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.
293 related articles for article (PubMed ID: 29335023)
21. Clinical and molecular investigation in Chinese patients with glutaric aciduria type I. Zhang Y; Li H; Ma R; Mei L; Wei X; Liang D; Wu L Clin Chim Acta; 2016 Jan; 453():75-9. PubMed ID: 26656312 [TBL] [Abstract][Full Text] [Related]
22. (1)H-MRS in glutaric aciduria type 1: impact of biochemical phenotype and age on the cerebral accumulation of neurotoxic metabolites. Harting I; Boy N; Heringer J; Seitz A; Bendszus M; Pouwels PJ; Kölker S J Inherit Metab Dis; 2015 Sep; 38(5):829-38. PubMed ID: 25860816 [TBL] [Abstract][Full Text] [Related]
24. Clinical course, early diagnosis, treatment, and prevention of disease in glutaryl-CoA dehydrogenase deficiency. Hoffmann GF; Athanassopoulos S; Burlina AB; Duran M; de Klerk JB; Lehnert W; Leonard JV; Monavari AA; Müller E; Muntau AC; Naughten ER; Plecko-Starting B; Superti-Furga A; Zschocke J; Christensen E Neuropediatrics; 1996 Jun; 27(3):115-23. PubMed ID: 8837070 [TBL] [Abstract][Full Text] [Related]
25. Teaching neuroimages: infant with glutaric aciduria type 1 presenting with infantile spasms and hypsarrhythmia. Young-Lin N; Shalev S; Glenn OA; Gardner M; Lee C; Wynshaw-Boris A; Gelfand AA Neurology; 2013 Dec; 81(24):e182-3. PubMed ID: 24323445 [TBL] [Abstract][Full Text] [Related]
26. [Perinatal asphyxia, hypoxic-ischemic encephalopathy and neurological sequelae in full-term newborns. II. Description and interrelation]. González de Dios J; Moya M Rev Neurol; 1996 Aug; 24(132):969-76. PubMed ID: 8755359 [TBL] [Abstract][Full Text] [Related]
27. Glutaric acidemia type 1: outcomes before and after expanded newborn screening. Viau K; Ernst SL; Vanzo RJ; Botto LD; Pasquali M; Longo N Mol Genet Metab; 2012 Aug; 106(4):430-8. PubMed ID: 22728054 [TBL] [Abstract][Full Text] [Related]
28. Prenatal diagnosis of fetal glutaric aciduria type 1 with rare compound heterozygous mutations in GCDH gene. Peng HH; Shaw SW; Huang KG Taiwan J Obstet Gynecol; 2018 Feb; 57(1):137-140. PubMed ID: 29458885 [TBL] [Abstract][Full Text] [Related]
29. Subependymal mass lesions and peripheral polyneuropathy in adult-onset glutaric aciduria type I. Herskovitz M; Goldsher D; Sela BA; Mandel H Neurology; 2013 Aug; 81(9):849-50. PubMed ID: 23884036 [TBL] [Abstract][Full Text] [Related]
30. Newborn screening: A disease-changing intervention for glutaric aciduria type 1. Boy N; Mengler K; Thimm E; Schiergens KA; Marquardt T; Weinhold N; Marquardt I; Das AM; Freisinger P; Grünert SC; Vossbeck J; Steinfeld R; Baumgartner MR; Beblo S; Dieckmann A; Näke A; Lindner M; Heringer J; Hoffmann GF; Mühlhausen C; Maier EM; Ensenauer R; Garbade SF; Kölker S Ann Neurol; 2018 May; 83(5):970-979. PubMed ID: 29665094 [TBL] [Abstract][Full Text] [Related]
31. Evaluation of the first 5 years of a glutaric aciduria type I neonatal screening programme in Asturias. Elola Pastor AI; Prieto García B; Díaz Martín JJ An Pediatr (Engl Ed); 2024 May; 100(5):318-324. PubMed ID: 38714461 [TBL] [Abstract][Full Text] [Related]
33. Rare presentation of a treatable disorder: glutaric aciduria type 1. Badve MS; Bhuta S; Mcgill J N Z Med J; 2015 Feb; 128(1409):61-4. PubMed ID: 25721963 [TBL] [Abstract][Full Text] [Related]
34. Impact of age at onset and newborn screening on outcome in organic acidurias. Heringer J; Valayannopoulos V; Lund AM; Wijburg FA; Freisinger P; Barić I; Baumgartner MR; Burgard P; Burlina AB; Chapman KA; I Saladelafont EC; Karall D; Mühlhausen C; Riches V; Schiff M; Sykut-Cegielska J; Walter JH; Zeman J; Chabrol B; Kölker S; J Inherit Metab Dis; 2016 May; 39(3):341-353. PubMed ID: 26689403 [TBL] [Abstract][Full Text] [Related]
35. Promising outcomes in glutaric aciduria type I patients detected by newborn screening. Lee CS; Chien YH; Peng SF; Cheng PW; Chang LM; Huang AC; Hwu WL; Lee NC Metab Brain Dis; 2013 Mar; 28(1):61-7. PubMed ID: 23104440 [TBL] [Abstract][Full Text] [Related]
36. Clinical, biochemical and molecular findings of 24 Brazilian patients with glutaric acidemia type 1: 4 novel mutations in the GCDH gene. Sitta A; Guerreiro G; de Moura Coelho D; da Rocha VV; Dos Reis BG; Sousa C; Vilarinho L; Wajner M; Vargas CR Metab Brain Dis; 2021 Feb; 36(2):205-212. PubMed ID: 33064266 [TBL] [Abstract][Full Text] [Related]
37. Brain MRI findings as an important diagnostic clue in glutaric aciduria type 1. Nunes J; Loureiro S; Carvalho S; Pais RP; Alfaiate C; Faria A; Garcia P; Diogo L Neuroradiol J; 2013 Apr; 26(2):155-61. PubMed ID: 23859237 [TBL] [Abstract][Full Text] [Related]
38. Two inborn errors of metabolism in a newborn: glutaric aciduria type I combined with isobutyrylglycinuria. Popek M; Walter M; Fernando M; Lindner M; Schwab KO; Sass JO Clin Chim Acta; 2010 Dec; 411(23-24):2087-91. PubMed ID: 20836999 [TBL] [Abstract][Full Text] [Related]
39. Mild phenotype of glutaric aciduria type 1 in polish patients - novel data from a group of 13 cases. Pokora P; Jezela-Stanek A; Różdżyńska-Świątkowska A; Jurkiewicz E; Bogdańska A; Szymańska E; Rokicki D; Ciara E; Rydzanicz M; Stawiński P; Płoski R; Tylki-Szymańska A Metab Brain Dis; 2019 Apr; 34(2):641-649. PubMed ID: 30570710 [TBL] [Abstract][Full Text] [Related]