street Hospital, London, UK., Khan T; Program in Genetics and Genome Biology, SickKids Research Institute, Toronto, ON, Canada., Koh J; Epilepsy Genetics Program, Division of Epilepsy and Neurophysiology, Department of Neurology, Boston Children's Hospital, Boston, MA, USA., Liang NSY; Department of Genetic Counselling, Hospital for Sick Children, Toronto, ON, Canada; Department of Molecular Genetics, University of Toronto, Toronto, ON, Canada., McRae L; Division of Neurology, Department of Paediatrics, Hospital for Sick Children, Toronto, ON, Canada., Nesbitt SE; North Thames Genomic Laboratory Hub, Great Ormond Street NHS Foundation Trust, London, UK; Genetics and Genomic Medicine, UCL Great Ormond Street Institute of Child Health, London, UK., Oby BT; Epilepsy Genetics Program, Division of Epilepsy and Neurophysiology, Department of Neurology, Boston Children's Hospital, Boston, MA, USA., Paternoster B; North Thames Genomic Laboratory Hub, Great Ormond Street NHS Foundation Trust, London, UK., Patton A; Department of Paediatrics, Frimley Park Hospital, Frimley Health NHS Foundation Trust, Frimley, UK., Rose G; North Thames Genomic Laboratory Hub, Great Ormond Street NHS Foundation Trust, London, UK., Scotchman E; North Thames Genomic Laboratory Hub, Great Ormond Street NHS Foundation Trust, London, UK., Valentine R; Epilepsy Genetics Program, Division of Epilepsy and Neurophysiology, Department of Neurology, Boston Children's Hospital, Boston, MA, USA., Wiltrout KN; Epilepsy Genetics Program, Division of Epilepsy and Neurophysiology, Department of Neurology, Boston Children's Hospital, Boston, MA, USA; Department of Neurology, Harvard Medical School, Boston, MA, USA., Hayeems RZ; Program in Child Health Evaluative Sciences, SickKids Research Institute, Toronto, ON, Canada; Institute of Health Policy, Management, and Evaluation, University of Toronto, Toronto, ON, Canada., Jain P; Division of Neurology, Department of Paediatrics, Hospital for Sick Children, Toronto, ON, Canada; Department of Paediatrics, Temerty Faculty of Medicine, University of Toronto, Toronto, ON, Canada., Lunke S; Victorian Clinical Genetics Service, Melbourne, VIC, Australia; Murdoch Children's Research Institute, Melbourne, VIC, Australia; Department of Pathology, University of Melbourne, Melbourne, VIC, Australia., Marshall CR; Division of Genome Diagnostics, Hospital for Sick Children, Toronto, ON, Canada; Department of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, ON, Canada., Rockowitz S; The Manton Center for Orphan Disease Research, Division of Genetics and Genomics, Boston Children's Hospital, Boston, MA, USA; Research Computing, Boston Children's Hospital, Boston, MA, USA; Division of Genetics and Genomics, Boston Children's Hospital, Boston, MA, USA., Sebire NJ; DRIVE Centre, Great Ormond Street Hospital for Children, London, UK., Stark Z; Victorian Clinical Genetics Service, Melbourne, VIC, Australia; Department of Paediatrics, University of Melbourne, Melbourne, VIC, Australia., White SM; Victorian Clinical Genetics Service, Melbourne, VIC, Australia; Department of Paediatrics, University of Melbourne, Melbourne, VIC, Australia., Chitty LS; North Thames Genomic Laboratory Hub, Great Ormond Street NHS Foundation Trust, London, UK; Genetics and Genomic Medicine, UCL Great Ormond Street Institute of Child Health, London, UK., Cross JH; Department of Neurology, Great Ormond Street Hospital, London, UK; Developmental Neurosciences, UCL Great Ormond Street Institute of Child Health, London, UK., Scheffer IE; Murdoch Children's Research Institute, Melbourne, VIC, Australia; Department of Paediatrics, University of Melbourne, Melbourne, VIC, Australia; Department of Medicine, University of Melbourne, Melbourne, VIC, Australia; Austin Health, and Florey Institute of Neuroscience and Mental Health, Melbourne, VIC, Australia; Department of Neurology, Royal Children's Hospital, Melbourne, VIC, Australia., Chau V; Division of Neurology, Department of Paediatrics, Hospital for Sick Children, Toronto, ON, Canada; Department of Paediatrics, Temerty Faculty of Medicine, University of Toronto, Toronto, ON, Canada., Costain G; Program in Genetics and Genome Biology, SickKids Research Institute, Toronto, ON, Canada; Department of Molecular Genetics, University of Toronto, Toronto, ON, Canada; Department of Paediatrics, Temerty Faculty of Medicine, University of Toronto, Toronto, ON, Canada; Division of Clinical and Metabolic Genetics, Department of Paediatrics, Hospital for Sick Children, Toronto, ON, Canada., Poduri A; Epilepsy Genetics Program, Division of Epilepsy and Neurophysiology, Department of Neurology, Boston Children's Hospital, Boston, MA, USA; Department of Neurology, Harvard Medical School, Boston, MA, USA., Howell KB; Murdoch Children's Research Institute, Melbourne, VIC, Australia; Department of Neurology, Royal Children's Hospital, Melbourne, VIC, Australia., McTague A; Department of Neurology, Great Ormond Street Hospital, London, UK; Developmental Neurosciences, Zayed Centre for Research into Rare Disease in Children, UCL Great Ormond Street Institute of Child Health, London, UK. Electronic address: a.mctague@ucl.ac.uk.

