-
1
-
-
0000066755
-
Acyl-coenzyme A dehydrogenases
-
F. Muller, editor. CRC Press, Boca Raton, FL
-
Engel, P. C. 1992. Acyl-coenzyme A dehydrogenases. In Chemistry and Biochemistry of Flavoenzymes. F. Muller, editor. CRC Press, Boca Raton, FL. 597-655.
-
(1992)
Chemistry and Biochemistry of Flavoenzymes
, pp. 597-655
-
-
Engel, P.C.1
-
2
-
-
0025814952
-
Inborn errors of fatty acid oxidation in man
-
Rhead, W. J. 1991. Inborn errors of fatty acid oxidation in man. Clin. Biochem. 24:319-329.
-
(1991)
Clin. Biochem.
, vol.24
, pp. 319-329
-
-
Rhead, W.J.1
-
3
-
-
0026718314
-
Fatty acid oxidation disorders: A new class of metabolic diseases
-
Hale, D. E., and M. J. Bennett. 1992. Fatty acid oxidation disorders: a new class of metabolic diseases. J. Pediatr. 121:1-11.
-
(1992)
J. Pediatr.
, vol.121
, pp. 1-11
-
-
Hale, D.E.1
Bennett, M.J.2
-
4
-
-
0026658581
-
Molecular basis of mitochondrial fatty acid oxidation defects
-
Coates, P. M., and K. Tanaka. 1992. Molecular basis of mitochondrial fatty acid oxidation defects. J. Lipid Res. 33:1099-1110.
-
(1992)
J. Lipid Res.
, vol.33
, pp. 1099-1110
-
-
Coates, P.M.1
Tanaka, K.2
-
5
-
-
0025695583
-
Molecular characterization of inherited medium-chain acyl-CoA dehydrogenase deficiency
-
Kelly, D. P., A. J. Whelan, M. L. Ogden, R. Alpers, Z. Zhang, G. Bellus, N. Gregersen, I. Dorland, and A. W. Strauss. 1990. Molecular characterization of inherited medium-chain acyl-CoA dehydrogenase deficiency. Proc. Natl. Acad. Sci. USA. 87:9236-9240.
-
(1990)
Proc. Natl. Acad. Sci. USA
, vol.87
, pp. 9236-9240
-
-
Kelly, D.P.1
Whelan, A.J.2
Ogden, M.L.3
Alpers, R.4
Zhang, Z.5
Bellus, G.6
Gregersen, N.7
Dorland, I.8
Strauss, A.W.9
-
6
-
-
0025010623
-
Molecular basis of medium-chain acyl-coenzyme A dehydrogenase deficiency
-
Yokota, I., Y. Indo, P. M. Coates, and K. Tanaka. 1990. Molecular basis of medium-chain acyl-coenzyme A dehydrogenase deficiency. J. Clin. Invest. 86:1000-1003.
-
(1990)
J. Clin. Invest.
, vol.86
, pp. 1000-1003
-
-
Yokota, I.1
Indo, Y.2
Coates, P.M.3
Tanaka, K.4
-
7
-
-
0020363432
-
In vitro fibrobtast studies in a patient with C6-C10 dicarboxylic aciduria: Evidence for a defect in general acyl-CoA dehydrogenase
-
Kolvraa, S., N. Gregersen, E. Christensen, and N. Hobolth. 1982. In vitro fibrobtast studies in a patient with C6-C10 dicarboxylic aciduria: evidence for a defect in general acyl-CoA dehydrogenase. Clin. Chim. Acta. 126:53-67.
-
(1982)
Clin. Chim. Acta
, vol.126
, pp. 53-67
-
-
Kolvraa, S.1
Gregersen, N.2
Christensen, E.3
Hobolth, N.4
-
9
-
-
0021053314
-
Medium-chain acyl-CoA dehydrogenase deficiency in children with non-ketotic hypoglycemia and low carnitine levels
-
Stanley, C. A., D. E. Hale, P. M. Coates, C. L. Hall, B. E. Corkey, W. Yang, R. I. Kelley, E. L. Gonzalez, J. R. Williamson, and L. Baker. 1983. Medium-chain acyl-CoA dehydrogenase deficiency in children with non-ketotic hypoglycemia and low carnitine levels. Pediatr. Res. 17:877-884.
