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Results: 1-25 | 26-50 | 51-75 | 76-98
Results: 1-25/98
CONGENITAL MYASTHENIC SYNDROMES - GENE MUTATION
Authors: OHNO K ENGEL AG
Citation: K. Ohno et Ag. Engel, CONGENITAL MYASTHENIC SYNDROMES - GENE MUTATION, Neuromuscular disorders, 8(2), 1998, pp. 12-13
QUINIDINE NORMALIZES THE OPEN DURATION OF SLOW-CHANNEL MUTANTS OF THEACETYLCHOLINE-RECEPTOR
Authors: FUKUDOME T OHNO K BRENGMAN JM ENGEL AG
Citation: T. Fukudome et al., QUINIDINE NORMALIZES THE OPEN DURATION OF SLOW-CHANNEL MUTANTS OF THEACETYLCHOLINE-RECEPTOR, NeuroReport, 9(8), 1998, pp. 1907-1911
CONGENITAL MYASTHENIC SYNDROMES - EXPERIMENTS OF NATURE
Authors: ENGEL AG OHNO K SINE SM
Citation: Ag. Engel et al., CONGENITAL MYASTHENIC SYNDROMES - EXPERIMENTS OF NATURE, J PHYSL-PAR, 92(2), 1998, pp. 113-117
MODE SWITCHING KINETICS PRODUCED BY A NATURALLY-OCCURRING MUTATION INTHE CYTOPLASMIC LOOP OF THE HUMAN ACETYLCHOLINE-RECEPTOR EPSILON-SUBUNIT
Authors: MILONE M WANG HL OHNO K PRINCE R FUKUDOME T SHEN XM BRENGMAN JM GRIGGS RC SINE SM ENGEL AG
Citation: M. Milone et al., MODE SWITCHING KINETICS PRODUCED BY A NATURALLY-OCCURRING MUTATION INTHE CYTOPLASMIC LOOP OF THE HUMAN ACETYLCHOLINE-RECEPTOR EPSILON-SUBUNIT, Neuron, 20(3), 1998, pp. 575-588
MYOPATHY, MYASTHENIA, AND EPIDERMOLYSIS-BULLOSA SIMPLEX DUE TO PLECTIN DEFICIENCY
Authors: BANWELL BL FUKUDOME T SHEN XM STILLING G RUSSELL J ENGEL AG
Citation: Bl. Banwell et al., MYOPATHY, MYASTHENIA, AND EPIDERMOLYSIS-BULLOSA SIMPLEX DUE TO PLECTIN DEFICIENCY, Annals of neurology, 44(3), 1998, pp. 83-83
MYASTHENIC SYNDROMES IN TURKISH KINSHIPS DUE TO MUTATIONS IN THE ACETYLCHOLINE-RECEPTOR
Authors: OHNO K ANLAR B OZDIRIM E BRENGMAN JM DEBLEECKER JL ENGEL AG
Citation: K. Ohno et al., MYASTHENIC SYNDROMES IN TURKISH KINSHIPS DUE TO MUTATIONS IN THE ACETYLCHOLINE-RECEPTOR, Annals of neurology, 44(2), 1998, pp. 234-241
AMYLOID MYOPATHY - AN UNDERDIAGNOSED ENTITY
Authors: SPULER S EMSLIESMITH A ENGEL AG
Citation: S. Spuler et al., AMYLOID MYOPATHY - AN UNDERDIAGNOSED ENTITY, Annals of neurology, 43(6), 1998, pp. 719-728
QUINIDINE SULFATE THERAPY FOR THE SLOW-CHANNEL CONGENITAL MYASTHENIC SYNDROME
Authors: HARPER CM ENGEL AG