مؤلفون مشاركون: Gene-STEPS Study Group, IPCHiP Executive Committee

المصدر: The Lancet. Neurology [Lancet Neurol] 2023 Sep; Vol. 22 (9), pp. 812-825.

نوع المنشور: Multicenter Study; Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: Lancet Pub. Group Country of Publication: England NLM ID: 101139309 Publication Model: Print Cited Medium: Internet ISSN: 1474-4465 (Electronic) Linking ISSN: 14744422 NLM ISO Abbreviation: Lancet Neurol Subsets: MEDLINE

مواضيع طبية MeSH: Seizures, Febrile* , Epilepsy*/diagnosis , Epilepsy*/genetics, Male ; Female ; Infant, Newborn ; Humans ; Child ; Pilot Projects ; Cohort Studies ; Feasibility Studies ; Ontario

المؤلفون: Liang NSY; Department of Genetic Counselling, The Hospital for Sick Children, Toronto, ON M5G 1X8, Canada.; Division of Clinical and Metabolic Genetics, The Hospital for Sick Children, Toronto, ON M5G 1X8, Canada., Watts-Dickens A; Department of Genetic Counselling, The Hospital for Sick Children, Toronto, ON M5G 1X8, Canada.; Division of Clinical and Metabolic Genetics, The Hospital for Sick Children, Toronto, ON M5G 1X8, Canada.; Department of Molecular Genetics, University of Toronto, Toronto, ON M5S 1A8, Canada., Chitayat D; Division of Clinical and Metabolic Genetics, The Hospital for Sick Children, Toronto, ON M5G 1X8, Canada.; Department of Molecular Genetics, University of Toronto, Toronto, ON M5S 1A8, Canada., Babul-Hirji R; Department of Genetic Counselling, The Hospital for Sick Children, Toronto, ON M5G 1X8, Canada.; Division of Clinical and Metabolic Genetics, The Hospital for Sick Children, Toronto, ON M5G 1X8, Canada.; Department of Molecular Genetics, University of Toronto, Toronto, ON M5S 1A8, Canada., Chakraborty P; Newborn Screening Ontario, Ottawa, ON K1H 8M8, Canada., Hayeems RZ; Child Health Evaluative Sciences, The Hospital for Sick Children, Toronto, ON M5G 1X8, Canada.; Health Policy, Management and Evaluation, University of Toronto, ON M5T 3M6, Canada.

المصدر: Children (Basel, Switzerland) [Children (Basel)] 2023 Aug 09; Vol. 10 (8). Date of Electronic Publication: 2023 Aug 09.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: MDPI AG Country of Publication: Switzerland NLM ID: 101648936 Publication Model: Electronic Cited Medium: Print ISSN: 2227-9067 (Print) Linking ISSN: 22279067 NLM ISO Abbreviation: Children (Basel) Subsets: PubMed not MEDLINE

