-
1
-
-
0035312549
-
Molecular mechanisms of memory acquisition, consolidation and retrieval
-
DOI 10.1016/S0959-4388(00)00194-X
-
Abel T, Lattal KM. 2001. Molecular mechanisms of memory acquisition, consolidation and retrieval. Curr Opin Neurobiol 11:180-187. (Pubitemid 32289404)
-
(2001)
Current Opinion in Neurobiology
, vol.11
, Issue.2
, pp. 180-187
-
-
Abel, T.1
Lattal, K.M.2
-
2
-
-
0037738587
-
Restless legs syndrome: Diagnostic criteria, special considerations and epidemiology. A report from the restless legs syndrome diagnosis and epidemiology workshop at the National Institutes of Health
-
Restless Legs Syndrome Diagnosis and Epidemiology workshop at the National Institutes of Health, International Restless Legs Syndrome Study Group
-
Allen RP, Picchietti D, Hening WA, Trenkwalder C, Walters AS, Montplaisi J, Restless Legs Syndrome Diagnosis and Epidemiology workshop at the National Institutes of Health, International Restless Legs Syndrome Study Group. 2003. Restless legs syndrome: Diagnostic criteria, special considerations and epidemiology. A report from the restless legs syndrome diagnosis and epidemiology workshop at the National Institutes of Health. Sleep Med 4:101-119.
-
(2003)
Sleep Med
, vol.4
, pp. 101-119
-
-
Allen, R.P.1
Picchietti, D.2
Hening, W.A.3
Trenkwalder, C.4
Walters, A.S.5
Montplaisi, J.6
-
3
-
-
24944512531
-
Narp immunostaining of human hypocretin (orexin) neurons: Loss in narcolepsy
-
DOI 10.1212/01.wnl.0000175219.01544.c8
-
Blouin AM, Thannickal TC, Worley PF, Baraban JM, Reti IM, Siegel JM. 2005. Narp immunostaining of human hypocretin (orexin) neurons: Loss in narcolepsy. Neurology 65:1189-1192. (Pubitemid 41508209)
-
(2005)
Neurology
, vol.65
, Issue.8
, pp. 1189-1192
-
-
Blouin, A.M.1
Thannickal, T.C.2
Worley, P.F.3
Baraban, J.M.4
Reti, I.M.5
Siegel, J.M.6
-
4
-
-
0038691989
-
Autosomal dominant restless legs syndrome maps on chromosome 14q
-
DOI 10.1093/brain/awg137
-
Bonati MT, Ferini-Strambi L, Aridon P, Oldani A, Zucconi M, Casari G. 2003. Autosomal dominant restless legs syndrome maps on chromosome14q. Brain 126:1485-1492. (Pubitemid 36644391)
-
(2003)
Brain
, vol.126
, Issue.6
, pp. 1485-1492
-
-
Bonati, M.T.1
Ferini-Strambi, L.2
Aridon, P.3
Oldani, A.4
Zucconi, M.5
Casari, G.6
-
5
-
-
33947112891
-
Interaction between the angiotensin-converting enzyme gene insertion/deletion polymorphism and obstructive sleep apnoea as a mechanism for hypertension
-
DOI 10.1097/HJH.0b013e328017f6d5, PII 0000487220070400000008
-
Bostrom KB, Hedner J, Melander O, Grote L, Gullberg B, Rastam L, Groop L, Lindblad U. 2007. Interaction between the angiotensin-converting enzyme gene insertion/deletion polymorphism and obstructive sleep apnoea as a mechanism for hypertension. J Hypertens 25:779-783. (Pubitemid 46398872)
-
(2007)
Journal of Hypertension
, vol.25
, Issue.4
, pp. 779-783
-
-
Bostrom, K.B.1
Hedner, J.2
Melander, O.3
Grote, L.4
Gullberg, B.5
Rastam, L.6
Groop, L.7
Lindblad, U.8
-
6
-
-
0002108048
-
Normal human sleep: Anoverview
-
Kryger MH, Roth T, Dement WC, editors. Philadelphia: Saunders
-
Carskadon MA, Dement WC. 2000. Normal human sleep: Anoverview. In: Kryger MH, Roth T, Dement WC, editors. Principles and practice of sleep medicine. Philadelphia: Saunders. pp. 15-25.
-
(2000)
Principles and Practice of Sleep Medicine
, pp. 15-25
-
-
Carskadon, M.A.1
Dement, W.C.2
-
7
-
-
0002683659
-
Monitoring and staging human sleep
-
Kryger MH, Roth T, Dement WC, editors. Philadelphia: Saunders
-
Carskadon MA, Rechtschaffen A. 2000. Monitoring and staging human sleep. In: Kryger MH, Roth T, Dement WC, editors. Principles and practice of sleep medicine. Philadelphia: Saunders. pp. 1197-1215.
-
(2000)
Principles and Practice of Sleep Medicine
, pp. 1197-1215
-
-
Carskadon, M.A.1
Rechtschaffen, A.2
-
8
-
-
2342527865
-
Genomewide Linkage Scan Identifies a Novel Susceptibility Locus for Restless Legs Syndrome on Chromosome 9p
-
DOI 10.1086/420772
-
Chen S, Ondo WG, Rao S, Li L, Chen Q, Wang Q. 2004. Genomewide linkage scan identifies a novel susceptibility locus for restless legs syndrome on chromosome 9p. Am J Hum Genet 74:876-885. (Pubitemid 38568962)
-
(2004)
American Journal of Human Genetics
, vol.74
, Issue.5
, pp. 876-885
-
-
Chen, S.1
Ondo, W.G.2
Rao, S.3
Li, L.4
Chen, Q.5
Wang, Q.6
-
9
-
-
70449347454
-
Reply to Ray and Weeks: Linkage for restless legs syndrome on chromosome 9p is significant
-
Chen S, Li L, Rao S, Ondo WG, Wang Q. 2005. Reply to Ray and Weeks: Linkage for restless legs syndrome on chromosome 9p is significant. Am J Hum Genet 76:707-710.
-
(2005)
Am J Hum Genet
, vol.76
, pp. 707-710
-
-
Chen, S.1
Li, L.2
Rao, S.3
Ondo, W.G.4
Wang, Q.5
-
10
-
-
0021034398
-
The structure of the occurrence of rapid eye movements in paradoxical sleep is similar in homozygotic twins
-
Chouvet G, Blois R, Debilly G, Jouvet M. 1983. The structure of the occurrence of rapid eye movements in paradoxical sleep is similar in homozygotic twins. C R Seances Acad Sci III 296:1063-1068.
