• 17p duplicated Charcot-Marie-Tooth 1A: characteristics of a new population
• A case of IgM paraproteinemic neuropathy associated with anti-sulfated glucuronic paragloboside (SGPG) IgG antibody without anti-myelin-associated glycoprotein (MAG) activity
• A molecular genetic update of inherited distal motor neuropathies
• A neurophysiological study of large- and small-diameter nerve fibers in the hands of hemodialysis patients
• A novel missense pathogenic variant in NEFH causing rare Charcot-Marie-Tooth neuropathy type 2CC
• A point of view: The need to identify an antigen in psyconeuroimmunological disorders
• A splice altering variant in NDRG1 gene causes Charcot-Marie-Tooth disease, type 4D
• Acetyl-L-carnitine in diabetic polyneuropathy: experimental and clinical data
• Activity-dependent conduction block in multifocal motor neuropathy: magnetic fatigue test
• Adducted thumb as an isolated morphologic finding: an early sonographic sign of impaired neurodevelopment: A STROBE compliant study
• Anconeus Epitrochlearis Muscle Associated With Cubital Tunnel Syndrome: A Case Series
• Assessment of hand function in a patient with chronic sensory demyelinating neuropathy
• Association between Early Neuroretinal Dysfunction and Peripheral Motor Unit Loss in Patients with Type 1 Diabetes Mellitus
• Association of PRPS1 Mutations with Disease Phenotypes
• Atypical clinical presentation of ataxia telangiectasia
• Autoimmune phenomena in patients with myelodysplastic syndromes and chronic myelomonocytic leukemia
• Candida infection in hip alloarthroplasty
• Cardiovascular autonomic function and sympathetic skin response in chronic inflammatory demyelinating polyradiculoneuropathy
• Charcot-Marie-Tooth disease and intracellular traffic
• Charcot-Marie-Tooth disease: emerging mechanisms and therapies
• Chronic inflammatory demyelinating polyneuropathy in a patient with hyperIgEaemia
• Chronic inflammatory demyelinating polyneuropathy in childhood--a case with markedly hypertrophic nerves and pes cavus
• Clinical features and pathophysiological basis of sensory neuronopathies (ganglionopathies)
• Contralateral electrodiagnosis in patients with abnormal median distal sensory latency
• Correction of an amyotrophic dorsal face of hands due to neurological disease with autologous fat cells transplant: An original case
• CRASH syndrome: mutations in L1CAM correlate with severity of the disease
• Defective axonal transport of Rab7 GTPase results in dysregulated trophic signaling
• Delayed health effects of pesticides: review of current epidemiological knowledge
• Diagnostic accuracy of laser-evoked potentials in diabetic neuropathy
• Diagnostic challenges in chronic inflammatory demyelinating polyradiculoneuropathy
• Duplication of the PMP22 gene in 17p partial trisomy patients with Charcot-Marie-Tooth type-1 neuropathy
• Dysfunction of small myelinated afferents in diabetic polyneuropathy, as assessed by laser evoked potentials
• Electrodiagnostic findings in amyotrophic lateral sclerosis: Variation with region of onset and utility of thoracic paraspinal muscle examination
• Ethnic and population differences in the genetic predisposition to human obesity
• Evidence for somatic and germline mosaicism in CRASH syndrome
• Focal chronic inflammatory demyelinating polyradiculoneuropathy: Onset, course, and distinct features
• Ganglionopathies: evolving concept and ideas on management
• Genetic diagnosis and molecular pathology of inherited neuropathy
• Genotype/phenotype correlations in AARS-related neuropathy in a cohort of patients from the United Kingdom and Ireland
• Hereditary motor and sensory neuropathy associated with auditory neuropathy in a Gypsy family
• Hereditary motor and sensory neuropathy associated with auditory neuropathy in a Gypsy family
• Hereditary neuropathy: variety of disease-causing genes and progress of molecular genetic diagnosis
• High-frequency Ultrasonography of the Digital and Palmar Nerve Branches of the Hand in Peripheral Nerve Diseases
• Historical and pathological overview of Castleman disease
• HNPP: not only entrapment sites. Ultrasound digital nerve abnormalities in a guitar player
• Hydration and packing are crucial to amyloidogenesis as revealed by pressure studies on transthyretin variants that either protect or worsen amyloid disease
• Identical twins with mental retardation, dysarthria, progressive spastic paraplegia, and brachydactyly type E: a new syndrome or variant of Fitzsimmons-Guilbert syndrome?
