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Results:
1-12
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Results: 12
Authors:
Cox, KB
Hamm, DA
Millington, DS
Matern, D
Vockley, J
Rinaldo, P
Pinkert, CA
Rhead, WJ
Lindsey, JR
Wood, PA
Citation: Kb. Cox et al., 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 GEN, 10(19), 2001, pp. 2069-2077
Authors:
Smith, WE
Millington, DS
Koeberl, DD
Lesser, PS
Citation: We. Smith et al., Glutaric acidemia, type I, missed by newborn screening in an infant with dystonia following promethazine administration, PEDIATRICS, 107(5), 2001, pp. 1184-1187
Authors:
Matern, D
Hart, P
Murtha, AP
Vockley, J
Gregersen, N
Millington, DS
Treem, WR
Citation: D. Matern et al., Acute fatty liver of pregnancy associated with short-chain acyl-coenzyme Adehydrogenase deficiency, J PEDIAT, 138(4), 2001, pp. 585-588
Authors:
Center, SA
Harte, J
Watrous, D
Reynolds, A
Watson, TDG
Markwell, PJ
Millington, DS
Wood, PA
Yeager, AE
Erb, HN
Citation: Sa. Center et al., The clinical and metabolic effects of rapid weight loss in obese pet cats and the influence of supplemental oral L-carnitine, J VET INT M, 14(6), 2000, pp. 598-608
Authors:
Van Hove, JLK
Kahler, SG
Feezor, MD
Ramakrishna, JP
Hart, P
Treem, WR
Shen, JJ
Matern, D
Millington, DS
Citation: Jlk. Van Hove et al., Acylcarnitines in plasma and blood spots of patients with long-chain 3-hydroxyacyl-coenzyme A dehydrogenase defiency, J INH MET D, 23(6), 2000, pp. 571-582
Authors:
Shen, JJ
Matern, D
Millington, DS
Hillman, S
Feezor, MD
Bennett, MJ
Qumsiyeh, M
Kahler, SG
Chen, YT
Van Hove, JLK
Citation: Jj. Shen et al., Acylcarnitines in fibroblasts of patients with long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency and other fatty acid oxidation disorders, J INH MET D, 23(1), 2000, pp. 27-44
Authors:
Stevens, RD
Hillman, SL
Worthy, S
Sanders, D
Millington, DS
Citation: Rd. Stevens et al., Assay for free and total carnitine in human plasma using tandem mass spectrometry, CLIN CHEM, 46(5), 2000, pp. 727-729
Authors:
An, Y
Young, SP
Hillman, SL
Van Hove, JLK
Chen, YT
Millington, DS
Citation: Y. An et al., Liquid chromatographic assay for a glucose tetrasaccharide, a putative biomarker for the diagnosis of Pompe disease, ANALYT BIOC, 287(1), 2000, pp. 136-143
Authors:
Rose, M
Matern, D
Millington, DS
Lehnert, W
Citation: M. Rose et al., Untypical case of multiple acyl-CoA-dehydrogenase deficiency, KLIN PADIAT, 211(5), 1999, pp. 413-416
Authors:
Ahmad, A
Kahler, SG
Kishnani, PS
Artigas-Lopez, M
Pappu, AS
Steiner, R
Millington, DS
Van Hove, JLK
Citation: A. Ahmad et al., Treatment of pyruvate carboxylase deficiency with high doses of citrate and aspartate, AM J MED G, 87(4), 1999, pp. 331-338
Authors:
Matern, D
Strauss, AW
Hillman, SL
Mayatepek, E
Millington, DS
Trefz, FK
Citation: D. Matern et al., Diagnosis of mitochondrial trifunctional protein deficiency in a blood spot from the newborn screening card by tandem mass spectrometry and DNA analysis, PEDIAT RES, 46(1), 1999, pp. 45-49
Authors:
Kurtz, DM
Rinaldo, P
Rhead, WJ
Tian, LQ
Millington, DS
Vockley, J
Hamm, DA
Brix, AE
Lindsey, JR
Pinkert, CA
O'Brien, WE
Wood, PA
Citation: Dm. Kurtz et al., Targeted disruption of mouse long-chain acyl-CoA dehydrogenase gene reveals crucial roles for fatty acid oxidation, P NAS US, 95(26), 1998, pp. 15592-15597
Risultati:
1-12
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