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Results:
1-7
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Results: 7
Authors:
Dipchand, AI
Tein, I
Robinson, B
Benson, LN
Citation: Ai. Dipchand et al., Maternally inherited hypertrophic cardiomyopathy: A manifestation of mitochondrial DNA mutations - Clinical course in two families, PEDIAT CARD, 22(1), 2001, pp. 14-22
Authors:
Tein, I
Citation: I. Tein, Metabolic disease in the fetus predisposes to maternal hepatic complications of pregnancy, PEDIAT RES, 47(1), 2000, pp. 6-8
Authors:
Raha, S
Merante, F
Shoubridge, E
Myint, AT
Tein, I
Benson, L
Johns, T
Robinson, BH
Citation: S. Raha et al., Repopulation of rho(0) cells with mitochondria from a patient with a mitochondrial DNA point mutation in tRNA(Gly) results in respiratory chain dysfunction, HUM MUTAT, 13(3), 1999, pp. 245-254
Authors:
Tein, I
Citation: I. Tein, Neonatal metabolic myopathies, SEM PERINAT, 23(2), 1999, pp. 125-151
Authors:
Tein, I
Vajsar, J
MacMillan, L
Sherwood, WG
Citation: I. Tein et al., Long-chain L-3-hydroxyacyl-coenzyme A dehydrogenase deficiency neuropathy:Response to cod liver oil, NEUROLOGY, 52(3), 1999, pp. 640-643
Authors:
Tein, I
Haslam, RHA
Rhead, WJ
Bennett, MJ
Becker, LE
Vockley, J
Citation: I. Tein et al., Short-chain acyl-CoA dehydrogenase deficiency - A cause of ophthalmoplegiaand multicore myopathy, NEUROLOGY, 52(2), 1999, pp. 366-372
Authors:
Lamhonwah, AM
Tein, I
Citation: Am. Lamhonwah et I. Tein, GFP-human high-affinity carnitine transporter OCTN2 protein: Subcellular localization and functional restoration of carnitine uptake in mutant cell lines with the carnitine transporter defect, BIOC BIOP R, 264(3), 1999, pp. 909-914
Risultati:
1-7
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