Tomaculous Neuropathy Latest Advances

PMP22-Related Neuropathies: A Systematic Review.

Journal: Genes

Published: September 29, 2025

Aberrant Molecular Myelin Architecture in Charcot-Marie-Tooth Disease Type 1A and Hereditary Neuropathy With Liability to Pressure Palsies.

Journal: Glia

Published: June 04, 2025

Copy Number Variations in a Case with Intractable Epilepsy, Intellectual Disability, and Hereditary Neuropathy with Liability to Pressure Palsies Having a 17p12 Deletion.

Journal: Internal medicine (Tokyo, Japan)

Published: April 13, 2025

Literature review of clinical analysis of hereditary neuropathy with liability to pressure palsies.

Journal: Journal of neurology

Published: October 24, 2024

Video head impulse test findings in patients with peripheral myelin protein 22 related neuropathies.

Journal: Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology

Published: June 20, 2024

Clinical and molecular genetic characteristics of 24 families of hereditary neuropathy with liability to pressure palsy and literature review.

Journal: Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences

Published: March 03, 2024

Loss of YAP in Schwann cells improves HNPP pathophysiology.

Journal: Glia

Published: February 29, 2024

Hereditary Neuropathy with Liability to Pressure Palsy and Vocal Cord Paralysis After Pulmonary Lobectomy: A Case Report.

Journal: A&A practice

Published: February 27, 2024

Targeting PI3K/Akt/mTOR signaling in rodent models of PMP22 gene-dosage diseases.

Journal: EMBO molecular medicine

Published: May 22, 2023

Monomelic Multifocal Neuropathy: An Unrecognized Electrophysiological Feature of Hereditary Neuropathy with Liability to Pressure Palsies in Childhood.

Journal: Neurology India

Published: May 06, 2023

Thyroid Eye Disease-Compressive Optic Neuropathy

Journal: Die Ophthalmologie

Published: May 05, 2023

Noncanonical splice-site variant in peripheral myelin protein 22 gene (PMP22) in a patient with hereditary neuropathy with liability to pressure palsies.

Journal: Journal of the peripheral nervous system : JPNS

Published: March 07, 2023

Tomaculous Neuropathy Latest Advances

Find the Latest Research About Tomaculous Neuropathy

PMP22-Related Neuropathies: A Systematic Review.

PMP22-Related Neuropathies: A Systematic Review.

Aberrant Molecular Myelin Architecture in Charcot-Marie-Tooth Disease Type 1A and Hereditary Neuropathy With Liability to Pressure Palsies.

Aberrant Molecular Myelin Architecture in Charcot-Marie-Tooth Disease Type 1A and Hereditary Neuropathy With Liability to Pressure Palsies.

Copy Number Variations in a Case with Intractable Epilepsy, Intellectual Disability, and Hereditary Neuropathy with Liability to Pressure Palsies Having a 17p12 Deletion.

Copy Number Variations in a Case with Intractable Epilepsy, Intellectual Disability, and Hereditary Neuropathy with Liability to Pressure Palsies Having a 17p12 Deletion.

Literature review of clinical analysis of hereditary neuropathy with liability to pressure palsies.

Literature review of clinical analysis of hereditary neuropathy with liability to pressure palsies.

Video head impulse test findings in patients with peripheral myelin protein 22 related neuropathies.

Video head impulse test findings in patients with peripheral myelin protein 22 related neuropathies.

Clinical and molecular genetic characteristics of 24 families of hereditary neuropathy with liability to pressure palsy and literature review.

Clinical and molecular genetic characteristics of 24 families of hereditary neuropathy with liability to pressure palsy and literature review.

Loss of YAP in Schwann cells improves HNPP pathophysiology.

Loss of YAP in Schwann cells improves HNPP pathophysiology.

Hereditary Neuropathy with Liability to Pressure Palsy and Vocal Cord Paralysis After Pulmonary Lobectomy: A Case Report.

Hereditary Neuropathy with Liability to Pressure Palsy and Vocal Cord Paralysis After Pulmonary Lobectomy: A Case Report.

Targeting PI3K/Akt/mTOR signaling in rodent models of PMP22 gene-dosage diseases.

Targeting PI3K/Akt/mTOR signaling in rodent models of PMP22 gene-dosage diseases.

Monomelic Multifocal Neuropathy: An Unrecognized Electrophysiological Feature of Hereditary Neuropathy with Liability to Pressure Palsies in Childhood.

Monomelic Multifocal Neuropathy: An Unrecognized Electrophysiological Feature of Hereditary Neuropathy with Liability to Pressure Palsies in Childhood.

Thyroid Eye Disease-Compressive Optic Neuropathy

Thyroid Eye Disease-Compressive Optic Neuropathy

Noncanonical splice-site variant in peripheral myelin protein 22 gene (PMP22) in a patient with hereditary neuropathy with liability to pressure palsies.

Noncanonical splice-site variant in peripheral myelin protein 22 gene (PMP22) in a patient with hereditary neuropathy with liability to pressure palsies.