부산대학교 도서관

Rannikko, Irina; Jaaskelainen, Erika; Miettunen, Jouko; Ahmed, Anthony O.; Veijola, Juha; Remes, Anne M.; Murray, Graham K.; Husa, Anja P.; Jarvelin, Marjo-Riitta; Isohanni, Matti; Haapea, Marianne

CLINICAL NEUROPSYCHOLOGIST; JAN 2 2016, 30 1, p17-p50, 34p.

Sahlsten, Hanna; Isohanni, Johan; Haapaniemi, Jorma; Salonen, Jaakko; Paavola, Janika; Loyttyniemi, Eliisa; Johansson, Reijo; Jaaskelainen, Satu K.

INTERNATIONAL JOURNAL OF AUDIOLOGY; DEC 2 2015, 54 12, p899-p909, 11p.

Ylikallio, Emil; Kim, Doyoun; Isohanni, Pirjo; Auranen, Mari; Kim, Eunjoon; Lonnqvist, Tuula; Tyynismaa, Henna

EUROPEAN JOURNAL OF HUMAN GENETICS; OCT 2015, 23 10, p1427-p1430, 4p.

Guo, Joyce Y.; Huhtaniska, Sanna; Miettunen, Jouko; Jaaskelainen, Erika; Kiviniemi, Vesa; Nikkinen, Juha; Moilanen, Jani; Haapea, Marianne; Maki, Pirjo; Jones, Peter B.; Veijola, Juha; Isohanni, Matti; Murray, Graham K.

SCHIZOPHRENIA RESEARCH; OCT 2015, 168 1-2, p297-p304, 8p.

Rannikko, Irina; Haapea, Marianne; Miettunen, Jouko; Veijola, Juha; Murray, Graham K.; Barnett, Jennifer H.; Husa, Anja P.; Jones, Peter B.; Isohanni, Matti; Jaaskelainen, Erika

PSYCHIATRY RESEARCH; AUG 30 2015, 228 3, p671-p679, 9p.

Anttonen, Anna-Kaisa; Hilander, Taru; Linnankivi, Tarja; Isohanni, Pirjo; French, Rachel L.; Liu, Yuchen; Simonovic, Miljan; Soell, Dieter; Somer, Mirja; Muth-Pawlak, Dorota; Corthals, Garry L.; Laari, Anni; Ylikallio, Emil; Lahde, Marja; Valanne, Leena; Lonnqvist, Tuula; Pihko, Helena; Paetau, Anders; Lehesjoki, Anna-Elina; Suomalainen, Anu; Tyynismaa, Henna

NEUROLOGY; JUL 28 2015, 85 4, p306-p315, 10p.

Moilanen, J.; Huhtaniska, S.; Haapea, M.; Jaaskelainen, E.; Veijola, J.; Isohanni, M.; Koponen, H.; Miettunen, J.

EUROPEAN PSYCHIATRY; JUL 2015, 30 5, p598-p605, 8p.

