-
1
-
-
0031914110
-
Simultaneous analysis of plasma free fatty acids and their 3-hydroxy analogs in fatty acid β-oxidation disorders
-
Costa C.G., Dorland L., Holwerda U., de Almeida I.T., Poll-The B.T., Jakobs C., Duran M. Simultaneous analysis of plasma free fatty acids and their 3-hydroxy analogs in fatty acid β-oxidation disorders. Clin. Chem. 44:1998;463-471.
-
(1998)
Clin. Chem.
, vol.44
, pp. 463-471
-
-
Costa, C.G.1
Dorland, L.2
Holwerda, U.3
De Almeida, I.T.4
Poll-The, B.T.5
Jakobs, C.6
Duran, M.7
-
2
-
-
0033801802
-
Acylcarnitines in plasma and blood spots of patients with long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency
-
Van Hove J.L., Kahler S.G., Feezor M.D., Ramakrishna J.P., Hart P., Treem W.R., Shen J.J., Matern D., Millington D.S. Acylcarnitines in plasma and blood spots of patients with long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency. J. Inherit. Metab. Dis. 23:2000;571-582.
-
(2000)
J. Inherit. Metab. Dis.
, vol.23
, pp. 571-582
-
-
Van Hove, J.L.1
Kahler, S.G.2
Feezor, M.D.3
Ramakrishna, J.P.4
Hart, P.5
Treem, W.R.6
Shen, J.J.7
Matern, D.8
Millington, D.S.9
-
3
-
-
0033004986
-
Recognition and management of fatty acid oxidation defects: A series of 107 patients
-
Saudubray J.M., Martin D., de Lonlay P., Touati G., Poggi-Travert F., Bonnet D., Jouvet P., Boutron M., Slama A., Vianey-Saban C., Bonnefont J.P., Rabier D., Kamoun P., Brivet M. Recognition and management of fatty acid oxidation defects: a series of 107 patients. J. Inherit. Metab. Dis. 22:1999;488-502.
-
(1999)
J. Inherit. Metab. Dis.
, vol.22
, pp. 488-502
-
-
Saudubray, J.M.1
Martin, D.2
De Lonlay, P.3
Touati, G.4
Poggi-Travert, F.5
Bonnet, D.6
Jouvet, P.7
Boutron, M.8
Slama, A.9
Vianey-Saban, C.10
Bonnefont, J.P.11
Rabier, D.12
Kamoun, P.13
Brivet, M.14
-
4
-
-
0032957435
-
Dietary management of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency (LCHADD). A case report and survey
-
Gillingham M., Van Calcar S.C., Ney D.M., Wolff J., Harding C.O. Dietary management of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency (LCHADD). A case report and survey. J. Inherit. Metab. Dis. 22:1999;123-131.
-
(1999)
J. Inherit. Metab. Dis.
, vol.22
, pp. 123-131
-
-
Gillingham, M.1
Van Calcar, S.C.2
Ney, D.M.3
Wolff, J.4
Harding, C.O.5
-
5
-
-
0033519714
-
A fetal fatty-acid oxidation disorder as a cause of liver disease in pregnant women
-
Ibdah J.A., Bennett M.J., Rinaldo P., Zhao Y., Gibson B., Sims H.F., Strauss A.W. A fetal fatty-acid oxidation disorder as a cause of liver disease in pregnant women. N. Engl. J. Med. 340:1999;1723-1731.
-
(1999)
N. Engl. J. Med.
, vol.340
, pp. 1723-1731
-
-
Ibdah, J.A.1
Bennett, M.J.2
Rinaldo, P.3
Zhao, Y.4
Gibson, B.5
Sims, H.F.6
Strauss, A.W.7
-
6
-
-
0028888960
-
The molecular basis of pediatric long chain 3-hydroxyacyl-CoA dehydrogenase deficiency associated with maternal acute fatty liver of pregnancy
-
Sims H.F., Brackett J.C., Powell C.K., Treem W.R., Hale D.E., Bennett M.J., Gibson B., Shapiro S., Strauss A.W. The molecular basis of pediatric long chain 3-hydroxyacyl-CoA dehydrogenase deficiency associated with maternal acute fatty liver of pregnancy. Proc. Natl. Acad. Sci. USA. 92:1995;841-845.
