• A case of Balo's concentric sclerosis showing the attenuation of the Balo lesion after ofatumumab treatment: A case report
• A case-report of Balo concentric sclerosis transformed into definite multiple sclerosis
• A de novo GABRB2 variant associated with myoclonic status epilepticus and rhythmic high-amplitude delta with superimposed (poly) spikes (RHADS)
• A new entity in the NARS2 variant: the first reported case of type 1 diabetes mellitus associated with the phenotype
• A new pathogenic POLG variant
• A SARS-CoV-2 Omicron outbreak among crew members on a cruise ship in Germany in early 2022
• Acute Disseminated Encephalomyelitis with Baló-like Lesion by Scorpion Sting: Case Report
• Age of Onset and Disease Course in Biopsy-Proven Minimal Change Disease: An Analysis From the Cure Glomerulonephropathy Network
• AJKD Atlas of Renal Pathology: Pierson Syndrome
• Alpers-Huttenlocher Syndrome
• Alpers-Huttenlocher Syndrome
• Antibody signatures in patients with histopathologically defined multiple sclerosis patterns
• Antiphospholipid Antibodies (aPL) and Thrombotic Microangiopathy for the Diagnosis of aPL Nephropathy: You Can't Have One Without the Other
• Assessing somatization in urologic chronic pelvic pain syndrome
• Astrocytic pathology in Alpers' syndrome
• Atypical inflammatory demyelinating lesions and atypical multiple sclerosis
• Balo concentric sclerosis in a 23-year-old man
• Balo concentric sclerosis: Literature review and report of two cases
• Balo's concentric sclerosis
• Balo's concentric sclerosis - A rare entity within the spectrum of demyelinating diseases
• Balo's concentric sclerosis is immunologically distinct from multiple sclerosis: results from retrospective analysis of almost 150 lumbar punctures
• Balo's concentric sclerosis presenting asymptomatically in a child: clinico-radiological-pathological correlation
• Balo's concentric sclerosis: An atypical demyelinating disease in pediatrics
• Balo's concentric sclerosis: an update and comprehensive literature review
• Balo's concentric sclerosis: Case report
• Biophysical characterization Of Alpers encephalopathy associated mutants of human mitochondrial phenylalanyl-tRNA synthetase
• Case 250: Alpers-Huttenlocher Syndrome
• Characterizing Viral Infection by Electron Microscopy: Lessons from the Coronavirus Disease 2019 Pandemic
• Classical Onion Bulb-Like Appearance in Balo's Concentric Sclerosis
• Clinical and biochemical characteristics of atypical variants of multiple sclerosis
• Clinical and genetic characteristics of 62 children with mitochondrial epilepsy
• Clinical and molecular spectrum associated with Polymerase-γ related disorders
• Clinical and Radiologic Features, Pathology, and Treatment of Balo Concentric Sclerosis
• Clinical Attributes and Electroencephalogram Analysis of Patients With Varying Alpers' Syndrome Genotypes
• Clinicopathologic Findings of CARS2 Mutation
• Defining the molecular correlate of arteriolar hyalinosis in kidney disease progression by integration of single cell transcriptomic analysis and pathology scoring
• Delineating selective vulnerability of inhibitory interneurons in Alpers' syndrome
• Differentiating rhythmic high-amplitude delta with superimposed (poly) spikes from extreme delta brushes: limitations of standardized nomenclature and implications for patient management
• Dissecting the neuronal vulnerability underpinning Alpers' syndrome: a clinical and neuropathological study
• Distinct microglial and macrophage distribution patterns in the concentric and lamellar lesions in Baló's disease and neuromyelitis optica spectrum disorders
• Do changes in dysfunctional posttraumatic cognitions differentially predict PTSD symptom clusters?
• Efficacy and safety of sparsentan versus irbesartan in patients with IgA nephropathy (PROTECT): 2-year results from a randomised, active-controlled, phase 3 trial
• Episodic Memories Among Irritable Bowel Syndrome (IBS) Patients: An Important Aspect of the IBS Symptom Experience
• Etiology and clinical features of epilepsia partialis continua: an analysis of six cases
• FARS2 (Phenylalanyl-tRNA Synthetase 2) Deficiency: A Novel Mutation Associated with EEG Phenotype of Epilepsy of Infancy with Migrating Focal Seizures (EIMFS)
• First description of Schilder's disease : Paul Ferdinand Schilder and his struggle for the delimitation of a new entity
• From Balo's concentric sclerosis to multiple sclerosis: a series of 6 patients
• Global boundedness and stability for a chemotaxis model of Bolo's concentric sclerosis
• Heterogeneity of Balo's concentric sclerosis: a study of eight cases with different therapeutic concepts
• Human transmissible spongiform encephalopathies: historic view
• Imaging of Fulminant Demyelinating Disorders of the Central Nervous System
• Inaugural tumor-like multiple sclerosis: clinical presentation and medium-term outcome in 87 patients
• Insights into Lewy body disease from rare neurometabolic disorders
• Is the Intestine a Portal of Entry for the Serious COVID-19 Complications of Endotoxemia and Thrombosis?
