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Results: 1-13 |
Results: 13
Identification and functional analysis of mutations in the hypocretin (Orexin) genes of narcoleptic canines (vol 11, pg 531, 2001)
Authors: Hungs, M Fan, J Lin, L Lin, XY Grigoriadis, D Maki, RA Mignot, E
Citation: M. Hungs et al., Identification and functional analysis of mutations in the hypocretin (Orexin) genes of narcoleptic canines (vol 11, pg 531, 2001), GENOME RES, 11(5), 2001, pp. 919-919
Identification and functional analysis of mutations in the Hypocretin (Orexin) genes of narcoleptic canines
Authors: Hungs, M Fan, J Lin, L Lin, XY Maki, RA Mignot, E
Citation: M. Hungs et al., Identification and functional analysis of mutations in the Hypocretin (Orexin) genes of narcoleptic canines, GENOME RES, 11(4), 2001, pp. 531-539
Repetitive transcranial magnetic stimulation effects on language function depend on the stimulation parameters
Authors: Sparing, R Mottaghy, FM Hungs, M Brugmann, M Foltys, H Huber, W Topper, R
Citation: R. Sparing et al., Repetitive transcranial magnetic stimulation effects on language function depend on the stimulation parameters, J CL NEURPH, 18(4), 2001, pp. 326-330
Hypocretin/orexin, sleep and narcolepsy
Authors: Hungs, M Mignot, E
Citation: M. Hungs et E. Mignot, Hypocretin/orexin, sleep and narcolepsy, BIOESSAYS, 23(5), 2001, pp. 397-408
Narcolepsy and the HLA region
Authors: Lin, L Hungs, M Mignot, E
Citation: L. Lin et al., Narcolepsy and the HLA region, J NEUROIMM, 117(1-2), 2001, pp. 9-20
Polymorphisms in the vicinity of the hypocretin/orexin are not associated with human narcolepsy
Authors: Hungs, M Lin, L Okun, M Mignot, E
Citation: M. Hungs et al., Polymorphisms in the vicinity of the hypocretin/orexin are not associated with human narcolepsy, NEUROLOGY, 57(10), 2001, pp. 1893-1895
A mutation in a case of early onset narcolepsy and a generalized absence of hypocretin peptides in human narcoleptic brains
Authors: Peyron, C Faraco, J Rogers, W Ripley, B Overeem, S Charnay, Y Nevsimalova, S Aldrich, M Reynolds, D Albin, R Li, R Hungs, M Pedrazzoli, M Padigaru, M Kucherlapati, M Fan, J Maki, R Lammers, GJ Bouras, C Kucherlapati, R Nishino, S Mignot, E
Citation: C. Peyron et al., A mutation in a case of early onset narcolepsy and a generalized absence of hypocretin peptides in human narcoleptic brains, NAT MED, 6(9), 2000, pp. 991-997
rTMS induces brief events of muscle atonia in patients with narcolepsy
Authors: Hungs, M Mottaghy, FM Sparing, R Zuchner, S Boroojerdi, B Topper, R
Citation: M. Hungs et al., rTMS induces brief events of muscle atonia in patients with narcolepsy, SLEEP, 23(8), 2000, pp. 1099-1104
Spontaneous intracranial hypotension: A rare cause of chronic headache
Authors: Hungs, M Schoen, SW Topper, R Noth, J
Citation: M. Hungs et al., Spontaneous intracranial hypotension: A rare cause of chronic headache, F NEUR PSYC, 67(9), 1999, pp. 387-390
Increased susceptibility to sporadic Parkinson's disease by a certain combined alpha-synuclein/apolipoprotein E genotype
Authors: Kruger, R Vieira-Saecker, AMM Kuhn, W Berg, D Muller, T Kuhnl, N Fuchs, GA Storch, A Hungs, M Woitalla, D Przuntek, H Epplen, JT Schols, L Riess, O
Citation: R. Kruger et al., Increased susceptibility to sporadic Parkinson's disease by a certain combined alpha-synuclein/apolipoprotein E genotype, ANN NEUROL, 45(5), 1999, pp. 611-617
Facilitation of picture naming after repetitive transcranial magnetic stimulation
Authors: Mottaghy, FM Hungs, M Brugmann, M Sparing, R Boroojerdi, B Foltys, H Huber, W Topper, R
Citation: Fm. Mottaghy et al., Facilitation of picture naming after repetitive transcranial magnetic stimulation, NEUROLOGY, 53(8), 1999, pp. 1806-1812
X-linked dominant Charcot-Marie-Tooth neuropathy: clinical, electrophysiological, and morphological phenotype in four families with different connexin32 mutations
Authors: Senderek, J Hermanns, B Bergmann, C Boroojerdi, B Bajbouj, M Hungs, M Ramaekers, VT Quasthoff, S Karch, D Schroder, JM
Citation: J. Senderek et al., X-linked dominant Charcot-Marie-Tooth neuropathy: clinical, electrophysiological, and morphological phenotype in four families with different connexin32 mutations, J NEUR SCI, 167(2), 1999, pp. 90-101
Age dependence of interhemispheric inhibition of the motor cortex in humans
Authors: Boroojerdi, B Hungs, M Topper, R Noth, J
Citation: B. Boroojerdi et al., Age dependence of interhemispheric inhibition of the motor cortex in humans, KLIN NEUROP, 29(2), 1998, pp. 112-116
Risultati: 1-13 |