-
(1995)
Proc. Natl. Acad. Sci. USA
, vol.92
, pp. 841-845
-
-
Sims, H.F.1
Brackett, J.C.2
Powell, C.K.3
Treem, W.R.4
Hale, D.E.5
Bennett, M.J.6
Gibson, B.7
Shapiro, S.8
Strauss, A.W.9
-
7
-
-
0028013251
-
Acute fatty liver of pregnancy and long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency
-
Treem W.R., Rinaldo P., Hale D.E., Stanley C.A., Millington D.S., Hyams J.S., Jackson S., Turnbull D.M. Acute fatty liver of pregnancy and long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency. Hepatology. 19:1994;339-345.
-
(1994)
Hepatology
, vol.19
, pp. 339-345
-
-
Treem, W.R.1
Rinaldo, P.2
Hale, D.E.3
Stanley, C.A.4
Millington, D.S.5
Hyams, J.S.6
Jackson, S.7
Turnbull, D.M.8
-
8
-
-
0035718040
-
Quantitative determination of plasma c8-c26 total fatty acids for the biochemical diagnosis of nutritional and metabolic disorders
-
Lagerstedt S.A., Hinrichs D.R., Batt S.M., Magera M.J., Rinaldo P., McConnell J.P. Quantitative determination of plasma c8-c26 total fatty acids for the biochemical diagnosis of nutritional and metabolic disorders. Mol. Genet. Metab. 73:2001;38-45.
-
(2001)
Mol. Genet. Metab.
, vol.73
, pp. 38-45
-
-
Lagerstedt, S.A.1
Hinrichs, D.R.2
Batt, S.M.3
Magera, M.J.4
Rinaldo, P.5
McConnell, J.P.6
-
9
-
-
0021186576
-
Will dietary ω-3 fatty acids change the composition of human milk?
-
Harris W.S., Connor W.E., Lindsey S. Will dietary ω-3 fatty acids change the composition of human milk? Am. J. Clin. Nutr. 40:1984;780-785.
-
(1984)
Am. J. Clin. Nutr.
, vol.40
, pp. 780-785
-
-
Harris, W.S.1
Connor, W.E.2
Lindsey, S.3
-
11
-
-
0034782503
-
Gestational, pathologic and biochemical differences between very long-chain acyl-CoA dehydrogenase deficiency and long-chain acyl-CoA dehydrogenase deficiency in the mouse
-
Cox K.B., Hamm D.A., Millington D.S., Matern D., Vockley J., Rinaldo P., Pinkert C.A., Rhead W.J., Lindsey J.R., Wood P.A. Gestational, pathologic and biochemical differences between very long-chain acyl-CoA dehydrogenase deficiency and long-chain acyl-CoA dehydrogenase deficiency in the mouse. Hum. Mol. Genet. 10:2001;2069-2077.
-
(2001)
Hum. Mol. Genet.
, vol.10
, pp. 2069-2077
-
-
Cox, K.B.1
Hamm, D.A.2
Millington, D.S.3
Matern, D.4
Vockley, J.5
Rinaldo, P.6
Pinkert, C.A.7
Rhead, W.J.8
Lindsey, J.R.9
Wood, P.A.10
-
13
-
-
0031710569
-
Dietary sources of nutrients among US children, 1989-1991
-
Subar A.F., Krebs-Smith S.M., Cook A., Kahle L.L. Dietary sources of nutrients among US children, 1989-1991. Pediatrics. 102:1998;913-923.
-
(1998)
Pediatrics
, vol.102
, pp. 913-923
-
-
Subar, A.F.1
Krebs-Smith, S.M.2
Cook, A.3
Kahle, L.L.4
-
14
-
-
0033956203
-
Acylcarnitines in fibroblasts of patients with long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency and other fatty acid oxidation disorders
-
Shen J.J., Matern D., Millington D.S., Hillman S., Feezor M.D., Bennett M.J., Qumsiyeh M., Kahler S.G., Chen Y.T., Van Hove J.L. Acylcarnitines in fibroblasts of patients with long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency and other fatty acid oxidation disorders. J. Inherit. Metab. Dis. 23:2000;27-44.
-
(2000)
J. Inherit. Metab. Dis.
, vol.23
, pp. 27-44
-
-
Shen, J.J.1
Matern, D.2
Millington, D.S.3
Hillman, S.4
Feezor, M.D.5
Bennett, M.J.6
Qumsiyeh, M.7
Kahler, S.G.8
Chen, Y.T.9
Van Hove, J.L.10
-
15
-
-
0022506829
-
Diet-induced essential fatty acid deficiency in ambulatory patient with type I diabetes mellitus
-
Piper C.M., Carroll P.B., Dunn F.L. Diet-induced essential fatty acid deficiency in ambulatory patient with type I diabetes mellitus. Diab. Care. 9:1986;291-293.
