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Christoph Kamm

University of Rostock
University of Tübingen

56

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Neues zur Genetik von Dystonien: Mutationen in den Genen VPS16 und VPS41 als Ursache einer Dystonie mit Beeinträchtigung der Fusion lysosomaler Vesikel

2021
- Christoph Kamm
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The ARCA Registry: A Collaborative Global Platform for Advancing Trial Readiness in Autosomal Recessive Cerebellar Ataxias.

2021 Frontiers in Neurology
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Serum creatine kinase and creatinine in adult spinal muscular atrophy under nusinersen treatment.

2021 Annals of clinical and translational neurology
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Nusinersen in adults with 5q spinal muscular atrophy: a non-interventional, multicentre, observational cohort study.

2020 Lancet Neurology
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Prominent White Matter Involvement in Multiple System Atrophy of Cerebellar Type

2020 Movement Disorders
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Frequency and risk factors of antibody-induced secondary failure of botulinum neurotoxin therapy.

2020 Neurology
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Validation of a self‐completed Dystonia Non‐Motor Symptoms Questionnaire

2019 Annals of clinical and translational neurology
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Spinale Muskelatrophie – Expertenempfehlungen zur Behandlung von erwachsenen Patienten mit Nusinersen

2019 Fortschritte Der Neurologie Psychiatrie
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Patient-Reported Prevalence of Non-motor Symptoms Is Low in Adult Patients Suffering From 5q Spinal Muscular Atrophy

2019 Frontiers in Neurology
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A novel heterozygous variant in ERLIN2 causes autosomal dominant pure hereditary spastic paraplegia

2018 European Journal of Neurology
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