-
(1983)
C R Seances Acad Sci III
, vol.296
, pp. 1063-1068
-
-
Chouvet, G.1
Blois, R.2
Debilly, G.3
Jouvet, M.4
-
11
-
-
24944518715
-
Concomitant loss of dynorphin, NARP, and orexin in narcolepsy
-
DOI 10.1212/01.WNL.0000168173.71940.ab
-
Crocker A, Espana RA, Papadopoulou M, Saper CB, Faraco J, Sakurai T, Honda M, Mignot E, Scammell TE. 2005. Concomitant loss of dynorphin, NARP, and orexin in narcolepsy. Neurology 65:1184-1188. (Pubitemid 41508208)
-
(2005)
Neurology
, vol.65
, Issue.8
, pp. 1184-1188
-
-
Crocker, A.1
Espana, R.A.2
Papadopoulou, M.3
Saper, C.B.4
Faraco, J.5
Sakurai, T.6
Honda, M.7
Mignot, E.8
Scammell, T.E.9
-
12
-
-
4444287267
-
A narcolepsy susceptibility locus maps to a 5Mb region of chromosome 21q
-
DOI 10.1002/ana.20208
-
Dauvilliers Y, Blouin JL, Neidhart E, Carlander B, Eliaou JF, Antonarakis SE, Billiard M, Tafti M. 2004. A narcolepsy susceptibility locus maps to a 5Mb region of chromosome 21q. Ann Neurol 56:382-388. (Pubitemid 39166557)
-
(2004)
Annals of Neurology
, 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
-
13
-
-
0001383694
-
Action potentials of the brain in normal persons and in normal states of cerebral activity
-
Davis H, Davis P. 1936. Action potentials of the brain in normal persons and in normal states of cerebral activity. Arch Neurol Psychiat 36:1214-1224.
-
(1936)
Arch Neurol Psychiat
, vol.36
, pp. 1214-1224
-
-
Davis, H.1
Davis, P.2
-
14
-
-
10444279116
-
Genetic influences in self-reported symptoms of obstructive sleep apnoea and restless legs: A twin study
-
Desai AV, Cherkas LF, Spector TD, Williams AJ. 2004. Genetic influences in self-reported symptoms of obstructive sleep apnoea and restless legs: A twin study. Twin Res 7:589-595.
-
(2004)
Twin Res
, vol.7
, pp. 589-595
-
-
Desai, A.V.1
Cherkas, L.F.2
Spector, T.D.3
Williams, A.J.4
-
15
-
-
0035208888
-
Identification of a major susceptibility locus for restless legs syndrome on chromosome 12q
-
DOI 10.1086/324649
-
Desautels A, Turecki G, Montplaisir J, Sequeira A, Verner A, Rouleau GA. 2001a. Identification of a major susceptibility locus for restless legs syndrome on chromosome 12q. Am J Hum Genet 69:1266-1270. (Pubitemid 33124208)
-
(2001)
American Journal of Human Genetics
, vol.69
, Issue.6
, pp. 1266-1270
-
-
Desautels, A.1
Turecki, G.2
Montplaisir, J.3
Sequeira, A.4
Verner, A.5
Rouleau, G.A.6
-
16
-
-
0035833952
-
Dopaminergic neurotransmission and restless legs syndrome: A genetic association analysis
-
Desautels A, Turecki G, Montplaisir J, Ftouhi-Paquin N, Michaud M, Chouinard VA, Rouleau GA. 2001b. Dopaminergic neurotransmission and restless legs syndrome: A genetic association analysis. Neurology 57:1304-1306. (Pubitemid 32947393)
-
(2001)
Neurology
, vol.57
, Issue.7
, pp. 1304-1306
-
-
Desautels, A.1
Turecki, G.2
Montplaisir, J.3
Ftouhi-Paquin, N.4
Michaud, M.5
Chouinard, V.A.6
Rouleau, G.A.7
-
17
-
-
0037162352
-
Evidence for a genetic association between monoamine oxidase a and restless legs syndrome
-
Desautels A, Turecki G, Montplaisir J, Brisebois K, Sequeira A, Adam B, Rouleau GA. 2002. Evidence for a genetic association between monoamine oxidase A and restless legs syndrome. Neurology 59:215-219. (Pubitemid 34779180)
-
(2002)
Neurology
, vol.59
, Issue.2
, pp. 215-219
-
-
Desautels, A.1
Turecki, G.2
Montplaisir, J.3
Brisebois, K.4
Sequeira, A.5
Adam, B.6
Rouleau, G.A.7
-
18
-
-
20144387708
-
Restless legs syndrome: Confirmation of linkage to chromosome 12q, genetic heterogeneity, and evidence of complexity
-
DOI 10.1001/archneur.62.4.591
-
Desautels A, Turecki G, Montplaisir J, Xiong L, Walters AS, Ehrenberg BL, Brisebois K, Desautels AK, Gingras Y, Johnson WG, Lugaresi E, Coccagna G, Picchietti DL, Lazzarini A, Rouleau GA. 2005. Restless legs syndrome: Confirmation of linkage to chromosome 12q, genetic heterogeneity, and evidence of complexity. Arch Neurol 62:591-596. (Pubitemid 40489891)
-
(2005)
Archives of Neurology
, vol.62
, Issue.4
, pp. 591-596
-
-
Desautels, A.1
Turecki, G.2
Montplaisir, J.3
Xiong, L.4
Walters, A.S.5
Ehrenberg, B.L.6
Brisebois, K.7
Desautels, A.K.8
Gingras, Y.9
Johnson, W.G.10
Lugaresi, E.11
Coccagna, G.12
Picchietti, D.L.13
Lazzarini, A.14
Rouleau, G.A.15
-
20
-
-
0018754405
-
Sleep and dream characteristics in twins
-
Roma
-
Gedda L, Brenci G. 1979. Sleep and dream characteristics in twins. Acta Genet Med Gemellol (Roma) 28:237-239.
-
(1979)
Acta Genet Med Gemellol
, vol.28
, pp. 237-239
-
-
Gedda, L.1
Brenci, G.2
-
21
-
-
0020959797
-
Twins living apart test: Progress report
-
Roma
-
Gedda L, Brenci G. 1983. Twins living apart test: Progress report. Acta Genet Med Gemellol (Roma) 32:17-22.
