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Results: 1-6 |
Results: 6

Authors: Koeppen, AH Dickson, AC
Citation: Ah. Koeppen et Ac. Dickson, Iron in the Hallervorden-Spatz syndrome, PED NEUROL, 25(2), 2001, pp. 148-155

Authors: Koeppen, AH
Citation: Ah. Koeppen, Untitled, J NEUR SCI, 187(1-2), 2001, pp. 107-107

Authors: Coffeen, CM McKenna, CE Koeppen, AH Plaster, NM Maragakis, N Mihalopoulos, J Schwankhaus, JD Flanigang, KM Gregg, RG Ptacek, LJ Fu, YH
Citation: Cm. Coffeen et al., Genetic localization of an autosomal dominant leukodystrophy mimicking chronic progressive multiple sclerosis to chromosome 5q31, HUM MOL GEN, 9(5), 2000, pp. 787-793

Authors: Koeppen, AH
Citation: Ah. Koeppen, Untitled, J NEUR SCI, 163(1), 1999, pp. 4-5

Authors: Koeppen, AH Dickson, AC Lamarche, JB Robitaille, Y
Citation: Ah. Koeppen et al., Synapses in the hereditary ataxias, J NE EXP NE, 58(7), 1999, pp. 748-764

Authors: Uemichi, T Uitti, RJ Koeppen, AH Donat, JR Benson, MD
Citation: T. Uemichi et al., Oculoleptomeningeal amyloidosis associated with a new transthyretin variant Ser64, ARCH NEUROL, 56(9), 1999, pp. 1152-1155
Risultati: 1-6 |