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7. Hallervorden-Spatz syndrome in two siblings diagnosed by clinical features and magnetic resonance imaging. Tiamkao S; Nitinavakarn B; Jitpimolmard S J Med Assoc Thai; 2000 Dec; 83(12):1535-40. PubMed ID: 11253896 [TBL] [Abstract][Full Text] [Related]
11. Adult onset Hallervorden-Spatz disease with psychotic symptoms. del Valle-López P; Pérez-García R; Sanguino-Andrés R; González-Pablos E Actas Esp Psiquiatr; 2011; 39(4):260-2. PubMed ID: 21769749 [TBL] [Abstract][Full Text] [Related]
12. First cases in the Czech Republic of the Hallervorden-Spatz disease resulting from mutation in the pantothenate kinase 2 gene. Zumrová A; Krepelová A; Kyncl M; Maríková T; Prosková M; Cíbochová R; Sebronová V; Komárek V Neuro Endocrinol Lett; 2005 Jun; 26(3):213-8. PubMed ID: 15990724 [TBL] [Abstract][Full Text] [Related]
13. [Hallervorden-Spatz syndrome. Indicative findings in cranial computerized and magnetic resonance tomography for intra vitam diagnosis]. Kurlemann G; Bongartz G; Kuchelmeister K; Palm DG Monatsschr Kinderheilkd; 1991 Sep; 139(9):626-8. PubMed ID: 1745254 [TBL] [Abstract][Full Text] [Related]
14. The first Vietnamese patient who presented late onset of pantothenate kinase-associated neurodegeneration diagnosed by whole exome sequencing: A case report. Tran VK; Vu CD; Tran HA; Lien NTK; Tung NV; Lan NN; Tran HT; Hoang NH Medicine (Baltimore); 2023 Oct; 102(43):e34853. PubMed ID: 37904482 [TBL] [Abstract][Full Text] [Related]
17. [Importance of magnetic resonance in the diagnosis of Hallervorden- Spatz disease: presentation of a case with familial history]. Pérez Sempere A; Martínez Menéndez B; Villaverde Amundarain FJ; Calandre Hoenigsfeld L; Bermejo Pareja F Neurologia; 1990; 5(7):252-3. PubMed ID: 2288756 [No Abstract] [Full Text] [Related]
18. Pantothenate kinase-associated neurodegeneration (PKAN): molecular confirmation of a Turkish patient with a rare frameshift mutation in the coding region of the PANK2 gene. Cangül H; Ozdemir O; Yakut T; Okan M; Morgan NV; Baytan B; Kurian MA; Spiegel R; Maher ER Turk J Pediatr; 2009; 51(2):161-5. PubMed ID: 19480328 [TBL] [Abstract][Full Text] [Related]
19. [Tourettism, hemiballism and juvenile Parkinsonism: expanding the clinical spectrum of the neurodegeneration associated to pantothenate kinase deficiency (Hallervorden Spatz syndrome)]. Carod-Artal FJ; Vargas AP; Marinho PB; Fernandes-Silva TV; Portugal D Rev Neurol; 2004 Feb 16-29; 38(4):327-31. PubMed ID: 14997456 [TBL] [Abstract][Full Text] [Related]