Carlo Wilke
19PUBLICATIONS
76CO-AUTHORS
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Publications (19)
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|Jul 09, 2024
Deciphering Distinct Genetic Risk Factors for FTLD-TDP Pathological Subtypes via Whole-Genome Sequencing.Cyril Pottier, Fahri Küçükali, Matt Baker
|Nov 14, 2023
Stage-Dependent Biomarker Changes in Spinocerebellar Ataxia Type 3.Jennifer Faber, Moritz Berger, Carlo Wilke
|Aug 14, 2023
Intronic FGF14 GAA repeat expansions are a common cause of downbeat nystagmus syndromes: frequency, phenotypic profile, and 4-aminopyridine treatment response.David Pellerin, Felix Heindl, Carlo Wilke
|Aug 02, 2023
As Frequent as Polyglutamine Spinocerebellar Ataxias: SCA27B in a Large German Autosomal Dominant Ataxia Cohort.Holger Hengel, David Pellerin, Carlo Wilke
|Jul 03, 2023
Intronic FGF14 GAA repeat expansions are a common cause of ataxia syndromes with neuropathy and bilateral vestibulopathy.David Pellerin, Carlo Wilke, Andreas Traschütz
|May 11, 2023
GAA-FGF14 ataxia (SCA27B): phenotypic profile, natural history progression and 4-aminopyridine treatment response.Carlo Wilke, David Pellerin, David Mengel
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Frequent Collaborators
17 joint publications
Matthis Synofzik
3 joint publications
Henry Houlden
3 joint publications
Andreas Traschütz
3 joint publications
David Pellerin
2 joint publications
Luis Pereira de Almeida
2 joint publications
Sergi Beltran
2 joint publications
Steven Laurie
2 joint publications
Holm Graessner
2 joint publications
Adrian Danek
2 joint publications
Harro Seelaar
