부산대학교 도서관

Wang Y; Children's Hospital of Fudan University and Institutes of Biomedical Sciences of Fudan University, Shanghai, China.; Xu Y; Department of Pediatrics, Henan Key Laboratory of Child Brain Injury and Henan Pediatric Clinical Research Center, The Third Affiliated Hospital and Institute of Neuroscience of Zhengzhou University, Zhengzhou, China.; Zhou C; Rehabilitation Department, Henan Key Laboratory of Child Genetics and Metabolism, Children's Hospital of Zhengzhou University, Zhengzhou, China.; Cheng Y; Children's Hospital of Fudan University and Institutes of Biomedical Sciences of Fudan University, Shanghai, China.; Shanghai Center for Women and Children's Health, Shanghai, China.; Qiao N; State Key Laboratory of Medical Genomics, Shanghai Institute of Hematology, National Research Center for Translational Medicine (Shanghai), and School of Life Sciences and Biotechnology, Shanghai Jiao Tong University, Shanghai, China.; Shang Q; Rehabilitation Department, Henan Key Laboratory of Child Genetics and Metabolism, Children's Hospital of Zhengzhou University, Zhengzhou, China.; Xia L; Department of Pediatrics, Henan Key Laboratory of Child Brain Injury and Henan Pediatric Clinical Research Center, The Third Affiliated Hospital and Institute of Neuroscience of Zhengzhou University, Zhengzhou, China.; Song J; Department of Pediatrics, Henan Key Laboratory of Child Brain Injury and Henan Pediatric Clinical Research Center, The Third Affiliated Hospital and Institute of Neuroscience of Zhengzhou University, Zhengzhou, China.; Gao C; Rehabilitation Department, Henan Key Laboratory of Child Genetics and Metabolism, Children's Hospital of Zhengzhou University, Zhengzhou, China.; Qiao Y; Children's Hospital of Fudan University and Institutes of Biomedical Sciences of Fudan University, Shanghai, China.; Department of Pediatrics, Henan Key Laboratory of Child Brain Injury and Henan Pediatric Clinical Research Center, The Third Affiliated Hospital and Institute of Neuroscience of Zhengzhou University, Zhengzhou, China.; Zhang X; Department of Pediatrics, Henan Key Laboratory of Child Brain Injury and Henan Pediatric Clinical Research Center, The Third Affiliated Hospital and Institute of Neuroscience of Zhengzhou University, Zhengzhou, China.; Li M; Department of Pediatrics, Henan Key Laboratory of Child Brain Injury and Henan Pediatric Clinical Research Center, The Third Affiliated Hospital and Institute of Neuroscience of Zhengzhou University, Zhengzhou, China.; Ma C; Rehabilitation Department, Henan Key Laboratory of Child Genetics and Metabolism, Children's Hospital of Zhengzhou University, Zhengzhou, China.; Fan Y; Children's Hospital of Fudan University and Institutes of Biomedical Sciences of Fudan University, Shanghai, China.; Peng X; Department of Pediatrics, Henan Key Laboratory of Child Brain Injury and Henan Pediatric Clinical Research Center, The Third Affiliated Hospital and Institute of Neuroscience of Zhengzhou University, Zhengzhou, China.; Wu S; Department of Neurosurgery, The Affiliated Zhongshan Hospital of Fudan University, Shanghai, China.; Lv N; Rehabilitation Department, Henan Key Laboratory of Child Genetics and Metabolism, Children's Hospital of Zhengzhou University, Zhengzhou, China.; Li B; Department of Pediatrics, Henan Key Laboratory of Child Brain Injury and Henan Pediatric Clinical Research Center, The Third Affiliated Hospital and Institute of Neuroscience of Zhengzhou University, Zhengzhou, China.; Sun Y; Department of Pediatrics, Henan Key Laboratory of Child Brain Injury and Henan Pediatric Clinical Research Center, The Third Affiliated Hospital and Institute of Neuroscience of Zhengzhou University, Zhengzhou, China.; Zhang B; Department of Pediatrics, Henan Key Laboratory of Child Brain Injury and Henan Pediatric Clinical Research Center, The Third Affiliated Hospital and Institute of Neuroscience of Zhengzhou University, Zhengzhou, China.; Li T; Department of Pediatrics, Henan Key Laboratory of Child Brain Injury and Henan Pediatric Clinical Research Center, The Third Affiliated Hospital and Institute of Neuroscience of Zhengzhou University, Zhengzhou, China.; Li H; Department of Pediatrics, Henan Key Laboratory of Child Brain Injury and Henan Pediatric Clinical Research Center, The Third Affiliated Hospital and Institute of Neuroscience of Zhengzhou University, Zhengzhou, China.; Zhang J; Children's Hospital of Fudan University and Institutes of Biomedical Sciences of Fudan University, Shanghai, China.; Shanghai Center for Women and Children's Health, Shanghai, China.; Su Y; Children's Hospital of Fudan University and Institutes of Biomedical Sciences of Fudan University, Shanghai, China.; Li Q; Children's Hospital of Fudan University and Institutes of Biomedical Sciences of Fudan University, Shanghai, China.; Yuan J; Department of Pediatrics, Henan Key Laboratory of Child Brain Injury and Henan Pediatric Clinical Research Center, The Third Affiliated Hospital and Institute of Neuroscience of Zhengzhou University, Zhengzhou, China.; Liu L; Children's Hospital of Fudan University and Institutes of Biomedical Sciences of Fudan University, Shanghai, China.; Moreno-De-Luca A; Department of Radiology, Neuroradiology Section, Kingston Health Sciences Centre, Queen's University Faculty of Health Sciences, Kingston, Ontario, Canada.; MacLennan AH; Robinson Research Institute and Adelaide Medical School, The University of Adelaide, Adelaide, South Australia, Australia.; Gecz J; Robinson Research Institute and Adelaide Medical School, The University of Adelaide, Adelaide, South Australia, Australia.; Zhu D; Department of Pediatrics, Henan Key Laboratory of Child Brain Injury and Henan Pediatric Clinical Research Center, The Third Affiliated Hospital and Institute of Neuroscience of Zhengzhou University, Zhengzhou, China.; Wang X; Centre for Perinatal Medicine and Health, Institute of Clinical Science, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.; Zhu C; Department of Pediatrics, Henan Key Laboratory of Child Brain Injury and Henan Pediatric Clinical Research Center, The Third Affiliated Hospital and Institute of Neuroscience of Zhengzhou University, Zhengzhou, China. changlian.zhu@neuro.gu.se.; Xing Q; Children's Hospital of Fudan University and Institutes of Biomedical Sciences of Fudan University, Shanghai, China. qhxing@fudan.edu.cn.; Shanghai Center for Women and Children's Health, Shanghai, China. qhxing@fudan.edu.cn.