-
(1983)
Pediatr. Res.
, vol.17
, pp. 877-884
-
-
Stanley, C.A.1
Hale, D.E.2
Coates, P.M.3
Hall, C.L.4
Corkey, B.E.5
Yang, W.6
Kelley, R.I.7
Gonzalez, E.L.8
Williamson, J.R.9
Baker, L.10
-
10
-
-
0026322069
-
985A-to-G transition, and identification of five infrequent mutations in the medium-chain acyl-CoA dehydrogenase (MCAD) gene in 55 patients with MCAD deficiency
-
985A-to-G transition, and identification of five infrequent mutations in the medium-chain acyl-CoA dehydrogenase (MCAD) gene in 55 patients with MCAD deficiency. Am. J. Hum. Genet. 49:1280-1291.
-
(1991)
Am. J. Hum. Genet.
, vol.49
, pp. 1280-1291
-
-
Yokota, I.1
Coates, P.M.2
Hale, D.E.3
Rinaldo, P.4
Tanaka, K.5
-
11
-
-
84915975559
-
Mutations causing medium-chain acyl-CoA dehydrogenase deficiency: A collaborative compilation of the data from 172 patients
-
Wiley-Liss, New York
-
Workshop on Molecular Aspects of MCAD Deficiency. 1992. Mutations causing medium-chain acyl-CoA dehydrogenase deficiency: a collaborative compilation of the data from 172 patients. In New Developments in Fatty Acid Oxidation. P. M. Coates and K. Tanaka, editors. Wiley-Liss, New York. 449-456.
-
(1992)
New Developments in Fatty Acid Oxidation
, pp. 449-456
-
-
Coates, P.M.1
Tanaka, K.2
-
12
-
-
0021873302
-
Long-chain acyl-coenzyme A dehydrogenase deficiency: An inherited cause of non-ketotic hypoglycemia
-
Hale, D. E., M. Batshaw, P. M. Coates, F. E. Frerman, S. I. Goodman, I. Singh, and C. A. Stanley. 1985. Long-chain acyl-coenzyme A dehydrogenase deficiency: an inherited cause of non-ketotic hypoglycemia. Pediatr. Res. 19:666-671.
-
(1985)
Pediatr. Res.
, vol.19
, pp. 666-671
-
-
Hale, D.E.1
Batshaw, M.2
Coates, P.M.3
Frerman, F.E.4
Goodman, S.I.5
Singh, I.6
Stanley, C.A.7
-
13
-
-
0025913135
-
Immunochemical characterization of variant long-chain acyl-CoA dehydrogenase in cultured fibroblasts from nine patients with long-chain acyl-CoA dehydrogenase deficiency
-
Indo. Y., P. M. Coates, D. E. Hale, and K. Tanaka. 1991. Immunochemical characterization of variant long-chain acyl-CoA dehydrogenase in cultured fibroblasts from nine patients with long-chain acyl-CoA dehydrogenase deficiency. Pediatr. Res. 30:211-215.
-
(1991)
Pediatr. Res.
, vol.30
, pp. 211-215
-
-
Indo, Y.1
Coates, P.M.2
Hale, D.E.3
Tanaka, K.4
-
14
-
-
0023248335
-
Short-chain acyl-CoA dehydrogenase deficiency: Clinical and biochemical studies in two patients
-
Amendt, B. A., C. Greene, L. Sweetman, J. Cloherty, V. Shin, A. Moon, L. Teel, and W. J. Rhead. 1987. Short-chain acyl-CoA dehydrogenase deficiency: clinical and biochemical studies in two patients. J. Clin. Invest. 79:1303-1309.
