162 related articles for article (PubMed ID: 33853092)
1. Psychiatric symptoms in an adolescent reveal a novel compound heterozygous mutation of the PANK2 gene in the atypical PKAN syndrome.
González Huerta LM; Gómez González S; Toral López J
Psychiatr Genet; 2021 Jun; 31(3):95-99. PubMed ID: 33853092
[TBL] [Abstract][Full Text] [Related]
2. Clinical, imaging, and molecular findings in a sample of Mexican families with pantothenate kinase-associated neurodegeneration.
Morales-Briceño H; Chacón-Camacho OF; Pérez-González EA; Arteaga-Vázquez J; Rodríguez-Violante M; Cervantes-Arriaga A; Pérez-Rodríguez L; Zenteno JC; Mutchinick OM
Clin Genet; 2015 Mar; 87(3):259-65. PubMed ID: 24712887
[TBL] [Abstract][Full Text] [Related]
3. A novel gene mutation in PANK2 in a patient with an atypical form of pantothenate kinase-associated neurodegeneration.
Pérez-González EA; Chacón-Camacho OF; Arteaga-Vázquez J; Zenteno JC; Mutchinick OM
Eur J Med Genet; 2013 Nov; 56(11):606-8. PubMed ID: 24075960
[TBL] [Abstract][Full Text] [Related]
4. Novel Compound Heterozygous Mutation in PANK2 in a Patient with an Atypical Form of Pantothenate Kinase Associated Neurodegeneration and His Family.
Yuan J; Zhanga C; Qiao S; Wang A; Zhang S
Neurol India; 2022; 70(2):737-739. PubMed ID: 35532650
[TBL] [Abstract][Full Text] [Related]
5. Novel PANK2 mutation in a Chinese boy with PANK2-associated neurodegeneration: A case report and review of Chinese cases.
Zhang Y; Zhou D; Yang T
Medicine (Baltimore); 2019 Jan; 98(4):e14122. PubMed ID: 30681573
[TBL] [Abstract][Full Text] [Related]
6. Basal ganglia calcification and novel compound heterozygous mutations in the PANK2 gene in a Chinese boy with classic Pantothenate kinase-associated neurodegeneration: A case report.
Shi X; Zheng F; Ye X; Li X; Zhao Q; Lin Z; Hu Y; Wang J
Medicine (Baltimore); 2018 Apr; 97(15):e0316. PubMed ID: 29642163
[TBL] [Abstract][Full Text] [Related]
7. Novel compound heterozygous PANK2 gene mutations in a Chinese patient with atypical pantothenate kinase-associated neurodegeneration.
Cheng Y; Liu YT; Yang ZH; Yang J; Shi CH; Xu YM
Int J Neurosci; 2018 Dec; 128(12):1109-1113. PubMed ID: 29962256
[TBL] [Abstract][Full Text] [Related]
8. CLINICAL EFFECT OF A MUTATION (p.Glu322Asp, c.966 G>T) IN PANK2 GENE IN A FAMILY WITH ATYPICAL PANTOTHENATE KINASE-ASSOCIATED NEURODEGENERATION.
Ayas ZO; Karkucak M; Ocal RO; Yakut T
Genet Couns; 2016; 27(4):489-494. PubMed ID: 30226968
[TBL] [Abstract][Full Text] [Related]
9. Novel PANK2 gene mutations in two Chinese siblings with atypical pantothenate kinase-associated neurodegeneration.
Shan J; Wen B; Zhu J; Lin P; Zheng J; Yan C
Neurol Sci; 2013 Apr; 34(4):561-3. PubMed ID: 22930366
[TBL] [Abstract][Full Text] [Related]
10. Novel PANK2 mutation discovered among South East Asian children living in Thailand affected with pantothenate kinase associated neurodegeneration.
Sakpichaisakul K; Saengow VE; Suwanpratheep P; Rongnoparat K; Panthan B; Trachoo O
J Clin Neurosci; 2019 Aug; 66():187-190. PubMed ID: 31088771
[TBL] [Abstract][Full Text] [Related]
11. Novel homozygous PANK2 mutation causing atypical pantothenate kinase-associated neurodegeneration (PKAN) in a Cypriot family.