Publisher: Nature Publishing Company Country of Publication: United States NLM ID: 9502015 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1546-170X (Electronic) Linking ISSN: 10788956 NLM ISO Abbreviation: Nat Med Subsets: MEDLINE

MacLennan AH; Wilson DH; Taylor AW; MacLennan, A H; Wilson, D H; Taylor, A W

Lancet. 3/2/1996, Vol. 347 Issue 9001, p569-573. 5p.

van Eyk C; The Robinson Research Institute, The University of Adelaide, Adelaide, South Australia, Australia.; Adelaide Medical School, The University of Adelaide, Adelaide, South Australia, Australia.; MacLennan SC; Adelaide Medical School, The University of Adelaide, Adelaide, South Australia, Australia.; Neurology Department, Women's & Children's Hospital, Adelaide, South Australia, Australia.; MacLennan AH; The Robinson Research Institute, The University of Adelaide, Adelaide, South Australia, Australia.

Publisher: American Medical Association Country of Publication: United States NLM ID: 101589544 Publication Model: Print Cited Medium: Internet ISSN: 2168-6211 (Electronic) Linking ISSN: 21686203 NLM ISO Abbreviation: JAMA Pediatr Subsets: MEDLINE

Kayumi S; Adelaide Medical School, The University of Adelaide, Adelaide, South Australia, Australia; Robinson Research Institute, The University of Adelaide, Adelaide, South Australia, Australia.; Pérez-Jurado LA; Genetics Service, Hospital del Mar Medical Research Institute (IMIM), Network Research Centre for Rare Diseases (CIBERER), Barcelona, Spain; Department of Medicine and Life Sciences, Universitat Pompeu Fabra, Barcelona, Spain.; Palomares M; Instituto de Genética Médica y Molecular (INGEMM), La Paz University Hospital, Network Research Centre for Rare Diseases (CIBERER), Madrid, Spain.; Rangu S; Albert Einstein College of Medicine, Bronx, NY; Section of Dermatology, Children's Hospital of Philadelphia, Philadelphia, PA.; Sheppard SE; Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, PA; Division of Intramural Research, Eunice Kennedy Shriver National Institute of Child Health and Human Development, Bethesda, MD.; Chung WK; Departments of Pediatrics and Medicine, Columbia University Irving Medical Center, New York, NY.; Kruer MC; Pediatric Movement Disorders Program, Division of Pediatric Neurology, Barrow Neurological Institute, Phoenix Children's Hospital, Phoenix, AZ; Departments of Child Health, Neurology, and Cellular & Molecular Medicine, and Program in Genetics, University of Arizona College of Medicine-Phoenix, Phoenix, AZ.; Kharbanda M; Wessex Clinical Genetics Service, Southampton University Hospitals NHS Foundation Trust, Princess Anne Hospital, Southampton, United Kingdom.; Amor DJ; Department of Paediatrics, Melbourne Medical School, The University of Melbourne, Parkville, Victoria, Australia; Murdoch Children's Research Institute, Parkville, Victoria, Australia.; McGillivray G; Murdoch Children's Research Institute, Parkville, Victoria, Australia.; Cohen JS; Department of Neurology and Developmental Medicine, Kennedy Krieger Institute, Baltimore, MD; Department of Neurology, Johns Hopkins University School of Medicine, Kennedy Krieger Institute, Baltimore, MD.; García-Miñaúr S; Instituto de Genética Médica y Molecular (INGEMM), La Paz University Hospital, Network Research Centre for Rare Diseases (CIBERER), Madrid, Spain.; van Eyk CL; Adelaide Medical School, The University of Adelaide, Adelaide, South Australia, Australia; Robinson Research Institute, The University of Adelaide, Adelaide, South Australia, Australia.; Harper K; Adelaide Medical School, The University of Adelaide, Adelaide, South Australia, Australia; Robinson Research Institute, The University of Adelaide, Adelaide, South Australia, Australia.; Jolly LA; Robinson Research Institute, The University of Adelaide, Adelaide, South Australia, Australia; Adelaide Biomedical School, The University of Adelaide, Adelaide, South Australia, Australia.; Webber DL; Adelaide Medical School, The University of Adelaide, Adelaide, South Australia, Australia; Robinson Research Institute, The University of Adelaide, Adelaide, South Australia, Australia.; Barnett CP; Paediatric and Reproductive Genetics Unit, Women's and Children's