-
(1983)
Acta Genet Med Gemellol
, vol.32
, pp. 17-22
-
-
Gedda, L.1
Brenci, G.2
-
22
-
-
0035830409
-
A prepro-orexin gene polymorphism is associated with narcolepsy
-
Gencik M, Dahmen N, Wieczorek S, Kasten M, Bierbrauer J, Anghelescu I, Szegedi A, Menezes Saecker AM, Epplen JT. 2001. A prepro-orexin gene polymorphism is associated with narcolepsy. Neurology 56:115-117. (Pubitemid 32059665)
-
(2001)
Neurology
, vol.56
, Issue.1
, pp. 115-117
-
-
Gencik, M.1
Dahmen, N.2
Wieczorek, S.3
Kasten, M.4
Bierbrauer, J.5
Anghelescu, I.6
Szegedi, A.7
Menezes Saecker, A.M.8
Epplen, J.T.9
-
23
-
-
0006060459
-
Ueber den Schlaf von Zwillingen
-
Geyer H. 1937. Ueber den Schlaf von Zwillingen. Z Indukt Abstamm Verebungsl 78:524-527.
-
(1937)
Z Indukt Abstamm Verebungsl
, vol.78
, pp. 524-527
-
-
Geyer, H.1
-
24
-
-
4143049097
-
APOE epsilon4 is associated with obstructive sleep apnea/hypopnea: The Sleep Heart Health Study
-
Gottlieb DJ, DeStefano AL, Foley DJ, Mignot E, Redline S, Givelber RJ, Young T. 2004. APOE epsilon4 is associated with obstructive sleep apnea/ hypopnea: The Sleep Heart Health Study. Neurology 63:664-668. (Pubitemid 39100822)
-
(2004)
Neurology
, vol.63
, Issue.4
, pp. 664-668
-
-
Gottlieb, D.J.1
Destefano, A.L.2
Foley, D.J.3
Mignot, E.4
Redline, S.5
Givelber, R.J.6
Young, T.7
-
25
-
-
34547610061
-
APOE epsilon4 allele, cognitive dysfunction, and obstructive sleep apnea in children
-
DOI 10.1212/01.wnl.0000265818.88703.83, PII 0000611420070717000004
-
Gozal D, Capdevila OS, Kheirandish-Gozal L, Crabtree VM. 2007. APOE epsilon-4 allele, cognitive dysfunction, and obstructive sleep apnea in children. Neurology 69:243-249. (Pubitemid 47205685)
-
(2007)
Neurology
, vol.69
, Issue.3
, pp. 243-249
-
-
Gozal, D.1
Capdevila, O.S.2
Kheirandish-Gozal, L.3
Crabtree, V.M.4
-
26
-
-
0025184217
-
Evidence for genetic influences on sleep disturbance and sleep pattern in twins
-
Heath AC, Kendler KS, Eaves LJ, Martin NG. 1990. Evidence for genetic influences on sleep disturbance and sleep pattern in twins. Sleep 13:318-335.
-
(1990)
Sleep
, vol.13
, pp. 318-335
-
-
Heath, A.C.1
Kendler, K.S.2
Eaves, L.J.3
Martin, N.G.4
-
27
-
-
33748456545
-
Sleep, dreaming, and wakefulness
-
Squire LR, Bloom FE, McConnell SK, Roberts JL, Spitzer NC, Zigmond MJ, editors. 2nd edition. Amsterdam: Academic Press
-
Hobson JA, Pace-Schott EF. 2003. Sleep, dreaming, and wakefulness. In: Squire LR, Bloom FE, McConnell SK, Roberts JL, Spitzer NC, Zigmond MJ, editors. Fundamental neuroscience. 2nd edition. Amsterdam: Academic Press. pp. 1085-1108.
-
(2003)
Fundamental Neuroscience
, pp. 1085-1108
-
-
Hobson, J.A.1
Pace-Schott, E.F.2
-
28
-
-
20444372942
-
Restless legs syndrome: A community-based study of prevalence, severity, and risk factors
-
DOI 10.1212/01.WNL.0000163996.64461.A3
-
Hogl B, Kiechl S, Willeit J, Saletu M, Frauscher B, Seppi K, Muller J, Rungger G, Gasperi A, Wenning G, Poewe W. 2005. Restless legs syndrome: A community-based study of prevalence, severity, and risk factors. Neurology 64:1920-1924. (Pubitemid 40800707)
-
(2005)
Neurology
, vol.64
, Issue.11
, pp. 1920-1924
-
-
Hogl, B.1
Kiechl, S.2
Willeit, J.3
Saletu, M.4
Frauscher, B.5
Seppi, K.6
Muller, J.7
Rungger, G.8
Gasperi, A.9
Wenning, G.10
Poewe, W.11
-
29
-
-
0022512644
-
Sleep characteristics in twins
-
Hori A. 1986. Sleep characteristics in twins. Jpn J Psychiatry Neurol 40:35-46.
-
(1986)
Jpn J Psychiatry Neurol
, vol.40
, pp. 35-46
-
-
Hori, A.1
-
31
-
-
33744534836
-
Periodic leg movements in sleep and periodic limb movement disorder: Prevalence, clinical significance and treatment
-
DOI 10.1016/j.smrv.2005.12.003, PII S1087079205001437
-
Hornyak M, Feige B, Riemann D, Voderholzer U. 2006. Periodic leg movements in sleep and periodic limb movement disorder: Prevalence, clinical significance and treatment. Sleep Med Rev 10:169-177. (Pubitemid 44177433)
-
(2006)
Sleep Medicine Reviews
, vol.10
, Issue.3
, pp. 169-177
-
-
Hornyak, M.1
Feige, B.2
Riemann, D.3
Voderholzer, U.4
-
32
-
-
0035960658
-
Polymorphisms in the vicinity of the hypocretin/orexin are not associated with human narcolepsy
-
Hungs M, Lin L, Okun M, Mignot E. 2001. Polymorphisms in the vicinity of the hypocretin/orexin are not associated with human narcolepsy. Neurology 57:1893-1895. (Pubitemid 33096703)
-
(2001)
Neurology
, vol.57
, Issue.10
, pp. 1893-1895
-
-
Hungs, M.1
Lin, L.2
Okun, M.3
Mignot, E.4
-
33
-
-
3042742483
-
-
International Classification of Sleep Disorders. Rochester, Minnesota: American Academy of Sleep Medicine
-
International Classification of Sleep Disorders. 2005. Version 2: Diagnostic and coding manual. Rochester, Minnesota: American Academy of Sleep Medicine.