Citation: Cm. Harper et Ag. Engel, QUINIDINE SULFATE THERAPY FOR THE SLOW-CHANNEL CONGENITAL MYASTHENIC SYNDROME, Annals of neurology, 43(4), 1998, pp. 480-484
T-CELL HETEROGENEITY IN MUSCLE LESIONS OF INCLUSION-BODY MYOSITIS
Authors: BENDER A BEHRENS L ENGEL AG HOHLFELD R
Citation: A. Bender et al., T-CELL HETEROGENEITY IN MUSCLE LESIONS OF INCLUSION-BODY MYOSITIS, Journal of neuroimmunology, 84(1), 1998, pp. 86-91
DUCHENNE DYSTROPHY - ELECTRON-MICROSCOPIC FINDINGS POINTING TO ABASICOR EARLY ABNORMALITY IN THE PLASMA-MEMBRANE OF THE MUSCLE-FIBER
Authors: MOKRI B ENGEL AG
Citation: B. Mokri et Ag. Engel, DUCHENNE DYSTROPHY - ELECTRON-MICROSCOPIC FINDINGS POINTING TO ABASICOR EARLY ABNORMALITY IN THE PLASMA-MEMBRANE OF THE MUSCLE-FIBER, Neurology, 51(1), 1998, pp. 1-1
DUCHENNE-DYSTROPHY - ELECTRON-MICROSCOPIC FINDINGS POINTING TO A BASIC OR EARLY ABNORMALITY IN THE PLASMA-MEMBRANE OF THE MUSCLE-FIBER (REPRINTED FROM NEUROLOGY, VOL 25, 1975)
Authors: MOKRI B ENGEL AG
Citation: B. Mokri et Ag. Engel, DUCHENNE-DYSTROPHY - ELECTRON-MICROSCOPIC FINDINGS POINTING TO A BASIC OR EARLY ABNORMALITY IN THE PLASMA-MEMBRANE OF THE MUSCLE-FIBER (REPRINTED FROM NEUROLOGY, VOL 25, 1975), Neurology, 51(1), 1998, pp. 1111-1120
CONGENITAL MYASTHENIC SYNDROMES (CMS) DUE TO NULL MUTATIONS IN ACETYLCHOLINE-RECEPTOR (ACHR) EPSILON-SUBUNIT GENE IN TURKISH KINSHIPS
Authors: ANIAR B OHNO K OZDIRIM E BRENGMAN JM DEBLEECKER JL ENGEL AG
Citation: B. Aniar et al., CONGENITAL MYASTHENIC SYNDROMES (CMS) DUE TO NULL MUTATIONS IN ACETYLCHOLINE-RECEPTOR (ACHR) EPSILON-SUBUNIT GENE IN TURKISH KINSHIPS, Neurology, 50(4), 1998, pp. 67001-67001
SLOW-CHANNEL CONGENITAL MYASTHENIC SYNDROME (SCCMS) CAUSED BY A NOVELMUTATION IN THE ACETYLCHOLINE-RECEPTOR (ACHR) EPSILON-SUBUNIT
Authors: OHNO K MILONE M BRENGMAN JM LOMONACO M EVOLI A TONALI PA ENGEL AG
Citation: K. Ohno et al., SLOW-CHANNEL CONGENITAL MYASTHENIC SYNDROME (SCCMS) CAUSED BY A NOVELMUTATION IN THE ACETYLCHOLINE-RECEPTOR (ACHR) EPSILON-SUBUNIT, Neurology, 50(4), 1998, pp. 67002-67002
LOW-AFFINITY FAST-CHANNEL CONGENITAL MYASTHENIC SYNDROME (CMS) CAUSEDBY NEW MISSENSE MUTATIONS IN THE ACETYLCHOLINE-RECEPTOR (ACHR) ALPHA-SUBUNIT
Authors: MILONE M OHNO K BRENGMAN JM BATOCCHI AP TONALI PA ENGEL AG