-
(1987)
J. Clin. Invest.
, vol.79
, pp. 1303-1309
-
-
Amendt, B.A.1
Greene, C.2
Sweetman, L.3
Cloherty, J.4
Shin, V.5
Moon, A.6
Teel, L.7
Rhead, W.J.8
-
15
-
-
0021633607
-
Short-chain acyl-CoA dehydrogenase deficiency associated with a lipid-storage myopathy and secondary camitine deficiency
-
Turnbull, D. M., K. Bartlett, D. L. Stevens, K. G. M. M. Albert, G. J. Gibson, M. A. Johnson, A. J. McCulloch, and H. S. A. Sherratt. 1984. Short-chain acyl-CoA dehydrogenase deficiency associated with a lipid-storage myopathy and secondary camitine deficiency. N. Engl. J. Med. 311:1232-1236.
-
(1984)
N. Engl. J. Med.
, vol.311
, pp. 1232-1236
-
-
Turnbull, D.M.1
Bartlett, K.2
Stevens, D.L.3
Albert, K.G.M.M.4
Gibson, G.J.5
Johnson, M.A.6
McCulloch, A.J.7
Sherratt, H.S.A.8
-
16
-
-
0023875592
-
Genetic deficiency of short-chain acyl-coenzyme A dehydrogenase in cultured fibroblasts from a patient with muscle carnitine deficiency and severe skeletal muscle weakness
-
Coates, P. M., D. E. Hale, G. Finocchiaro, K. Tanaka, and S. M. Winter. 1988. Genetic deficiency of short-chain acyl-coenzyme A dehydrogenase in cultured fibroblasts from a patient with muscle carnitine deficiency and severe skeletal muscle weakness. J. Clin. Invest. 81:171-175.
-
(1988)
J. Clin. Invest.
, vol.81
, pp. 171-175
-
-
Coates, P.M.1
Hale, D.E.2
Finocchiaro, G.3
Tanaka, K.4
Winter, S.M.5
-
17
-
-
0025325156
-
Identification of two variant short-chain acyl-coenzyme A dehydrogenase alleles, each containing a different point mutation in a patient with short-chain acyl-coenzyme A dehydrogenase deficiency
-
Natio, E., Y. Indo, and K. Tanaka. 1990. Identification of two variant short-chain acyl-coenzyme A dehydrogenase alleles, each containing a different point mutation in a patient with short-chain acyl-coenzyme A dehydrogenase deficiency. J. Clin. Invest. 85:1575-1582.
-
(1990)
J. Clin. Invest.
, vol.85
, pp. 1575-1582
-
-
Natio, E.1
Indo, Y.2
Tanaka, K.3
-
18
-
-
0024453488
-
Short-chain acyl-coenzyme A dehydrogenase (SCAD) deficiency: Immunochemical demonstration of molecular heterogeneity due to variant SCAD with differing stability
-
Naito, E., Y. Indo, and K. Tanaka. 1989. Short-chain acyl-coenzyme A dehydrogenase (SCAD) deficiency: immunochemical demonstration of molecular heterogeneity due to variant SCAD with differing stability. J. Clin. Invest. 84:1671-1674.
-
(1989)
J. Clin. Invest.
, vol.84
, pp. 1671-1674
-
-
Naito, E.1
Indo, Y.2
Tanaka, K.3
-
19
-
-
0021795143
-
Defects in the metabolism of fatty acids in the sudden infant death syndrome
-
Howat, A. J., M. J. Bennett, S. Variend, L. Shaw, and P. C. Engel. 1985. Defects in the metabolism of fatty acids in the sudden infant death syndrome. Br. Med. J. 290:1771-1775.
-
(1985)
Br. Med. J.
, vol.290
, pp. 1771-1775
-
-
Howat, A.J.1
Bennett, M.J.2
Variend, S.3
Shaw, L.4
Engel, P.C.5
-
20
-
-
0023850314
-
Acyl-coenzyme A dehydrogenase deficiency in heart tissue from infants who died unexpectedly with fatty change in the liver
-
Allison, F., M. J. Bennett, S. Variend, and P. C. Engel. 1988. Acyl-coenzyme A dehydrogenase deficiency in heart tissue from infants who died unexpectedly with fatty change in the liver. Br. Med. J. 296:11-20.
-
(1988)
Br. Med. J.
