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1 Lambert Eaton myasthenic syndrome and acquired neuromyot
2 Lambert et al question our retrospective and holistic ep
3 Lambert et al. make clever use of psoriasis patient gene
4 Lambert et al. reported that silicate ions catalyze the
5 Lambert-Eaton myasthenic syndrome (LEMS) is a paraneopla
6 Lambert-Eaton myasthenic syndrome (LEMS) is an autoimmun
7 Lambert-Eaton myasthenic syndrome (LEMS) is an autoimmun
8 Lambert-Eaton myasthenic syndrome IgG did not selectivel
9 mplitudes were correlated with decibel and 1/Lambert DLS for the central 18 degrees of the visual fie
10 ensitivities (both in logarithmic [dB] and 1/Lambert scales [1/L]), were investigated with components
11 There was a linear correlation between 1/Lambert DLS and PERG amplitude (transient PERG: R(2) = 0
12 im area, and a linear relationship between 1/Lambert DLS and PERG amplitude and neuroretinal rim area
13 There was a linear correlation between 1/Lambert DLS and temporal neuroretinal rim area (R(2) = 0
14 .75%, and -0.78% per year for decibel DLS, 1/Lambert DLS, transient PERG, and SS PERG, respectively.
17 limbic encephalitis, 3 cerebellar ataxia, 2 Lambert-Eaton myasthenic syndrome, 1 autonomic neuropath
19 ataxia type 2, spinocerebellar ataxia 6, and Lambert-Eaton myasthenic syndrome), and the skeletal mus
21 nase antibody-positive myasthenia gravis and Lambert-Eaton myasthenic syndrome are about 20 times les
26 ia gravis can be associated with thymoma and Lambert-Eaton myasthenic syndrome with small-cell lung c
32 microscopic optical path lengths, both Beer-Lambert's law and the law of superposition were found to
33 e obtained, quantitatively obeying both Beer-Lambert's law and the law of superposition, despite the
35 on in the ITO, causing a deviation from Beer-Lambert absorption that results in an optimum ITO thickn
38 on plots are assessed in the context of Beer-Lambert's law and provide combined with time-dependent d
41 so establishes that deviations from the Beer-Lambert law can be expected when (a) the light source is
42 in coincide with those predicted by the Beer-Lambert law for a range of ferricyanide concentrations f
47 ration of analytes-as postulated by the Beer-Lambert law-is one of the fundamental assumptions that m
52 sing from either the energy loss of the Beer-Lambert-Bouguer transmission law or the evanescent penet
60 equency relation is established by employing Lambert's special function or alternatively using linear
63 o coimmunogenic tumor antigens, for example, Lambert-Eaton syndrome (P/Q-type Ca(2+) channel antibody
64 d JMG, 141 (38.7%) had CMS, and 6 (1.7%) had Lambert-Eaton syndrome, diagnosed at a median age of 13.
65 ation patients without clinically identified Lambert-Eaton myasthenic syndrome had P/Q-type voltage-g
68 iated with small-cell lung cancer, including Lambert-Eaton myasthenic syndrome (LEMS) and paraneoplas
70 ciated with Waldenstrom's macroglobulinemia, Lambert-Eaton myasthenic syndrome, and multifocal motor
71 d/or signs were present in 18 of 23 (78%) of Lambert-Eaton myasthenic syndrome (LEMS) patients evalua
72 ations, although 1 developed a fatal case of Lambert Eaton myasthenic syndrome following ICI treatmen
73 d GV-58 in a passive transfer mouse model of Lambert-Eaton myasthenic syndrome and have shown that we
75 t, some PNSs such as sensory neuronopathy or Lambert-Eaton myasthenic syndrome rarely occur in lympho
77 syn I, DeMarini DM, Caldwell JC, Kavlock RJ, Lambert P, Hecht SS, Bucher JR, Stewart BW, Baan R, Cogl
82 and demonstrated an autoimmune basis for the Lambert Eaton myasthenic syndrome and 'seronegative' mya
83 ubtype that is targeted by antibodies in the Lambert-Eaton myasthenic syndrome has been identified, a
85 ced improvement in several patients with the Lambert-Eaton myasthenic syndrome and myasthenia gravis
87 There was one treatment-related death due to Lambert-Eaton syndrome in a PD-L1-negative patient durin
90 ls of gabapentin funded by Pfizer and Warner-Lambert's subsidiary, Parke-Davis (hereafter referred to
91 thenic syndrome and have shown that weakened Lambert-Eaton myasthenic syndrome-model neuromuscular sy
92 ample, P/Q-type Ca(2+)-channel antibody with Lambert-Eaton syndrome (n = 5), anti-neuronal nuclear an