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Results: 1-9 |
Results: 9
July 2001: 58-year-old man with a temporal bone mass - Diagnosis - Giant cholesterol granuloma of the petrous portion of the temporal bone with a small component of coexistent cholesteatoma
Authors: Havlik, DM Hart, BL Becher, MW
Citation: Dm. Havlik et al., July 2001: 58-year-old man with a temporal bone mass - Diagnosis - Giant cholesterol granuloma of the petrous portion of the temporal bone with a small component of coexistent cholesteatoma, BRAIN PATH, 12(1), 2002, pp. 133
Oculopharyngeal muscular dystrophy in Hispanic new Mexicans
Authors: Becher, MW Morrison, L Davis, LE Maki, WC King, MK Bicknell, JM Reinert, BL Bartolo, C Bear, DG
Citation: Mw. Becher et al., Oculopharyngeal muscular dystrophy in Hispanic new Mexicans, J AM MED A, 286(19), 2001, pp. 2437-2440
Sudden death due to primary diffuse leptomeningeal gliomatosis
Authors: Havlik, DM Becher, MW Nolte, KB
Citation: Dm. Havlik et al., Sudden death due to primary diffuse leptomeningeal gliomatosis, J FOREN SCI, 46(2), 2001, pp. 392-395
Mechanisms of neuronal death in Huntington's disease
Authors: Koliatsos, VE Portera-Cailliau, C Schilling, G Borchelt, DB Becher, MW Ross, CA
Citation: Ve. Koliatsos et al., Mechanisms of neuronal death in Huntington's disease, CONT NEUROS, 2001, pp. 93-111
Intranuclear inclusions in oculopharyngeal muscular dystrophy contain poly(A) binding protein 2
Authors: Becher, MW Kotzuk, JA Davis, LE Bear, DG
Citation: Mw. Becher et al., Intranuclear inclusions in oculopharyngeal muscular dystrophy contain poly(A) binding protein 2, ANN NEUROL, 48(5), 2000, pp. 812-815
Intranuclear inclusions and neuritic aggregates in transgenic mice expressing a mutant N-terminal fragment of huntingtin (vol 8, pg 397, 1999)
Authors: Schilling, G Becher, MW Sharp, AH Jinnah, HA Duan, K Kotzuk, JA Slunt, HH Ratovitski, T Cooper, JK Jenkins, NA Copeland, NG Price, DL Ross, CA Borchelt, DR
Citation: G. Schilling et al., Intranuclear inclusions and neuritic aggregates in transgenic mice expressing a mutant N-terminal fragment of huntingtin (vol 8, pg 397, 1999), HUM MOL GEN, 8(5), 1999, pp. 943-943
Intranuclear inclusions and neuritic aggregates in transgenic mice expressing a mutant N-terminal fragment of huntingtin
Authors: Schilling, G Becher, MW Sharp, AH Jinnah, HA Duan, K Kotzuk, JA Slunt, HH Ratovitski, T Cooper, JK Jenkins, NA Copeland, NG Price, DL Ross, CA Borchelt, DR
Citation: G. Schilling et al., Intranuclear inclusions and neuritic aggregates in transgenic mice expressing a mutant N-terminal fragment of huntingtin, HUM MOL GEN, 8(3), 1999, pp. 397-407
Kearns-Sayre syndrome with features of Pearson's marrow-pancreas syndrome and a novel 2905-base pair mitochondrial DNA deletion
Authors: Becher, MW Wills, ML Noll, WM Hurko, O Price, DL
Citation: Mw. Becher et al., Kearns-Sayre syndrome with features of Pearson's marrow-pancreas syndrome and a novel 2905-base pair mitochondrial DNA deletion, HUMAN PATH, 30(5), 1999, pp. 577-581
Transglutaminase aggregates huntingtin into nonamyloidogenic polymers, andits enzymatic activity increases in Huntington's disease brain nuclei
Authors: Karpuj, MV Garren, H Slunt, H Price, DL Gusella, J Becher, MW Steinman, L
Citation: Mv. Karpuj et al., Transglutaminase aggregates huntingtin into nonamyloidogenic polymers, andits enzymatic activity increases in Huntington's disease brain nuclei, P NAS US, 96(13), 1999, pp. 7388-7393
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