Hospital, Adelaide, South Australia, Australia.; Santos-Simarro F; Instituto de Genética Médica y Molecular (INGEMM), La Paz University Hospital, Network Research Centre for Rare Diseases (CIBERER), Madrid, Spain.; Pacio-Míguez M; Instituto de Genética Médica y Molecular (INGEMM), La Paz University Hospital, Network Research Centre for Rare Diseases (CIBERER), Madrid, Spain.; Pozo AD; Instituto de Genética Médica y Molecular (INGEMM), La Paz University Hospital, Network Research Centre for Rare Diseases (CIBERER), Madrid, Spain.; Bakhtiari S; Pediatric Movement Disorders Program, Division of Pediatric Neurology, Barrow Neurological Institute, Phoenix Children's Hospital, Phoenix, AZ; Departments of Child Health, Neurology, and Cellular & Molecular Medicine, and Program in Genetics, University of Arizona College of Medicine-Phoenix, Phoenix, AZ.; Deardorff M; Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, PA; Robert's Individualized Medical Genetics Center, Children's Hospital of Philadelphia, Philadelphia, PA; Departments of Pathology and Laboratory Medicine and Pediatrics, Children's Hospital Los Angeles, Keck School of Medicine of the University of Southern California, Los Angeles, CA.; Dubbs HA; Division of Neurology, Children's Hospital of Philadelphia, Philadelphia, PA.; Izumi K; Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, PA; Robert's Individualized Medical Genetics Center, Children's Hospital of Philadelphia, Philadelphia, PA; Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA.; Grand K; Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, PA; Department of Pediatrics, Medical Genetics, Cedars-Sinai Medical Center, Los Angeles, CA.; Gray C; Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, PA; Robert's Individualized Medical Genetics Center, Children's Hospital of Philadelphia, Philadelphia, PA.; Mark PR; Spectrum Health Medical Genetics, Grand Rapids, MI.; Bhoj EJ; Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, PA; Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA.; Li D; Center for Applied Genomics, Children's Hospital of Philadelphia Research Institute, Philadelphia, PA.; Ortiz-Gonzalez XR; Paediatric and Reproductive Genetics Unit, Women's and Children's Hospital, Adelaide, South Australia, Australia; Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA.; Keena B; Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, PA.; Zackai EH; Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, PA; Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA.; Goldberg EM; Division of Neurology, Children's Hospital of Philadelphia, Philadelphia, PA; Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA.; Perez de Nanclares G; Molecular (epi)genetics lab, Bioaraba Research Health Institute, Araba University Hospital, Vitoria-Gasteiz, Spain.; Pereda A; Molecular (epi)genetics lab, Bioaraba Research Health Institute, Araba University Hospital, Vitoria-Gasteiz, Spain.; Llano-Rivas I; Department of Genetics, Hospital de Cruces, Barakaldo, Spain.; Arroyo I; Servicio de Neonatología, Hospital San Pedro de Alcántara, Cáceres, Spain.; Fernández-Cuesta MÁ; Neuropediatrics, Hospital Universitario de Basurto, Bilbao, Vizcaya, Spain.; Thauvin-Robinet C; Centre de Référence Anomalies du Développement et Syndromes Malformatifs et Centre de Référence Déficiences Intellectuelles de Causes Rares, FHU TRANSLAD, CHU Dijon Bourgogne, Dijon, France; L'Unité Fonctionnelle Innovation en Diagnostic Génomique des Maladies Rares, Laboratoire de Génétique Chromosomique et Moléculaire, FHU-TRANSLAD, CHU Dijon Bourgogne, Dijon, France; INSERM - Bourgogne Franche-Comté University, UMR 1231 GAD Team, Genetics of Developmental Disorders, Dijon, France.; Faivre L; Centre de Référence Anomalies du Développement et Syndromes Malformatifs et Centre de Référence Déficiences Intellectuelles de Causes Rares, FHU TRANSLAD, CHU Dijon Bourgogne, Dijon, France; L'Unité Fonctionnelle Innovation en Diagnostic Génomique des Maladies Rares, Laboratoire de Génétique Chromosomique et Moléculaire, FHU-TRANSLAD, CHU Dijon Bourgogne, Dijon, France.; Garde A; Centre de Référence Anomalies du Développement et Syndromes Malformatifs et Centre de Référence