• Ketogenic Diet in the Treatment of Super-Refractory Status Epilepticus at a Pediatric Intensive Care Unit: A Single-Center Experience
• Lethal NARS2-Related Disorder Associated With Rapidly Progressive Intractable Epilepsy and Global Brain Atrophy
• Long-term Outcome of Schilder Disease Treated With Interferon-beta
• Long-term Outcome of Schilder Disease Treated With Interferon-β
• Magnetic Resonance Characteristics of Balo Concentric Sclerosis in Children
• MRI signs of CNS demyelinating diseases
• MRI study of Balo's concentric sclerosis before and after corticosteroid therapy
• Multicenter Clinicopathologic Correlation of Kidney Biopsies Performed in COVID-19 Patients Presenting With Acute Kidney Injury or Proteinuria
• Myelinoclastic diffuse sclerosis (Schilder's disease) is immunologically distinct from multiple sclerosis: results from retrospective analysis of 92 lumbar punctures
• Myelodysplastic syndrome-associated spliceosome gene mutations enhance innate immune signaling
• Nerve-Wracking Eye Puzzle: A Rare Case of Alpers-Huttenlocher Syndrome
• Novel variants in the NARS2 gene as a cause of infantile-onset severe epilepsy leading to fatal refractory status epilepticus: case study and literature review
• Nucleoside supplements as treatments for mitochondrial DNA depletion syndrome
• Opercular Syndrome: A Rare Presentation of Schilder's Variant of Multiple Sclerosis
• Pathways to healing: Plants with therapeutic potential for neurodegenerative diseases
• Pediatric Balo Concentric Sclerosis Response to Dimethyl Fumarate
• Pediatric tumefactive multiple sclerosis case (with balo-like lesions), diagnostic and treatment challenges
• POLG gene mutation. Clinico-neuropathological study
• POLG-related disorders and their neurological manifestations
• Population-based study of rare epilepsy incidence in a US urban population
• Radiologically Isolated Syndrome: An Atypical Presentation of Balo's Concentric Sclerosis in a Patient with the Meniere's Disease
• Recent perspectives of pediatric mitochondrial diseases
• Recurrent schilder's disease
• Reversible symptoms present in a patient with Balo's concentric sclerosis
• Rod bipolar cell dysfunction in POLG retinopathy
• Safety and efficacy of deoxycytidine/deoxythymidine combination therapy in POLG-related disorders: 6-month interim results of an open-label, single arm, phase 2 trial
• Schilder's disease
• Simplifying the clinical classification of polymerase gamma (POLG) disease based on age of onset; studies using a cohort of 155 cases
• Specific EEG markers in POLG1 Alpers' syndrome
• Status epilepticus in a pregnant patient with a previously unrecognized POLG-associated disease
• The effects of nuclear DNA mutations on mitochondrial function
• The frequency of mitochondrial polymerase gamma related disorders in a large Polish population cohort
• The genotypic and phenotypic spectrum of PARS2-related infantile-onset encephalopathy
• The mitochondrial epilepsies
• The NAD(+) Precursor Nicotinamide Riboside Rescues Mitochondrial Defects and Neuronal Loss in iPSC derived Cortical Organoid of Alpers' Disease
• The phenotypic variability and natural history of NARS2 associated disease
• The Significance of Hematuria in Podocytopathies
• The Y831C Mutation of the <em>POLG</em> Gene in Dementia
• Torsional Nystagmus and Oscillopsia as Initial Presentation of Balo's Concentric Sclerosis
• TSPO PET With 18F-GE-180 to Differentiate Variants of Multiple Sclerosis: Relapsing-Remitting Multiple Sclerosis, Tumefactive Demyelination, and Balo's Concentric Sclerosis
• Tumefactive Demyelination Lesions: Report on three cases
• Tumefactive inflammatory leukoencephalopathy in cocaine users: Report of three cases
• TUMOR-LIKE EFFECT AS INITIAL PRESENTATION OF PEDIATRIC MULTIPLE SCLEROSIS
• Valproic acid for myoclonic epilepsy in POLG1 carriers can be fatal
• Vitamin B12 absorption and malabsorption
• Why Is This Auntminnie a Diagnostic Conundrum?: A Knowledge-Based Approach to Balo's Concentric Sclerosis From Reports of 3 Cases and Pooled Data From 68 Other Patients in the Literature