-
(2005)
Version 2: Diagnostic and Coding Manual
-
-
-
34
-
-
0035854022
-
Association between apolipoprotein e epsilon4 and sleep-disordered breathing in adults
-
Kadotani H, Kadotani T, Young T, Peppard PE, Finn L, Colrain IM, Murphy GM Jr, Mignot E. 2001. Association between apolipoprotein E epsilon4 and sleep-disordered breathing in adults. JAMA 285: 2888-2890. (Pubitemid 32537353)
-
(2001)
Journal of the American Medical Association
, vol.285
, Issue.22
, pp. 2888-2890
-
-
Kadotani, H.1
Kadotani, T.2
Young, T.3
Peppard, P.E.4
Finn, L.5
Colrain, I.M.6
Murphy Jr., G.M.7
Mignot, E.8
-
35
-
-
1242317710
-
The glutamate/neutral amino acid transporter family SLC1: Molecular, physiological and pharmacological aspects
-
DOI 10.1007/s00424-003-1146-4, The ABCs of Solute Carriers: Physiological, Pathological and Therapeutic Implications of Human Membrane Transport Proteins
-
Kanai Y, Hediger MA. 2004. The glutamate/neutral amino acid transporter family SLC1: Molecular, physiological and pharmacological aspects. Pflugers Arch 447:469-479. (Pubitemid 38241433)
-
(2004)
Pflugers Archiv European Journal of Physiology
, vol.447
, Issue.5
, pp. 469-479
-
-
Kanai, Y.1
Hediger, M.A.2
-
36
-
-
33746472884
-
Genomewide association analysis of human narcolepsy and a new resistance gene
-
DOI 10.1086/505539
-
Kawashima M, Tamiya G, Oka A, Hohjoh H, Juji T, Ebisawa T, Honda Y, Inoko H, Tokunaga K. 2006. Genomewide association analysis of human narcolepsy and a new resistance gene. Am J Hum Genet 79:252-263. (Pubitemid 44141824)
-
(2006)
American Journal of Human Genetics
, vol.79
, Issue.2
, pp. 252-263
-
-
Kawashima, M.1
Tamiya, G.2
Oka, A.3
Hohjoh, H.4
Juji, T.5
Ebisawa, T.6
Honda, Y.7
Inoko, H.8
Tokunaga, K.9
-
37
-
-
0022749581
-
Characterization of a human gene inducible by alpha- and beta-interferons and its expression in mouse cells
-
Kelly JM, Porter AC, Chernajovsky Y, Gilbert CS, Stark GR, Kerr IM. 1986. Characterization of a human gene inducible by alpha- and beta-interferons and its expression in mouse cells. EMBO J 5:1601-1606.
-
(1986)
EMBO J
, vol.5
, pp. 1601-1606
-
-
Kelly, J.M.1
Porter, A.C.2
Chernajovsky, Y.3
Gilbert, C.S.4
Stark, G.R.5
Kerr, I.M.6
-
38
-
-
33847735100
-
Family-based association study of the restless legs syndrome loci 2 and 3 in a European population
-
DOI 10.1002/mds.21254
-
Kemlink D, Polo O, Montagna P, Provini F, Stiasny-Kolster K, Oertel W, de Weerd A, Nevsimalova S, Sonka K, Högl B, Frauscher B, Poewe W, Trenkwalder C, Pramstaller PP, Ferini-Strambi L, Zucconi M, Konofal E, Arnulf I, Hadjigeorgiou GM, Happe S, Klein C, Hiller A, Lichtner P, Meitinger T, Müller-Myshok B, Winkelmann J. 2007. Family-based association study of the restless legs syndrome loci 2 and 3 in a European population. Mov Disord 22:207-212. (Pubitemid 46374763)
-
(2007)
Movement Disorders
, vol.22
, Issue.2
, pp. 207-212
-
-
Kemlink, D.1
Polo, O.2
Montagna, P.3
Provini, F.4
Stiasny-Kolster, K.5
Oertel, W.6
De Weerd, A.7
Nevsimalova, S.8
Sonka, K.9
Hogl, B.10
Frauscher, B.11
Poewe, W.12
Trenkwalder, C.13
Pramstaller, P.P.14
Ferini-Strambi, L.15
Zucconi, M.16
Konofal, E.17
Arnulf, I.18
Hadjigeorgiou, G.M.19
Happe, S.20
Klein, C.21
Hiller, A.22
Lichtner, P.23
Meitinger, T.24
Muller-Myshok, B.25
Winkelmann, J.26
more..
-
39
-
-
42149093971
-
Suggestive evidence for linkage for restless legs syndrome on chromosome 19p13
-
Kemlink D, Plazzi G, Vetrugno R, Provini F, Polo O, Stiasny-Kolster K, Oertel W, Nevsimalova S, Sonka K, Högl B, Frauscher B, Hadjigeorgiou GM, Pramstaller PP, Lichtner P, Meitinger T, Müller-Myshok B, Winkelmann J, Montagna P. 2008. Suggestive evidence for linkage for restless legs syndrome on chromosome 19p13. Neurogenetics 9:75-82.
-
(2008)
Neurogenetics
, vol.9
, pp. 75-82
-
-
Kemlink, D.1
Plazzi, G.2
Vetrugno, R.3
Provini, F.4
Polo, O.5
Stiasny-Kolster, K.6
Oertel, W.7
Nevsimalova, S.8
Sonka, K.9
Högl, B.10
Frauscher, B.11
Hadjigeorgiou, G.M.12
Pramstaller, P.P.13
Lichtner, P.14
Meitinger, T.15
Müller-Myshok, B.16
Winkelmann, J.17
Montagna, P.18
-
40
-
-
18444418887
-
Mode of inheritance and susceptibility locus for restless legs syndrome, on chromosome 12q [2] (multiple letters)
-
DOI 10.1086/341097
-
Kock N, Culjkovic B, Maniak S, Schilling K, Muller B, Zuhlke C, Ozelius L, Klein C, Pramstaller PP, Kramer PL. 2002. Mode of inheritance and susceptibility locus for restless legs syndrome, on chromosome 12q. Am J Hum Genet 71:205-208. (Pubitemid 34734726)
-
(2002)
American Journal of Human Genetics
, vol.71
, Issue.1
, pp. 205-208
-
-
Kock, N.1
Culjkovic, B.2
Maniak, S.3
Schilling, K.4
Muller, B.5
Zuhlke, C.6
Ozelius, L.7
Klein, C.8
Pramstaller, P.P.9
Kramer, P.L.10
Desautels, A.11
Turecki, G.12
Montplaisir, J.13
Rouleau, G.A.14
-
41
-
-
32044474687
-
Apolipoprotein e and obstructive sleep apnea: Evaluating whether a candidate gene explains a linkage peak
-
DOI 10.1002/gepi.20127
-
Larkin EK, Patel SR, Redline S, Mignot E, Elston RC, Hallmayer J. 2006. Apolipoprotein E and obstructive sleep apnea: Evaluating whether a candidate gene explains a linkage peak. Genet Epidemiol 30:101-110. (Pubitemid 43201583)
-
(2006)
Genetic Epidemiology
, vol.30
, Issue.2
, pp. 101-110
-
-
Larkin, E.K.1
Patel, S.R.2
Redline, S.3
Mignot, E.4
Elston, R.C.5
Hallmayer, J.6
-
42
-
-
14644421238
-
The intelligence and the electroencephalograms of normal and epileptic twins
-
Lennox W, Gibbs E. 1944. The intelligence and the electroencephalograms of normal and epileptic twins. Trans Am Neurol Assoc 70:182-184.