Tanteles GA; Spanou-Aristidou E; Antoniou C; Christophidou-Anastasiadou V; Kleopa KA
J Neurol Sci; 2014 May; 340(1-2):233-6. PubMed ID: 24655737
[TBL] [Abstract][Full Text] [Related]
12. Novel compound heterozygous mutations in the PANK2 gene in a Chinese patient with atypical pantothenate kinase-associated neurodegeneration.
Zhang YH; Tang BS; Zhao AL; Xia K; Long ZG; Guo JF; Westaway SK; Hayflick SJ
Mov Disord; 2005 Jul; 20(7):819-21. PubMed ID: 15747360
[TBL] [Abstract][Full Text] [Related]
13. Atypical pantothenate kinase-associated neurodegeneration with PANK2 mutations : clinical description and a review of the literature.
Pan S; Zhu C
Neurocase; 2020 Jun; 26(3):175-182. PubMed ID: 32310012
[TBL] [Abstract][Full Text] [Related]
14. Genetic heterogeneity in patients with pantothenate kinase-associated neurodegeneration and classic magnetic resonance imaging eye-of-the-tiger pattern.
Valentino P; Annesi G; Cirò Candiano IC; Annesi F; Civitelli D; Tarantino P; Naso F; Spadafora P; Carrideo S; De Marco EV; Consoli D; Zappia M; Gambardella A; Quattrone A
Mov Disord; 2006 Feb; 21(2):252-4. PubMed ID: 16149094
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. Siblings with the adult-onset slowly progressive type of pantothenate kinase-associated neurodegeneration and a novel mutation, Ile346Ser, in PANK2: clinical features and (99m)Tc-ECD brain perfusion SPECT findings.
Doi H; Koyano S; Miyatake S; Matsumoto N; Kameda T; Tomita A; Miyaji Y; Suzuki Y; Sawaishi Y; Kuroiwa Y
J Neurol Sci; 2010 Mar; 290(1-2):172-6. PubMed ID: 20006850
[TBL] [Abstract][Full Text] [Related]
17. Pantothenate kinase-associated neurodegeneration in Korea: recurrent R440P mutation in PANK2 and outcome of deep brain stimulation.
Lim BC; Ki CS; Cho A; Hwang H; Kim KJ; Hwang YS; Kim YE; Yun JY; Jeon BS; Lim YH; Paek SH; Chae JH
Eur J Neurol; 2012 Apr; 19(4):556-61. PubMed ID: 22103354
[TBL] [Abstract][Full Text] [Related]
18. Clinical and genetic features of PKAN patients in a tertiary centre in Turkey.
Akcakaya NH; Iseri SU; Bilir B; Battaloglu E; Tekturk P; Gultekin M; Akar G; Yigiter R; Hanagasi H; Alp R; Cagirici S; Eraksoy M; Ozbek U; Yapici Z
Clin Neurol Neurosurg; 2017 Mar; 154():34-42. PubMed ID: 28113101
[TBL] [Abstract][Full Text] [Related]
19. Indian-subcontinent NBIA: unusual phenotypes, novel PANK2 mutations, and undetermined genetic forms.
Aggarwal A; Schneider SA; Houlden H; Silverdale M; Paudel R; Paisan-Ruiz C; Desai S; Munshi M; Sanghvi D; Hardy J; Bhatia KP; Bhatt M
Mov Disord; 2010 Jul; 25(10):1424-31. PubMed ID: 20629144
[TBL] [Abstract][Full Text] [Related]
20. Genetic, clinical, and radiographic delineation of Hallervorden-Spatz syndrome.
Hayflick SJ; Westaway SK; Levinson B; Zhou B; Johnson MA; Ching KH; Gitschier J
N Engl J Med; 2003 Jan; 348(1):33-40. PubMed ID: 12510040
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]