Citation: M. Milone et al., LOW-AFFINITY FAST-CHANNEL CONGENITAL MYASTHENIC SYNDROME (CMS) CAUSEDBY NEW MISSENSE MUTATIONS IN THE ACETYLCHOLINE-RECEPTOR (ACHR) ALPHA-SUBUNIT, Neurology, 50(4), 1998, pp. 67004-67004
UNEXPECTED SARCOLEMMAL COMPLEMENT MEMBRANE ATTACK COMPLEX DEPOSITS ONNONNECROTIC MUSCLE-FIBERS IN MUSCULAR-DYSTROPHIES
Authors: SPULER S ENGEL AG
Citation: S. Spuler et Ag. Engel, UNEXPECTED SARCOLEMMAL COMPLEMENT MEMBRANE ATTACK COMPLEX DEPOSITS ONNONNECROTIC MUSCLE-FIBERS IN MUSCULAR-DYSTROPHIES, Neurology, 50(1), 1998, pp. 41-46
HUMAN END-PLATE ACETYLCHOLINESTERASE DEFICIENCY CAUSED BY MUTATIONS IN THE COLLAGEN-LIKE TAIL SUBUNIT (COLQ) OF THE ASYMMETRIC ENZYME
Authors: OHNO K BRENGMAN J TSUJINO A ENGEL AG
Citation: K. Ohno et al., HUMAN END-PLATE ACETYLCHOLINESTERASE DEFICIENCY CAUSED BY MUTATIONS IN THE COLLAGEN-LIKE TAIL SUBUNIT (COLQ) OF THE ASYMMETRIC ENZYME, Proceedings of the National Academy of Sciences of the United Statesof America, 95(16), 1998, pp. 9654-9659
RETINOCOCHLEOCEREBRAL VASCULOPATHY
Authors: PETTY GW ENGEL AG YOUNGE BR DUFFY J YANAGIHARA T LUCCHINETTI CF BARTLESON JD PARISI JE KASPERBAUER JL RODRIGUEZ M
Citation: Gw. Petty et al., RETINOCOCHLEOCEREBRAL VASCULOPATHY, Medicine, 77(1), 1998, pp. 12-40
CONGENITAL MYASTHENIC SYNDROMES DUE TO HETEROALLELIC NONSENSE MISSENSE MUTATIONS IN THE ACETYLCHOLINE-RECEPTOR EPSILON-SUBUNIT GENE - IDENTIFICATION AND FUNCTIONAL-CHARACTERIZATION OF 6 NEW MUTATIONS/
Authors: OHNO K QUIRAM PA MILONE M WANG HL HARPER MC PRUITT JN BRENGMAN JM PAO L FISCHBECK KH CRAWFORD TO SINE SM ENGEL AG
Citation: K. Ohno et al., CONGENITAL MYASTHENIC SYNDROMES DUE TO HETEROALLELIC NONSENSE MISSENSE MUTATIONS IN THE ACETYLCHOLINE-RECEPTOR EPSILON-SUBUNIT GENE - IDENTIFICATION AND FUNCTIONAL-CHARACTERIZATION OF 6 NEW MUTATIONS/, Human molecular genetics, 6(5), 1997, pp. 753-766
SMI-31 IMMUNOREACTIVITY IN INCLUSION-BODY MYOSITIS
Authors: SPULER S ENGEL AG
Citation: S. Spuler et Ag. Engel, SMI-31 IMMUNOREACTIVITY IN INCLUSION-BODY MYOSITIS, Annals of neurology, 42(5), 1997, pp. 815-815
SLOW-CHANNEL MYASTHENIC SYNDROME CAUSED BY ENHANCED ACTIVATION, DESENSITIZATION, AND AGONIST BINDING-AFFINITY ATTRIBUTABLE TO MUTATION IN THE M2 DOMAIN OF THE ACETYLCHOLINE-RECEPTOR ALPHA-SUBUNIT
Authors: MILONE M WANG HL OHNO K FUKUDOME T PRUITT JN BREN N SINE SM ENGEL AG
