1. T Sakuma,N Sugiyama,T Ichiki,M Kobayashi,Y Wada,D Nohara. (1991-02-01) Analysis of acylcarnitines in maternal urine for prenatal diagnosis of glutaric aciduria type 2.. Prenatal diagnosis, 11 ((2)): (77-82). [PMID:2062823] |
2. S Pontremoli,E Melloni,M Michetti,B Sparatore,F Salamino,N Siliprandi,B L Horecker. (1987-11-13) Isovalerylcarnitine is a specific activator of calpain of human neutrophils.. Biochemical and biophysical research communications, 148 ((3)): (1189-1195). [PMID:2825678] |
3. D S Millington,C R Roe,D A Maltby,F Inoue. (1987-01-01) Endogenous catabolism is the major source of toxic metabolites in isovaleric acidemia.. The Journal of pediatrics, 110 ((1)): (56-60). [PMID:3794887] |
4. R A Chalmers,C R Roe,T E Stacey,C L Hoppel. (1984-12-01) Urinary excretion of l-carnitine and acylcarnitines by patients with disorders of organic acid metabolism: evidence for secondary insufficiency of l-carnitine.. Pediatric research, 18 ((12)): (1325-1328). [PMID:6441143] |
5. F Salamino,F Di Lisa,A B Burlina,R Menabŏ,R Barbato,R De Tullio,N Siliprandi. (1994-08-01) Involvement of erythrocyte calpain in glycine- and carnitine-treated isovaleric acidemia.. Pediatric research, 36 ((2)): (182-186). [PMID:7970932] |
6. M H Fries,P Rinaldo,E Schmidt-Sommerfeld,E Jurecki,S Packman. (1996-09-01) Isovaleric acidemia: response to a leucine load after three weeks of supplementation with glycine, L-carnitine, and combined glycine-carnitine therapy.. The Journal of pediatrics, 129 ((3)): (449-452). [PMID:8804338] |
7. M Fontaine,G Briand,L Vallée,G Ricart,P Degand,P Divry,C Vianey-Saban,J Vamecq. (1996-08-30) Acylcarnitine removal in a patient with acyl-CoA beta-oxidation deficiency disorder: effect of L-carnitine therapy and starvation.. Clinica chimica acta; international journal of clinical chemistry, 252 ((2)): (109-122). [PMID:8853559] |
8. C R Roe,S D Cederbaum,D S Roe,R Mardach,A Galindo,L Sweetman. (1999-01-16) Isolated isobutyryl-CoA dehydrogenase deficiency: an unrecognized defect in human valine metabolism.. Molecular genetics and metabolism, 65 ((4)): (264-271). [PMID:9889013] |
9. F Ferrara,A Bertelli,M Falchi. (2005-07-22) Evaluation of carnitine, acetylcarnitine and isovalerylcarnitine on immune function and apoptosis.. Drugs under experimental and clinical research, 31 ((3)): (109-114). [PMID:16033249] |
10. Judit Bene,Katalin Komlósi,Viktória Havasi,Gábor Talián,Beáta Gasztonyi,Krisztina Horváth,Gyula Mózsik,Béla Hunyady,Béla Melegh,Mária Figler. (2006-01-28) Changes of plasma fasting carnitine ester profile in patients with ulcerative colitis.. World journal of gastroenterology, 12 ((1)): (110-113). [PMID:16440427] |
11. Evan L Pannkuk,Evagelia C Laiakis,Kirandeep Gill,Shreyans K Jain,Khyati Y Mehta,Denise Nishita,Kim Bujold,James Bakke,Janet Gahagen,Simon Authier,Polly Chang,Albert J Fornace. (2019-03-08) Liquid Chromatography-Mass Spectrometry-Based Metabolomics of Nonhuman Primates after 4 Gy Total Body Radiation Exposure: Global Effects and Targeted Panels.. Journal of proteome research, 18 ((5)): (2260-2269). [PMID:30843397] |
12. David Meierhofer. (2019-08-16) Acylcarnitine profiling by low-resolution LC-MS.. PloS one, 14 ((8)): (e0221342-e0221342). [PMID:31415665] |
13. Y Shigematsu,Y Kikawa,M Sudo,H Kanaoka,M Fujioka,M Dan. (1991-12-16) Prenatal diagnosis of isovaleric acidemia by fast atom bombardment and tandem mass spectrometry.. Clinica chimica acta; international journal of clinical chemistry, 203 ((2-3)): (369-374). [PMID:1777996] |
14. K Kidouchi,T Niwa,D Nohara,K Asai,N Sugiyama,H Morishita,M Kobayashi,Y Wada. (1988-04-29) Urinary acylcarnitines in a patient with neonatal multiple acyl-CoA dehydrogenation deficiency, quantified by a carboxylic acid analyzer with a reversed-phase column.. Clinica chimica acta; international journal of clinical chemistry, 173 ((3)): (263-272). [PMID:3383426] |
15. J E Abdenur,N A Chamoles,A E Guinle,A B Schenone,A N Fuertes. (1998-10-08) Diagnosis of isovaleric acidaemia by tandem mass spectrometry: false positive result due to pivaloylcarnitine in a newborn screening programme.. Journal of inherited metabolic disease, 21 ((6)): (624-630). [PMID:9762597] |
16. Dietrich Matern,Miao He,Susan A Berry,Piero Rinaldo,Chester B Whitley,Pia P Madsen,Sandra C van Calcar,Richard C Lussky,Brage S Andresen,Jon A Wolff,Jerry Vockley. (2003-07-03) Prospective diagnosis of 2-methylbutyryl-CoA dehydrogenase deficiency in the Hmong population by newborn screening using tandem mass spectrometry.. Pediatrics, 112 ((1 Pt 1)): (74-78). [PMID:12837870] |