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kw.\*:("Hydroxymethylglutaryl-CoA lyase")

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3-hydroxy-3-methylglutaryl-coenzyme A lyase deficiency : biochemical studies and family investigation of four generationsBARASH, V; MANDEL, H; SELLA, S et al.Journal of inherited metabolic disease. 1990, Vol 13, Num 2, pp 156-164, issn 0141-8955, 9 p.Article

Increased plasma amylase in the family of a patient with 3-hydroxy-3-methylglutaryl-coenzyme A lyase deficiencyPLÖCHL, E; COLOMBO, J. P; WERMUTH, B et al.Clinical chemistry (Baltimore, Md.). 1992, Vol 38, Num 2, pp 307-309, issn 0009-9147Article

Sudden death in an infant with 3-hydroxy-3-methylglutaryl-CoA lyase deficiencyRIBES, A; BRIONES, P; VILASECA, M. A et al.Journal of inherited metabolic disease. 1990, Vol 13, Num 5, pp 752-753, issn 0141-8955, 2 p.Article

3-METHYL-3-BUTENOIC ACID: AN ARTEFACT IN THE URINARY METABOLIC PATTERN OF PATIENTS WITH 3-HYDROXY-3-METHYL-GLUTARYL-COA LYASE DEFICIENCYJAKOBS C; BOJASCH M; DURAN M et al.1980; CLIN. CHIM. ACTA; NLD; DA. 1980; VOL. 106; NO 1; PP. 85-89; BIBL. 12 REF.Article

PURIFICATION AND CHARACTERIZATION OF AVIAN LIVER 3-HYDROXY-3-METHYLGLUTARYL COENZYME A LYASEKRAMER PR; MIZIORKO HM.1980; J. BIOL. CHEM.; ISSN 0021-9258; USA; DA. 1980; VOL. 255; NO 22; PP. 11023-11028; BIBL. 27 REF.Article

Cerebral MRI in 3-hydroxy-3-methylglutaryl-coenzyme A lyase deficiency : case reportFERRIS, N. J; TIEN, R. D.Neuroradiology (Berlin. Print). 1993, Vol 35, Num 7, pp 559-560, issn 0028-3940Article

3-Hydroxy-3-methylglutaryl coenzyme A lyase deficiencyGÜNEL, M; COSKUN, T; TOKATLI, A et al.Journal of inherited metabolic disease. 1993, Vol 16, Num 6, pp 1062-1063, issn 0141-8955Article

3-hydroxy-3-methylglutaryldithio-CoA : utility of an alternative substrate in elucidation of a role for HMG-CoA lyase's cation activatorHRUZ, P. W; ANDERSON, V. E; MIZIORKO, H. M et al.Biochimica et biophysica acta. Protein structure and molecular enzymology. 1993, Vol 1162, Num 1-2, pp 149-154, issn 0167-4838Article

Déficit et hydroxy-méthylglutaryl-coenzyme A lyase révélé par un syndrome de Reye chez une fille de 3 ans = 3-hydroxy-3-methylglutaryl-Coenzyme A lyase deficiency presenting as a Reye's syndrome in a 3 years old girlKARCHER, C; ROUSSELOT, J. M; LEFEBVRE, E et al.Pédiatrie (Marseille). 1993, Vol 48, Num 5, pp 385-387, issn 0031-4021Article

Pseudomonas mevalonii 3-hydroxy-3-methylglutaryl-CoA lyase : characterization of the isolated recombinant protein and investigation of the enzyme's cation requirementsNARASIMHAN, C; MIZIORKO, H. M.Biochemistry (Easton). 1992, Vol 31, Num 45, pp 11224-11230, issn 0006-2960Article

3-Hydroxy-3-methylglutaryl-CoA-lyase deficiencyPLOECHL, E; BACHMANN, C; COLOMBO, J. P et al.Journal of inherited metabolic disease. 1989, Vol 12, Num 3, issn 0141-8955, 343 [1 p.]Article

3-Hydroxy-3-methylglutaryl-coenzyme A lyase deficiencyMOSES, S. W; AVIRAM, M; GEIGER, R et al.Journal of inherited metabolic disease. 1989, Vol 12, Num 3, pp 341-342, issn 0141-8955Article

