Accès ouvert
2023
article
OpenAlex
Stefan Braune, Sandra Bluemich, Carola Bruns, Petra Dirks et autres
BACKGROUND: Primary progressive multiple sclerosis (PPMS) is characterised by gradual worsening of disability from symptom onset. Knowledge about the natural course of PPMS remains limited. METHODS: PPMS patients from the German NeuroTransData (NTD) MS registry with data from 56 outpatient practices were …
ru, de, ch
(code pays fourni par la source)
2017
other
OpenAlex
Stephan Gierer
Accès ouvert
2015
article
OpenAlex
Dietmar Rudolf Thal, Stephan L. Zuchner, Stephan Gierer, Claudia Schulte et autres
Mutations in the SPG7 gene are the most frequent cause of autosomal recessive hereditary spastic paraplegias and spastic ataxias. Ala510Val is the most common SPG7 mutation, with a frequency of up to 1% in the general population. Here we report the clinical, …
de, be, us
(code pays fourni par la source)
2011
book-chapter
OpenAlex
Konrad Scheglmann, Stephanie Gierer, Stephan Gierer, Manfred Stöhr et autres
de
(code pays fourni par la source)
2006
book-chapter
OpenAlex
Konrad Scheglmann, Stephanie Gierer, Stephan Gierer, Manfred Stöhr
us, de
(code pays fourni par la source)
1999
book-chapter
OpenAlex
Konrad Scheglmann, Stephanie Gierer, Stephan Gierer, Manfred Stöhr