Tim W Rattay

9PUBLICATIONS
59CO-AUTHORS
Gene mappingPeripheral nervous systemNeurology and neuromuscular diseasesMetabolic medicineMemory and attention
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Publications (9)

|Feb 14, 2026
Loss-of-function variants in the CAPN1 activator CD99L2 cause X-linked spastic ataxia.

Benita Menden, Rana D Incebacak Eltemur, German Demidov

|Apr 26, 2022
The prodromal phase of hereditary spastic paraplegia type 4: the preSPG4 cohort study.

Tim W Rattay, Maximilian Völker, Maren Rautenberg

|Feb 16, 2022
Characteristics of serum neurofilament light chain as a biomarker in hereditary spastic paraplegia type 4.

Christoph Kessler, Lina Maria Serna-Higuita, Carlo Wilke

|Jul 09, 2021
Chromium and cobalt intoxication mimicking mitochondriopathy.

Tim W Rattay, Torsten Kluba, Ludger Schöls

|Oct 27, 2020
PolyQ-expanded ataxin-3 protein levels in peripheral blood mononuclear cells correlate with clinical parameters in SCA3: a pilot study.

Kathrin Gonsior, Gabriele Anna Kaucher, Patrik Pelz

|Oct 25, 2019
Non-motor symptoms are relevant and possibly treatable in hereditary spastic paraplegia type 4 (SPG4).

Tim W Rattay, Andreas Boldt, Maximilian Völker

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Frequent Collaborators

4 joint publications

Matthis Synofzik

2 joint publications

Holger Hengel

2 joint publications

Olaf Riess

1 joint publications

Alexandra Durr