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1 ced in cockroach (Ritzmann) and fish escape (Eaton) systems can be predicted based on the activity of
2 hD in nutritional biochemistry with Hamilton Eaton at the University of Connecticut followed by postd
5 nstrated an autoimmune basis for the Lambert Eaton myasthenic syndrome and 'seronegative' myasthenia.
10 encephalitis, 3 cerebellar ataxia, 2 Lambert-Eaton myasthenic syndrome, 1 autonomic neuropathy, and 1
12 ibody-positive myasthenia gravis and Lambert-Eaton myasthenic syndrome are about 20 times less common
15 s can be associated with thymoma and Lambert-Eaton myasthenic syndrome with small-cell lung cancer.
16 ype 2, spinocerebellar ataxia 6, and Lambert-Eaton myasthenic syndrome), and the skeletal muscle ryan
30 nogenic tumor antigens, for example, Lambert-Eaton syndrome (P/Q-type Ca(2+) channel antibody) and pe
31 41 (38.7%) had CMS, and 6 (1.7%) had Lambert-Eaton syndrome, diagnosed at a median age of 13.5, 5.1,
32 tients without clinically identified Lambert-Eaton myasthenic syndrome had P/Q-type voltage-gated cal
35 th small-cell lung cancer, including Lambert-Eaton myasthenic syndrome (LEMS) and paraneoplastic cere
36 ith Waldenstrom's macroglobulinemia, Lambert-Eaton myasthenic syndrome, and multifocal motor neuropat
38 ns were present in 18 of 23 (78%) of Lambert-Eaton myasthenic syndrome (LEMS) patients evaluated at t
39 in a passive transfer mouse model of Lambert-Eaton myasthenic syndrome and have shown that weakened L
40 PNSs such as sensory neuronopathy or Lambert-Eaton myasthenic syndrome rarely occur in lymphomas, whe
42 Previous work has demonstrated that Lambert-Eaton syndrome (LES) antibodies reduce calcium currents
43 ovement in several patients with the Lambert-Eaton myasthenic syndrome and myasthenia gravis but had
44 hat is targeted by antibodies in the Lambert-Eaton myasthenic syndrome has been identified, and there
48 s one treatment-related death due to Lambert-Eaton syndrome in a PD-L1-negative patient during phase
49 yndrome and have shown that weakened Lambert-Eaton myasthenic syndrome-model neuromuscular synapses a
51 /Q-type Ca(2+)-channel antibody with Lambert-Eaton syndrome (n = 5), anti-neuronal nuclear antibody t
52 ustrated by 'COREX' and the Wako-Saito-Munoz-Eaton (WSME) model, the Framework Rigidity Optimized Dyn
53 ecent generalization of the Wako-Saito-Munoz-Eaton model with support for group-transfer free energie
55 The model is a continuation of the Munoz-Eaton model to include the intermittency of contacts bet
60 st my beloved wife and life partner, Suzanne Eaton to a senseless act of violence, and all assumption
61 three singular omnidirectional devices: the Eaton lens, the generalized Maxwell Fish-Eye, and the in
62 ed 4-aryl-5-(sulfonamidovinyl)pyrroles using Eaton's reagent provides 2,3-dihydrobenzo[e]indoles havi