• Insights into the pharmaceuticals and mechanisms of neurological orphan diseases: Current Status and future expectations
• Insulin deficiency rather than hyperglycemia accounts for impaired neurotrophic responses and nerve fiber regeneration in type 1 diabetic neuropathy
• Involvement of the peripheral nervous system in HIV infection: electromyographic study and nerve conduction velocity
• L1CAM whole gene deletion in a child with L1 syndrome
• MASA syndrome: clinical variability and linkage analysis
• MASA syndrome: new clinical features and linkage analysis using DNA probes
• Median-ulnar anastomosis to thenar, hypothenar, and first dorsal interosseous muscles: collision technique confirmation
• Metabolic biology of 3-methylglutaconic acid-uria: a new perspective
• Molecular genetics of autosomal-recessive axonal Charcot-Marie-Tooth neuropathies
• MRI and SPECT findings in a case of metronidazole-induced reversible acute cerebellar ataxia
• Muscle fiber conduction abnormalities in early diabetic polyneuropathy
• Near-infrared spectrophotoscopy of finger venules in assessment of autonomic dysfunction
• Neurobehavioral and clinical effects in workers exposed to CS(2)
• Neurofilament light polypeptide gene N98S mutation in mice leads to neurofilament network abnormalities and a Charcot-Marie-Tooth Type 2E phenotype
• Neurological manifestations of antiphospholipid antibody syndrome
• Neuropathic Pain as Main Manifestation of <em>POLG</em>-Related Disease: A Case Report
• Neuropathic pain in Charcot-Marie-Tooth disease: A clinical and laser-evoked potential study
• Neuropathology of diabetic neuropathy and its correlations with neurophysiology
• New syndrome: clavicle hypoplasia, facial dysmorphism, severe myopia, single central incisor and peripheral neuropathy
• Normative Values for Electrochemical Skin Conductance Measurements for Quantitative Assessment of Sudomotor Function in Healthy Indian Adults
• Novel GARS mutation presenting as autosomal dominant intermediate Charcot-Marie-Tooth disease
• Novel mutations in the L1CAM gene support the complexity of L1 syndrome
• Occupational risk caused by ultrasound in medicine
• Optic Nerve Demyelination in IgG4 Anti-Neurofascin 155 Antibody-Positive Combined Central and Peripheral Demyelination Syndrome
• Outcome measures for Charcot-Marie-Tooth disease: clinical and neurofunctional assessment in children
• Partial trisomy 17p12pter, associated with pre and postnatal growth retardation, dysmorphic facial and digital features, developmental delay, and signs of HMSN1 in early childhood
• Patterns and severity of conduction abnormalities in Guillain-Barre syndrome
• Pitt-Hopkins syndrome in a boy with Charcot Marie Tooth disease type 1A: a rare co-occurrence of 2 genetic disorders
• Properties of cutaneous afferents during recovery from Guillain-Barré syndrome
• Proximal motor conduction evaluated by transcranial magnetic stimulation in acquired inflammatory demyelinating neuropathies
• Quantitative assessment of cardiovascular autonomic function in Guillain-Barre syndrome
• Quantitative sensory testing of thermal and vibratory perception in familial dysautonomia
• Refsum disease: a defect in the alpha-oxidation of phytanic acid in peroxisomes
• Reversal of longstanding neurological deficits after a late release of tethered spinal cord
• Reversible conduction failure on the deep tendon reflex response recording in early Guillain-Barré syndrome
• Roussy-Lévy syndrome is a phenotypic variant of Charcot-Marie-Tooth syndrome IA associated with a duplication on chromosome 17p11.2
• Seven Years of Selective Genetic Screening Program and Follow-Up of Asymptomatic Carriers With Hereditary Transthyretin Amyloidosis in Bulgaria
• Shoulder capsulitis in type I and II diabetic patients: association with diabetic complications and related diseases
• Silver syndrome variant of hereditary spastic paraplegia: A locus to 4p and allelism with SPG4
• Skeletal abnormalities in Refsum's disease (heredopathia atactica polyneuritiformis)
• Spastic paraplegia, dysarthria, brachydactyly, and cone shaped epiphyses: confirmation of the Fitzsimmons syndrome
• Spectral-domain optical coherence tomography findings in Alström syndrome
• SSR abnormalities in chronic alcoholics
• Sympathetic skin response in diabetic neuropathy
• Syndrome disintegration: Exome sequencing reveals that Fitzsimmons syndrome is a co-occurrence of multiple events
• The interrelation of vascular, neurological and functional disorders in the hand of rheumatoid arthritis patients
• The neuropathy of Dejerine and Sottas: report of an Indian family
• Troyer syndrome: a combination of central brain abnormality and motor neuron disease?
• Ulnar neuropathy in the forearm: A possible complication of diabetes mellitus
• Ultrasound in the diagnosis of ulnar neuropathy at the cubital tunnel
• Underestimated associated features in CMT neuropathies: clinical indicators for the causative gene?
• Vibrotactile function of the hand in compression and vibration-induced neuropathy. Sensibility index--a new measure
• X-linked dominant hereditary motor and sensory neuropathy