Fahr’s Disease Presenting with Non-febrile Epileptic Seizures: Case Report and Systematic Literature Review

References (19)

1. 1 Mutations in SLC20A2 link familial idiopathic basal ganglia calcification with phosphate homeostasis [DOI]
2. 2 Mutations in the gene encoding PDGF-B cause brain calcifications in humans and mice [DOI]
3. 3 Mutations in XPR1 cause primary familial brain calcification associated with altered phosphate export [DOI]
4. 4 Fahr’s syndrome: literature review of current evidence [DOI]
5. 5 Bilateral striopallidodentate calcinosis: Clinical characteristics of patients seen in a registry [DOI]
6. 6 Phenotypic spectrum of probable and genetically-confirmed idiopathic basal ganglia calcification [DOI]
7. 7 Basal ganglia calcifications (Fahr’s syndrome): related conditions and clinical features [DOI]
8. 8 Mutations in SLC20A2 are a major cause of familial idiopathic basal ganglia calcification [DOI]
9. 9 Deconstructing Fahr's disease/syndrome of brain calcification in the era of new genes [DOI]
10. 10 The significance of the incidental finding of basal ganglia calcification on computed tomography. [DOI]
11. 11 MRI demonstration and CT correlation of the brain in patients with idiopathic intracerebral calcification [DOI]
12. 12 Neuropsychological Alterations in Patients With Computed Tomography--Detected Basal Ganglia Calcification [DOI]
13. 13 Fahr's Disease or Fahr's Syndrome?
14. 14 Brain calcifications induce neurological dysfunction that can be reversed by a bone drug [DOI]
15. 15 Fahr's Syndrome: A Report of Two Cases
16. 16 FAHR'S Sy ndrome: A rare Neurodegenerative Disorder [DOI]
17. 17 Case Report: An Incidental Finding of Fahr's Disease in a Patient with Hypochondria [DOI]
18. 18 Fahr's Disease: A Case Report [DOI]
19. 19 Clinical Presentation of the Epileptic Patients at People Medical College Hospital, Nawabshah, Pakistan [DOI]

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