, vol.296
, pp. 11-20
-
-
Allison, F.1
Bennett, M.J.2
Variend, S.3
Engel, P.C.4
-
21
-
-
0026518372
-
Novel fatty acid β-oxidation enzymes in rat liver mitochondria. I. Purification and properties of very-long-chain acyl-coenzyme A dehydrogenase
-
Izai, K., Y. Uchida, T. Orii, S. Yamatmoto, and T. Hashimoto. 1992. Novel fatty acid β-oxidation enzymes in rat liver mitochondria. I. Purification and properties of very-long-chain acyl-coenzyme A dehydrogenase. J. Biol. Chem. 267:1027-1033.
-
(1992)
J. Biol. Chem.
, vol.267
, pp. 1027-1033
-
-
Izai, K.1
Uchida, Y.2
Orii, T.3
Yamatmoto, S.4
Hashimoto, T.5
-
22
-
-
0027295763
-
A novel disease with deficiency of mitochondrial very-long-chain acyl-CoA dehydrogenase
-
Aoyama, T., Y. Uchida, R. I. Kelley, M. Marble, K. Hofman, J. H. Tonsgard, W. J. Rhead, and T. Hashimoto. 1993. A novel disease with deficiency of mitochondrial very-long-chain acyl-CoA dehydrogenase. Biochem. Biophys. Res. Commun. 191:1369-1372.
-
(1993)
Biochem. Biophys. Res. Commun.
, vol.191
, pp. 1369-1372
-
-
Aoyama, T.1
Uchida, Y.2
Kelley, R.I.3
Marble, M.4
Hofman, K.5
Tonsgard, J.H.6
Rhead, W.J.7
Hashimoto, T.8
-
23
-
-
0027207327
-
Identification of very-long-chain acyl-CoA dehydrogenase deficiency in three patients previously diagnosed with long-chain acyl-CoA dehydrogenase deficiency
-
Yamaguchi, S., Y. Indo, P. M. Coates, T. Hashimoto, and K. Tanaka. 1993. Identification of very-long-chain acyl-CoA dehydrogenase deficiency in three patients previously diagnosed with long-chain acyl-CoA dehydrogenase deficiency. Pediatr. Res. 34:111-113.
-
(1993)
Pediatr. Res.
, vol.34
, pp. 111-113
-
-
Yamaguchi, S.1
Indo, Y.2
Coates, P.M.3
Hashimoto, T.4
Tanaka, K.5
-
24
-
-
0025851939
-
Defect in fatty acid oxidation: Laboratory and pathologic findings in a patient
-
Tonsgard, J. H., J. K. Stephens, W. J. Rhead, D. Penn, A. L. Horwitz, B. S. Kirschner, P. F. Whitington, S Berger, and M. E. Tripp. 1991. Defect in fatty acid oxidation: laboratory and pathologic findings in a patient. Pediatr. Neurol. 7:125-130.
-
(1991)
Pediatr. Neurol.
, vol.7
, pp. 125-130
-
-
Tonsgard, J.H.1
Stephens, J.K.2
Rhead, W.J.3
Penn, D.4
Horwitz, A.L.5
Kirschner, B.S.6
Whitington, P.F.7
Berger, S.8
Tripp, M.E.9
-
25
-
-
0025025196
-
The long-chain acyl-CoA dehydrogenase deficiency
-
K. Tanaka and P. M. Coates, editors. Alan R. Liss Inc., New York
-
Hale, D. E., C. A. Stanley, and P. M. Coates. 1990. The long-chain acyl-CoA dehydrogenase deficiency. In Fatty Acid Oxidation: Clinical, Biochemical and Molecular Aspects. K. Tanaka and P. M. Coates, editors. Alan R. Liss Inc., New York. 303-311.
-
(1990)
Fatty Acid Oxidation: Clinical, Biochemical and Molecular Aspects
, pp. 303-311
-
-
Hale, D.E.1
Stanley, C.A.2
Coates, P.M.3
-
26
-
-
0025025197
-
Genetic defects of acyl-CoA dehydrogenases: Studies using an electron transfer flavoprotein reduction assay
-
K. Tanaka and P. M. Coates, editors. Alan R. Liss Inc., New York
-
Hale, D. E., C. A. Stanley, and P. M. Coates. 1990. Genetic defects of acyl-CoA dehydrogenases: studies using an electron transfer flavoprotein reduction assay. In Fatty Acid Oxidation: Clinical, Biochemical and Molecular Aspects. K. Tanaka and P. M. Coates, editors. Alan R. Liss Inc., New York. 333-348.