Déficiences Intellectuelles de Causes Rares, FHU TRANSLAD, CHU Dijon Bourgogne, Dijon, France.; Mazel B; Centre de Référence Anomalies du Développement et Syndromes Malformatifs et Centre de Référence Déficiences Intellectuelles de Causes Rares, FHU TRANSLAD, CHU Dijon Bourgogne, Dijon, France.; Bruel AL; L'Unité Fonctionnelle Innovation en Diagnostic Génomique des Maladies Rares, Laboratoire de Génétique Chromosomique et Moléculaire, FHU-TRANSLAD, CHU Dijon Bourgogne, Dijon, France; INSERM - Bourgogne Franche-Comté University, UMR 1231 GAD Team, Genetics of Developmental Disorders, Dijon, France.; Tress ML; Bioinformatics Unit, Spanish National Cancer Research Centre (CNIO), Madrid, Spain.; Brilstra E; Department of Genetics, University Medical Center Utrecht, Utrecht, the Netherlands.; Fine AS; Department of Neurology and Developmental Medicine, Kennedy Krieger Institute, Baltimore, MD; Department of Neurology, Johns Hopkins University School of Medicine, Kennedy Krieger Institute, Baltimore, MD.; Crompton KE; Department of Paediatrics, Melbourne Medical School, The University of Melbourne, Parkville, Victoria, Australia; Murdoch Children's Research Institute, Parkville, Victoria, Australia.; Stegmann APA; Department of Clinical Genetics, Maastricht University Medical Center, Maastricht, the Netherlands.; Sinnema M; Department of Clinical Genetics, Maastricht University Medical Center, Maastricht, the Netherlands.; Stevens SCJ; Department of Clinical Genetics, Maastricht University Medical Center, Maastricht, the Netherlands.; Nicolai J; Department of Neurology, Maastricht University Medical Center, Maastricht, the Netherlands.; Lesca G; Department of Medical Genetics, Hospices Civils de Lyon, Lyon, France.; Lion-François L; Department of Pediatric Neurology, Hospices Civils de Lyon, Lyon, France.; Haye D; Department of Medical Genetics, Hospices Civils de Lyon, Lyon, France.; Chatron N; Department of Medical Genetics, Hospices Civils de Lyon, Lyon, France.; Piton A; Department of Medical genetics, Hopitaux Universitaires de Strasbourg, France.; Nizon M; Service de Génétique Médicale, CHU Nantes, Nantes, France.; Cogne B; Service de Génétique Médicale, CHU Nantes, Nantes, France.; Srivastava S; Department of Neurology, Rosamund Stone Zander Translational Neuroscience Center, Boston Children's Hospital, Harvard Medical School, Boston, MA.; Bassetti J; Department of Pediatrics, Division of Medical Genetics, Weill Cornell Medicine, New York, NY.; Muss C; Nemours/A.I duPont Hospital for Children, Wilmington, DE.; Gripp KW; Nemours/A.I duPont Hospital for Children, Wilmington, DE.; Procopio RA; Department of Ophthalmology, Wills Eye Hospital, Philadelphia, PA.; Millan F; GeneDX, Gaithersburg, MD.; Morrow MM; GeneDX, Gaithersburg, MD.; Assaf M; Banner Children's Specialists Neurology Clinic, Glendale, AZ.; Moreno-De-Luca A; Department of Radiology, Autism & Developmental Medicine Institute, Genomic Medicine Institute, Geisinger, Danville, PA.; Joss S; West of Scotland Clinical Genetics Service, Glasgow, United Kingdom.; Hamilton MJ; West of Scotland Clinical Genetics Service, Glasgow, United Kingdom.; Bertoli M; Northern Genetics Service, Newcastle upon Tyne, United Kingdom.; Foulds N; Wessex Clinical Genetics Service, Southampton University Hospitals NHS Foundation Trust, Princess Anne Hospital, Southampton, United Kingdom.; McKee S; Northern Ireland Regional Genetics Centre, Belfast, United Kingdom.; MacLennan AH; Adelaide Medical School, The University of Adelaide, Adelaide, South Australia, Australia; Robinson Research Institute, The University of Adelaide, Adelaide, South Australia, Australia.; Gecz J; Adelaide Medical School, The University of Adelaide, Adelaide, South Australia, Australia; Robinson Research Institute, The University of Adelaide, Adelaide, South Australia, Australia; South Australian Health and Medical Research Institute, Adelaide, South Australia, Australia.; Corbett MA; Adelaide Medical School, The University of Adelaide, Adelaide, South Australia, Australia; Robinson Research Institute, The University of Adelaide, Adelaide, South Australia, Australia. Electronic address: mark.corbett@adelaide.edu.au.