Nucleotide sequence and expression in Escherichia coli of the 3-hydroxy-3-methylglutaryl coenzyme A lyase gene of Pseudomonas mevaloniiANDERSON, D. H; RODWELL, V. W.Journal of bacteriology. 1989, Vol 171, Num 12, pp 6468-6472, issn 0021-9193Article

3-Hydroxy-3-methylglutaryl-coenzyme A lyase deficiency: report of five new patientsGIBSON, K. M; BREUER, J; CONDE, C et al.Journal of inherited metabolic disease. 1988, Vol 11, Num 1, pp 76-87, issn 0141-8955Article

3-hydroxy-3-methylglutaryl coenzyme A lyase (HL) : cloning of human and chicken liver HL cDNAs and characterization of a mutation causing human HL deficiencyMITCHELL, G. A; ROBERT, M.-F; MIZIORKO, H. M et al.The Journal of biological chemistry (Print). 1993, Vol 268, Num 6, pp 4376-4381, issn 0021-9258Article

3-hydroxy-3-methylglutaric aciduria in portuguese populationVILARINHO, L; CARDOSO, M. L; RABIER, D et al.Journal of inherited metabolic disease. 1993, Vol 16, Num 1, pp 154-155, issn 0141-8955Article

3-Methylglutaconyl-CoA hydratase, 3-methylcrotonyl-CoA carboxylase and 3-hydroxy-3-methylglutaryl-CoA lyase deficiencies: a coupled enzyme assay useful for their detectionNARISAWA, K; GIBSON, K. M; SWEETMAN, L et al.Clinica chimica acta. 1989, Vol 184, Num 1, pp 57-64, issn 0009-8981Article

3-Hydroxy-3-methylglutaryl-CoA lyase deficiency as detected by radiochemical assay in cell extracts by thin-layer chromatography, and identification of three new casesGIBSON, K. M; LEE, C. F; KAMALI, V et al.Clinical chemistry (Baltimore, Md.). 1990, Vol 36, Num 2, pp 297-303, issn 0009-9147Article

Enzymatic diagnosis of 3-hydroxy-3-methylglutaryl-CoA lyase deficiency with high-performance liquid chromatographyKIKUCHI, M; NARISAWA, K; TADA, K et al.Clinica chimica acta. 1990, Vol 189, Num 3, pp 297-301, issn 0009-8981, 5 p.Article

Rapid diagnosis of 3-hydroxy-3-methylglutaryl-coenzyme A lyase deficiency via enzyme activity measurements in leukocytes of platelets using a simple spectrophotometric methodWANDERS, R. J. A; ZOETERS, P. H. M; SCHUTGENS, R. B. H et al.Clinica chimica acta. 1990, Vol 189, Num 3, pp 327-334, issn 0009-8981, 8 p.Article

Partial purification and characterization of membrane-associated 3-hydroxy-3-methylglutaryl-coenzyme A lyase from radish seedlingsWEBER, T; BACH, T. J.Zeitschrift für Naturforschung. C. A journal of biosciences. 1993, Vol 48, Num 5-6, pp 444-450, issn 0939-5075Article

3-Hydroxy-3-methylglutaryl coenzyme A lyase : affinity labeling of the Pseudomonas mevalonii enzyme and assignment of cysteine-237 to the active siteHRUZ, P. W; CHAKRAVARTHY NARASIMHAN; MIZIORKO, H. M et al.Biochemistry (Easton). 1992, Vol 31, Num 29, pp 6842-6847, issn 0006-2960Article

Inhibiteurs de l'HMG-CoA réductase et rhabdomyolyse : hypothèses physiopathologiques, conséquences thérapeutiques = Inhibitors of HMG-CoA reductase and rhabdomyolysis: physiopathological hypotheses, therapeutic implicationsMARQUES-VIDAL, P; VEDRENNE, C; GRANIER, P et al.STV. Sang thrombose vaisseaux. 1991, Vol 3, Num 8, pp 503-594, issn 0999-7385Article

Measurement of 3-hydroxy-3-methylglutaryl-CoA clyase activity in amniotic cells and in chorionic rilliBARASH, V; ELPELEG, O; SHEFFER, R et al.Prenatal diagnosis. 1988, Vol 8, Num 9, issn 0197-3851, 691Article

A new case of 3-hydroxy-3-methylglutaryl-coenzyme A lyase deficiencyMARKLOVA, E; VERNER, P; PEHAL, F et al.Journal of inherited metabolic disease. 1987, Vol 10, Num 4, issn 0141-8955, 399Article

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