-
1
-
-
33846432297
-
ICSD-2: International Classification of Sleep Disorders
-
American Academy of Sleep Medicine, Westchester, IL
-
American Academy of Sleep Medicine. ICSD-2: International Classification of Sleep Disorders. Diagnostic and Coding Manual. 2nd ed (2005), American Academy of Sleep Medicine, Westchester, IL
-
(2005)
Diagnostic and Coding Manual. 2nd ed
-
-
American Academy of Sleep Medicine1
-
2
-
-
0017808506
-
Genetic study of the narcoleptic syndrome
-
Baraitser M., and Parkes J.D. Genetic study of the narcoleptic syndrome. J. Med. Genet. 15 (1978) 254-259
-
(1978)
J. Med. Genet.
, vol.15
, pp. 254-259
-
-
Baraitser, M.1
Parkes, J.D.2
-
3
-
-
0028597385
-
Family studies in narcolepsy
-
Billiard M., Pasquie-Magnetto V., Heckman M., Carlander B., Besset A., Zachariev Z., Eliaou J.F., and Malafosse A. Family studies in narcolepsy. Sleep 17 8 Suppl. (1994) S54-S59
-
(1994)
Sleep
, vol.17
, Issue.8 SUPPL
-
-
Billiard, M.1
Pasquie-Magnetto, V.2
Heckman, M.3
Carlander, B.4
Besset, A.5
Zachariev, Z.6
Eliaou, J.F.7
Malafosse, A.8
-
5
-
-
4444287267
-
A narcolepsy susceptibility locus maps to a 5 Mb region of chromosome 21q
-
Dauvilliers Y., Blouin J.L., Neidhart E., Carlander B., Eliaou J.F., Antonarakis S.E., Billiard M., and Tafti M. A narcolepsy susceptibility locus maps to a 5 Mb region of chromosome 21q. Ann. Neurol. 56 3 (2004) 382-388
-
(2004)
Ann. Neurol.
, vol.56
, Issue.3
, pp. 382-388
-
-
Dauvilliers, Y.1
Blouin, J.L.2
Neidhart, E.3
Carlander, B.4
Eliaou, J.F.5
Antonarakis, S.E.6
Billiard, M.7
Tafti, M.8
-
6
-
-
0024387830
-
Familial patterns of narcolepsy
-
Guilleminault C., Mignot E., and Grumet F.C. Familial patterns of narcolepsy. Lancet 2 8676 (1989) 1376-1379
-
(1989)
Lancet
, vol.2
, Issue.8676
, pp. 1376-1379
-
-
Guilleminault, C.1
Mignot, E.2
Grumet, F.C.3
-
7
-
-
0034784993
-
Low cerebrospinal fluid hypocretin levels found in familial narcolepsy
-
Hartwig G., Harsh J., Ripley B., Nishino S., and Mignot E. Low cerebrospinal fluid hypocretin levels found in familial narcolepsy. Sleep Med. 2 5 (2001) 451-453
-
(2001)
Sleep Med.
, vol.2
, Issue.5
, pp. 451-453
-
-
Hartwig, G.1
Harsh, J.2
Ripley, B.3
Nishino, S.4
Mignot, E.5
-
10
-
-
0026603899
-
DQ (rather than DR) gene marks susceptibility to narcolepsy
-
Matsuki K., Grumet F.C., Lin X., Gelb M., Guilleminault C., Dement W.C., and Mignot E. DQ (rather than DR) gene marks susceptibility to narcolepsy. Lancet 339 (1992) 1052
-
(1992)
Lancet
, vol.339
, pp. 1052
-
-
Matsuki, K.1
Grumet, F.C.2
Lin, X.3
Gelb, M.4
Guilleminault, C.5
Dement, W.C.6
Mignot, E.7
-
11
-
-
0031912090
-
Genetic and familial aspects of narcolepsy
-
Mignot E. Genetic and familial aspects of narcolepsy. Neurology 50 (1998) 16-22
-
(1998)
Neurology
, vol.50
, pp. 16-22
-
-
Mignot, E.1
-
12
-
-
0031283162
-
HLA DQB1*0602 is associated with cataplexy in 509 narcoleptic patients
-
Mignot E., Hayduk R., Black J., Grumet F.C., and Guilleminault C. HLA DQB1*0602 is associated with cataplexy in 509 narcoleptic patients. Sleep 20 11 (1997) 1012-1020
-
(1997)
Sleep
, vol.20
, Issue.11
, pp. 1012-1020
-
-
Mignot, E.1
Hayduk, R.2
Black, J.3
Grumet, F.C.4
Guilleminault, C.5
-
13
-
-
0032492409
-
Reduction of REM sleep latency associated with HLA-DQB1*0602 in normal adults
-
Mignot E., Young T., Lin L., Finn L., and Palta M. Reduction of REM sleep latency associated with HLA-DQB1*0602 in normal adults. Lancet 351 (1998) 727
-
(1998)
Lancet
, vol.351
, pp. 727
-
-
Mignot, E.1
Young, T.2
Lin, L.3
Finn, L.4
Palta, M.5
-
14
-
-
0036791834
-
The role of cerebrospinal fluid hypocretin measurement in the diagnosis of narcolepsy and other hypersomnias
-
Mignot E., Lammers G.J., Ripley B., Okun M., Nevsimalova S., Overeem S., Vankova J., Black J., Harsh J., Bassetti C., Schrader H., and Nishino S. The role of cerebrospinal fluid hypocretin measurement in the diagnosis of narcolepsy and other hypersomnias. Arch. Neurol. 59 10 (2002) 1553-1562
-
(2002)
Arch. Neurol.