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

Martin M; Aide aux Parents d'Enfants souffrants du Syndrome de l'AntiConvulsivant, Pollestres, France.; Hill C; Service de Biostatistique et d'Epidémiologie, Gustave Roussy, Paris-Saclay University, Villejuif, France.; Bewley S; Department of Women & Children's Health, King's College London, London, UK.; MacLennan AH; Australian Collaborative Cerebral Palsy Research Group, Robinson Research Institute, University of Adelaide, Adelaide, Australia.; Braillon A; Amiens, France.

Publisher: John Wiley & Sons, Inc Country of Publication: United States NLM ID: 101701004 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 2472-1727 (Electronic) NLM ISO Abbreviation: Birth Defects Res Subsets: MEDLINE

Purbrick B; Stranks K; Sum C; Maclennan AH

Climacteric. Jun2012, Vol. 15 Issue 3, p288-293. 6p.

Archer DF; Sturdee DW; Baber R; de Villiers TJ; Pines A; Freedman RR; Gompel A; Hickey M; Hunter MS; Lobo RA; Lumsden MA; Maclennan AH; Maki P; Palacios S; Shah D; Villaseca P; Warren M

Climacteric. Oct2011, Vol. 14 Issue 5, p515-528. 14p.

O'Callaghan ME; MacLennan AH; Gibson CS; McMichael GL; Haan EA; Broadbent JL; Goldwater PN; Dekker GA; Australian Collaborative Cerebral Palsy Research Group (CORPORATE AUTHOR); O'Callaghan, Michael E; MacLennan, Alastair H; Gibson, Catherine S; McMichael, Gai L; Haan, Eric A; Broadbent, Jessica L; Goldwater, Paul N; Dekker, Gustaaf A

Obstetrics & Gynecology. Sep2011, Vol. 118 Issue 3, p576-582. 7p.

O'Callaghan ME; MacLennan AH; Gibson CS; McMichael GL; Haan EA; Broadbent J; Priest K; Goldwater PN; Dekker GA; Australian Collaborative Cerebral Palsy Research Group (CORPORATE AUTHOR)

Journal of Paediatrics & Child Health. Mar2011, Vol. 47 Issue 3, p99-110. 12p.

Welton AJ; Vickers MR; Kim J; Ford D; Lawton BA; MacLennan AH; Meredith SK; Martin J; Meade TW; WISDOM (Women's International Study of Long Duration Oestrogen After the Menopause) Team (CORPORATE AUTHOR)

BMJ: British Medical Journal (International Edition). 9/6/2008, Vol. 337 Issue 7669, p550-553. 4p.