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1

Contribution to a book

Minnerop, Martina
2022

2

Journal Article

Validation of a German version of the Cerebellar Cognitive Affective/Schmahmann Syndrome Scale: preliminary version and study protocol

Thieme, A.
2020

Neurological research and practice, 2 (2020) S. 39

OpenAccess OpenAccess

3

Reference values for the Cerebellar Cognitive Affective Syndrome Scale: Age and education matter.

Thieme, A.
2020

OpenAccess

4

Journal Article

Investigation of Visual System Involvement in Spinocerebellar Ataxia Type 14.

Ihl, Thomas
2020

The Cerebellum, 19 (2020) S. 469-482

OpenAccess OpenAccess

5

Journal Article

Tracking the brain in myotonic dystrophies: A 5-year longitudinal follow-up study

Gliem, Carla
2019

PLOS ONE, 14 (2019) 3, S. e0213381 -

OpenAccess OpenAccess

6

Journal Article

Reply: Biallelic POLR3A variants confirmed as a frequent cause of hereditary ataxia and spastic paraparesis.

Minnerop, Martina
2019

Brain, 142 (2019) 4, S. e13

OpenAccess OpenAccess

7

Deformation-based morphometry in a german multicenter SCA14 cohort reveals structural changes in cerebellum and forebrain

Pieperhoff, Peter
2019

OpenAccess OpenAccess

8

From bench to bedside: STN-deep brain stimulation is effective in SCA3 with parkinsonian symptoms

Minnerop, Martina
2019

9

Imaging of the cerebellar nuclei in spinocerebellar ataxia type 6

Jäschke, D.
2019

10

Journal Article

Cerebellar Involvement in DYT-THAP1 Dystonia.

Nikolov, Petyo
2019

The Cerebellum, 18 (2019) 5, S. 969-971

11

Journal Article

Current Progress in CNS Imaging of Myotonic Dystrophy

Minnerop, Martina
2018

Frontiers in neurology, 9 (2018) S. 646

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12

Neuropsychological characteristics of spinocerebellar ataxia type 14

Lux, Silke
2018

13

Conference Presentation

Neurometabolische Veränderungen in Spinozerebellärer Ataxie Typ 14 und 1

Grosch, A.
2018

14

Multi-modal multi-centre MRI study of rare spinocerebellar ataxia type 14

Grinberg, Farida
2018

15

Neuropsychological characteristics of spinocerebellar ataxia type 14

Bußenis, L.
2018

16

Journal Article

Reply: POLR3A variants in hereditary spastic paraplegia and ataxia

Minnerop, Martina
2018

Brain, 141 (2018) 1, S. e2

OpenAccess OpenAccess

17

Journal Article

Hypomorphic mutations in POLR3A are a frequent cause of sporadic and recessive spastic ataxia.

Minnerop, Martina
2017

Brain, 140 (2017) 6, S. 1561 - 1578

18

Conference Presentation

Familiäre Gangstörung

Minnerop, Martina
2017

19

Conference Presentation

Multi-modal multi-centre MRI study of rare spinocerebellar ataxia, type 14

Grinberg, Farida
2017

20

Journal Article

Expanded phenotype and hippocampal involvement in a novel compound heterozygosity of adult PLA2G6 associated neurodegeneration (PARK14)

Michelis, Joan Philipp
2017

Parkinsonism & related disorders, 37 (2017) S. 111-113

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