Callyn A. Kirk

CMT subtypes and disease burden in patients enrolled in the Inherited Neuropathies Consortium natural history study: a cross-sectional analysis

Jun Yu Li, R. Finkel, S. Züchner, 2014, Journal of Neurology, Neurosurgery & Psychiatry.

Modifier Gene Candidates in Charcot-Marie-Tooth Disease Type 1A: A Case-Only Genome-Wide Association Study

F. Baas, S. Züchner, G. Beecham, 2019, Journal of neuromuscular diseases.

Variation in SIPA1L2 is correlated with phenotype modification in Charcot– Marie– Tooth disease type 1A

F. Baas, S. Züchner, G. Beecham, 2019, Annals of neurology.

A longitudinal study of CMT1A using Rasch analysis based CMT neuropathy and examination scores

R. Finkel, S. Züchner, F. Muntoni, 2020, Neurology.

Quality-of-life in Charcot–Marie–Tooth disease: The patient’s perspective

D. Herrmann, M. Shy, Denise Shereff, 2014, Neuromuscular Disorders.