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Results: 1-10 |
Results: 10
INCLUSION-BODY MYOSITIS - NO EVIDENCE THAT APOPTOSIS PLAYS A SIGNIFICANT PATHOGENIC ROLE
Authors: HUTCHINSON DO
Citation: Do. Hutchinson, INCLUSION-BODY MYOSITIS - NO EVIDENCE THAT APOPTOSIS PLAYS A SIGNIFICANT PATHOGENIC ROLE, Neurology, 50(4), 1998, pp. 4013-4013
A MATTER OF DEGREES
Authors: HUTCHINSON DO
Citation: Do. Hutchinson, A MATTER OF DEGREES, Chemical engineering progress, 93(12), 1997, pp. 9-9
NEW MUTATIONS IN ACETYLCHOLINE-RECEPTOR SUBUNIT GENES REVEAL HETEROGENEITY IN THE SLOW-CHANNEL CONGENITAL MYASTHENIC SYNDROME
Authors: ENGEL AG OHNO K MILONE M WANG HL NAKANO S BOUZAT C PRUITT JN HUTCHINSON DO BRENGMAN JM BREN N SIEB JP SINE SM
Citation: Ag. Engel et al., NEW MUTATIONS IN ACETYLCHOLINE-RECEPTOR SUBUNIT GENES REVEAL HETEROGENEITY IN THE SLOW-CHANNEL CONGENITAL MYASTHENIC SYNDROME, Human molecular genetics, 5(9), 1996, pp. 1217-1227
INTESTINAL PSEUDOOBSTRUCTION, MYASTHENIA-GRAVIS, AND THYMOMA
Authors: ANDERSON NE HUTCHINSON DO NICHOLSON GI AITCHESON F NIXON JM
Citation: Ne. Anderson et al., INTESTINAL PSEUDOOBSTRUCTION, MYASTHENIA-GRAVIS, AND THYMOMA, Neurology, 47(4), 1996, pp. 985-987
CONGENITAL MYASTHENIC SYNDROME CAUSED BY PROLONGED ACETYLCHOLINE-RECEPTOR CHANNEL OPENINGS DUE TO A MUTATION IN THE M2 DOMAIN OF THE EPSILON-SUBUNIT
Authors: OHNO K HUTCHINSON DO MILONE M BRENGMAN JM BOUZAT C SINE SM ENGEL AG
Citation: K. Ohno et al., CONGENITAL MYASTHENIC SYNDROME CAUSED BY PROLONGED ACETYLCHOLINE-RECEPTOR CHANNEL OPENINGS DUE TO A MUTATION IN THE M2 DOMAIN OF THE EPSILON-SUBUNIT, Proceedings of the National Academy of Sciences of the United Statesof America, 92(3), 1995, pp. 758-762
PATCH-CLAMP ANALYSIS OF THE PROPERTIES OF ACETYLCHOLINE-RECEPTOR CHANNELS AT THE NORMAL HUMAN END-PLATE
Authors: MILONE M HUTCHINSON DO ENGEL AG
Citation: M. Milone et al., PATCH-CLAMP ANALYSIS OF THE PROPERTIES OF ACETYLCHOLINE-RECEPTOR CHANNELS AT THE NORMAL HUMAN END-PLATE, Muscle & nerve, 17(12), 1994, pp. 1364-1369
A CONGENITAL MYASTHENIC SYNDROME (CMS) WITH A NONSENSE MUTATION IN THE EPSILON(E)-SUBUNIT OF THE ACETYLCHOLINE-RECEPTOR (ACHR)
Authors: OHNO K ENGEL AG BRENGMAN JM HUTCHINSON DO GRIGGS RC
Citation: K. Ohno et al., A CONGENITAL MYASTHENIC SYNDROME (CMS) WITH A NONSENSE MUTATION IN THE EPSILON(E)-SUBUNIT OF THE ACETYLCHOLINE-RECEPTOR (ACHR), Neurology, 44(4), 1994, pp. 10000188-10000188
PATCH-CLAMP ANALYSIS OF THE SLOW-CHANNEL MYASTHENIC SYNDROME (SCMS)
Authors: HUTCHINSON DO NAKANO S SIEB JP ENGEL AG
Citation: Do. Hutchinson et al., PATCH-CLAMP ANALYSIS OF THE SLOW-CHANNEL MYASTHENIC SYNDROME (SCMS), Neurology, 43(4), 1993, pp. 180-181
CONGENITAL MYASTHENIC SYNDROME WITH ACETYLCHOLINE-RECEPTOR (ACHR) DEFICIENCY AND INCREASED QUANTAL RELEASE
Authors: SIEB JP HUTCHINSON DO NAKANO S GROOVER RV ENGEL AG
Citation: Jp. Sieb et al., CONGENITAL MYASTHENIC SYNDROME WITH ACETYLCHOLINE-RECEPTOR (ACHR) DEFICIENCY AND INCREASED QUANTAL RELEASE, Neurology, 43(4), 1993, pp. 180-180
CONGENITAL END-PLATE ACETYLCHOLINESTERASE DEFICIENCY
Authors: HUTCHINSON DO WALLS TJ NAKANO S CAMP S TAYLOR P HARPER CM GROOVER RV PETERSON HA JAMIESON DG ENGEL AG
Citation: Do. Hutchinson et al., CONGENITAL END-PLATE ACETYLCHOLINESTERASE DEFICIENCY, Brain, 116, 1993, pp. 633-653
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