학술논문
'학술논문'
에서 검색결과 667건 | 목록
1~10
Academic Journal
N. Guffon; M. Pettazzoni; N. Pangaud; C. Garin; G. Lina-Granade; C. Plault; C. Mottolese; R. Froissart; A. Fouilhoux
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-20 (2021)
Academic Journal
Guffon, N.; Pettazzoni, M.; Pangaud, N.; Garin, C.; Lina-Granade, G.; Plault, C.; Mottolese, C.; Froissart, R.; Fouilhoux, A.
Orphanet Journal of Rare Diseases. 16(1)
Academic Journal
Braunlin E; Department of Pediatrics, University of Minnesota, Minneapolis, MN, USA.; Bay L; Hospital Nacional de Pediatría J. P. Garrahan, Ciudad Autónoma de Buenos Aires, Buenos Aires, Argentina.; Guffon N; Centre de Référence des Maladies Héréditaires du Métabolisme, Hôpital Femme Mère Enfant, Lyon, France.; Yang M; Formerly Epidemiology and Biostatistics, Sanofi, Cambridge, MA, USA.; Pangaud N; Cardiology, Louis Pradel Hospital, Hospices Civils de Lyon, Lyon, France.; Clarke LA; Department of Medical Genetics and the British Columbia Children's Hospital Research Institute, University of British Columbia, Vancouver, BC, Canada.
Publisher: Cambridge University Press Country of Publication: England NLM ID: 9200019 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1467-1107 (Electronic) Linking ISSN: 10479511 NLM ISO Abbreviation: Cardiol Young Subsets: MEDLINE
Academic Journal
Wraith, JE; Scarpa, M; Beck, M; Bodamer, OA; De Meirleir, L; Guffon, N; Lund, AM; Malm, G; Van der Ploeg, AT; Zeman, J
European journal of pediatrics. 167(3):267-277
Academic Journal
Heard, JM; Bellettato, C; Lingen, C; Scarpa, M; Debray, FG; Nassogne, MC; van Coster, R; De Meirleir, L; Eyskens, F; Morava, E; Baric, I; Kozich, V; Lund, AM; Germain, D; Belmatoug, N; Guffon, N; Labrune, P; Gouya, L; De Lonlay, P; Schiff, M; Dobbelaere, D; Chabrol, B; Ploeckinger, U; Das, AM; Spiekerkoetter, U; Rutsch, F; Mohnike, K; Hahn, A; Kolker, S; Ullrich, K; Hennermann, J; Balogh, I; Bembi, B; Donati, MA; Gasperini, S; Parenti, G; Salviati, A; Vici, CD; Di Rocco, M; Cefalo, G; Burlina, A; Ceccarini, G; Federico, A; Van der Ploeg, A; Rubio-Gozalbo, ME; Van Spronsen, F; Visser, G; Bosch, A; Tangeraas, T; Sanderberg, S; Kiec-Wilk, B; Gaspar, AMSM; Martins, E; Silva, EMFR; Matos, LMDFD; Azevedo, O; Tansek, MZ; Couce-Pico, ML; Cazorla, AG; Azuara, LAE; Del Toro-Riera, M; Silva, MTG; Lajic, S; Darin, N; Deegan, P; Vijay, S; Chronopolou, E; Jones, S; Chakrapani, A; Hiwot, T
Orphanet journal of rare diseases. 14(1):119
Muenzer J; University of North Carolina at Chapel Hill, Chapel Hill, NC, USA. Electronic address: muenzer@med.unc.edu.; Burton BK; Ann & Robert H. Lurie Children's Hospital of Chicago, Northwestern University, Chicago, IL, USA.; Harmatz P; UCSF Benioff Children's Hospital Oakland, Oakland, CA, USA.; Gutiérrez-Solana LG; Infant Jesus Children's Hospital, Madrid, Spain.; Ruiz-Garcia M; National Institute of Pediatrics, Mexico City, Mexico.; Jones SA; St Mary's Hospital, Manchester University NHS Foundation Trust, University of Manchester, Manchester, UK.; Guffon N; Reference Center for Inherited Metabolic Diseases, Hospices Civils de Lyon, Lyon, France.; Inbar-Feigenberg M; University of Toronto, Toronto, ON, Canada; The Hospital for Sick Children, Toronto, ON, Canada.; Bratkovic D; Women's and Children's Hospital, North Adelaide, SA, Australia.; Hale M; Takeda Development Center Americas, Inc., Cambridge, MA, USA; Hale Scientific Statistics, LLC, Beaverton, OR, USA.; Wu Y; Takeda Development Center Americas, Inc., Lexington, MA, USA.; Yee KS; Takeda Development Center Americas, Inc., Cambridge, MA, USA.; Whiteman DAH; Takeda Development Center Americas, Inc., Lexington, MA, USA.; Alexanderian D; Takeda Development Center Americas, Inc., Lexington, MA, USA; Affinia Therapeutics, Inc., Waltham, MA, USA.
