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Tim W Rattay

9PUBLICATIONS

59CO-AUTHORS

Gene mappingLinguistic structures (incl. phonology, morphology and syntax)Peripheral nervous systemNeurology and neuromuscular diseasesMetabolic medicine

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Publications (9)

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|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

|May 25, 2022

"Ears of the lynx" sign and thin corpus callosum on MRI in heterozygous SPG11 mutation carriers.

Tim W Rattay, Ludger Schöls, Lena Zeltner

|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

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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

1 joint publications

Jeannette Hübener-Schmid

1 joint publications

Christoph Kessler

1 joint publications

Carlo Wilke

1 joint publications

David Mengel

1 joint publications

Ludger Schöls

1 joint publications

Tobias Lindig

Frequent Collaborators

4 joint publications

Matthis Synofzik

2 joint publications

Holger Hengel

2 joint publications

Olaf Riess

1 joint publications

Alexandra Durr

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