Patient pathways for rare diseases in Europe: ataxia as an example

Vallortigara, Julie; Greenfield, Julie; Hunt, Barry; Hoffman, Deborah; Reinhard, Carola; Graessner, Holm; Federico, Antonio; Quoidbach, Vinciane; Morris, Steve; Giunti, Paola

dc.contributor.author	Reinhard, Carola
dc.contributor.author	Graessner, Holm
dc.date.accessioned	2024-06-11T08:33:49Z
dc.date.available	2024-06-11T08:33:49Z
dc.date.issued	2023
dc.identifier.issn	1750-1172
dc.identifier.uri	http://hdl.handle.net/10900/154159
dc.language.iso	en	de_DE
dc.publisher	London : Bmc	de_DE
dc.relation.uri	http://dx.doi.org/10.1186/s13023-023-02907-y	de_DE
dc.subject.ddc	570	de_DE
dc.subject.ddc	610	de_DE
dc.title	Patient pathways for rare diseases in Europe: ataxia as an example	de_DE
dc.type	Article	de_DE
utue.quellen.id	20240124000000_00728
utue.personen.roh	Vallortigara, Julie
utue.personen.roh	Greenfield, Julie
utue.personen.roh	Hunt, Barry
utue.personen.roh	Hoffman, Deborah
utue.personen.roh	Reinhard, Carola
utue.personen.roh	Graessner, Holm
utue.personen.roh	Federico, Antonio
utue.personen.roh	Quoidbach, Vinciane
utue.personen.roh	Morris, Steve
utue.personen.roh	Giunti, Paola
dcterms.isPartOf.ZSTitelID	Orphanet Journal of Rare Diseases	de_DE
dcterms.isPartOf.ZS-Issue	Article 328	de_DE
dcterms.isPartOf.ZS-Volume	18 (1)	de_DE
utue.fakultaet	04 Medizinische Fakultät	de_DE