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Results: 1-13 |
Results: 13
Mitochondrial DNA depletion associated with partial complex II and IV deficiencies and 3-methylglutaconic aciduria
Authors: Scaglia, F Sutton, VR Bodamer, OAF Vogel, H Shapira, SK Naviaux, RK Vladutiu, GD
Citation: F. Scaglia et al., Mitochondrial DNA depletion associated with partial complex II and IV deficiencies and 3-methylglutaconic aciduria, J CHILD NEU, 16(2), 2001, pp. 136-138
Atypical presentation of Amniotic Band Sequence
Authors: Bodamer, OAF Popek, EJ Bacino, C
Citation: Oaf. Bodamer et al., Atypical presentation of Amniotic Band Sequence, AM J MED G, 100(2), 2001, pp. 100-102
Adult-onset combined methylmalonic aciduria and homocystinuria (cblC)
Authors: Bodamer, OAF Rosenblatt, DS Appel, SH Beaudet, AL
Citation: Oaf. Bodamer et al., Adult-onset combined methylmalonic aciduria and homocystinuria (cblC), NEUROLOGY, 56(8), 2001, pp. 1113-1113
Uses of stable isotopes in clinical diagnosis and research in the paediatric population
Authors: Bodamer, OAF Halliday, D
Citation: Oaf. Bodamer et D. Halliday, Uses of stable isotopes in clinical diagnosis and research in the paediatric population, ARCH DIS CH, 84(5), 2001, pp. 444-448
Deletion (9) (p13.1 p21.1)
Authors: Scaglia, F Bodamer, OAF Berend, SA Adam, LR Shaffer, LG
Citation: F. Scaglia et al., Deletion (9) (p13.1 p21.1), AM J MED G, 91(2), 2000, pp. 113-115
Protein, glucose and energy metabolism in Gaucher disease type I (vol 23, pg 86, 2000)
Authors: Bodamer, OAF Vellodi, A
Citation: Oaf. Bodamer et A. Vellodi, Protein, glucose and energy metabolism in Gaucher disease type I (vol 23, pg 86, 2000), J INH MET D, 23(5), 2000, pp. 474-474
Psychiatric symptoms of inherited metabolic disease
Authors: Estrov, Y Scaglia, F Bodamer, OAF
Citation: Y. Estrov et al., Psychiatric symptoms of inherited metabolic disease, J INH MET D, 23(1), 2000, pp. 2-6
Protein, glucose and energy metabolism in Gaucher disease type I
Authors: Bodamer, OAF Vellodi, A
Citation: Oaf. Bodamer et A. Vellodi, Protein, glucose and energy metabolism in Gaucher disease type I, J INH MET D, 23(1), 2000, pp. 86-87
The effects of L-alanine supplementation in late-onset glycogen storage disease type II
Authors: Bodamer, OAF Halliday, D Leonard, JV
Citation: Oaf. Bodamer et al., The effects of L-alanine supplementation in late-onset glycogen storage disease type II, NEUROLOGY, 55(5), 2000, pp. 710-712
Resting energy expenditure in disorders of propionate metabolism
Authors: Feillet, F Bodamer, OAF Dixon, MA Sequeira, S Leonard, JV
Citation: F. Feillet et al., Resting energy expenditure in disorders of propionate metabolism, J PEDIAT, 136(5), 2000, pp. 659-663
Measurement of carbon dioxide production in very low birth weight babies
Authors: Kingdon, CC Mitchell, F Bodamer, OAF Williams, AF
Citation: Cc. Kingdon et al., Measurement of carbon dioxide production in very low birth weight babies, ARCH DIS CH, 83(1), 2000, pp. F50-F55
Importance of measuring plasma cholesterol precursors
Authors: Bodamer, OAF Craigen, WJ
Citation: Oaf. Bodamer et Wj. Craigen, Importance of measuring plasma cholesterol precursors, AM J MED G, 82(2), 1999, pp. 199-199
Sublingual therapy for cobalamin deficiency
Authors: Bodamer, OAF Scaglia, F
Citation: Oaf. Bodamer et F. Scaglia, Sublingual therapy for cobalamin deficiency, LANCET, 354(9189), 1999, pp. 1562-1562
Risultati: 1-13 |