-
(1990)
Fatty Acid Oxidation: Clinical, Biochemical and Molecular Aspects
, pp. 333-348
-
-
Hale, D.E.1
Stanley, C.A.2
Coates, P.M.3
-
27
-
-
0009482260
-
Electrophoretic transfer of proteins from acrylamide gels to nitrocellulose sheet
-
Towbin, H., T. Staehelin, and J. Gordon. 1979. Electrophoretic transfer of proteins from acrylamide gels to nitrocellulose sheet. Proc. Natl. Acad. Sci. USA. 76:4350-4354.
-
(1979)
Proc. Natl. Acad. Sci. USA
, vol.76
, pp. 4350-4354
-
-
Towbin, H.1
Staehelin, T.2
Gordon, J.3
-
28
-
-
0027993542
-
Peroxisomal acyl-coenzyme A oxidase is a rate-limiting enzyme in a very-long-chain fatty acid β-oxidation system
-
Aoyama, T., M. Souri, T. Kamijo, S. Ushikubo, and T. Hashimoto. 1994. Peroxisomal acyl-coenzyme A oxidase is a rate-limiting enzyme in a very-long-chain fatty acid β-oxidation system. Biochem. Biophys. Res. Commun. 201:1541-1547.
-
(1994)
Biochem. Biophys. Res. Commun.
, vol.201
, pp. 1541-1547
-
-
Aoyama, T.1
Souri, M.2
Kamijo, T.3
Ushikubo, S.4
Hashimoto, T.5
-
29
-
-
0028229531
-
Rat very-long-chain acyl-CoA dehydrogenase, a novel mitochondrial acyl-CoA dehydrogenase gene product, is a rate-limiting enzyme in long-chain fatty acid β-oxidation system: CDNA and deduced amino acid sequence and distinct specificities of the cDNA-expressed protein
-
Aoyama, T., I. Ueno, T. Kamijo, and T. Hashimoto. 1994. Rat very-long-chain acyl-CoA dehydrogenase, a novel mitochondrial acyl-CoA dehydrogenase gene product, is a rate-limiting enzyme in long-chain fatty acid β-oxidation system: cDNA and deduced amino acid sequence and distinct specificities of the cDNA-expressed protein. J. Biol. Chem. 269:19088-19094.
-
(1994)
J. Biol. Chem.
, vol.269
, pp. 19088-19094
-
-
Aoyama, T.1
Ueno, I.2
Kamijo, T.3
Hashimoto, T.4
-
30
-
-
0019742255
-
Purification and properties of rat liver acyl-CoA dehydrogenases and electron transfer flavoprotein
-
Furuta, S., S. Miyazawa, and T. Hashimoto. 1981. Purification and properties of rat liver acyl-CoA dehydrogenases and electron transfer flavoprotein. J. Biochem. 90:1739-1750.
-
(1981)
J. Biochem.
, vol.90
, pp. 1739-1750
-
-
Furuta, S.1
Miyazawa, S.2
Hashimoto, T.3
-
31
-
-
0025374115
-
An acyl-coenzyme A dehydrogenase assay utilizing the ferricenium ion
-
Lehman, T. C., D. E. Hale, A. Bhala, and C. Thorpe. 1990. An acyl-coenzyme A dehydrogenase assay utilizing the ferricenium ion. Anal. Biochem. 186:280-284.
-
(1990)
Anal. Biochem.
, vol.186
, pp. 280-284
-
-
Lehman, T.C.1
Hale, D.E.2
Bhala, A.3
Thorpe, C.4
-
32
-
-
49749184695
-
The microestimation of succinate and the extinction coefficient of cytochrome c
-
Massey, V. 1959. The microestimation of succinate and the extinction coefficient of cytochrome c. Biochim. Biophys. Acta. 34:255-256.
