| P50 | author | Frank Baas | Q30111686 |
| P2093 | author name string | Camiel Verhamme | |
| | Anneloor L.M.A. ten Asbroek | |
| | Ivo N. van Schaik | |
| | John R. Muddle | |
| | Michelle Nourallah | |
| | Rosalind H.M. King | |
| | Ruud Wolterman | |
| P2860 | cites work | Distal axonopathy in peripheral nerves of PMP22-mutant mice | Q48147302 |
| | The natural history of Charcot-Marie-Tooth type 1A in adults: a 5-year follow-up study | Q48429094 |
| | Qualitative and quantitative morphology of human sural nerve at different ages | Q48430348 |
| | PMP22 overexpression causes dysmyelination in mice. | Q48483173 |
| | Clinical, electrophysiological and molecular genetic characteristics of 93 patients with X-linked Charcot-Marie-Tooth disease | Q48779070 |
| | Identical point mutations of PMP-22 in Trembler-J mouse and Charcot-Marie-Tooth disease type 1A | Q55671003 |
| | Different Intracellular Pathomechanisms Produce Diverse Myelin Protein Zero Neuropathies in Transgenic Mice | Q57650102 |
| | Duplication in chromosome 17p11.2 in Charcot-Marie-Tooth neuropathy type 1a (CMT 1a) | Q58183892 |
| | Demyelinating and axonal features of Charcot-Marie-Tooth disease with mutations of myelin-related proteins (PMP22, MPZ and Cx32): a clinicopathological study of 205 Japanese patients | Q28217188 |
| | Shortened internodal length of dermal myelinated nerve fibres in Charcot-Marie-Tooth disease type 1A. | Q33567193 |
| | Copy number variations are a rare cause of non-CMT1A Charcot-Marie-Tooth disease | Q33833588 |
| | Neurological dysfunction and axonal degeneration in Charcot-Marie-Tooth disease type 1A. | Q33907007 |
| | Copy number variation upstream of PMP22 in Charcot-Marie-Tooth disease | Q34328787 |
| | Behavioral and functional analysis of mouse phenotype: SHIRPA, a proposed protocol for comprehensive phenotype assessment | Q34441265 |
| | Schwann cells as regulators of nerve development | Q34470057 |
| | Mechanisms for nonrecurrent genomic rearrangements associated with CMT1A or HNPP: rare CNVs as a cause for missing heritability | Q34544478 |
| | Axonal pathology precedes demyelination in a mouse model of X-linked demyelinating/type I Charcot-Marie Tooth neuropathy | Q34554468 |
| | Comparison of a new pmp22 transgenic mouse line with other mouse models and human patients with CMT1A. | Q34713834 |
| | Neurophysiologic abnormalities in children with Charcot-Marie-Tooth disease type 1A. | Q34849353 |
| | Disease mechanisms in inherited neuropathies | Q35209953 |
| | Phenotypic clustering in MPZ mutations | Q35623626 |
| | The formation of peripheral myelin protein 22 aggregates is hindered by the enhancement of autophagy and expression of cytoplasmic chaperones | Q35762256 |
| | Oligodendroglial modulation of fast axonal transport in a mouse model of hereditary spastic paraplegia. | Q36322059 |
| | The function of RhoGTPases in axon ensheathment and myelination | Q37040608 |
| | Peripheral myelin protein 22 is regulated post-transcriptionally by miRNA-29a | Q37268768 |
| | Development of the Schwann cell lineage: from the neural crest to the myelinated nerve | Q37273618 |
| | Chapter 2: Development of the peripheral nerve. | Q37580149 |
| | Charcot-Marie-Tooth disease and related neuropathies: mutation distribution and genotype-phenotype correlation | Q38292207 |
| | Peripheral myelin protein 22 is in complex with alpha6beta4 integrin, and its absence alters the Schwann cell basal lamina. | Q40325105 |
| | Unmedullated fibers originating in dorsal root ganglia | Q41834741 |
| | PMP22 expression in dermal nerve myelin from patients with CMT1A. | Q41908068 |
| | The postspike positivity of unmedullated fibers of dorsal root origin | Q42945904 |
| | Induced myelination and demyelination in a conditional mouse model of Charcot-Marie-Tooth disease type 1A. | Q43594474 |
| | Longitudinal conduction studies in hereditary motor and sensory neuropathy type 1. | Q45039279 |
| | Construction of a mouse model of Charcot-Marie-Tooth disease type 1A by pronuclear injection of human YAC DNA. | Q45877689 |
| | Connexin32-null mice develop demyelinating peripheral neuropathy | Q47700279 |
| P433 | issue | 5 | |
| P921 | main subject | pathology | Q7208 |
| | overexpression | Q61643320 |
| P304 | page(s) | 386-398 | |
| P577 | publication date | 2011-05-01 | |
| P1433 | published in | Journal of Neuropathology & Experimental Neurology | Q15716771 |
| P1476 | title | Myelin and Axon Pathology in a Long-Term Study ofPMP22-Overexpressing Mice | |
| P478 | volume | 70 | |