Maas RR; Translational Metabolic Laboratory, Department of Laboratory Medicine, Radboud University Medical Center, Nijmegen, the Netherlands.; Iwanicka-Pronicka K; Department of Audiology and Phoniatrics, Children's Memorial Health Institute, Warsaw, Poland.; Kalkan Ucar S; Division of Metabolic Disease, Ege University Medical Faculty, Department of Pediatrics, Izmir, Turkey.; Alhaddad B; Institute of Human Genetics, Technische UniversitätMünchen, Munich, Germany.; AlSayed M; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.; Department of Anatomy and Cell Biology, College of Medicine, Alfaisal University, Riyadh, Saudi Arabia.; Al-Owain MA; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.; Department of Anatomy and Cell Biology, College of Medicine, Alfaisal University, Riyadh, Saudi Arabia.; Al-Zaidan HI; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.; Department of Anatomy and Cell Biology, College of Medicine, Alfaisal University, Riyadh, Saudi Arabia.; Balasubramaniam S; Western Sydney Genetics Program, Children's Hospital at Westmead, Sydney, New South Wales, Australia.; Discipline of Genetic Medicine & Paediatrics and Child Health, University of Sydney, Sydney, New South Wales, Australia.; Barić I; Department of Pediatrics, University Hospital Center, Zagreb, Croatia.; School of Medicine, University of Zagreb, Zagreb, Croatia.; Bubshait DK; Department of Pediatrics, College of Medicine, Imam Abdulrahman Bin Faisal University, Dammam, Saudi Arabia.; Burlina A; Division of Inherited Metabolic Diseases, Department of Pediatrics, University Hospital of Padua, Padua, Italy.; Christodoulou J; Neurodevelopmental Genomics Research Group, Murdoch Children's Research Institute, and Department of Paediatrics, Melbourne Medical School, University of Melbourne, Melbourne, Victoria, Australia.; Genetic Metabolic Disorders Research Unit and Western Sydney Genetics Program, Children's Hospital at Westmead, Sydney, New South Wales, Australia.; Discipline of Child and Adolescent Health and Genetic Medicine, Sydney Medical School, University of Sydney, Sydney, New South Wales, Australia.; Chung WK; Departments of Pediatrics and Medicine, Columbia University, New York, NY.; Colombo R; Institute of Clinical Biochemistry, Faculty of Medicine, Catholic University of the Sacred Heart, Rome, Italy.; Center for the Study of Rare Hereditary Diseases, Niguarda Ca' Granda Metropolitan Hospital, Milan, Italy.; Darin N; Department of Pediatrics, Institute of Clinical Sciences, University of Gothenburg, Queen Silvia's Children's Hospital, Gothenburg, Sweden.; Freisinger P; Childrens Hospital, Klinikum Reutlingen, Reutlingen, Germany.; Garcia Silva MT; Inborn Errors of Metabolism and Mitochondrial Disease Unit, '12 de Octubre' University Hospital, Avenida de Cordoba sn, 28041 Madrid, Spain. Rare Diseases Biomedical Research Centre (CIBERER), Madrid, Spain.; Complutense University, Madrid, Spain.; Grunewald S; Metabolic Medicine Department, Great Ormond Street Hospital for Children National Health Service Foundation Trust, University College London Institute of Child Health, London, United Kingdom.; Haack TB; Institute of Human Genetics, Technische UniversitätMünchen, Munich, Germany.; Institute of Medical Genetics and Applied Genomics, Tübingen, Germany.; van Hasselt PM; Wilhelmina Children's Hospital Utrecht, University Medical Center Utrecht, Utrecht, the Netherlands.; Hikmat O; Department of Pediatrics, Haukeland University Hospital, Bergen, Norway.; Department of Clinical Medicine (K1), University of Bergen, Bergen, Norway.; Hörster F; Department of General Pediatrics, Division of Neuropediatrics and Pediatric Metabolic Medicine, University Hospital Heidelberg, Heidelberg, Germany.; Isohanni P; Children's Hospital, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.; Research Programs Unit, Molecular Neurology, Biomedicum Helsinki, University of Helsinki, Helsinki, Finland.; Ramzan K; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.; Department of Anatomy and Cell Biology, College of Medicine, Alfaisal University, Riyadh, Saudi Arabia.; Kovacs-Nagy R; Institute of Human Genetics, Technische UniversitätMünchen, Munich, Germany.; Krumina Z; Department of Biology and Microbiology, Riga Stradin's University, Riga, Latvia.; Martin-Hernandez E; Inborn Errors of Metabolism and Mitochondrial Disease Unit, '12 de Octubre' University