-
(1944)
Trans Am Neurol Assoc
, vol.70
, pp. 182-184
-
-
Lennox, W.1
Gibbs, E.2
-
43
-
-
77957217441
-
The brain-wave pattern and hereditary trait
-
Lennox W, Gibbs E, Gibbs F. 1945. The brain-wave pattern and hereditary trait. J Heredity 36:233-243.
-
(1945)
J Heredity
, vol.36
, pp. 233-243
-
-
Lennox, W.1
Gibbs, E.2
Gibbs, F.3
-
44
-
-
2542595563
-
The 14q restless legs syndrome locus in the French Canadian population
-
DOI 10.1002/ana.20140
-
Levchenko A, Montplaisir JY, Dube MP, Riviere JB, St-Onge J, Turecki G, Xiong L, Thibodeau P, Desautels A, Verlaan DJ, Rouleau GA. 2004. The 14q restless legs syndrome locus in the French Canadian population. Ann Neurol 55:887-891. (Pubitemid 38702587)
-
(2004)
Annals of Neurology
, vol.55
, Issue.6
, pp. 887-891
-
-
Levchenko, A.1
Montplaisir, J.-Y.2
Dube, M.-P.3
Riviere, J.-B.4
St-Onge, J.5
Turecki, G.6
Xiong, L.7
Thibodeau, P.8
Desautels, A.9
Verlaan, D.J.10
Rouleau, G.A.11
-
45
-
-
33748696387
-
A novel autosomal dominant restless legs syndrome locus maps to chromosome 20p13
-
DOI 10.1212/01.wnl.0000233991.20410.b6, PII 0000611420060912000042
-
Levchenko A, Provost S, Montplaisir JY, Xiong L, St-Onge J, Thibodeau P, Riviere JB, Desautels A, Turecki G, Dube MP, Rouleau GA. 2006. A novel autosomal dominant restless legs syndrome locus maps to chromosome 20p13. Neurology 67:900-901. (Pubitemid 44394216)
-
(2006)
Neurology
, vol.67
, Issue.5
, pp. 900-901
-
-
Levchenko, A.1
Provost, S.2
Montplaisir, J.Y.3
Xiong, L.4
St-Onge, J.5
Thibodeau, P.6
Riviere, J.B.7
Desautels, A.8
Turecki, G.9
Dube, M.P.10
Rouleau, G.A.11
-
46
-
-
0037396082
-
Linkage analysis of the candidate genes of familial restless legs syndrome
-
Li J, Hu LD, Wang WJ, Chen YG, Kong XY. 2003. Linkage analysis of the candidate genes of familial restless legs syndrome. Yi Chuan Xue Bao 30:325-329. (Pubitemid 36505799)
-
(2003)
Acta Genetica Sinica
, vol.30
, Issue.4
, pp. 325-329
-
-
Li, J.1
Hu, L.-D.2
Wang, W.-J.3
Chen, Y.-G.4
Kong, X.-Y.5
-
47
-
-
33747037830
-
RLS3: Fine-mapping of an autosomal dominant locus in a family with intrafamilial heterogeneity
-
DOI 10.1212/01.wnl.0000224886.65213.b5, PII 0000611420060725000033
-
Liebetanz KM, Winkelmann J, Trenkwalder C, Putz B, Dichgans M, Gasser T, Muller-Myhsok B. 2006. RLS3: Fine-mapping of an autosomal dominant locus in a family with intrafamilial heterogeneity. Neurology 67:320-321. (Pubitemid 44305424)
-
(2006)
Neurology
, vol.67
, Issue.2
, pp. 320-321
-
-
Liebetanz, K.M.1
Winkelmann, J.2
Trenkwalder, C.3
Putz, B.4
Dichgans, M.5
Gasser, T.6
Muller-Myhsok, B.7
-
48
-
-
0033057814
-
EEG sleep patterns in twins
-
Linkowski P. 1999. EEG sleep patterns in twins. J Sleep Res 1:11-13.
-
(1999)
J Sleep Res
, vol.1
, pp. 11-13
-
-
Linkowski, P.1
-
49
-
-
0024467138
-
EEG sleep patterns in man: A twin study
-
Linkowski P, Kerkhofs M, Hauspie R, Susanne C, Mendlewicz J. 1989. EEG sleep patterns in man: A twin study. Electroencephalogr Clin Neurophysiol 73:279-284. (Pubitemid 19237091)
-
(1989)
Electroencephalography and Clinical Neurophysiology
, vol.73
, Issue.4
, pp. 279-284
-
-
Linkowski, P.1
Kerkhofs, M.2
Hauspie, R.3
Susanne, C.4
Mendlewicz, J.5
-
51
-
-
40349112722
-
Evidence for linkage of restless legs syndrome to chromosome 9p: Are there two distinct loci?
-
Lohmann-Hedrich K, Neumann A, Kleensang A, Lohnau T, Muhle H, Djarmati A, Konig IR, Pramstaller PP, Schwinger E, Kramer PL, Ziegler A, Stephani U, Klein C. 2008. Evidence for linkage of restless legs syndrome to chromosome 9p: Are there two distinct loci? Neurology 70:686-694.
-
(2008)
Neurology
, vol.70
, pp. 686-694
-
-
Lohmann-Hedrich, K.1
Neumann, A.2
Kleensang, A.3
Lohnau, T.4
Muhle, H.5
Djarmati, A.6
Konig, I.R.7
Pramstaller, P.P.8
Schwinger, E.9
Kramer, P.L.10
Ziegler, A.11
Stephani, U.12
Klein, C.13
-
52
-
-
0023870835
-
Familial 'sleep apnea plus' syndrome: Report of a family
-
Manon-Espaillat R, Gothe B, Adams N, Newman C, Ruff R. 1988. Familial 'sleep apnea plus' syndrome: Report of a family. Neurology 38:190-193.
