• A Case of Apoplexy Attack-Like Neuropathy due to Hereditary Neuropathy with Liability to Pressure Palsies in a Patient Diagnosed with Chronic Cerebral Infarction
• A case of hereditary neuropathy with liability to pressure palsies due to push-up exercise
• A Case of Severe Early-Onset Neuropathy Caused by a Compound Heterozygous Deletion of the PMP22 Gene: Clinical and Neurographic Aspects
• A case report of hereditary neuropathy with liability to pressure palsies accompanied by type 2 diabetes mellitus and psoriasis
• A Correlation between Upper Extremity Compressive Neuropathy and Nerve Compression Headache
• A dual role for Integrin α6β4 in modulating hereditary neuropathy with liability to pressure palsies
• A Functional and Neuropathological Testing Paradigm Reveals New Disability-Based Parameters and Histological Features for P0180-190-Induced Experimental Autoimmune Neuritis in C57BL/6 Mice
• A New Point Mutation in the PMP22 Gene in a Family Suffering From Atypical HNPP
• Afferent Visual Pathway Affection in Patients with PMP22 Deletion-Related Hereditary Neuropathy with Liability to Pressure Palsies
• An 18-year-old man of hereditary neuropathy with liability to pressure palsies presenting with bilateral brachial plexopathy during military training
• Anconeus Epitrochlearis Muscle Associated With Cubital Tunnel Syndrome: A Case Series
• Anesthetic Considerations of Hereditary Neuropathy With Liability to Pressure Palsies in an Obstetric Patient: A Case Report
• Asymptomatic Retinal Vein Occlusion in a 13-Year-Old With Heterozygous Deletion of the PMP22 Gene and a Diagnosis of Hereditary Neuropathy With Liability to Pressure Palsies
• Avian riboflavin deficiency causes reliably reproducible peripheral nerve demyelination and, with vitamin supplementation, rapid remyelination
• Characterisation of pain in people with hereditary neuropathy with liability to pressure palsy
• Chronic peripheral nerve compression disrupts paranodal axoglial junctions
• Clemastine improves electrophysiologic and histomorphometric changes through promoting myelin repair in a murine model of compression neuropathy
• Clinical and molecular genetic characteristics of 24 families of hereditary neuropathy with liability to pressure palsy and literature review
• Clinical and neurophysiological findings in patients with hereditary neuropathy with liability to pressure palsy and chromosome 17p11.2 deletion
• Clinical Reasoning: A 15-year-old boy with bilateral wrist pain in the setting of weight loss
• Clinical Reasoning: A teenager with left arm weakness
• Clinical, electrophysiological, genetic, and imaging features of six Chinese Han patients with hereditary neuropathy with liability to pressure palsies (HNPP)
• Common Compression Neuropathies
• Comparison of clinical and electrophysiological features of patients with hereditary neuropathy with liability to pressure palsies with or without pain
• Compression neuropathy of common peroneal nerve caused by a popliteal cyst: A case report
• Compression of Root Level in a Patient with Hereditary Neuropathy with Liability to Pressure Palsy Diagnosed by Magnetic Resonance Imaging
• Compressive Neuropathy: A Consequence of Mal-Positioning during Labour?
• Davidenkow syndrome: A phenotypic variant of hereditary neuropathy with liability to pressure palsies
• Decompression with Brachioradialis Tenotomy Improves Pain and Quality of Life in Patients with Radial Sensory Nerve Compression
• Diabetes mellitus as a risk factor for compression neuropathy: a longitudinal cohort study from southern Sweden
• Dosage effects of PMP22 on nonmyelinating Schwann cells in hereditary neuropathy with liability to pressure palsies
• Effect of Intrathecal Baclofen on Delayed-Onset Paroxysmal Dystonia due to Compression Injury Resulting From Congenital and Progressive Spinal Bone Deformities in Chondrodysplasia Punctata
• Electrodiagnostic Characterization of Hereditary Neuropathy With Liability to Pressure Palsies
• Evaluating the interreader agreement and intrareader reproducibility of Visual Field Defects in Thyroid Eye Disease- Compressive Optic Neuropathy
• Evaluation of neurological testing for hand-arm vibration syndrome
• Fatigue in patients with hereditary neuropathy with liability to pressure palsies
• Fibular nerve palsy after hip replacement: Not only surgeon responsibility. Hereditary neuropathy with liability to pressure palsies (HNPP) a rare cause of nerve liability
• Frequency of hereditary neuropathy with liability to pressure palsies (HNPP) due to 17p11.2 deletion in a Korean newborn population
• Hand compression neuropathy: An assessment guide
• Hand manifestations of neurological disease: some alternatives to consider
• Hereditary neuropathy with liability to pressure palsies
• Hereditary neuropathy with liability to pressure palsies (HNPP): Intrafamilial phenotypic variability and early childhood refusal to walk as the presenting symptom
• Hereditary neuropathy with liability to pressure palsies in childhood: Case series and literature update
• Hereditary neuropathy with liability to pressure palsies in childhood: Report of three cases
• Hereditary neuropathy with liability to pressure palsies mimicking chronic inflammatory demyelinating polyneuropathy
• Hereditary neuropathy with liability to pressure palsies misdiagnosed as Guillain-Barré Syndrome: A case report
• Hereditary Neuropathy with Liability to Pressure Palsies: A Rare Condition That Presents with Common Symptoms: A Case Report
• Hereditary Neuropathy With Liability to Pressure Palsies: Diverse Phenotypes in Childhood
• Hereditary neuropathy with liability to pressure palsy (HNPP): report of a family with a new point mutation in PMP22 gene
• Hereditary Neuropathy with Liability to Pressure Palsy and Vocal Cord Paralysis After Pulmonary Lobectomy: A Case Report
• Hereditary neuropathy with liability to pressure palsy presenting as a bilateral brachial plexopathy
• Heterotopic Ossification After Revision Carpal Tunnel Release Causing Mixed Ulnar and Median Compression Neuropathy
• HNPP: not only entrapment sites. Ultrasound digital nerve abnormalities in a guitar player
• IgG4-related disease presenting as hypertrophic pachymeningitis and compressive optic neuropathy
• Intravenous Immunoglobulin in Treatment of Hereditary Neuropathy With Liability to Pressure Palsy
• Is the diagnosis written in the palm? Compression neuropathy from a walking frame
• Laryngeal and phrenic nerve involvement in a patient with hereditary neuropathy with liability to pressure palsies (HNPP)
• Length-dependent MRI of hereditary neuropathy with liability to pressure palsies
• Lesions of the anterior interosseous nerve: differentiating between compression neuropathy and neuritis
• Lipomas of the Brachial Plexus: A Case Series and Review of the Literature
• Marfanoid Habitus in an Adolescent With Hereditary Neuropathy With Liability to Pressure Palsies: A Novel Association?
