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Results:
1-11
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Results: 11
Authors:
Oexle, K
Kohlschutter, A
Citation: K. Oexle et A. Kohlschutter, Cause of progression in Duchenne muscular dystrophy: Impaired differentiation more probable than replicative aging, NEUROPEDIAT, 32(3), 2001, pp. 123-129
Authors:
Durken, M
Herrnring, C
Finckh, B
Nagel, S
Nielsen, P
Fischer, R
Berger, HM
Moison, RMW
Pichlmeier, U
Kohlschutter, B
Zander, AR
Kohlschutter, A
Citation: M. Durken et al., Impaired plasma antioxidative defense and increased nontransferrin-bound iron during high-dose chemotherapy and radiochemotherapy preceding bone marrow transplantation, FREE RAD B, 28(6), 2000, pp. 887-894
Authors:
Schuelke, M
Elsner, A
Finckh, B
Kohlschutter, A
Hubner, C
Brigelius-Flohe, R
Citation: M. Schuelke et al., Urinary alpha-tocopherol metabolites in alpha-tocopherol transfer protein-deficient patients, J LIPID RES, 41(10), 2000, pp. 1543-1551
Authors:
Das, AM
Jolly, RD
Kohlschutter, A
Citation: Am. Das et al., Anomalies of mitochondrial ATP synthase regulation in four different typesof neuronal ceroid lipofuscinosis, MOL GEN MET, 66(4), 1999, pp. 349-355
Authors:
Goebel, HH
Schochet, SS
Jaynes, M
Bruck, W
Kohlschutter, A
Hentati, F
Citation: Hh. Goebel et al., Progress in neuropathology of the neuronal ceroid lipofuscinoses, MOL GEN MET, 66(4), 1999, pp. 367-372
Authors:
Hofman, I
Kohlschutter, A
Santavuori, P
Gottlob, I
Goebel, HH
Lake, BD
Schutgens, RBH
Greene, NDE
Leung, KY
Mitchison, HM
Munroe, PB
Taschner, PEM
Citation: I. Hofman et al., Juvenile NCL, BIOM HLTH R, 33, 1999, pp. 55-76
Authors:
Kohlschutter, A
Lake, BD
Citation: A. Kohlschutter et Bd. Lake, NCL variants without genetic assignment, BIOM HLTH R, 33, 1999, pp. 125-127
Authors:
Williams, RE
Kohlschutter, A
Santavuori, P
Mole, SE
Lake, BD
Citation: Re. Williams et al., NCL diagnostic algorithms, BIOM HLTH R, 33, 1999, pp. 149-151
Authors:
Cossee, M
Durr, A
Schmitt, M
Dahl, N
Trouillas, P
Allinson, P
Kostrzewa, M
Nivelon-Chevallier, A
Gustavson, KH
Kohlschutter, A
Muller, U
Mandel, JL
Brice, A
Koenig, M
Cavalcanti, F
Tammaro, A
De Michele, G
Filla, A
Cocozza, S
Labuda, M
Montermini, L
Poirier, J
Pandolfo, M
Citation: M. Cossee et al., Friedreich's ataxia: Point mutations and clinical presentation of compoundheterozygotes, ANN NEUROL, 45(2), 1999, pp. 200-206
Authors:
Steen, C
Baumgartner, ER
Duran, M
Lehnert, W
Suormala, T
Fingerhut, R
Stehn, M
Kohlschutter, A
Citation: C. Steen et al., Metabolic stroke in isolated 3-methylcrotonyl-CoA carboxylase deficiency, EUR J PED, 158(9), 1999, pp. 730-733
Authors:
Finckh, B
Kontush, A
Commentz, J
Hubner, C
Burdelski, M
Kohlschutter, A
Citation: B. Finckh et al., High-performance liquid chromatography coulometric electrochemical detection of ubiquinol 10, ubiquinone 10, carotenoids, and tocopherols in neonatalplasma, METH ENZYM, 299, 1999, pp. 341-348
Risultati:
1-11
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