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1 MSLTs were conducted following nocturnal polysomnography
4 considered diagnostic without the use of an MSLT; absence of short REML, however, requires a subsequ
5 among OSA patients predict 2omSOREMPs on an MSLT that follows nocturnal polysomnography, we reviewed
6 patients with nocturnal polysomnography and MSLT, including 25 with narcolepsy with cataplexy (N+C),
7 Sensitivity and specificity of NPSG REML and MSLT as diagnostic tests for narcolepsy/hypocretin defic
8 ting characteristic curves for NPSG REML and MSLT findings (sleep studies performed between May 1976
12 thickness <1 mm with a Clark level > or =IV (MSLT criterion); LM/SL performed between June 1, 1985, a
16 tified with the multiple sleep latency test (MSLT) and survival analysis was used to assess the risk
18 omSOREMPs) on a Multiple Sleep Latency Test (MSLT) raise the possibility of narcolepsy, patients with
20 t with a normal multiple sleep latency test (MSLT) result, or if MSLT is not interpretable, conclusiv
25 ase, the success of SN identification in the MSLT group was independent of the center's case volume o
26 the randomization phase, each center in the MSLT was required to finish a 30-case learning phase wit
27 examined the accuracy of LM/SL/SCLND in the MSLT, using the experience of the organizing center (Joh
28 % CI = 1.9 to 12.7), a 5-min decrease in the MSLT-derived mean sleep latency (OR = 1.9, 95% CI = 1.3
31 M) latency during NPSG, were sleepier on the MSLT and reported increased sleepiness, hypnagogic hallu
33 Multicenter Selective Lymphadenectomy Trial (MSLT) 5 years ago to evaluate the survival of patients w
34 Multicenter Selective Lymphadenectomy Trial (MSLT-I) to compare 2 treatment approaches: wide excision
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