Hospital, Avenida de Cordoba sn, 28041 Madrid, Spain. Rare Diseases Biomedical Research Centre (CIBERER), Madrid, Spain.; Complutense University, Madrid, Spain.; Mayr JA; Department of Pediatrics, Salzburg State Hospitals and Paracelsus Medical University, Salzburg, Austria.; McClean P; Leeds Teaching Hospitals National Health Service Trust, Leeds, United Kingdom.; De Meirleir L; Pediatric Neurology, Brussels University Hospital, Brussels, Belgium.; Naess K; Department of Pediatric Neurology, Karolinska University Hospital, Stockholm, Sweden.; Ngu LH; Division of Clinical Genetics, Department of Genetics, Kuala Lumpur Hospital, Kuala Lumpur, Malaysia.; Pajdowska M; Department of Clinical Biochemistry, Radioimmunology, and Experimental Medicine, Children's Memorial Health Institute, Warsaw, Poland.; Rahman S; University College London Great Ormond Street Institute of Child Health, London, United Kingdom.; Riordan G; Department of Pediatric Neurology, Red Cross War Memorial Children's Hospital, Cape Town, South Africa.; Riley L; Genetic Metabolic Disorders Research Unit and Western Sydney Genetics Program, Children's Hospital at Westmead, Sydney, New South Wales, Australia.; Discipline of Child and Adolescent Health and Genetic Medicine, Sydney Medical School, University of Sydney, Sydney, New South Wales, Australia.; Roeben B; Department of Neurodegeneration, Hertie Institute for Clinical Brain Research, University of Tübingen, Tübingen, Germany.; German Center for Neurodegenerative Diseases (DZNE), Tübingen, Germany.; Rutsch F; Department of General Pediatrics, Münster University Children's Hospital, Münster, Germany.; Santer R; Department of Pediatrics, University Medical Center Eppendorf, Hamburg, Germany.; Schiff M; Reference Center for Inherited Metabolic Diseases, AP-HP, Robert Debré Hospital, University Paris Diderot-Sorbonne Paris Cité, Paris, France AND INSERM U1141, Paris, France.; Seders M; Department of Human Genetics, Radboud University Medical Center, Nijmegen, the Netherlands.; Sequeira S; Metabolic Unit, Dona Estefânia Hospital, Lisbon, Portugal.; Sperl W; Department of Pediatrics, Salzburg State Hospitals and Paracelsus Medical University, Salzburg, Austria.; Staufner C; Department of General Pediatrics, Division of Neuropediatrics and Pediatric Metabolic Medicine, University Hospital Heidelberg, Heidelberg, Germany.; Synofzik M; Department of Neurodegeneration, Hertie Institute for Clinical Brain Research, University of Tübingen, Tübingen, Germany.; German Center for Neurodegenerative Diseases (DZNE), Tübingen, Germany.; Taylor RW; Wellcome Centre for Mitochondrial Research, Institute of Neuroscience, The Medical School, Newcastle University, Newcastle upon Tyne, United Kingdom.; Trubicka J; Department of Medical Genetics, Children's Memorial Health Institute, Warsaw, Poland.; Tsiakas K; Department of Pediatrics, University Medical Center Eppendorf, Hamburg, Germany.; Unal O; Division of Metabolic Diseases, Hacettepe University Children's Hospital, Ankara, Turkey.; Wassmer E; Birmingham Children's Hospital, Birmingham, United Kingdom.; Wedatilake Y; University College London Great Ormond Street Institute of Child Health, London, United Kingdom.; Wolff T; Nottingham University Hospitals National Health Service Trust, Nottingham Children's Hospital, Nottingham, United Kingdom.; Prokisch H; Institute of Human Genetics, Technische UniversitätMünchen, Munich, Germany.; Institute of Human Genetics, Helmholtz Center Munich, Neuherberg, Germany.; Morava E; Hayward Genetics Center and Department of Pediatrics, Tulane University Medical School, New Orleans, LA.; Pronicka E; Department of Pediatrics, Nutrition and Metabolic Diseases, Children's Memorial Health Institute, Warsaw, Poland.; Wevers RA; Translational Metabolic Laboratory, Department of Laboratory Medicine, Radboud University Medical Center, Nijmegen, the Netherlands.; de Brouwer AP; Department of Human Genetics, Radboud University Medical Center, Nijmegen, the Netherlands.; Donders Institute for Brain, Cognition, and Behavior, Radboud University Medical Center, Nijmegen, the Netherlands.; Wortmann SB; Institute of Human Genetics, Technische UniversitätMünchen, Munich, Germany.; Department of Pediatrics, Salzburg State Hospitals and Paracelsus Medical University, Salzburg, Austria.; Institute of Human Genetics, Helmholtz Center Munich, Neuherberg, Germany.

