164 related articles for article (PubMed ID: 1691326)
1. [3-hydroxy-3-methylglutaraturia. Clinical aspects, follow-up and therapy in a young child].
Plöchl E; Bachmann C; Colombo JP; Gibson KM
Klin Padiatr; 1990; 202(2):76-80. PubMed ID: 1691326
[TBL] [Abstract][Full Text] [Related]
2. 3-Hydroxy-3-methylglutaric aciduria: response to carnitine therapy and fat and leucine restriction.
Dasouki M; Buchanan D; Mercer N; Gibson KM; Thoene J
J Inherit Metab Dis; 1987; 10(2):142-6. PubMed ID: 2443756
[TBL] [Abstract][Full Text] [Related]
3. [Late onset 3-HMG-CoA lyase deficiency: a rare but treatable disorder].
Pierron S; Giudicelli H; Moreigne M; Khalfi A; Touati G; Caruba C; Rolland MO; Acquaviva C
Arch Pediatr; 2010 Jan; 17(1):10-3. PubMed ID: 19932602
[TBL] [Abstract][Full Text] [Related]
4. [3-hydroxy-3-methylglutaric aciduria and recurrent Reye-like syndrome].
Eirís J; Ribes A; Fernández-Prieto R; Rodríguez-García J; Rodríguez-Segade S; Castro-Gago M
Rev Neurol; 1998 Jun; 26(154):911-4. PubMed ID: 9658458
[TBL] [Abstract][Full Text] [Related]
5. [3-hydroxy-3-methylglutaraciduria (case report of a female Turkish sisters with 3-hydroxy-3- methylglutaryl-Coenzyme A lyase deficiency].
Koling S; Kalhoff H; Schauerte P; Lehnert W; Diekmann L
Klin Padiatr; 2000; 212(3):113-6. PubMed ID: 10916782
[TBL] [Abstract][Full Text] [Related]
6. 3-Hydroxy-3-methylglutaryl-CoA lyase deficiency: absence of clinical symptoms due to a self-imposed dietary fat and protein restriction.
Bakker HD; Wanders RJ; Schutgens RB; Abeling NG; van Gennip AH
J Inherit Metab Dis; 1993; 16(6):1061-2. PubMed ID: 8127066
[No Abstract] [Full Text] [Related]
7. 3-hydroxy-3-methylglutaryl-CoA lyase deficiency in an adult with leukoencephalopathy.
Bischof F; Nägele T; Wanders RJ; Trefz FK; Melms A
Ann Neurol; 2004 Nov; 56(5):727-30. PubMed ID: 15505778
[TBL] [Abstract][Full Text] [Related]
8. 3-Hydroxy-3-methylglutaric aciduria.
Greene CL; Cann HM; Robinson BH; Gibson KM; Sweetman L; Holm J; Nyhan WL
J Neurogenet; 1984 Apr; 1(2):165-73. PubMed ID: 6085636
[TBL] [Abstract][Full Text] [Related]
9. [Macrocephaly and dystonic cerebral palsy in a child with type I glutaric aciduria].
Plöchl E; Christensen E; Colombo JP; Weiss-Wichert P; Wenger E
Padiatr Padol; 1991; 26(2):97-101. PubMed ID: 1945471
[TBL] [Abstract][Full Text] [Related]
10. A case of organic aciduria--suspected 3-hydroxy-3-methylglutaric aciduria.
Kulczycka H; Mielniczuk Z; Kamińska H; Lewanowicz W; Pronicka E
Mater Med Pol; 1991; 23(4):312-4. PubMed ID: 1726825
[TBL] [Abstract][Full Text] [Related]
11. Prenatal diagnosis of 3-hydroxy-3-methylglutaric aciduria by GC-MS and enzymology on cultured amniocytes and chorionic villi.
Chalmers RA; Tracey BM; Mistry J; Stacey TE; McFadyen IR
J Inherit Metab Dis; 1989; 12(3):286-92. PubMed ID: 2482386
[TBL] [Abstract][Full Text] [Related]
12. Identification of 3-methylglutarylcarnitine. A new diagnostic metabolite of 3-hydroxy-3-methylglutaryl-coenzyme A lyase deficiency.
Roe CR; Millington DS; Maltby DA
J Clin Invest; 1986 Apr; 77(4):1391-4. PubMed ID: 3958190
[TBL] [Abstract][Full Text] [Related]
13. A neonatal case of 3-hydroxy-3-methylglutaric-coenzyme A lyase deficiency.
Santarelli F; Cassanello M; Enea A; Poma F; D'Onofrio V; Guala G; Garrone G; Puccinelli P; Caruso U; Porta F; Spada M
Ital J Pediatr; 2013 May; 39():33. PubMed ID: 23705938
[TBL] [Abstract][Full Text] [Related]
14. 3-hydroxy-3-methylglutaric aciduria: a new assay of 3-hydroxy-3-methylglutaryl-coa lyase using high performance liquid chromatography.
Gibson KM; Sweetman L; Nyhan WL; Page TM; Greene C; Cann HM
Clin Chim Acta; 1982 Dec; 126(2):171-81. PubMed ID: 6185253
[TBL] [Abstract][Full Text] [Related]
15. 3-Hydroxy-3-methylglutaryl-CoA lyase in human skin fibroblasts: study of its properties and deficient activity in 3-hydroxy-3-methylglutaric aciduria patients using a simple spectrophotometric method.
Wanders RJ; Schutgens RB; Zoeters PH
Clin Chim Acta; 1988 Jan; 171(1):95-101. PubMed ID: 2450702
[TBL] [Abstract][Full Text] [Related]
16. Gas-chromatographic/mass spectrometric detection of 3-hydroxy-3-methylglutaryl-CoA lyase deficiency in double first cousins.
Norman EJ; Denton MD; Berry HK
Clin Chem; 1982 Jan; 28(1):137-40. PubMed ID: 7055897
[TBL] [Abstract][Full Text] [Related]
17. [Macrocephaly as the initial manifestation of glutaryl-CoA-dehydrogenase deficiency (glutaric aciduria type I)].
Trefz FK; Hoffmann GF; Mayatepek E; Lichter-Konecki U; Weisser J; Otten A; Wendel U; Rating D; Bremer HJ
Monatsschr Kinderheilkd; 1991 Nov; 139(11):754-8. PubMed ID: 1775140
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. 3-Hydroxy-3-methylglutaryl-CoA lyase deficiency studied using 2-dimensional proton nuclear magnetic resonance spectroscopy.
Iles RA; Jago JR; Williams SR; Chalmers RA
FEBS Lett; 1986 Jul; 203(1):49-53. PubMed ID: 2424790
[TBL] [Abstract][Full Text] [Related]
20. Clinical and biochemical observations on a child with a deficiency of 3-hydroxy-3-methylglutaryl coenzyme A lyase.
Ketel A; Ket JL; Schutgens RB; Duran M; Wadman SK
J Inherit Metab Dis; 1980; 3(3):89-90. PubMed ID: 6158624
[No Abstract] [Full Text] [Related]
[Next] [New Search]
