Chantal Marie Elisabeth Tallaksen

Emeritus
ved Nevrologisk avdeling ved Universitetet i Oslo
Overlege
ved Nevrologisk avdeling ved Oslo universitetssykehus HF

Resultater Resultater

Survival and severity in dominant cerebellar ataxias.

Monin, Marie-Lorraine; Tezenas du Montcel, Sophie; Marelli, Cecilia; Cazeneuve, Cecile; Charles, Perrine; Tallaksen, Chantal Marie Elisabeth; Forlani, Sylvie; Stevanin, Giovanni; Brice, Alexis; Durr, Alexandra. 2015, Annals of clinical and translational neurology. CHU-MONTP, UPMC, UIO, OUS, PITIEVitenskapelig artikkel

Evolution of Clinical Outcome Measures and Biomarkers in Sporadic Adult-Onset Degenerative Ataxia.

Oender, Demet; Faber, Jennifer; Wilke, Carlo; Schaprian, Tamara; Lakghomi, Asadeh; Mengel, David; Schöls, Ludger; Traschütz, Andreas; Fleszar, Zofia; Dufke, Claudia mfl.. 2023, Movement Disorders. LM, UK-ESSEN, MEDINNSBRU, UdSFIdN, UIO, TYSKLAND, UR, OM, RFB, ETVitenskapelig artikkel

Standardized Assessment of Hereditary Ataxia Patients in Clinical Studies.

Paap, Brigitte K.; Roeske, Sandra; Durr, Alexandra; Schöls, Ludger; Ashizawa, Tetsuo; Boesch, Sylvia; Bunn, Lisa M.; Delatycki, Martin B.; Giunti, Paola; Lehéricy, Stéphane mfl.. 2016, Movement Disorders Clinical Practice. SORBONNE, UTOKYO, USA, UK-ESSEN, UMCN, PT, MEDINNSBRU, AUSTIN, OUS, DZNE, RFB, UNIKLINIK, ULDB, RCH, UOP, UIO, PITIE, ITALIA, UCLVitenskapelig artikkel

Clinical, neuropathological, and genetic characterization of STUB1 variants in cerebellar ataxias: a frequent cause of predominant cognitive impairment.

Roux, Thomas; Barbier, Mathieu; Papin, Mélanie; Davoine, Claire-Sophie; Sayah, Sabrina; Coarelli, Giulia; Charles, Perrine; Marelli, Cecilia; Parodi, Livia; Tranchant, Christine mfl.. 2020, Genetics in Medicine. IRCCS, UdP, ISRAEL, UA, SERBIA, Udd, UNISTRA, LIBANON, BULGARIA, PORTUGAL, UdMI, UK-ESSEN, UMCN, UdSdT, ALGERIE, UdSdP, OUS, UIA, MAROKKO, ET, UdSdRLS, UdSFIdN, JE, SPANIA, UBORDEAUX, IRCCSMEDEA, UPMC, NYCU, UFdRGdS, TYSKLAND, KI, PITIE, AP-HP, MEDINNSBRU, SAUDIARAB, ACH, UVSR, UOC, KU, FRANKRIKE, ULDB, COLOMBIA, IGR, UdF, LUMC, ITALIA, NRC, UCL, SYRIAVitenskapelig artikkel

Correction: Clinical, neuropathological, and genetic characterization of STUB1 variants in cerebellar ataxias: a frequent cause of predominant cognitive impairment (Genetics in Medicine, (2020), 22, 11, (1851-1862), 10.1038/s41436-020-0899-x).

Roux, Thomas; Barbier, Mathieu; Papin, Mélanie; Davoine, Claire-Sophie; Sayah, Sabrina; Coarelli, Giulia; Charles, Perrine; Marelli, Cecilia; Parodi, Livia; Tranchant, Christine mfl.. 2021, Genetics in Medicine. ISRAEL, SPANIA, UA, UBORDEAUX, SERBIA, Udd, UPMC, EGYPT, UNISTRA, NYCU, TYSKLAND, UFdRGdS, LIBANON, PITIE, KI, AP-HP, PORTUGAL, BULGARIA, UdMI, UK-ESSEN, MEDINNSBRU, UMCN, SAUDIARAB, ACH, UVSR, UdSdT, UOC, KU, ALGERIE, OUS, UIA, UdSdP, MAROKKO, FRANKRIKE, UdSdRLS, ET, ULDB, COLOMBIA, IGR, UdF, SUDAN, UdSFIdN, LUMC, ITALIA, UCL, SYRIAErrata

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