Publisher: Wiley-Liss Country of Publication: United States NLM ID: 7707449 Publication Model: Print Cited Medium: Internet ISSN: 1531-8249 (Electronic) Linking ISSN: 03645134 NLM ISO Abbreviation: Ann Neurol Subsets: MEDLINE

Isohanni, Matti; Miettunen, Jouko; Maki, Pirjo; Murray, Graham K.; Ridler, Khanum; Lauronen, Erika; Moilanen, Kristiina; Alaraisanen, Antti; Haapea, Marianne; Isohanni, Irene; Ivleva, Elena; Tamminga, Carol; McGrath, John; Koponen, Hannu

WORLD PSYCHIATRY; OCT 2006, 5 3, p168-p171, 4p.

Hikmat O; Department of Pediatrics, Haukeland University Hospital, Bergen, Norway.; Department of Clinical Medicine (K1), University of Bergen, Bergen, Norway.; Naess K; Center for Inherited Metabolic Diseases, Karolinska University Hospital, Stockholm, Sweden.; Department of Medical Biochemistry and Biophysics, Karolinska Institute, Stockholm, Sweden.; Engvall M; Center for Inherited Metabolic Diseases, Karolinska University Hospital, Stockholm, Sweden.; Department of Molecular Medicine and Surgery, Karolinska Institute, Stockholm, Sweden.; Klingenberg C; Department of Pediatric and Adolescent Medicine, University Hospital of North Norway, Tromso, Norway.; Pediatric Research Group, Department of Clinical Medicine, UiT-Arctic University of Norway, Tromso, Norway.; Rasmussen M; Women and Children's Division, Department of Clinical Neurosciences for Children, Oslo University Hospital, Oslo, Norway.; Unit for Congenital and Hereditary Neuromuscular Disorders, Department of Neurology, Oslo University Hospital, Oslo, Norway.; Tallaksen CME; Department of Neurology, Oslo University Hospital, Oslo, Norway.; Institute of Clinical Medicine, Faculty of Medicine, University of Oslo, Oslo, Norway.; Brodtkorb E; Department of Neuroscience, Norwegian University of Science and Technology, Trondheim, Norway.; Department of Neurology and Clinical Neurophysiology, St. Olav's University Hospital, Trondheim, Norway.; Fiskerstrand T; Department of Medical Genetics and Molecular Medicine, Haukeland University Hospital, Bergen, Norway.; Department of Clinical Science (K2), University of Bergen, Bergen, Norway.; Isohanni P; Department of Pediatric Neurology, Children's Hospital, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.; Research Programs Unit, Molecular Neurology, Biomedicum Helsinki, University of Helsinki, Helsinki, Finland.; Uusimaa J; PEDEGO Research Unit and Biocenter Oulu, University of Oulu, Oulu, Finland.; Department of Children and Adolescents, Medical Research Center, Oulu University Hospital, Oulu, Finland.; Darin N; Department of Pediatrics, Queen Silvia Children's Hospital, University of Gothenburg, Gothenburg, Sweden.; Rahman S; Mitochondrial Research Group, University College London Great Ormond Street Institute of Child Health, London, UK.; Metabolic Unit, Great Ormond Street Hospital for Children, National Health Service Foundation Trust, London, UK.; Bindoff LA; Department of Clinical Medicine (K1), University of Bergen, Bergen, Norway.; Department of Neurology, Haukeland University Hospital, Bergen, Norway.

Publisher: Blackwell Science Country of Publication: United States NLM ID: 2983306R Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1528-1167 (Electronic) Linking ISSN: 00139580 NLM ISO Abbreviation: Epilepsia Subsets: MEDLINE