-
(1959)
Biochim. Biophys. Acta
, vol.34
, pp. 255-256
-
-
Massey, V.1
-
33
-
-
0026690145
-
Peroxisomal and mitochondrial enzymes
-
P. M. Coates and K. Tanaka, editors. Wiley-Liss, Inc., New York
-
Hashimoto, T. 1992. Peroxisomal and mitochondrial enzymes. In New Developments in Fatty Acid Oxidation. P. M. Coates and K. Tanaka, editors. Wiley-Liss, Inc., New York. 19-32.
-
(1992)
New Developments in Fatty Acid Oxidation
, pp. 19-32
-
-
Hashimoto, T.1
-
34
-
-
0021970335
-
Purification and characterization of short-chain, medium-chain, and long-chain acyl-CoA dehydrogenases from rat liver mitochondria: Isolation of the holo- And apoenzymes and conversion of the apoenzyme to the holoenzyme
-
Ikeda, Y., K. Okamura-Ikeda, and K. Tanaka. 1985. Purification and characterization of short-chain, medium-chain, and long-chain acyl-CoA dehydrogenases from rat liver mitochondria: isolation of the holo- and apoenzymes and conversion of the apoenzyme to the holoenzyme. J. Biol. Chem. 260.1311-1325.
-
(1985)
J. Biol. Chem.
, vol.260
, pp. 1311-1325
-
-
Ikeda, Y.1
Okamura-Ikeda, K.2
Tanaka, K.3
-
35
-
-
0028353551
-
Mitochondrial trifunctional protein deficiency: Catalytic heterogeneity of the mutant enzyme in two patients
-
Kamijo, T., R. J. A. Wanders, J. M. Saudubray, T. Aoyama, A. Komiyama, and T. Hashimoto. 1994. Mitochondrial trifunctional protein deficiency: catalytic heterogeneity of the mutant enzyme in two patients. J. Clin. Invest. 93:1740-1747.
-
(1994)
J. Clin. Invest.
, vol.93
, pp. 1740-1747
-
-
Kamijo, T.1
Wanders, R.J.A.2
Saudubray, J.M.3
Aoyama, T.4
Komiyama, A.5
Hashimoto, T.6
-
36
-
-
0021111556
-
Separation and properties of five distinct acyl-CoA dehydrogenases from rat liver mitochondria: Identification of a new 2-methyl branched chain acyl-CoA dehydrogenase
-
Ikeda, Y., C. Dabrowski, and K. Tanaka. 1983. Separation and properties of five distinct acyl-CoA dehydrogenases from rat liver mitochondria: identification of a new 2-methyl branched chain acyl-CoA dehydrogenase. J. Biol. Chem. 258:1066-1076.
-
(1983)
J. Biol. Chem.
, vol.258
, pp. 1066-1076
-
-
Ikeda, Y.1
Dabrowski, C.2
Tanaka, K.3
-
37
-
-
0027404491
-
Very long chain acyl-CoA dehydrogenase deificiency: Identification of a new inborn error of mitochondrial fatty acid oxidation in fibroblasts
-
Bertand, C., C. Largilliere, M. T. Zabot, M. Mathieu, and C. Vianey-Saban. 1993. Very long chain acyl-CoA dehydrogenase deificiency: identification of a new inborn error of mitochondrial fatty acid oxidation in fibroblasts. Biochem. Biophys. Acta. 1180:327-329.
-
(1993)
Biochem. Biophys. Acta
, vol.1180
, pp. 327-329
-
-
Bertand, C.1
Largilliere, C.2
Zabot, M.T.3
Mathieu, M.4
Vianey-Saban, C.5
-
38
-
-
0019830914
-
Systemic carnitine deficiency presenting as endocardial fibroelastosis: A treatable cardiomyopathy
-
Tripp, M. E., M. L. Katcher, H. A. Peters, E. F. Gilbert, S. Arya, R. J. Hodach, and A. L. Shug. 1981. Systemic carnitine deficiency presenting as endocardial fibroelastosis: a treatable cardiomyopathy. N. Engl. J. Med. 305:385-390.