المؤلفون: Hayeems RZ; Child Health Evaluative Sciences, Peter Gilgan Centre for Research and Learning, The Hospital for Sick Children, Toronto, Ontario, Canada; Institute of Health Policy Management and Evaluation, University of Toronto, Toronto, Ontario, Canada. Electronic address: robin.hayeems@sickkids.ca., Luca S; Child Health Evaluative Sciences, Peter Gilgan Centre for Research and Learning, The Hospital for Sick Children, Toronto, Ontario, Canada., Chad L; Division of Clinical and Metabolic Genetics, The Hospital for Sick Children, Toronto, Ontario, Canada; Department of Pediatrics, University of Toronto, Toronto, Ontario, Canada., Quercia N; Division of Clinical and Metabolic Genetics, The Hospital for Sick Children, Toronto, Ontario, Canada; Department of Genetic Counselling, The Hospital for Sick Children, Toronto, Ontario, Canada; Department of Molecular Genetics, Temerty Faculty of Medicine, University of Toronto, Toronto, Ontario, Canada., Xiao B; Child Health Evaluative Sciences, Peter Gilgan Centre for Research and Learning, The Hospital for Sick Children, Toronto, Ontario, Canada., Hossain A; Biostatistics, Design and Analysis Unit, The Hospital for Sick Children, Toronto, Ontario, Canada., Meyn MS; Center for Human Genomics and Precision Medicine, The University of Wisconsin School of Medicine and Public Health, Madison, Wisconsin, USA., Pullenayegum E; Child Health Evaluative Sciences, Peter Gilgan Centre for Research and Learning, The Hospital for Sick Children, Toronto, Ontario, Canada; Dalla Lana School of Public Health, University of Toronto, Toronto, Ontario, Canada., Ungar WJ; Child Health Evaluative Sciences, Peter Gilgan Centre for Research and Learning, The Hospital for Sick Children, Toronto, Ontario, Canada; Institute of Health Policy Management and Evaluation, University of Toronto, Toronto, Ontario, Canada.

المصدر: Clinical therapeutics [Clin Ther] 2023 Aug; Vol. 45 (8), pp. 729-735. Date of Electronic Publication: 2023 Jul 27.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: Excerpta Medica Country of Publication: United States NLM ID: 7706726 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1879-114X (Electronic) Linking ISSN: 01492918 NLM ISO Abbreviation: Clin Ther Subsets: MEDLINE

المؤلفون: Ungar WJ; Program in Child Health Evaluative Sciences, Hospital for Sick Children Research Institute, Toronto, Ontario, Canada; Institute for Health Policy, Management and Evaluation, University of Toronto, Toronto, Ontario, Canada. Electronic address: wendy.ungar@sickkids.ca., Hayeems RZ; Program in Child Health Evaluative Sciences, Hospital for Sick Children Research Institute, Toronto, Ontario, Canada; Institute for Health Policy, Management and Evaluation, University of Toronto, Toronto, Ontario, Canada., Marshall CR; Genome Diagnostics, Department of Paediatric Laboratory Medicine, Hospital for Sick Children, Toronto, Ontario, Canada., Gillespie MK; Children's Hospital of Eastern Ontario Research Institute, University of Ottawa, Ottawa, Ontario, Canada., Szuto A; Division of Clinical and Metabolic Genetics, Hospital for Sick Children, Toronto, Ontario, Canada., Chisholm C; Department of Genetics, Children's Hospital of Eastern Ontario, Ottawa, Ontario, Canada., James Stavropoulos D; Genome Diagnostics, Department of Paediatric Laboratory Medicine, Hospital for Sick Children, Toronto, Ontario, Canada., Huang L; Department of Genetics, Children's Hospital of Eastern Ontario, Ottawa, Ontario, Canada., Jarinova O; Children's Hospital of Eastern Ontario Research Institute, University of Ottawa, Ottawa, Ontario, Canada; Department of Genetics, Children's Hospital of Eastern Ontario, Ottawa, Ontario, Canada., Wu V; Program in Child Health Evaluative Sciences, Hospital for Sick Children Research Institute, Toronto, Ontario, Canada., Tsiplova K; Program in Child Health Evaluative Sciences, Hospital for Sick Children Research Institute, Toronto, Ontario, Canada., Lau L; Genome Diagnostics, Department of Paediatric Laboratory Medicine, Hospital for Sick Children, Toronto, Ontario, Canada., Lee W; Institute for Health Policy, Management and Evaluation, University of Toronto, Toronto, Ontario, Canada; Division of Clinical and Metabolic Genetics, Hospital for Sick Children, Toronto, Ontario, Canada., Venkataramanan V; Program in Child Health Evaluative Sciences, Hospital for Sick Children Research Institute, Toronto, Ontario, Canada., Sawyer S; Department of Genetics, Children's Hospital of Eastern Ontario, Ottawa, Ontario, Canada., Mendoza-Londono R; Division of Clinical and Metabolic Genetics, Hospital for Sick Children, Toronto, Ontario, Canada., Somerville MJ; Genome Diagnostics, Department of Paediatric Laboratory Medicine, Hospital for Sick Children, Toronto, Ontario, Canada., Boycott KM; Children's Hospital of Eastern Ontario Research Institute, University of Ottawa, Ottawa, Ontario, Canada; Department of Genetics, Children's Hospital of Eastern Ontario, Ottawa, Ontario, Canada.