-
(1988)
Neurology
, vol.38
, pp. 190-193
-
-
Manon-Espaillat, R.1
Gothe, B.2
Adams, N.3
Newman, C.4
Ruff, R.5
-
53
-
-
0031464185
-
Nuclear cotransport mechanism of cytoplasmic human MxB protein
-
DOI 10.1074/jbc.272.51.32353
-
Melen K, Julkunen I. 1997. Nuclear cotransport mechanism of cytoplasmic human MxB protein. J Biol Chem 272:32353-32359. (Pubitemid 28011917)
-
(1997)
Journal of Biological Chemistry
, vol.272
, Issue.51
, pp. 32353-32359
-
-
Melen, K.1
Julkunen, I.2
-
54
-
-
4344609367
-
Sleep, sleep disorders and hypocretin (orexin)
-
Mignot E. 2004. Sleep, sleep disorders and hypocretin (orexin). Sleep Med 5:S2-S8.
-
(2004)
Sleep Med
, vol.5
-
-
Mignot, E.1
-
55
-
-
0034176716
-
Linkage of human narcolepsy with HLA association to chromosome 4p13-q21
-
DOI 10.1006/geno.2000.6143
-
Nakayama J, Miura M, Honda M, Miki T, Honda Y, Arinami T. 2000. Linkage of human narcolepsy with HLA association to chromosome 4p13-q21. Genomics 65:84-86. (Pubitemid 30249921)
-
(2000)
Genomics
, vol.65
, Issue.1
, pp. 84-86
-
-
Nakayama, J.1
Miura, M.2
Honda, M.3
Miki, T.4
Honda, Y.5
Arinami, T.6
-
56
-
-
23844554159
-
Nocturnal sleep apnea/hypopnea is associated with lower memory performance in APOE epsilon4 carriers
-
DOI 10.1212/01.wnl.0000173055.75950.bf
-
O'Hara R, Schroder CM, Kraemer HC, Kryla N, Cao C, Miller E, Schatzberg AF, Yesavage JA, Murphy GM Jr. 2005. Nocturnal sleep apnea/hypopnea is associated with lower memory performance in APOE epsilon-4 carriers. Neurology 65:642-644. (Pubitemid 41170736)
-
(2005)
Neurology
, vol.65
, Issue.4
, pp. 642-644
-
-
O'Hara, R.1
Schroder, C.M.2
Kraemer, H.C.3
Kryla, N.4
Cao, C.5
Miller, E.6
Schatzberg, A.F.7
Yesavage, J.A.8
Murphy Jr., G.M.9
-
57
-
-
0020629497
-
Genetic and environmental determination of human sleep
-
Partinen M, Kaprio J, Koskenvuo M, Putkonen P, Langinvainio H. 1983. Genetic and environmental determination of human sleep. Sleep 6:179-185.
-
(1983)
Sleep
, vol.6
, pp. 179-185
-
-
Partinen, M.1
Kaprio, J.2
Koskenvuo, M.3
Putkonen, P.4
Langinvainio, H.5
-
58
-
-
0033826856
-
A mutation in a case of early onset narcolepsy and a generalized absence of hypocretin peptides in human narcoleptic brains
-
Peyron C, Faraco J, Rogers W, Ripley B, Overeem S, Charnay Y, 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. 2000. A mutation in a case of early onset narcolepsy and a generalized absence of hypocretin peptides in human narcoleptic brains. Nature Med 6:991-997.
-
(2000)
Nature Med
, vol.6
, pp. 991-997
-
-
Peyron, C.1
Faraco, J.2
Rogers, W.3
Ripley, B.4
Overeem, S.5
Charnay, Y.6
Aldrich, M.7
Reynolds, D.8
Albin, R.9
Li, R.10
Hungs, M.11
Pedrazzoli, M.12
Padigaru, M.13
Kucherlapati, M.14
Fan, J.15
Maki, R.16
Lammers, G.J.17
Bouras, C.18
Kucherlapati, R.19
Nishino, S.20
Mignot, E.21
more..
-
59
-
-
33749005651
-
Linkage analysis identifies a novel locus for restless legs syndrome on chromosome 2q in a South Tyrolean population isolate
-
Pichler I, Marroni F, Volpato CB, Gusella JF, Klein C, Casari G, De Grandi A, Pramstaller PP. 2006. Linkage analysis identifies a novel locus for restless legs syndrome on chromosome 2q in a South Tyrolean population isolate. Am J Hum Genet 79:716-723.
-
(2006)
Am J Hum Genet
, vol.79
, pp. 716-723
-
-
Pichler, I.1
Marroni, F.2
Volpato, C.B.3
Gusella, J.F.4
Klein, C.5
Casari, G.6
De Grandi, A.7
Pramstaller, P.P.8
-
60
-
-
39049126446
-
The epidemiology of adult obstructive sleep apnea
-
DOI 10.1513/pats.200709-155MG
-
Punjabi NM. 2008. The epidemiology of adult obstructive sleep apnea. Proc Am Thorac Soc 5:136-143. (Pubitemid 351237871)
-
(2008)
Proceedings of the American Thoracic Society
, vol.5
, Issue.2
, pp. 136-143
-
-
Punjabi, N.M.1
-
61
-
-
15944376234
-
No convincing evidence of linkage for restless legs syndrome on chromosome 9p
-
Ray A, Weeks DE. 2005. No convincing evidence of linkage for restless legs syndrome on chromosome 9p. Am J Hum Genet 76:705-707.
-
(2005)
Am J Hum Genet
, vol.76
, pp. 705-707
-
-
Ray, A.1
Weeks, D.E.2
-
62
-
-
27344454837
-
A functional genetic variation of adenosine deaminase affects the duration and intensity of deep sleep in humans
-
DOI 10.1073/pnas.0505414102
-
Retey JV, Adam M, Honegger E, Khatami R, Luhmann UF, Jung HH, Berger W, Landolt HP. 2005. A function genetic variation of adenosine deaminase affects the duration and intensity of deep sleep in humans. Proc Natl Acad Sci 102:15676-15681. (Pubitemid 41528115)
-
(2005)
Proceedings of the National Academy of Sciences of the United States of America
, vol.102
, Issue.43
, pp. 15676-15681
-
-
Retey, J.V.1
Adam, M.2
Honegger, E.3
Khatami, R.4
Luhmann, U.F.O.5
Jung, H.H.6
Berger, W.7
Landolt, H.-P.8
-
63
-
-
0037623288
-
+-selective family of ion channels using a comprehensive alignment and the KcsA channel structure
-
Shealy RT, Murphy AD, Ramarathnam R, Jakobsson E, Subramaniam S. 2003. Sequence-function analysis of the K+-selective family of ion channels using a comprehensive alignment and the KcsA channel structure. Biophys J 84:2929-2942. (Pubitemid 36531745)
-
(2003)
Biophysical Journal
, vol.84
, Issue.5
, pp. 2929-2942
-
-
Shealy, R.T.1
Murphy, A.D.2
Ramarathnam, R.3
Jakobsson, E.4
Subramaniam, S.5
-
64
-
-
27644580795
-
Clues to the functions of mammalian sleep
-
Siegel JM. 2005. Clues to the functions of mammalian sleep. Nature 437:1264-1271.