• Median nerve compression neuropathy due to a closed osteocartilaginous tunnel at the distal upper arm: a case report
• Microvascular neural blood flow assessment for a chronic nerve compression neuropathy mouse model by fluorescein angiography
• Migraine Headaches in Patients with Upper Extremity Compressive Neuropathy
• Molecular genetic diagnosis and clinical features of hereditary neuropathy with liability to pressure palsies in Belarusian patients
• Monomelic Multifocal Neuropathy: An Unrecognized Electrophysiological Feature of Hereditary Neuropathy with Liability to Pressure Palsies in Childhood
• Multiple tendon transfer for a case of radial nerve palsy in hereditary neuropathy with liability to pressure palsy
• Muscle training-induced bilateral brachial plexopathy in an adolescent with sporadic hereditary neuropathy with liability to pressure palsies
• Myelin protein zero-related autosomal dominant peripheral neuropathy presenting as hereditary neuropathy with liability to pressure palsies
• Nerve wrapping for recurrent compression neuropathy: A systematic review
• New evidence for secondary axonal degeneration in demyelinating neuropathies
• Nociceptive and Neuronal Evaluation of the Sciatic Nerve of Wistar Rats Subjected to Compression Injury and Treated with Resistive Exercise
• Noncanonical splice-site variant in peripheral myelin protein 22 gene (PMP22) in a patient with hereditary neuropathy with liability to pressure palsies
• Pain and small-fiber affection in hereditary neuropathy with liability to pressure palsies (HNPP)
• Peripheral Myelin Protein 22 Gene Mutations in Charcot-Marie-Tooth Disease Type 1E Patients
• Peripheral neuropathy in diabetes: it's not always what it looks like
• Pmp22 super-enhancer deletion causes tomacula formation and conduction block in peripheral nerves
• Prevalence of Common Types of Compression Neuropathies in Qena Governorate/Egypt: A Population-Based Survey
• Prevalence of thoracic spine lesions masquerading as cauda equina syndrome: yield of a novel magnetic resonance imaging protocol
• Problems of the diagnosis and treatment of compression neuropathy of the median nerve: an analysis of typical medical practice
• Quality of life in hereditary neuropathy with liability to pressure palsies is as impaired as in Charcot-Marie-Tooth disease type 1A
• Radial Tunnel Syndrome: Case Report and Comprehensive Critical Review of a Compression Neuropathy Surrounded by Controversy
• Recommendations for Patients with Complex Nerve Injuries during the COVID-19 Pandemic
• Reply: A Correlation between Upper Extremity Compressive Neuropathy and Nerve Compression Headache
• Reverse End-to-Side Transfer to Ulnar Motor Nerve: Evidence From Preclinical and Clinical Studies
• Schwann Cell O-GlcNAc Glycosylation Is Required for Myelin Maintenance and Axon Integrity
• Somatotopic Fascicular Lesions of the Brachial Plexus Demonstrated by High-Resolution Magnetic Resonance Neurography
• Spinal anaesthesia for elective caesarean section in a patient with hereditary neuropathy with liability to pressure palsies
• Squatting-induced bilateral peroneal nerve palsy in a sewer pipe worker
• Targeting PI3K/Akt/mTOR signaling in rodent models of PMP22 gene-dosage diseases
• Teaching NeuroImage: Radial Compression Neuropathy Secondary to Accessory Belly of the Triceps Muscle
• The Belgian MicroArray Prenatal (BEMAPRE) database: A systematic nationwide repository of fetal genomic aberrations
• The Electrophysiologic and Ultrasonographic Change after Carpal Tunnel Release in a Patient with Hereditary Neuropathy with Liability to Pressure Palsy
• Thyroid Eye Disease-Compressive Optic Neuropathy
• Tract-Specific Diffusion Tensor Imaging Reveals Laterality of Neurological Symptoms in Patients with Cervical Compression Myelopathy
• Transient Exertional Compressive Radial Neuropathy in a Collegiate Baseball Pitcher: A Case Report
• Tuning PAK Activity to Rescue Abnormal Myelin Permeability in HNPP
• Utility of Carpal Tunnel Release and Ulnar Decompression in CMT1A and HNPP
• Vagus nerve pressure palsy in hereditary neuropathy with liability to pressure palsies confirmed by neurosonography
• Wrist drop in an arcade dancing game: Unusual sudden bilateral radial palsy