مؤلفون مشاركون: Genome Sequencing Ontario Secondary Findings Study Team

المصدر: Clinical therapeutics [Clin Ther] 2023 Aug; Vol. 45 (8), pp. 702-709. Date of Electronic Publication: 2023 Jul 14.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: Excerpta Medica Country of Publication: United States NLM ID: 7706726 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1879-114X (Electronic) Linking ISSN: 01492918 NLM ISO Abbreviation: Clin Ther Subsets: MEDLINE

المؤلفون: Currie GR; Department of Pediatrics, Health Research Innovation Centre, University of Calgary, Room 3C56, 3280 Hospital Drive NW, Calgary, AB, T2N 4Z6, Canada. currie@ucalgary.ca.; Department of Community Health Sciences, University of Calgary, Calgary, AB, Canada. currie@ucalgary.ca.; Alberta Children's Hospital Research Institute, University of Calgary, Calgary, AB, Canada. currie@ucalgary.ca., Gerber B; Department of Community Health Sciences, University of Calgary, Calgary, AB, Canada., Lorenzetti D; Department of Community Health Sciences, University of Calgary, Calgary, AB, Canada.; Health Sciences Library, University of Calgary, Calgary, AB, Canada., MacDonald K; Department of Community Health Sciences, University of Calgary, Calgary, AB, Canada., Benseler SM; Department of Pediatrics, Health Research Innovation Centre, University of Calgary, Room 3C56, 3280 Hospital Drive NW, Calgary, AB, T2N 4Z6, Canada.; Alberta Children's Hospital Research Institute, University of Calgary, Calgary, AB, Canada.; Alberta Health Services, Calgary, AB, Canada., Bernier FP; Alberta Children's Hospital Research Institute, University of Calgary, Calgary, AB, Canada.; Department of Medical Genetics, Alberta Children's Hospital, Calgary, AB, Canada., Boycott KM; Department of Genetics, Children's Hospital of Eastern Ontario, Ottawa, ON, Canada.; Children's Hospital of Eastern Ontario Research Institute, University of Ottawa, Ottawa, ON, Canada., Carias KV; Genome Alberta, Calgary, AB, Canada., Hamelin B; Ontario Genomics Institute, Toronto, ON, Canada., Hayeems RZ; Child Health Evaluative Sciences, Hospital for Sick Children, Toronto, ON, Canada.; Institute of Health Policy Management and Evaluation, University of Toronto, Toronto, ON, Canada., LeBlanc C; Department of Pediatrics, Faculty of Medicine, McGill University, Montreal, Quebec, Canada., Twilt M; Department of Pediatrics, Cumming School of Medicine, McCaig Institute for Bone and Joint Health, and the Alberta Children's Hospital Research Institute, University of Calgary, Calgary, AB, Canada., van Rooijen G; Genome Alberta, Calgary, AB, Canada., Wong-Rieger D; Canadian Organization for Rare Disorders (CORD), Toronto, ON, Canada., Yeung RSM; Departments of Paediatrics, Immunology and Medical Science, The Hospital for Sick Children, University of Toronto, Toronto, ON, Canada., Marshall DA; Department of Community Health Sciences, University of Calgary, Calgary, AB, Canada.; Alberta Children's Hospital Research Institute, University of Calgary, Calgary, AB, Canada.; McCaig Institute for Bone and Joint Health, University of Calgary, Calgary, AB, Canada.; O'Brien Institute for Public Health, University of Calgary, Calgary, AB, Canada.

المصدر: PharmacoEconomics [Pharmacoeconomics] 2023 Jul; Vol. 41 (7), pp. 803-818. Date of Electronic Publication: 2023 Apr 07.

نوع المنشور: Review; Journal Article; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: Adis, Springer International Country of Publication: New Zealand NLM ID: 9212404 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1179-2027 (Electronic) Linking ISSN: 11707690 NLM ISO Abbreviation: Pharmacoeconomics

مواضيع طبية MeSH: Rare Diseases*/therapy , Delivery of Health Care*, Humans ; Chronic Disease ; Socioeconomic Factors