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Results: 26-31/31
Authors:
Wilichowski, E
Pouwels, PJW
Frahm, J
Hanefeld, F
Citation: E. Wilichowski et al., Quantitative proton magnetic resonance spectroscopy of cerebral metabolic disturbances in patients with MELAS, NEUROPEDIAT, 30(5), 1999, pp. 256-263
Authors:
Borchert, A
Wilichowski, E
Hanefeld, F
Citation: A. Borchert et al., Supplementation with creatine monohydrate in children with mitochondrial encephalomyopathies, MUSCLE NERV, 22(9), 1999, pp. 1299-1300
Authors:
Pouwels, PJW
Brockmann, K
Kruse, B
Wilken, B
Wick, M
Hanefeld, F
Frahm, J
Citation: Pjw. Pouwels et al., Regional age dependence of human brain metabolites from infancy to adulthood as detected by quantitative localized proton MRS, PEDIAT RES, 46(4), 1999, pp. 474-485
Authors:
Pelin, K
Hilpela, P
Donner, K
Sewry, C
Akkari, PA
Wilton, SD
Wattanasirichaigoon, D
Bang, ML
Centner, T
Hanefeld, F
Odent, S
Fardeau, M
Urtizberea, JA
Muntoni, F
Dubowitz, V
Beggs, AH
Laing, NG
Labeit, S
de la Chapelle, A
Wallgren-Pettersson, C
Citation: K. Pelin et al., Mutations in the nebulin gene associated with autosomal recessive nemalinemyopathy, P NAS US, 96(5), 1999, pp. 2305-2310
Authors:
Wilichowski, E
Ohlenbusch, A
Hanefeld, F
Citation: E. Wilichowski et al., Characterization of the mitochondrial genome in childhood multiple sclerosis II. Multiple sclerosis without optic neuritis and LHON-associated genes, NEUROPEDIAT, 29(6), 1998, pp. 307-312
Authors:
Ohlenbusch, A
Wilichowski, E
Hanefeld, F
Citation: A. Ohlenbusch et al., Characterization of the mitochondrial genome in childhood multiple sclerosis III. Multiple sclerosis without optic neuritis and the non-LHON-associated genes, NEUROPEDIAT, 29(6), 1998, pp. 313-319