Pages that link to "Q37949887"
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The following pages link to Syndromes of neurodegeneration with brain iron accumulation (NBIA): an update on clinical presentations, histological and genetic underpinnings, and treatment considerations (Q37949887):
Displaying 50 items.
- Metals, oxidative stress and neurodegeneration: a focus on iron, manganese and mercury (Q26863224) (← links)
- Dystonic opisthotonus: a "red flag" for neurodegeneration with brain iron accumulation syndromes? (Q27005740) (← links)
- Pantothenate kinase 2 mutation with eye-of-the-tiger sign on magnetic resonance imaging in three siblings (Q28661582) (← links)
- Open-Label Fosmetpantotenate, a Phosphopantothenate Replacement Therapy in a Single Patient with Atypical PKAN. (Q30355488) (← links)
- Dystonia with brain manganese accumulation resulting from SLC30A10 mutations: a new treatable disorder (Q30540080) (← links)
- Neurodegeneration with Brain Iron Accumulation: Clinicoradiological Approach to Diagnosis (Q30882077) (← links)
- Abnormal high-frequency burst firing of cerebellar neurons in rapid-onset dystonia-parkinsonism (Q34091178) (← links)
- The pallidopyramidal syndromes: nosology, aetiology and pathogenesis (Q34336776) (← links)
- Eryptosis as a marker of Parkinson's disease (Q34585744) (← links)
- Cortical pencil lining in neuroferritinopathy: a diagnostic clue (Q35582411) (← links)
- Deficiency of Calcium-Independent Phospholipase A2 Beta Induces Brain Iron Accumulation through Upregulation of Divalent Metal Transporter 1 (Q35823121) (← links)
- Alternative approaches to modeling hereditary dystonias (Q35913791) (← links)
- Novel PLA2G6 mutations associated with an exonic deletion due to non-allelic homologous recombination in a patient with infantile neuroaxonal dystrophy. (Q36671171) (← links)
- Review: Insights into molecular mechanisms of disease in neurodegeneration with brain iron accumulation: unifying theories. (Q36800670) (← links)
- A delicate balance: Iron metabolism and diseases of the brain. (Q37023585) (← links)
- Profound morphological changes in the erythrocytes and fibrin networks of patients with hemochromatosis or with hyperferritinemia, and their normalization by iron chelators and other agents. (Q37458594) (← links)
- The systemic iron-regulatory proteins hepcidin and ferroportin are reduced in the brain in Alzheimer's disease (Q37485028) (← links)
- Blood Transcriptomic Meta-analysis Identifies Dysregulation of Hemoglobin and Iron Metabolism in Parkinson' Disease (Q37729558) (← links)
- Excess iron harms the brain: the syndromes of neurodegeneration with brain iron accumulation (NBIA). (Q38065116) (← links)
- Brain iron accumulation in aging and neurodegenerative disorders (Q38067144) (← links)
- Genetic diagnosis of hyperkinetic movement disorders (Q38088410) (← links)
- Pediatric movement disorders: Five new things (Q38103261) (← links)
- "Atypical" atypical parkinsonism: new genetic conditions presenting with features of progressive supranuclear palsy, corticobasal degeneration, or multiple system atrophy-a diagnostic guide (Q38110488) (← links)
- Polyphenols: multipotent therapeutic agents in neurodegenerative diseases (Q38120532) (← links)
- Pathophysiology and treatment of neurodegeneration with brain iron accumulation in the pediatric population (Q38124286) (← links)
- Developments in the role of transcranial sonography for the differential diagnosis of parkinsonism. (Q38501869) (← links)
- iPSC-derived neuronal models of PANK2-associated neurodegeneration reveal mitochondrial dysfunction contributing to early disease (Q38597809) (← links)
- A novel diagnostic approach to patients with myoclonus. (Q38629335) (← links)
- Early-onset torsion dystonia: a novel high-throughput yeast genetic screen for factors modifying protein levels of torsinAΔE. (Q38646083) (← links)
- Nomenclature of genetic movement disorders: Recommendations of the international Parkinson and movement disorder society task force (Q38808532) (← links)
- A Novel Nonsense Mutation in PANK2 Gene in Two Patients with Pantothenate Kinase-Associated Neurodegeneration (Q38868041) (← links)
- A Novel Deletion Mutation of Exon 2 of the C19orf12 Gene in an Omani Family with Mitochondrial Membrane Protein-Associated Neurodegeneration (MPAN). (Q39922187) (← links)
- Novel PANK2 mutation in the first Greek compound heterozygote patient with pantothenate-kinase-associated neurodegeneration. (Q41087124) (← links)
- Genetics and Pathophysiology of Neurodegeneration with Brain Iron Accumulation (NBIA). (Q41836301) (← links)
- Brain iron quantification by MRI in mitochondrial membrane protein-associated neurodegeneration under iron-chelating therapy (Q41915901) (← links)
- Late onset neurodegeneration with brain-iron accumulation presenting as parkinsonism (Q42182116) (← links)
- PANK2 and C19orf12 mutations are common causes of neurodegeneration with brain iron accumulation. (Q43503198) (← links)
- Psychopathology and hypodense basal ganglion lesions: early manifestation of cognitive-mnestic deficits in an 18-year-old male patient with familial neurodegeneration and iron accumulation in the brain (Q43596324) (← links)
- Mitochondrial membrane protein associated neurodegenration: a novel variant of neurodegeneration with brain iron accumulation (Q44356168) (← links)
- Clinical features of neurodegeneration with brain iron accumulation due to a C19orf12 gene mutation (Q44948255) (← links)
- Follow-up study of 25 Chinese children with PLA2G6-associated neurodegeneration (Q46348751) (← links)
- Neurodegeneration with brain iron accumulation: A case report (Q47129057) (← links)
- Iron metabolism and its detection through MRI in parkinsonian disorders: a systematic review. (Q48129184) (← links)
- First video report of static encephalopathy of childhood with neurodegeneration in adulthood (Q48172818) (← links)
- Transcranial Sonography in Mitochondrial Membrane Protein-Associated Neurodegeneration. (Q48239923) (← links)
- Iron - too much of a good thing. (Q48538867) (← links)
- Unraveling the Burden of Iron in Neurodegeneration: Intersections with Amyloid Beta Peptide Pathology. (Q51759208) (← links)
- Botulinum Toxin-A Injection in the Treatment of Spasticity in a Infantile-Onset Neurodegeneration With Brain Iron Accumulation: A Case Report. (Q54109535) (← links)
- Retinitis pigmentosa in pantothenate kinase-associated neurodegeneration. (Q54314029) (← links)
- Phenotypes and genotypes of patients with pantothenate kinase-associated neurodegeneration in Asian and Caucasian populations: 2 cases and literature review. (Q55369986) (← links)