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Results: 1-12 |
Results: 12
HEREDITARY MOTOR AND SENSORY NEUROPATHY TYPE 1A ASSOCIATED WITH SENSORINEURAL DEAFNESS
Authors: STONE J MORAN G WALLS TJ
Citation: J. Stone et al., HEREDITARY MOTOR AND SENSORY NEUROPATHY TYPE 1A ASSOCIATED WITH SENSORINEURAL DEAFNESS, Journal of Neurology, Neurosurgery and Psychiatry, 65(3), 1998, pp. 403-403
DRIVING AND STROKE - REPLY
Authors: CHINNERY PF TURNBULL DM WALLS TJ READING PJ
Citation: Pf. Chinnery et al., DRIVING AND STROKE - REPLY, Lancet, 350(9088), 1997, pp. 1402-1403
RECURRENT STROKES IN A 34-YEAR-OLD MAN
Authors: CHINNERY PF TURNBULL DM WALLS TJ READING PJ
Citation: Pf. Chinnery et al., RECURRENT STROKES IN A 34-YEAR-OLD MAN, Lancet, 350(9077), 1997, pp. 560-560
BREATHING PATTERN AWAKE AND ASLEEP IN PATIENTS WITH MYOTONIC-DYSTROPHY
Authors: VEALE D COOPER BG GILMARTIN JJ WALLS TJ GRIFFITH CJ GIBSON GJ
Citation: D. Veale et al., BREATHING PATTERN AWAKE AND ASLEEP IN PATIENTS WITH MYOTONIC-DYSTROPHY, The European respiratory journal, 8(5), 1995, pp. 815-818
MALIGNANT CEREBROVASCULAR THROMBOEMBOLIZATION BY PHAECHROMOCYTAMA
Authors: RAGHAVAN R INCE PG WALLS TJ GHOLKAR A DARK JH FOSTER JB
Citation: R. Raghavan et al., MALIGNANT CEREBROVASCULAR THROMBOEMBOLIZATION BY PHAECHROMOCYTAMA, Clinical neuropathology, 14(2), 1995, pp. 69-71
DEFECTS OF THE NEUROMUSCULAR-JUNCTION ASSOCIATED WITH IMPAIRED NEUROMUSCULAR-TRANSMISSION IN LIMB-GIRDLE MYASTHENIAS IN MAN
Authors: SLATER CR FAWCETT PRW GARDNERMEDWIN D LYONS PR WALLS TJ WOOD SJ YOUNG C
Citation: Cr. Slater et al., DEFECTS OF THE NEUROMUSCULAR-JUNCTION ASSOCIATED WITH IMPAIRED NEUROMUSCULAR-TRANSMISSION IN LIMB-GIRDLE MYASTHENIAS IN MAN, Journal of physiology, 489P, 1995, pp. 150-151
CEREBROTENDINOUS XANTHOMATOSIS IN 2 SISTERS - CASE-REPORTS AND MR-IMAGING
Authors: CHAKRAVERTY S GRIFFITHS PD WALLS TJ MCALLISTER VL
Citation: S. Chakraverty et al., CEREBROTENDINOUS XANTHOMATOSIS IN 2 SISTERS - CASE-REPORTS AND MR-IMAGING, Clinical Radiology, 50(2), 1995, pp. 117-119
CASE-REPORT - MULTIPLE THORACIC HEMANGIOMAS - A RARE CAUSE OF SPINAL-CORD COMPRESSION
Authors: WORTHY SA GHOLKAR A WALLS TJ TODD NV
Citation: Sa. Worthy et al., CASE-REPORT - MULTIPLE THORACIC HEMANGIOMAS - A RARE CAUSE OF SPINAL-CORD COMPRESSION, British journal of radiology, 68(811), 1995, pp. 770-772
NEWLY RECOGNIZED CONGENITAL MYASTHENIC SYNDROME-ASSOCIATED WITH HIGH-CONDUCTANCE AND FAST CLOSURE OF THE ACETYLCHOLINE-RECEPTOR CHANNEL
Authors: ENGEL AG UCHITEL OD WALLS TJ NAGEL A HARPER CM BODENSTEINER J
Citation: Ag. Engel et al., NEWLY RECOGNIZED CONGENITAL MYASTHENIC SYNDROME-ASSOCIATED WITH HIGH-CONDUCTANCE AND FAST CLOSURE OF THE ACETYLCHOLINE-RECEPTOR CHANNEL, Annals of neurology, 34(1), 1993, pp. 38-47
CONGENITAL MYASTHENIC SYNDROMES .1. DEFICIENCY AND SHORT OPEN-TIME OFTHE ACETYLCHOLINE-RECEPTOR
Authors: ENGEL AG NAGEL A WALLS TJ HARPER CM WAISBURG HA
Citation: Ag. Engel et al., CONGENITAL MYASTHENIC SYNDROMES .1. DEFICIENCY AND SHORT OPEN-TIME OFTHE ACETYLCHOLINE-RECEPTOR, Muscle & nerve, 16(12), 1993, pp. 1284-1292
CONGENITAL MYASTHENIC SYNDROMES .2. SYNDROME ATTRIBUTED TO ABNORMAL INTERACTION OF ACETYLCHOLINE WITH ITS RECEPTOR
Authors: UCHITEL O ENGEL AG WALLS TJ NAGEL A ATASSI MZ BRIL V
Citation: O. Uchitel et al., CONGENITAL MYASTHENIC SYNDROMES .2. SYNDROME ATTRIBUTED TO ABNORMAL INTERACTION OF ACETYLCHOLINE WITH ITS RECEPTOR, Muscle & nerve, 16(12), 1993, pp. 1293-1301
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
Risultati: 1-12 |