177 related articles for article (PubMed ID: 15351024)
1. Riboflavin-responsive glutaric aciduria type II with recurrent pancreatitis.
Liang WC; Tsai KB; Lai CL; Chen LH; Jong YJ
Pediatr Neurol; 2004 Sep; 31(3):218-21. PubMed ID: 15351024
[TBL] [Abstract][Full Text] [Related]
2. [Late-onset riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency (glutaric aciduria type II)].
Liang Y; Liu L; Wei H; Luo XP; Wang MT
Zhonghua Er Ke Za Zhi; 2003 Dec; 41(12):916-20. PubMed ID: 14723814
[TBL] [Abstract][Full Text] [Related]
3. Riboflavin responsive glutaric aciduria type II.
Gregersen N; Rhead W; Christensen E
Prog Clin Biol Res; 1990; 321():477-94. PubMed ID: 2183240
[No Abstract] [Full Text] [Related]
4. Recurrent hypoglycemia associated with glutaric aciduria type II in an adult.
Dusheiko G; Kew MC; Joffe BI; Lewin JR; Mantagos S; Tanaka K
N Engl J Med; 1979 Dec; 301(26):1405-9. PubMed ID: 514320
[TBL] [Abstract][Full Text] [Related]
5. [A case of riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency (glutaric aciduria type II)].
Tojo M; Gunji T; Yamaguchi S; Shimizu N; Koga Y; Nonaka I
No To Hattatsu; 2000 Mar; 32(2):163-8. PubMed ID: 10723193
[TBL] [Abstract][Full Text] [Related]
6. C6-C10-dicarboxylic aciduria: investigations of a patient with riboflavin responsive multiple acyl-CoA dehydrogenation defects.
Gregersen N; Wintzensen H; Christensen SK; Christensen MF; Brandt NJ; Rasmussen K
Pediatr Res; 1982 Oct; 16(10):861-8. PubMed ID: 7145508
[TBL] [Abstract][Full Text] [Related]
7. Acquired multiple Acyl-CoA dehydrogenase deficiency in 10 horses with atypical myopathy.
Westermann CM; Dorland L; Votion DM; de Sain-van der Velden MG; Wijnberg ID; Wanders RJ; Spliet WG; Testerink N; Berger R; Ruiter JP; van der Kolk JH
Neuromuscul Disord; 2008 May; 18(5):355-64. PubMed ID: 18406615
[TBL] [Abstract][Full Text] [Related]
8. Acute pancreatitis in a patient with glutaric acidemia type II.
Coşkun T; Göğüş S; Akçören Z; Tokatli A; Ozalp I
Turk J Pediatr; 1997; 39(3):379-85. PubMed ID: 9339118
[TBL] [Abstract][Full Text] [Related]
9. Magnetic resonance imaging findings of adult-onset glutaric aciduria type I.
Sonmez G; Mutlu H; Ozturk E; Sildiroglu HO; Keskin AT; Basekim CC; Kizilkaya E
Acta Radiol; 2007 Jun; 48(5):557-9. PubMed ID: 17520433
[TBL] [Abstract][Full Text] [Related]
10. [Glutaric aciduria type I: diagnosis in adulthood and phenotypic variability].
Corral I; Martínez Castrillo JC; Martínez-Pardo M; Gimeno A
Neurologia; 2001 Oct; 16(8):377-80. PubMed ID: 11738016
[TBL] [Abstract][Full Text] [Related]
11. [In utero macrocephaly as clinical manifestation of glutaric aciduria type I. Report of a novel mutation].
Mahfoud A; Domínguez CL; Rizzo C; Ribes A
Rev Neurol; 2004 Nov 16-30; 39(10):939-42. PubMed ID: 15573311
[TBL] [Abstract][Full Text] [Related]
12. [Macrocephaly the first manifestation of glutaric aciduria type I: the importance of early diagnosis].
Martínez Granero MA; Garcia Pérez A; Martínez-Pardo M; Parra E
Neurologia; 2005 Jun; 20(5):255-60. PubMed ID: 15954035
[TBL] [Abstract][Full Text] [Related]
13. So doctor, what exactly is wrong with my muscles? Glutaric aciduria type II presenting in a teenager.
Beresford MW; Pourfarzam M; Turnbull DM; Davidson JE
Neuromuscul Disord; 2006 Apr; 16(4):269-73. PubMed ID: 16527485
[TBL] [Abstract][Full Text] [Related]
14. Magnetic resonance spectroscopic characteristics of glutaric aciduria type II.
Firat AK; Karakas HM; Yakinci C
Dev Med Child Neurol; 2006 Oct; 48(10):847-50. PubMed ID: 16978466
[TBL] [Abstract][Full Text] [Related]
15. Glutaric aciduria type II: review of the phenotype and report of an unusual glomerulopathy.
Wilson GN; de Chadarévian JP; Kaplan P; Loehr JP; Frerman FE; Goodman SI
Am J Med Genet; 1989 Mar; 32(3):395-401. PubMed ID: 2658591
[TBL] [Abstract][Full Text] [Related]
16. Central nervous system and muscle involvement in an adolescent patient with riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency.
Ishii K; Komaki H; Ohkuma A; Nishino I; Nonaka I; Sasaki M
Brain Dev; 2010 Sep; 32(8):669-72. PubMed ID: 19783111
[TBL] [Abstract][Full Text] [Related]
17. Riboflavin-responsive glutaryl CoA dehydrogenase deficiency.
Chalmers RA; Bain MD; Zschocke J
Mol Genet Metab; 2006 May; 88(1):29-37. PubMed ID: 16377226
[TBL] [Abstract][Full Text] [Related]
18. Riboflavin-responsive lipid-storage myopathy and glutaric aciduria type II of early adult onset.
de Visser M; Scholte HR; Schutgens RB; Bolhuis PA; Luyt-Houwen IE; Vaandrager-Verduin MH; Veder HA; Oey PL
Neurology; 1986 Mar; 36(3):367-72. PubMed ID: 3951704
[TBL] [Abstract][Full Text] [Related]
19. [Type 1 glutaric aciduria: clinical and therapeutic implications].
Jiménez Caballero PE; Marsal Alonso C
Neurologia; 2007 Jun; 22(5):329-32. PubMed ID: 17508309
[TBL] [Abstract][Full Text] [Related]
20. [Glutaric aciduria type 1 with normal evolution: follow-up of one case until adult age].
Pascual-Castroviejo I; Pascual-Pascual SI; Merinero B; Ugarte M; Garcia-Segura JM; Viaño J; Velazquez R
Neurologia; 2005 May; 20(4):189-93. PubMed ID: 15891948
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