-
(1986)
Diab. Care
, vol.9
, pp. 291-293
-
-
Piper, C.M.1
Carroll, P.B.2
Dunn, F.L.3
-
16
-
-
0026468949
-
First year growth of preterm infants fed standard compared to marine oil n-3 supplemented formula
-
Carlson S.E., Cooke R.J., Werkman S.H., Tolley E.A. First year growth of preterm infants fed standard compared to marine oil. n-3 supplemented formula Lipids. 27:1992;901-907.
-
(1992)
Lipids
, vol.27
, pp. 901-907
-
-
Carlson, S.E.1
Cooke, R.J.2
Werkman, S.H.3
Tolley, E.A.4
-
17
-
-
0033038553
-
Docosahexaenoic acid and retinal function in children with long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency
-
Harding C.O., Gillingham M.B., van Calcar S.C., Wolff J.A., Verhoeve J.N., Mills M.D. Docosahexaenoic acid and retinal function in children with long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency. J. Inherit. Metab. Dis. 22:1999;276-280.
-
(1999)
J. Inherit. Metab. Dis.
, vol.22
, pp. 276-280
-
-
Harding, C.O.1
Gillingham, M.B.2
Van Calcar, S.C.3
Wolff, J.A.4
Verhoeve, J.N.5
Mills, M.D.6
-
18
-
-
0026023968
-
3-Hydroxydicarboxylic aciduria due to long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency associated with sudden neonatal death: Protective effect of medium-chain triglyceride treatment
-
Duran M., Wanders R.J., de Jager J.P., Dorland L., Bruinvis L., Ketting D., Ijlst L., van Sprang F.J. 3-Hydroxydicarboxylic aciduria due to long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency associated with sudden neonatal death: protective effect of medium-chain triglyceride treatment. Eur. J. Pediatr. 150:1991;190-195.
-
(1991)
Eur. J. Pediatr.
, vol.150
, pp. 190-195
-
-
Duran, M.1
Wanders, R.J.2
De Jager, J.P.3
Dorland, L.4
Bruinvis, L.5
Ketting, D.6
Ijlst, L.7
Van Sprang, F.J.8
-
19
-
-
0036071008
-
Treatment of cardiomyopathy and rhabdomyolysis in long-chain fat oxidation disorders using an anaplerotic odd-chain triglyceride
-
Roe C.R., Sweetman L., Roe D.S., David F., Brunengraber H. Treatment of cardiomyopathy and rhabdomyolysis in long-chain fat oxidation disorders using an anaplerotic odd-chain triglyceride. J. Clin. Invest. 110:2002;259-269.
-
(2002)
J. Clin. Invest.
, vol.110
, pp. 259-269
-
-
Roe, C.R.1
Sweetman, L.2
Roe, D.S.3
David, F.4
Brunengraber, H.5
-
20
-
-
0036140895
-
Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: Clinical presentation and follow-up of 50 patients
-
den Boer M.E., Wanders R.J., Morris A.A., Ijlst L., Heymans H.S., Wijburg F.A. Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: clinical presentation and follow-up of 50 patients. Pediatrics. 109:2002;99-104.
-
(2002)
Pediatrics
, vol.109
, pp. 99-104
-
-
Den Boer, M.E.1
Wanders, R.J.2
Morris, A.A.3
Ijlst, L.4
Heymans, H.S.5
Wijburg, F.A.6
-
21
-
-
0003598844
-
-
National Academy Press, Washington, DC
-
Food and Nutrition Board, National Institute of Medicine. Dietary Reference Intakes for Energy, Carbohydrate, Fiber, Fat, Fatty Acids, Cholesterol, Protein and Amino Acids (Macronutrients), National Academy Press, Washington, DC, 2002.
-
(2002)
Dietary Reference Intakes for Energy, Carbohydrate, Fiber, Fat, Fatty Acids, Cholesterol, Protein and Amino Acids (Macronutrients)
-
-
-
22
-
-
12444282175
-
Docosahexaenoic acid (DHA) supplementation does not prevent retinal degeneration in LCHAD deficiency
-
Harding C.O., Gillingham M., Connor W.E., Neuringer M., Weleber R.G. Docosahexaenoic acid (DHA) supplementation does not p+revent retinal degeneration in LCHAD deficiency. J. Inherit. Metab. Dis. 25:2002;71.
-
(2002)
J. Inherit. Metab. Dis.
, vol.25
, pp. 71
-
-
Harding, C.O.1
Gillingham, M.2
Connor, W.E.3
Neuringer, M.4
Weleber, R.G.5
|