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.
150 related articles for article (PubMed ID: 22840416)
1. L-2 hydroxyglutaric aciduria as a rare cause of leukencephalopathy in adults. Weimar C; Schlamann M; Krägeloh-Mann I; Schöls L Clin Neurol Neurosurg; 2013 Jun; 115(6):765-6. PubMed ID: 22840416 [No Abstract] [Full Text] [Related]
2. L-2-hydroxyglutaric aciduria diagnosed in a young adult with progressive cerebellar ataxia and facial dyskinesia. Marcel C; Mallaret M; Lagha-Boukbiza O; Kremer S; Echaniz-Laguna A; Tranchant C Rev Neurol (Paris); 2012 Feb; 168(2):187-91. PubMed ID: 22030381 [TBL] [Abstract][Full Text] [Related]
3. Clinical, neuroimaging, and genetic features of L-2-hydroxyglutaric aciduria in Arab kindreds. Faiyaz-Ul-Haque M; Al-Sayed MD; Faqeih E; Jamil M; Saeed A; Amoudi MS; Kaya N; Abalkhail H; Al-Abdullatif A; Rashed M; Al-Owain M; Peltekova I; Zaidi SH Ann Saudi Med; 2014; 34(2):107-14. PubMed ID: 24894778 [TBL] [Abstract][Full Text] [Related]
4. A successfully treated adult patient with L-2-hydroxyglutaric aciduria. Samuraki M; Komai K; Hasegawa Y; Kimura M; Yamaguchi S; Terada N; Yamada M Neurology; 2008 Mar; 70(13):1051-2. PubMed ID: 18362286 [No Abstract] [Full Text] [Related]
5. White matter abnormalities in an adult patient with l-2-hydroxyglutaric aciduria. Yamamoto T; Yoshioka S; Tsurusaki Y; Shino S; Shimojima K; Shigematsu Y; Takeuchi Y; Matsumoto N Brain Dev; 2016 Jan; 38(1):142-4. PubMed ID: 25982940 [TBL] [Abstract][Full Text] [Related]
6. Eyelid myoclonia with absence seizures in a child with l-2 hydroxyglutaric aciduria: findings of magnetic resonance imaging. Mete A; Isikay S; Sirikci A; Ozkur A; Bayram M Pediatr Neurol; 2012 Mar; 46(3):195-7. PubMed ID: 22353300 [TBL] [Abstract][Full Text] [Related]
7. Combined D-2- and L-2-hydroxyglutaric aciduria with neonatal onset encephalopathy: a third biochemical variant of 2-hydroxyglutaric aciduria? Muntau AC; Röschinger W; Merkenschlager A; van der Knaap MS; Jakobs C; Duran M; Hoffmann GF; Roscher AA Neuropediatrics; 2000 Jun; 31(3):137-40. PubMed ID: 10963100 [TBL] [Abstract][Full Text] [Related]
8. Peripheral neuropathy in a patient with D-2-hydroxyglutaric aciduria. Haliloglu G; Temucin CM; Oguz KK; Celiker A; Coskun T; Sass JO; Fischer J; Topcu M J Inherit Metab Dis; 2009 Dec; 32 Suppl 1():S21-5. PubMed ID: 19169842 [TBL] [Abstract][Full Text] [Related]
10. [L-2-hydroxyglutaric aciduria caused by a new mutation in the L2HGDH gene]. Saifullina EV; Zakharova EY; Kurkina MV; Magzhanov RV; Gaisina EV; Zakirova EN Zh Nevrol Psikhiatr Im S S Korsakova; 2017; 117(4):81-85. PubMed ID: 28617386 [TBL] [Abstract][Full Text] [Related]
11. 3-Methylglutaconic aciduria type I redefined: a syndrome with late-onset leukoencephalopathy. Wortmann SB; Kremer BH; Graham A; Willemsen MA; Loupatty FJ; Hogg SL; Engelke UF; Kluijtmans LA; Wanders RJ; Illsinger S; Wilcken B; Cruysberg JR; Das AM; Morava E; Wevers RA Neurology; 2010 Sep; 75(12):1079-83. PubMed ID: 20855850 [TBL] [Abstract][Full Text] [Related]
12. Gliomatosis cerebri in L-2-hydroxyglutaric aciduria. London F; Jeanjean A Acta Neurol Belg; 2015 Dec; 115(4):749-51. PubMed ID: 25997888 [No Abstract] [Full Text] [Related]
13. A novel compound heterozygous mutation of the L2HGDH gene in a Chinese boy with L-2-hydroxyglutaric aciduria: case report and literature review. Zhang Y; Wang C; Yang K; Wang S; Tian G; Chen Y Neurol Sci; 2018 Oct; 39(10):1697-1703. PubMed ID: 29980873 [TBL] [Abstract][Full Text] [Related]
14. [L-2-hydroxyglutaric aciduria: report on two cases]. Wagner S; Vianey-Saban C; Salomons GS; Schmitt E; Feillet F Arch Pediatr; 2014 Jan; 21(1):78-85. PubMed ID: 24321868 [TBL] [Abstract][Full Text] [Related]
15. L-2-hydroxyglutaric aciduria: a report of clinical, radiological, and genetic characteristics of two siblings from Egypt. Fayed AI; Mohamed MT; Abed E; Meshref M; Ali Mahmoud A Neurocase; 2024 Apr; 30(2):77-82. PubMed ID: 38795053 [TBL] [Abstract][Full Text] [Related]
16. A novel compound heterozygous mutation in a Chinese boy with L-2-hydroxyglutaric aciduria: a case study. Tai H; Zhang Z BMC Neurol; 2015 Jul; 15():117. PubMed ID: 26208971 [TBL] [Abstract][Full Text] [Related]
17. [Analysis of L2HGDH gene mutation in a patient with 2-hydroxyglutaric aciduria]. Deng Y; Tang G; Wen P; Wang G; Zhao C; Chen Z; Zhang X; Liu X; Cui D; Li C Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2016 Feb; 33(1):48-52. PubMed ID: 26829733 [TBL] [Abstract][Full Text] [Related]
18. Two novel L2HGDH mutations identified in a rare Chinese family with L-2-hydroxyglutaric aciduria. Peng W; Ma XW; Yang X; Zhang WQ; Yan L; Wang YX; Liu X; Wang Y; Feng ZC BMC Med Genet; 2018 Sep; 19(1):167. PubMed ID: 30217188 [TBL] [Abstract][Full Text] [Related]
19. A novel mutation as a cause of L-2-hydroxyglutaric aciduria. O'Connor G; King M; Salomons G; Jakobs C; Hardiman O J Neurol; 2009 Apr; 256(4):672-3. PubMed ID: 19444541 [No Abstract] [Full Text] [Related]
20. [D-2-hydroxyglutaric aciduria. Report of two cases]. Mahfoud A; Domínguez CL; Rashed M; Durán M; Rodríguez T; Rodríguez D; Landa V Invest Clin; 2009 Sep; 50(3):369-75. PubMed ID: 19961059 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]