, vol.59
, Issue.10
, pp. 1553-1562
-
-
Mignot, E.1
Lammers, G.J.2
Ripley, B.3
Okun, M.4
Nevsimalova, S.5
Overeem, S.6
Vankova, J.7
Black, J.8
Harsh, J.9
Bassetti, C.10
Schrader, H.11
Nishino, S.12
-
15
-
-
2642670334
-
Familial aspects of narcolepsy-cataplexy in the Czech Republic
-
Nevsimalova S., Mignot E., Sonka K., and Arrigoni J.L. Familial aspects of narcolepsy-cataplexy in the Czech Republic. Sleep 20 11 (1997) 1021-1026
-
(1997)
Sleep
, vol.20
, Issue.11
, pp. 1021-1026
-
-
Nevsimalova, S.1
Mignot, E.2
Sonka, K.3
Arrigoni, J.L.4
-
16
-
-
0033971611
-
Hypocretin (orexin) deficiency in human narcolepsy
-
Nishino S., Ripley B., Overeem S., Lammers G.J., and Mignot E. Hypocretin (orexin) deficiency in human narcolepsy. Lancet 355 (2000) 39-40
-
(2000)
Lancet
, vol.355
, pp. 39-40
-
-
Nishino, S.1
Ripley, B.2
Overeem, S.3
Lammers, G.J.4
Mignot, E.5
-
17
-
-
0031973895
-
HLA-DQB1*0602 homozygosity increases relative risk for narcolepsy but not disease severity in two ethnic groups U.S. Modafinil in Narcolepsy Multicenter Study Group
-
Pelin Z., Guilleminault C., Risch N., Grumet F.C., and Mignot E. HLA-DQB1*0602 homozygosity increases relative risk for narcolepsy but not disease severity in two ethnic groups U.S. Modafinil in Narcolepsy Multicenter Study Group. Tissue Antigens 51 (1998) 96-100
-
(1998)
Tissue Antigens
, vol.51
, pp. 96-100
-
-
Pelin, Z.1
Guilleminault, C.2
Risch, N.3
Grumet, F.C.4
Mignot, E.5
-
18
-
-
0030858847
-
HLA DR15 (DR2) and DQB1*0602 typing studies in 188 narcoleptic patients with cataplexy
-
Rogers A.E., Meehan J., Guilleminault C., Grumet F.C., and Mignot E. HLA DR15 (DR2) and DQB1*0602 typing studies in 188 narcoleptic patients with cataplexy. Neurology 48 (1997) 1550-1556
-
(1997)
Neurology
, vol.48
, pp. 1550-1556
-
-
Rogers, A.E.1
Meehan, J.2
Guilleminault, C.3
Grumet, F.C.4
Mignot, E.5
-
19
-
-
0036302041
-
The role of hypocretins (orexins) in sleep regulation and narcolepsy
-
Taheri S., Zeitzer J.M., and Mignot E. The role of hypocretins (orexins) in sleep regulation and narcolepsy. Annu. Rev. Neurosci. 25 (2002) 283-313
-
(2002)
Annu. Rev. Neurosci.
, vol.25
, pp. 283-313
-
-
Taheri, S.1
Zeitzer, J.M.2
Mignot, E.3
|