Citation: M. Milone et al., SLOW-CHANNEL MYASTHENIC SYNDROME CAUSED BY ENHANCED ACTIVATION, DESENSITIZATION, AND AGONIST BINDING-AFFINITY ATTRIBUTABLE TO MUTATION IN THE M2 DOMAIN OF THE ACETYLCHOLINE-RECEPTOR ALPHA-SUBUNIT, The Journal of neuroscience, 17(15), 1997, pp. 5651-5665
ACUTE QUADRIPLEGIC MYOPATHY - ANALYSIS OF MYOSIN ISOFORMS AND EVIDENCE FOR CALPAIN-MEDIATED PROTEOLYSIS
Authors: SHOWALTER CJ ENGEL AG
Citation: Cj. Showalter et Ag. Engel, ACUTE QUADRIPLEGIC MYOPATHY - ANALYSIS OF MYOSIN ISOFORMS AND EVIDENCE FOR CALPAIN-MEDIATED PROTEOLYSIS, Muscle & nerve, 20(3), 1997, pp. 316-322
QUINIDINE SULFATE IN THE TREATMENT OF THE SLOW CHANNEL CONGENITAL MYASTHENIC SYNDROME
Authors: HARPER CM ENGEL AG
Citation: Cm. Harper et Ag. Engel, QUINIDINE SULFATE IN THE TREATMENT OF THE SLOW CHANNEL CONGENITAL MYASTHENIC SYNDROME, Neurology, 48(3), 1997, pp. 1001-1001
QUINIDINE SULFATE (QS) NORMALIZES THE OPEN DURATION OF SLOW CHANNEL CONGENITAL MYASTHENIC SYNDROME (SCCMS) ACETYLCHOLINE-RECEPTOR (ACHR) CHANNELS EXPRESSED IN HUMAN EMBRYONIC KIDNEY (HEK) CELLS
Authors: FUKODOME T OHNO K BRENGMAN J ENGEL AG
Citation: T. Fukodome et al., QUINIDINE SULFATE (QS) NORMALIZES THE OPEN DURATION OF SLOW CHANNEL CONGENITAL MYASTHENIC SYNDROME (SCCMS) ACETYLCHOLINE-RECEPTOR (ACHR) CHANNELS EXPRESSED IN HUMAN EMBRYONIC KIDNEY (HEK) CELLS, Neurology, 48(3), 1997, pp. 1002-1002
CONGENITAL MYASTHENIC SYNDROMES (CMS) DUE TO HETEROALLELIC NONSENSE MISSENSE MUTATIONS IN THE ACETYLCHOLINE-RECEPTOR (ACHR) EPSILON-SUBUNITGENE - REPORT OF 5 NEW MUTATIONS/
Authors: OHNO K QUIRAM PA MILONE M WANG HL HARPER CM PRUITT JN BRENGMAN JM PAO L FISCHBECK K CRAWFORD TA SINE SM ENGEL AG FISCHBECK KH
Citation: K. Ohno et al., CONGENITAL MYASTHENIC SYNDROMES (CMS) DUE TO HETEROALLELIC NONSENSE MISSENSE MUTATIONS IN THE ACETYLCHOLINE-RECEPTOR (ACHR) EPSILON-SUBUNITGENE - REPORT OF 5 NEW MUTATIONS/, Neurology, 48(3), 1997, pp. 1003-1003
ABERRANT EXPRESSION OF CYCLIN-DEPENDENT KINASE-5 (CDK5) IN INCLUSION-BODY MYOSITIS (IBM)
Authors: NAKANO S ENGEL AG AKIGUCHI I KIMURA J
Citation: S. Nakano et al., ABERRANT EXPRESSION OF CYCLIN-DEPENDENT KINASE-5 (CDK5) IN INCLUSION-BODY MYOSITIS (IBM), Neurology, 48(3), 1997, pp. 2109-2109
Risultati: 1-25 | 26-50 | 51-75 | 76-98