These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

122 related articles for article (PubMed ID: 28150298)

  • 1. Twin-sisters with PLA2G6-associated neurodegeneration due to paternal isodisomy of the chromosome 22 following in vitro fertilization.
    Tello C; Darling A; Lupo V; Ortez CI; Pérez-Dueñas B; Espinós C
    Clin Genet; 2017 Jul; 92(1):117-118. PubMed ID: 28150298
    [No Abstract]   [Full Text] [Related]  

  • 2. Infantile neuroaxonal dystrophy caused by uniparental disomy.
    Solomons J; Ridgway O; Hardy C; Kurian MA; Jayawant S; Hughes S; Pretorius P; Németh AH
    Dev Med Child Neurol; 2014 Apr; 56(4):386-9. PubMed ID: 24628589
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A new PLA2G6 mutation in a family with infantile neuroaxonal dystrophy.
    Iannello G; Graziano C; Cenacchi G; Cordelli DM; Zuntini R; Papa V; Magistà AM; Gagliardi M; Procopio R; Quattrone A; Annesi G
    J Neurol Sci; 2017 Oct; 381():209-212. PubMed ID: 28991683
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Iron accumulation in syndromes of neurodegeneration with brain iron accumulation 1 and 2: causative or consequential?
    Schneider SA; Hardy J; Bhatia KP
    J Neurol Neurosurg Psychiatry; 2009 Jun; 80(6):589-90. PubMed ID: 19147629
    [No Abstract]   [Full Text] [Related]  

  • 5. Typical MRI features of PLA2G6 mutation-related phospholipase-associated neurodegeneration (PLAN)/infantile neuroaxonal dystrophy (INAD).
    Singh S; Mishra SC; Israrahmed A; Lal H
    BMJ Case Rep; 2021 Mar; 14(3):. PubMed ID: 33766980
    [No Abstract]   [Full Text] [Related]  

  • 6. [A novel homozygous mutation in PLA2G6 gene causes infantile neuroaxonal dystrophy in a case].
    Wang J; Wu W; Chen X; Zhang L; Wang X; Dong G
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2016 Feb; 33(1):64-7. PubMed ID: 26829737
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Follow-up study of 25 Chinese children with PLA2G6-associated neurodegeneration.
    Zhang P; Gao Z; Jiang Y; Wang J; Zhang F; Wang S; Yang Y; Xiong H; Zhang Y; Bao X; Xiao J; Wu X; Wu Y
    Eur J Neurol; 2013 Feb; 20(2):322-30. PubMed ID: 22934738
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Infantile neuroaxonal dystrophy and PLA2G6-associated neurodegeneration: An update for the diagnosis.
    Iodice A; Spagnoli C; Salerno GG; Frattini D; Bertani G; Bergonzini P; Pisani F; Fusco C
    Brain Dev; 2017 Feb; 39(2):93-100. PubMed ID: 27884548
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Widening the MRI Findings of PLA2G6-Associated Neurodegeneration.
    Vithayathil J; Adang L; Alves CAPF
    Neuropediatrics; 2021 Dec; 52(6):509-510. PubMed ID: 34256386
    [No Abstract]   [Full Text] [Related]  

  • 10. Oculogyric crises in PLA2G6 associated neurodegeneration.
    Rohani M; Shahidi G; Vali F; Lang AE; Slow E; Gahl WA; Behnam B
    Parkinsonism Relat Disord; 2018 Jul; 52():111-112. PubMed ID: 29574084
    [No Abstract]   [Full Text] [Related]  

  • 11. PLA2G6 mutations associated with a continuous clinical spectrum from neuroaxonal dystrophy to hereditary spastic paraplegia.
    Ozes B; Karagoz N; Schüle R; Rebelo A; Sobrido MJ; Harmuth F; Synofzik M; Pascual SIP; Colak M; Ciftci-Kavaklioglu B; Kara B; Ordóñez-Ugalde A; Quintáns B; Gonzalez MA; Soysal A; Zuchner S; Battaloglu E
    Clin Genet; 2017 Nov; 92(5):534-539. PubMed ID: 28295203
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Phenotypic spectrum of neurodegeneration associated with mutations in the PLA2G6 gene (PLAN).
    Kurian MA; Morgan NV; MacPherson L; Foster K; Peake D; Gupta R; Philip SG; Hendriksz C; Morton JE; Kingston HM; Rosser EM; Wassmer E; Gissen P; Maher ER
    Neurology; 2008 Apr; 70(18):1623-9. PubMed ID: 18443314
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Mouse models of human INAD by Pla2g6 deficiency.
    Wada H; Kojo S; Seino K
    Histol Histopathol; 2013 Aug; 28(8):965-9. PubMed ID: 23467909
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Case report of a novel homozygous splice site mutation in PLA2G6 gene causing infantile neuroaxonal dystrophy in a Sudanese family.
    Elsayed LEO; Mohammed IN; Hamed AAA; Elseed MA; Salih MAM; Yahia A; Siddig RA; Amin M; Koko M; Elbashir MI; Ibrahim ME; Brice A; Ahmed AE; Stevanin G
    BMC Med Genet; 2018 May; 19(1):72. PubMed ID: 29739362
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Infantile neuroaxonal dystrophy in a pair of Malaysian siblings with progressive cerebellar atrophy: Description of an expanded phenotype with novel PLA2G6 variants.
    Li L; Fong CY; Tay CG; Tae SK; Suzuki H; Kosaki K; Thong MK
    J Clin Neurosci; 2020 Jan; 71():289-292. PubMed ID: 31493991
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Neuroaxonal dystrophy in PLA2G6 knockout mice.
    Sumi-Akamaru H; Beck G; Kato S; Mochizuki H
    Neuropathology; 2015 Jun; 35(3):289-302. PubMed ID: 25950622
    [TBL] [Abstract][Full Text] [Related]  

  • 17. PLA2G6, encoding a phospholipase A2, is mutated in neurodegenerative disorders with high brain iron.
    Morgan NV; Westaway SK; Morton JE; Gregory A; Gissen P; Sonek S; Cangul H; Coryell J; Canham N; Nardocci N; Zorzi G; Pasha S; Rodriguez D; Desguerre I; Mubaidin A; Bertini E; Trembath RC; Simonati A; Schanen C; Johnson CA; Levinson B; Woods CG; Wilmot B; Kramer P; Gitschier J; Maher ER; Hayflick SJ
    Nat Genet; 2006 Jul; 38(7):752-4. PubMed ID: 16783378
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Disruption of Golgi morphology and altered protein glycosylation in PLA2G6-associated neurodegeneration.
    Davids M; Kane MS; He M; Wolfe LA; Li X; Raihan MA; Chao KR; Bone WP; Boerkoel CF; Gahl WA; Toro C
    J Med Genet; 2016 Mar; 53(3):180-9. PubMed ID: 26668131
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Neurons and astrocytes in an infantile neuroaxonal dystrophy (INAD) mouse model show characteristic alterations in glutamate-induced Ca
    Strokin M; Reiser G
    Neurochem Int; 2017 Sep; 108():121-132. PubMed ID: 28279750
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Validation of the finding of hypertrophy of the clava in infantile neuroaxonal dystrophy/PLA2G6 by biometric analysis.
    Al-Maawali A; Yoon G; Feigenbaum AS; Halliday WC; Clarke JT; Branson HM; Banwell BL; Chitayat D; Blaser SI
    Neuroradiology; 2016 Oct; 58(10):1035-1042. PubMed ID: 27516098
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.