• A West Nile Virus infection expressed as unilateral limb paralysis and complicated by Parsonage-Turner syndrome: a case report
• Absceso cerebral como manifestación inicial de Deficiencia especifica de anticuerpos
• An Assessment of the Reduction of Submental Fullness With ATX-101 (Deoxycholic Acid Injection) in the Expanded Safe Zone
• Approach to sialadenitis
• Bi-allelic SNAPC4 variants dysregulate global alternative splicing and lead to neuroregression and progressive spastic paraparesis
• Case report: Flail leg syndrome in familial amyotrophic lateral sclerosis with L144S <em>SOD1</em> mutation
• Characterization of Effect of Enterovirus D68 in 129/Sv Mice Deficient in IFN-α/β and/or IFN-γ Receptors
• COQ7 splice site variant causing a spastic paraparesis phenotype in siblings
• Developmental disorder and spastic paraparesis in two sisters with a TCF7L2 truncating variant inherited from a mosaic mother
• Early-onset familial Alzheimer's disease with spastic paraparesis associated with PSEN1 gene
• Efficacy of individualized homeopathic medicines in treatment of post-stroke hemiparesis: A randomized trial
• Efficacy of the Grit Scale Score in Predicting Voice Therapy Adherence and Outcomes
• End-stage crystalline maculopathy with retinal atrophy in Sjögren-Larsson syndrome: a case report and review of the literature
• Expanding the Clinical Spectrum of <em>UBTF</em>-Related Neurodevelopmental Disorder
• Family and literature analysis demonstrates phenotypic effect of two variants in the calpain-3 gene
• Frequency and Causes of Traumatic and Non-traumatic Spinal Injury Reported at Two Major Tertiary Care Hospitals of Khyber Pakhtunkhwa
• Hereditary spastic paraparesis due to SPG5/CYP7B1 mutation with potential therapeutic implications
• Hereditary Transthyretin Amyloidosis
• Iatrogenic Facial Nerve Injury in Head and Neck Surgery in the Presence of Intraoperative Facial Nerve Monitoring With Electromyography: A Systematic Review
• Intrathecal baclofen for the management of hereditary spastic paraparesis: a systematic review
• Living with glioblastoma - the need for integrated support based on experiences of chaos, loss of autonomy, and isolation in both patients and their relatives
• Medical management of feline emphysematous hepatitis-A case report
• Migraine Aura-Catch Me If You Can with EEG and MRI-A Narrative Review
• Migraine with prolonged aphasic aura associated with a CACNA1A mutation: A case report and narrative review
• Neuromuscular Practical Knowledge: Focus On Muscle Weakness
• Novel genetic variant in hereditary spastic paraparesis
• Oncocytic carcinoma of the thyroid: Conclusions from a 20-year patient cohort
• Palinacousis in amyloidosis: exploring the hallucinatory phenomenon in brain pathology-a case report
• Pelizaeus-Merzbacher Disease
• Pelizaeus-Merzbacher Disease
• Post-traumatic Delayed Bilateral Vocal Cord Paralysis Caused by Cervical Osteophytes: A Case Report
• Presentation and management of nervous system cavernous malformations in children: A systematic review and case report
• Ptosis Correction
• Ptosis Correction
• Recurrent sporadic malignant triton tumor in the carotid sheath in the absence of neurofibromatosis
• Recurrent Transient Ischemic Attacks and Stroke Due to Carotid Dissection During Air Travel: A Case Report
• Safety of Laryngeal Electromyography and Repetitive Stimulation
• Subclinical spinal muscular atrophy in a 60-year-old man
• TCL1-family negative T-cell prolymphocytic leukemia with rapid progression of extranodal disease despite a normal white blood cell count
• The CAPN3 p.Lys 254del variant is not always associated with dominant CAPN3-related muscular dystrophy
• The quality of life of teenagers living with cerebral palsy participating in conductive education
• Towards sustainable and humane dairy farming: A low-cost electrochemical sensor for on-site diagnosis of milk fever
• Treatment of spasticity