-
(2005)
Nature
, vol.437
, pp. 1264-1271
-
-
Siegel, J.M.1
-
65
-
-
0036815572
-
Genetic variation of apolipoproteins in North Indians
-
Singh PP, Singh M, Mastana SS. 2002. Genetic variation of apolipoproteins in North Indians. Hum Biol 74:673-682. (Pubitemid 35426680)
-
(2002)
Human Biology
, vol.74
, Issue.5
, pp. 673-682
-
-
Singh, P.P.1
Singh, M.2
Mastana, S.S.3
-
66
-
-
0025138795
-
Interferon-induced proteins and the antiviral state
-
Staeheli P. 1990. Interferon-induced proteins and the antiviral state. Adv Virus Res 38:147-200.
-
(1990)
Adv Virus Res
, vol.38
, pp. 147-200
-
-
Staeheli, P.1
-
67
-
-
0023779963
-
Genetic determination of the human EEG. Survey of recent results on twins reared together and apart
-
Stassen HH, Lykken DT, Propping P, Bomben G. 1988. Genetic determination of the human EEG. Survey of recent results on twins reared together and apart. Hum Genet 80:165-176.
-
(1988)
Hum Genet
, vol.80
, pp. 165-176
-
-
Stassen, H.H.1
Lykken, D.T.2
Propping, P.3
Bomben, G.4
-
68
-
-
34547926806
-
A genetic risk factor for periodic limb movements in sleep
-
DOI 10.1056/NEJMoa072743
-
Stefansson H, Rye DB, Hicks A, Petursson H, Ingason A, Thorgeirsson TE, Palsson S, Sigmundsson T, Sigurdsson AP, Eiriksdottir I, Soebech E, Bliwise D, Beck JM, Rosen A, Waddy S, Trotti LM, Iranzo A, Thambisetty M, Hardarson GA, Kristjansson K, Gudmundsson LJ, Thorsteinsdottir U, Kong A, Gulcher JR, Gudbjartsson D, Stefansson K. 2007. A genetic risk factor for periodic limb movements in sleep. N Engl J Med 357:639-647. (Pubitemid 47267233)
-
(2007)
New England Journal of Medicine
, vol.357
, Issue.7
, pp. 639-647
-
-
Stefansson, H.1
Rye, D.B.2
Hicks, A.3
Petursson, H.4
Ingason, A.5
Thorgeirsson, T.E.6
Palsson, S.7
Sigmundsson, T.8
Sigurdsson, A.P.9
Eiriksdottir, I.10
Soebech, E.11
Bliwise, D.12
Beck, J.M.13
Rosen, A.14
Waddy, S.15
Trotti, L.M.16
Iranzo, A.17
Thambisetty, M.18
Hardarson, G.A.19
Kristjansson, K.20
Gudmundsson, L.J.21
Thorsteinsdottir, U.22
Kong, A.23
Gulcher, J.R.24
Gudbjartsson, D.25
Stefansson, K.26
more..
-
69
-
-
0026553008
-
Localization of a gene for the human low voltage EEG on 20q and genetic heterogeneity
-
Steinlein O, Anokhin A, Yping M, Schalt E, Vogel F. 1992. Localization of a gene for the human low voltage EEG on 20q and genetic heterogeneity. Genomics 12:69-73.
-
(1992)
Genomics
, vol.12
, pp. 69-73
-
-
Steinlein, O.1
Anokhin, A.2
Yping, M.3
Schalt, E.4
Vogel, F.5
-
70
-
-
0012110908
-
The genetics of sleep disorders
-
Taheri S, Mignot E. 2002. The genetics of sleep disorders. Lancet Neurol 1:242-250.
-
(2002)
Lancet Neurol
, vol.1
, pp. 242-250
-
-
Taheri, S.1
Mignot, E.2
-
71
-
-
34547677716
-
Identification of differentially expressed genes in blood cells of narcolepsy patients
-
Tanaka S, Honda Y, Honda M. 2007. Identification of differentially expressed genes in blood cells of narcolepsy patients. Sleep 30:974-979. (Pubitemid 47221897)
-
(2007)
Sleep
, vol.30
, Issue.8
, pp. 974-979
-
-
Tanaka, S.1
Honda, Y.2
Honda, M.3
-
72
-
-
0032489347
-
Cloning and characterization of MUPP1, a novel PDZ domain protein
-
DOI 10.1016/S0014-5793(98)00141-0, PII S0014579398001410
-
Ullmer C, Schmuck K, Figge A, Lubbert H. 1998. Cloning and characterization of MUPP1, a novel PDZ domain protein. FEBS Lett 424:63-68. (Pubitemid 28130353)
-
(1998)
FEBS Letters
, vol.424
, Issue.1-2
, pp. 63-68
-
-
Ullmer, C.1
Schmuck, K.2
Figge, A.3
Lubbert, H.4
-
73
-
-
0030029838
-
Heritability of human brain functioning as assessed by electroencephalography
-
Van Beijsterveldt CE, Molenaar PC, de Geus EJ, Boomsma DI. 1996. Heritability of human brain functioning as assessed by electroencephalography. Am J Hum Genet 58:562-573. (Pubitemid 26062487)
-
(1996)
American Journal of Human Genetics
, vol.58
, Issue.3
, pp. 562-573
-
-
Van Beijsterveldt, C.E.M.1
Molenaar, P.C.M.2
De Geus, E.J.C.3
Boomsma, D.I.4
-
74
-
-
0014953006
-
The genetic basis of the normal human electroencephalogram (EEG)
-
Vogel F. 1970. The genetic basis of the normal human electroencephalogram (EEG). Humangenetik 10:91-114.
-
(1970)
Humangenetik
, vol.10
, pp. 91-114
-
-
Vogel, F.1
-
75
-
-
33748341110
-
Restless legs syndrome: Epidemiological and clinicogenetic study in a South Tyrolean population isolate
-
Vogl FD, Pichler I, Adel S, Pinggera GK, Bracco S, DeGrandi A, Volpato CB, Aridon P, Mayer T, Meitinger T, Klein C, Casari G, Pramstaller PP. 2006. Restless legs syndrome: Epidemiological and clinicogenetic study in a South Tyrolean population isolate. Mov Disord 21:1189-1195.
