Disease: Idiopathic basal ganglia calcification 1
- <em>MAP3K6</em> Mutations in a Neurovascular Disease Causing Stroke, Cognitive Impairment, and Tremor
- A - 104 Basal Ganglia Calcification, Hypothyroidism, and COVID-19: a Case of Possible Fahr's Syndrome
- A Case of Cerebral Large-Vessel Vasculitis Concomitant Fahr Syndrome in Systemic Lupus Erythematosus
- A Case of Non-ketotic Hyperglycemic Hemichorea and Fahr Syndrome
- A case report of a patient with primary familial brain calcification with a <em>PDGFRB</em> genetic variant
- A Case Report of Fahr's Disease and Its Clinical Heterogeneity
- A Japanese family with idiopathic basal ganglia calcification carrying a novel XPR1 variant
- A Patient With Fahr's Disease Who Presented Prominent Visuospatial Dysfunction
- A rare case of Fahr disease revealed by an epileptic seizure
- A rare case of spondyloarthropathy: Iatrogenic hypoparathyroidism
- Activating calcium-sensing receptor gene variants in China: a case report of hypocalcaemia and literature review
- Advanced Early-Onset Fahr's Disease: A Case Report
- Aneurysmal subarachnoid hemorrhage with PFBC and beta thalassemia: a case report
- Basal Ganglia Calcification: A Case Report of Two Siblings With Fahr's Disease
- Bilateral Basal Ganglia Calcifications Manifesting as Psychosis With Manic Features: A Case Report on Fahr's Syndrome
- Canadian national hypoparathyroidism registry: an overview of hypoparathyroidism in Canada
- Case report: 10 years follow-up of psychosis due to Fahr's disease complicated by a left temporal stroke
- Characteristics and therapeutic potential of sodium-dependent phosphate cotransporters in relation to idiopathic basal ganglia calcification
- Coronary artery calcification in a patient with Fahr disease
- Decoding brain calcifications: A single-center descriptive case series and examination of pathophysiological mechanisms
- Erratum: A Patient With Fahr's Disease Who Presented Prominent Visuospatial Dysfunction
- Fahr´s Syndrome; Pseudohypoparathyroidism Type Ib Masquerading as Epileptic Seizures
- Fahr's disease
- Fahr's disease in a patient with recurrent pneumonias, parkinsonism and dementia
- Fahr's disease linked to a novel mutation in MYORG variants manifesting as paroxysmal limb stiffness and dysarthria: Case report and literature review
- Fahr's disease presenting as Parkinson's disease along with dysphagia and dysarthria: A case report
- Fahr's disease with neuropsychiatric symptoms and intermittent course: a case report
- Fahr's Disease: Case Presentation With Facial Numbness
- Fahr's syndrome associated with hypoparathyroidism: A case report
- Fahr's syndrome due to hypoparathyroidism revisited: A case of parkinsonism and a review of all published cases
- Fahr's Syndrome: A Rare Case Presentation
- Familial idiopathic basal ganglia calcification with a heterozygous missense variant (c.902C>T/p.P307L) in SLC20A2 showing widespread cerebrovascular lesions
- Familial Idiopathic Basal Ganglia Calcification: A Father-Son Dyad Demonstrate Heterogeneity of Presentation and Disease Progression
- From seizures to cognitive dysfunction: A case report of Fahr syndrome in an Afghan patient
- Hypoparathyroidism and Fahr's Syndrome: A Case Series
- Idiopathic basal ganglia calcification presenting with obsessive-compulsive symptoms: A case report
- Idiopathic brain calcification in a patient with hereditary hemochromatosis
- Idiopathic young-onset Fahr's disease with schizophrenia-like presentation: a case report
- Infectious Diseases and Basal Ganglia Calcifications: A Cross-Sectional Study in Patients with Fahr's Disease and Systematic Review
- Intracerebral Calcifications Associated with Failure to Thrive and Macular Degeneration in an Adolescent: A Case Report
- New Evidence Suggests a Much Complex Classification for the Genetic Pattern of Inheritance in Primary Brain Calcification
- PDGF-BB is involved in phosphate regulation via the phosphate transporters in human neuroblastoma SH-SY5Y cells
- Pharmacology of Mammalian Na<sup>+</sup>-Dependent Transporters of Inorganic Phosphate
- Primary familial brain calcification presenting with parkinsonism and motor complications caused by a novel <em>SLC20A2</em> variant: a case report
- PSEN1/SLC20A2 double mutation causes early-onset Alzheimer's disease and primary familial brain calcification co-morbidity
- PSEUDOPSEUDOHYPOPARATHYROIDISM AS A CAUSE OF FAHR SYNDROME: HYPOPARATHYROIDISM NOT THE ONLY ONE
- Role of phosphate transporter PiT-2 in the pathogenesis of primary brain calcification
- SLC20A2-Associated Idiopathic basal ganglia calcification (Fahr disease): a case family report
- SLC20A2-Associated Idiopathic Basal Ganglia Calcification-Related Recurrent Psychosis Response to Low-Dose Antipsychotics: A Case Report and Literature Review
- The Association between Intracranial Calcifications and Symptoms in Patients with Primary Familial Brain Calcification
- The clinical and genetic spectrum of primary familial brain calcification
- The effects of etidronate on brain calcifications in Fahr's disease or syndrome: rationale and design of the randomised, placebo-controlled, double-blind CALCIFADE trial
- The first Japanese case of primary familial brain calcification caused by an MYORG variant
- The Genetics of Primary Familial Brain Calcification: A Literature Review
- Traumatic Brain Injury in the Setting of Fahr Syndrome
- XPR1 mutation related Fahr's disease presenting with a hemorrhagic stroke: a case report