-
(1981)
N. Engl. J. Med.
, vol.305
, pp. 385-390
-
-
Tripp, M.E.1
Katcher, M.L.2
Peters, H.A.3
Gilbert, E.F.4
Arya, S.5
Hodach, R.J.6
Shug, A.L.7
-
39
-
-
0025995690
-
Chronic cardiomyopathy and weakness or acute coma in children with a defect in carnitine uptake
-
Stanley, C. A., S. DeLeeuw, P. M. Coates, C. Vianey-Liaud, P. Divry, J. P. Bonnefont, J. M. Saudubray, M. Haymond, F. K. Trefz, G. N. Bremingstall, et al. 1991. Chronic cardiomyopathy and weakness or acute coma in children with a defect in carnitine uptake. Ann. Neurol. 30:700-716.
-
(1991)
Ann. Neurol.
, vol.30
, pp. 700-716
-
-
Stanley, C.A.1
DeLeeuw, S.2
Coates, P.M.3
Vianey-Liaud, C.4
Divry, P.5
Bonnefont, J.P.6
Saudubray, J.M.7
Haymond, M.8
Trefz, F.K.9
Bremingstall, G.N.10
-
40
-
-
0026715669
-
Approach to the patient with a fatty acid oxidation disorder
-
P. M. Coates and K. Tanaka, editors. Wiley-Liss, Inc., New York
-
Saudubray, J. M., G. Mitchell, J. P. Bonnefont, G. Schwartz, C. Nuttin, A. Munnich, M. Brivet, A. Vassault, F. Demaugre, D. Rabier, and C. Charpentier. 1992. Approach to the patient with a fatty acid oxidation disorder. In New Developments in Fatty Acid Oxidation. P. M. Coates and K. Tanaka, editors. Wiley-Liss, Inc., New York. 271-288.
-
(1992)
New Developments in Fatty Acid Oxidation
, pp. 271-288
-
-
Saudubray, J.M.1
Mitchell, G.2
Bonnefont, J.P.3
Schwartz, G.4
Nuttin, C.5
Munnich, A.6
Brivet, M.7
Vassault, A.8
Demaugre, F.9
Rabier, D.10
Charpentier, C.11
-
41
-
-
0024246260
-
Primary carnitine deficiency due to a failure of carnitine transport in kidney, muscle, and fibroblasts
-
Treem, W. R., C. A. Stanley, D. N. Finegold, D. E. Hale, and P. M. Coates. 1988. Primary carnitine deficiency due to a failure of carnitine transport in kidney, muscle, and fibroblasts. N. Engl. J. Med. 319:1331-1336.
-
(1988)
N. Engl. J. Med.
, vol.319
, pp. 1331-1336
-
-
Treem, W.R.1
Stanley, C.A.2
Finegold, D.N.3
Hale, D.E.4
Coates, P.M.5
-
42
-
-
0025906746
-
Infantile form of carnitine palmitoyltransferase II deficiency with hepatomuscular symptoms and sudden death
-
Demaugre, F., J. P. Bonnefont, M. Colonna, C. Cepanec, J. P. Leroux, and J. M. Saudubray. 1991. Infantile form of carnitine palmitoyltransferase II deficiency with hepatomuscular symptoms and sudden death. J. Clin. Invest. 87:859-864.
-
(1991)
J. Clin. Invest.
, vol.87
, pp. 859-864
-
-
Demaugre, F.1
Bonnefont, J.P.2
Colonna, M.3
Cepanec, C.4
Leroux, J.P.5
Saudubray, J.M.6
-
43
-
-
0024551414
-
Prophylaxis of early ventricular fibrillation by inhibition of acylcarnitine accumulation
-
Corr, P. B., M. H. Creer, K. A. Yamada, J. E. Saffitz, and B. E. Sobel. 1989. Prophylaxis of early ventricular fibrillation by inhibition of acylcarnitine accumulation. J. Clin. Invest. 83:927-936.
-
(1989)
J. Clin. Invest.
, vol.83
, pp. 927-936
-
-
Corr, P.B.1
Creer, M.H.2
Yamada, K.A.3
Saffitz, J.E.4
Sobel, B.E.5
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