CIDP, CMT1B, or CMT1B plus CIDP?

[1]  C. Briani,et al.  Sporadic hereditary neuropathies misdiagnosed as chronic inflammatory demyelinating polyradiculoneuropathy: Pitfalls and red flags , 2020, Journal of the peripheral nervous system : JPNS.

[2]  C. Zaidman,et al.  Nerve ultrasound in polyneuropathies , 2018, Muscle & nerve.

[3]  Stefano Tamburin,et al.  The spectrum of Charcot-Marie-Tooth disease due to myelin protein zero: An electrodiagnostic, nerve ultrasound and histological study , 2018, Clinical Neurophysiology.

[4]  P. Latour,et al.  Hereditary and inflammatory neuropathies: a review of reported associations, mimics and misdiagnoses , 2016, Journal of Neurology, Neurosurgery & Psychiatry.

[5]  R. Finkel,et al.  Genotype-phenotype characteristics and baseline natural history of heritable neuropathies caused by mutations in the MPZ gene. , 2015, Brain : a journal of neurology.

[6]  J. Lupski,et al.  The allelic spectrum of Charcot–Marie–Tooth disease in over 17,000 individuals with neuropathy , 2014, Molecular genetics & genomic medicine.

[7]  C. Angiari,et al.  Segmental conduction abnormalities and myelin thickenings in Val102/fs null mutation of MPZ gene , 2004, Neurology.

[8]  S. Sisodiya,et al.  Steroid responsive polyneuropathy in a family with a novel myelin protein zero mutation , 2000, Journal of neurology, neurosurgery, and psychiatry.

[9]  E. Bellone,et al.  HMSN III phenotype due to homozygous expression of a dominant HMSN II gene , 1992, Neurology.

[10]  R. Martini,et al.  Role of immune cells in animal models for inherited peripheral neuropathies , 2007, NeuroMolecular Medicine.

[11]  D. Sharp,et al.  Coexistent hereditary and inflammatory neuropathy. , 2004, Brain : a journal of neurology.