Publisher: Academic Press Country of Publication: United States NLM ID: 9805456 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1096-7206 (Electronic) Linking ISSN: 10967192 NLM ISO Abbreviation: Mol Genet Metab Subsets: PubMed not MEDLINE; MEDLINE
Academic Journal
D. Hughes; R. Giugliani; N. Guffon; S. A. Jones; K. E. Mengel; R. Parini; R. Matousek; S. M. Hawley; A. Quartel
Orphanet Journal of Rare Diseases, Vol 12, Iss 1, Pp 1-8 (2017)
Muenzer J; University of North Carolina at Chapel Hill, Chapel Hill, NC, USA. Electronic address: muenzer@med.unc.edu.; Burton BK; Ann & Robert H. Lurie Children's Hospital of Chicago, Northwestern University, Chicago, IL, USA.; Harmatz P; UCSF Benioff Children's Hospital Oakland, Oakland, CA, USA.; Gutiérrez-Solana LG; Infant Jesus Children's Hospital, Madrid, Spain.; Ruiz-Garcia M; National Institute of Pediatrics, Mexico City, Mexico.; Jones SA; St Mary's Hospital, Manchester University NHS Foundation Trust, University of Manchester, Manchester, UK.; Guffon N; Reference Center for Inherited Metabolic Diseases, Hospices Civils de Lyon, Lyon, France.; Inbar-Feigenberg M; University of Toronto, Toronto, ON, Canada; The Hospital for Sick Children, Toronto, ON, Canada.; Bratkovic D; Women's and Children's Hospital, North Adelaide, SA, Australia.; Hale M; Takeda Development Center Americas, Inc., Cambridge, MA, USA; Hale Scientific Statistics, LLC, Beaverton, OR, USA.; Wu Y; Takeda Development Center Americas, Inc., Lexington, MA, USA.; Yee KS; Takeda Development Center Americas, Inc., Cambridge, MA, USA.; Whiteman DAH; Takeda Development Center Americas, Inc., Lexington, MA, USA.; Alexanderian D; Takeda Development Center Americas, Inc., Lexington, MA, USA; Affinia Therapeutics, Inc., Waltham, MA, USA.
Publisher: Academic Press Country of Publication: United States NLM ID: 9805456 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1096-7206 (Electronic) Linking ISSN: 10967192 NLM ISO Abbreviation: Mol Genet Metab Subsets: PubMed not MEDLINE; MEDLINE
Academic Journal
Braunlin, E; Rosenfeld, H; Kampmann, C; Johnson, J; Beck, M; Giugliani, R; Guffon, N; Ketteridge, D; Miranda, CM Sá; Scarpa, M; Schwartz, IV; Teles, E Leão; Wraith, JE; Barrios, P; da Silva, E Dias; Kurio, G; Richardson, M; Gildengorin, G; Hopwood, JJ; Imperiale, M; Schatz, A; Decker, C; Harmatz, P; Group, MPS VI Study
Journal of Inherited Metabolic Disease. 36(2)
검색 결과 제한하기
제한된 항목
[검색어] Guffon, N.
발행연도 제한
-
학술DB(Database Provider)
저널명(출판물, Title)
출판사(Publisher)
자료유형(Source Type)
주제어
언어