Afferent Visual Pathway Affection in Patients with PMP22 Deletion-Related Hereditary Neuropathy with Liability to Pressure Palsies

DTI Study of Cerebral Normal-Appearing White Matter in Hereditary Neuropathy With Liability to Pressure Palsies (HNPP)

(2015) Wei-wei Wang et al.   MEDICINE

Reliability of Intra-Retinal Layer Thickness Estimates

(2015) Timm Oberwahrenbrock et al.   PLoS One

Optic and auditory pathway dysfunction in demyelinating neuropathies

(2014) M. Knopp et al.   ACTA NEUROLOGICA SCANDINAVICA

Relations of low contrast visual acuity, quality of life and multiple sclerosis functional composite: a cross-sectional analysis

(2014) Johann Schinzel et al.   BMC Neurology

PMP22 related neuropathies: Charcot-Marie-Tooth disease type 1A and Hereditary Neuropathy with liability to Pressure Palsies

(2014) Barbara W van Paassen et al.   Orphanet Journal of Rare Diseases

Abnormal junctions and permeability of myelin in PMP22-deficient nerves

(2013) Jiasong Guo et al.   ANNALS OF NEUROLOGY

Central nervous system abnormalities in patients with PMP22 gene mutations: a prospective study

(2012) J.-B. Chanson et al.   JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY

The OSCAR-IB Consensus Criteria for Retinal OCT Quality Assessment

(2012) Prejaas Tewarie et al.   PLoS One

Charcot–Marie–Tooth disease in Northern England: Figure 1

(2011) Charlotte Foley et al.   JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY

Conduction Block in PMP22 Deficiency

(2010) Y. Bai et al.   JOURNAL OF NEUROSCIENCE

Variable phenotypes are associated with PMP22 missense mutations

(2010) M. Russo et al.   NEUROMUSCULAR DISORDERS