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1 Ergebnisse
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Worldwide barriers to genetic testing for movement disorder:
Gatto, Emilia M
;
Walker, Ruth H
;
Gonzalez, Claudio
...
qt3pc6r51f. , 2021
Link:
https://escholarship.org/uc/item/3pc6r51f
RT Journal T1
Worldwide barriers to genetic testing for movement disorders
UL https://suche.suub.uni-bremen.de/peid=base-ftcdlib:oai:escholarship.org:ark:_13030_qt3pc6r51f&Exemplar=1&LAN=DE A1 Gatto, Emilia M A1 Walker, Ruth H A1 Gonzalez, Claudio A1 Cesarini, Martin A1 Cossu, Giovanni A1 Stephen, Christopher D A1 Balint, Bettina A1 Rodríguez‐Violante, Mayela A1 Jankovic, Joseph A1 Morgante, Francesca A1 Jinnah, Hyder A A1 Albanese, Alberto A1 Amorin, Ignacio A1 Bhatia, Kailash A1 Brandabur, Melanie A1 Canals, Francisca A1 Cardoso, Francisco A1 Cardozo, Adriana A1 Carvalho, Vanessa A1 Chade, Anabel A1 Chana, Pedro A1 Darling, Alejandra A1 Correia Guedes, Leonor A1 De la Cerda, Andrés A1 de Koning‐Tijssen, Marina A1 Della Coletta, Marcus V A1 Duquette, Antoine A1 Espay, Alberto A1 Etcheverry, Jose A1 Ferreira, Joaquim A1 Friedman, Jennifer A1 Fung, Victor A1 Ganos, Christos A1 Ruiz, Pedro Garcia A1 Gershanik, Oscar A1 Gross, Kenneth BV A1 Han‐Joon, Kim A1 Kaji, Ruyji A1 Kotschet, Katya A1 Rosa, Andres Lescano Da A1 Litvan, Irene A1 Lubarr, Naomi A1 Marano, Massimo A1 Josep Martí, Maria A1 Martinez Ramirez, Daniel A1 Miyasaki, Janis A1 Münchau, Alexander A1 Chesta, Daniela Muñoz A1 Pal, Pramod A1 Peralta, María Cecilia A1 Phielipp, Nicolás A1 Maria Riboldi, Giulietta A1 Oroz, María Cruz Rodríguez A1 Rodriguez‐Porcel, Federico A1 Sarva, Harini A1 Schoels, Ludger A1 Stamelou, Maria A1 Uribe Roca, Claudia PB eScholarship, University of California YR 2021 K1 Neurodegenerative K1 Genetic Testing K1 Clinical Research K1 Neurosciences K1 Genetics K1 Neurological K1 Asia K1 Europe K1 Humans K1 Middle East K1 Movement Disorders K1 Rare Movement Disorders Study Group of the International Parkinson Disease K1 Movement Disorders Society K1 Parkinson's disease K1 chorea K1 dystonia K1 genetic and inherited disorders K1 genetic diagnosis K1 whole exome sequencing K1 Clinical Sciences K1 Neurology & Neurosurgery JF qt3pc6r51f LK http://dx.doi.org/https://escholarship.org/uc/item/3pc6r51f DO https://escholarship.org/uc/item/3pc6r51f SF ELIB - SuUB Bremen
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