-
(2006)
Mov Disord
, vol.21
, pp. 1189-1195
-
-
Vogl, F.D.1
Pichler, I.2
Adel, S.3
Pinggera, G.K.4
Bracco, S.5
DeGrandi, A.6
Volpato, C.B.7
Aridon, P.8
Mayer, T.9
Meitinger, T.10
Klein, C.11
Casari, G.12
Pramstaller, P.P.13
-
76
-
-
0020503776
-
Relationships in sleep characteristics of identical and fraternal twins
-
Webb WB, Campbell SS. 1983. Relationships in sleep characteristics of identical and fraternal twins. Arch Gen Psychiatry 40:1093-1095.
-
(1983)
Arch Gen Psychiatry
, vol.40
, pp. 1093-1095
-
-
Webb, W.B.1
Campbell, S.S.2
-
77
-
-
33244486964
-
Evidence for further genetic heterogeneity and confirmation of RLS-1 in restless legs syndrome
-
DOI 10.1002/mds.20627
-
Winkelmann J, Lichtner P, Putz B, Trenkwalder C, Hauk S, Meitinger T, Strom T, Muller-Myhsok B. 2006. Evidence for further genetic locus heterogeneity and confirmation of RLS-1 in restless legs syndrome. Mov Disord 21:28-33. (Pubitemid 43273746)
-
(2006)
Movement Disorders
, vol.21
, Issue.1
, pp. 28-33
-
-
Winkelmann, J.1
Lichtner, P.2
Putz, B.3
Trenkwalder, C.4
Hauk, S.5
Meitinger, T.6
Strom, T.7
Muller-Myhsok, B.8
-
78
-
-
34547497308
-
Genome-wide association study of restless legs syndrome identifies common variants in three genomic regions
-
DOI 10.1038/ng2099, PII NG2099
-
Winkelmann J, Schormair B, Lichtner P, Ripke S, Xiong L, Jalilzadeh S, Fulda S, Putz B, Eckstein G, Hauk S, Trenkwalder C, Zimprich A, Stiasny-Kolster K, Oertel W, Bachmann CG, Paulus W, Peglau I, Eisensehr I, Montplaisir J, Turecki G, Rouleau G, Gieger C, Illig T, Wichmann HE, Holsboer F, Muller-Myhsok B, Meitinger T. 2007. Genome-wide association study of restless legs syndrome identifies common variants in three genomic regions. Nat Genet 39:1000-1006. (Pubitemid 47185185)
-
(2007)
Nature Genetics
, vol.39
, Issue.8
, pp. 1000-1006
-
-
Winkelmann, J.1
Schormair, B.2
Lichtner, P.3
Ripke, S.4
Xiong, L.5
Jalilzadeh, S.6
Fulda, S.7
Putz, B.8
Eckstein, G.9
Hauk, S.10
Trenkwalder, C.11
Zimprich, A.12
Stiasny-Kolster, K.13
Oertel, W.14
Bachmann, C.G.15
Paulus, W.16
Peglau, I.17
Eisensehr, I.18
Montplaisir, J.19
Turecki, G.20
Rouleau, G.21
Gieger, C.22
Illig, T.23
Wichmann, H.-E.24
Holsboer, F.25
Muller-Myhsok, B.26
Meitinger, T.27
more..
-
79
-
-
34248161525
-
Canadian restless legs syndrome twin study
-
DOI 10.1212/01.wnl.0000261016.90374.fd, PII 0000611420070508000016
-
Xiong L, Jang K, Montplaisir J, Levchenko A, Thibodeau P, Gaspar C, Turecki G, Rouleau GA. 2007a. Canadian restless legs syndrome twin study. Neurology 68:1631-1633. (Pubitemid 46717991)
-
(2007)
Neurology
, vol.68
, Issue.19
, pp. 1631-1633
-
-
Xiong, L.1
Jang, K.2
Montplaisir, J.3
Levchenko, A.4
Thibodeau, P.5
Gaspar, C.6
Turecki, G.7
Rouleau, G.A.8
-
80
-
-
35148838500
-
Molecular genetic studies of DMT1 on 12q in French-Canadian restless legs syndrome patients and families
-
DOI 10.1002/ajmg.b.30528
-
Xiong L, Dion P, Montplaisir J, Levchenko A, Thibodeau P, Karemera L, Riviere JB, St-Onge J, Gaspar C, Dube MP, Desautels A, Turecki G, Rouleau GA. 2007b. Molecular genetic studies of DMT1 on 12q in French -Canadian restless legs syndrome patients and families. Am J Med Genet Part B 144B:911-917. (Pubitemid 47547993)
-
(2007)
American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics
, vol.144
, Issue.7
, pp. 911-917
-
-
Xiong, L.1
Dion, P.2
Montplaisir, J.3
Levchenko, A.4
Thibodeau, P.5
Karemera, L.6
Riviere, J.-B.7
St-Onge, J.8
Gaspar, C.9
Dube, M.-P.10
Desautels, A.11
Turecki, G.12
Rouleau, G.A.13
-
81
-
-
0033804342
-
Angiotensin-converting enzyme gene insertion/deletion (I/D) polymorphism in hypertensive patients with different degrees of obstructive sleep apnea
-
Zhang J, Zhao B, Gesongluobu SY, Sun Y, Wu Y, Pei W, Ye J, Hui R, Liu L. 2000. Angiotensin-converting enzyme gene insertion/deletion (I/D) polymorphism in hypertensive patients with different degrees of obstructive sleep apnea. Hypertens Res 23:407-411. (Pubitemid 30742113)
-
(2000)
Hypertension Research
, vol.23
, Issue.5
, pp. 407-411
-
-
Zhang, J.1
Zhao, B.2
Gesongluobu3
Sun, Y.4
Wu, Y.5
Pei, W.6
Ye, J.7
Hui, R.8
Liu, L.9
-
82
-
-
0014002174
-
Sleep and dream patterns in twins. Markov analysis of a genetic trait
-
Zung WW, Wilson WP. 1966. Sleep and dream patterns in twins. Markov analysis of a genetic trait. Recent Adv Biol Psychiatry 9:119-130.
-
(1966)
Recent Adv Biol Psychiatry
, vol.9
, pp. 119-130
-
-
Zung, W.W.1
Wilson, W.P.2
|