-
1
-
-
0038364971
-
Sleep disorders
-
Nunes ML. Sleep disorders. J Pediatr (Rio J). 2002;78 Suppl 1:S63-72.
-
(2002)
J Pediatr (Rio J)
, vol.78
, Issue.SUPPL. 1
-
-
Nunes, M.L.1
-
2
-
-
34249701848
-
Narcolepsy and familial advanced sleep-phase syndrome: Molecular genetics of sleep disorders
-
Tafti M, Dauvilliers Y, Overeem S. Narcolepsy and familial advanced sleep-phase syndrome: molecular genetics of sleep disorders. Curr Opin Genet Dev. 2007;17:222-7.
-
(2007)
Curr Opin Genet Dev
, vol.17
, pp. 222-227
-
-
Tafti, M.1
Dauvilliers, Y.2
Overeem, S.3
-
3
-
-
29844445190
-
Sleep disturbances and teacher ratings of school achievement and temperament in children
-
Bruni O, Ferini-Strambi L, Russo PM, Antignani M, Innocenzi M, Ottaviano P, et al. Sleep disturbances and teacher ratings of school achievement and temperament in children. Sleep Med. 2006;7:43-8.
-
(2006)
Sleep Med
, vol.7
, pp. 43-48
-
-
Bruni, O.1
Ferini-Strambi, L.2
Russo, P.M.3
Antignani, M.4
Innocenzi, M.5
Ottaviano, P.6
-
4
-
-
35549003631
-
Quantitative genetics of sleep in inbred mice
-
Tafti M. Quantitative genetics of sleep in inbred mice. Dialogues Clin Neurosci. 2007;9:273-8.
-
(2007)
Dialogues Clin Neurosci
, vol.9
, pp. 273-278
-
-
Tafti, M.1
-
5
-
-
36248934760
-
Macromolecule biosynthesis: A key function of sleep
-
Mackiewicz M, Shockley KR, Romer MA, Galante RJ, Zimmerman JE, Naidoo N, et al. Macromolecule biosynthesis: a key function of sleep. Physiol Genomics. 2007;31:441-57.
-
(2007)
Physiol Genomics
, vol.31
, pp. 441-457
-
-
Mackiewicz, M.1
Shockley, K.R.2
Romer, M.A.3
Galante, R.J.4
Zimmerman, J.E.5
Naidoo, N.6
-
6
-
-
35748938782
-
Genome-wide association of sleep and circadian phenotypes
-
Gottlieb DJ, O'Connor GT, Wilk JB. Genome-wide association of sleep and circadian phenotypes. BMC Med Genet. 2007;8 Suppl 1:S9.
-
(2007)
BMC Med Genet
, vol.8
, Issue.SUPPL. 1
-
-
Gottlieb, D.J.1
O'Connor, G.T.2
Wilk, J.B.3
-
7
-
-
35748967283
-
PER2 controls circadian periods through nuclear localization in the suprachiasmatic nucleus
-
Miyazaki K, Wakabayashi M, Chikahisa S, Sei H, Ishida N. PER2 controls circadian periods through nuclear localization in the suprachiasmatic nucleus. Genes Cells. 2007;12:1225-34.
-
(2007)
Genes Cells
, vol.12
, pp. 1225-1234
-
-
Miyazaki, K.1
Wakabayashi, M.2
Chikahisa, S.3
Sei, H.4
Ishida, N.5
-
8
-
-
0002125950
-
Narcolepsy
-
Kryger MH, Roth T, Dement C, editors, Philadelphia: WB Saunders;
-
Guilleminaut C, Anagnos A. Narcolepsy. In: Kryger MH, Roth T, Dement C, editors. Principles and practice of sleep medicine. Philadelphia: WB Saunders; 2000. p. 676-92.
-
(2000)
Principles and practice of sleep medicine
, pp. 676-692
-
-
Guilleminaut, C.1
Anagnos, A.2
-
9
-
-
33748442450
-
Narcolepsy and the hypocretins
-
Wurtman RJ. Narcolepsy and the hypocretins. Metabolism. 2006; 55: S36-9.
-
(2006)
Metabolism
, vol.55
-
-
Wurtman, R.J.1
-
10
-
-
36348950837
-
Hypocretin/orexin: A molecular link between sleep, energy regulation and pleasure
-
Ganjavi H, Shapiro CM. Hypocretin/orexin: a molecular link between sleep, energy regulation and pleasure. J Neuropsychiatry Clin Neurosci. 2007;19:413-9.
-
(2007)
J Neuropsychiatry Clin Neurosci
, vol.19
, pp. 413-419
-
-
Ganjavi, H.1
Shapiro, C.M.2
-
11
-
-
34248149838
-
Clinical and neurobiological aspects of narcolepsy
-
Nishino S. Clinical and neurobiological aspects of narcolepsy. Sleep Med. 2007;8:373-99.
-
(2007)
Sleep Med
, vol.8
, pp. 373-399
-
-
Nishino, S.1
-
12
-
-
34547690718
-
CSF hypocretin-1 levels and clinical profiles in narcolepsy and idiophatic CNS hypersomnia in Norway
-
Heier MS, Evsiukova T, Vilming S, Gjerstad MD, Schrader H, Gautvik K. CSF hypocretin-1 levels and clinical profiles in narcolepsy and idiophatic CNS hypersomnia in Norway. Sleep. 2007;30:969-73.
-
(2007)
Sleep
, vol.30
, pp. 969-973
-
-
Heier, M.S.1
Evsiukova, T.2
Vilming, S.3
Gjerstad, M.D.4
Schrader, H.5
Gautvik, K.6
-
13
-
-
33744990828
-
Molecular genetics and treatment of narcolepsy
-
Dauvilliers Y, Tafti M. Molecular genetics and treatment of narcolepsy. Ann Med. 2006;38:252-62.
-
(2006)
Ann Med
, vol.38
, pp. 252-262
-
-
Dauvilliers, Y.1
Tafti, M.2
-
14
-
-
4744371580
-
The genetics of sleep disorders
-
Taheri S. The genetics of sleep disorders. Minerva Med. 2004;95:203-12.
-
(2004)
Minerva Med
, vol.95
, pp. 203-212
-
-
Taheri, S.1
-
15
-
-
33745714458
-
Follow-up of four narcolepsy patients treated with intravenous immunoglobulins
-
Dauvilliers Y. Follow-up of four narcolepsy patients treated with intravenous immunoglobulins. Ann Neurol. 2006;60:153.
-
(2006)
Ann Neurol
, vol.60
, pp. 153
-
-
Dauvilliers, Y.1
-
16
-
-
34547677716
-
Identification of differentially expressed genes in blood cells of narcoleptic patients
-
Tanaka S, Honda Y, Honda M. Identification of differentially expressed genes in blood cells of narcoleptic patients. Sleep. 2007;30:974-9.
-
(2007)
Sleep
, vol.30
, pp. 974-979
-
-
Tanaka, S.1
Honda, Y.2
Honda, M.3
-
17
-
-
33746472884
-
Genomewide association analysis of human narcolepsy and a new resistance gene
-
Kawashima M, Tamiya G, Oka A, Hohjoh H, Juji T, Ebisawa T, et al. Genomewide association analysis of human narcolepsy and a new resistance gene. Am J Hum Genet. 2006;79:252-63
-
(2006)
Am J Hum Genet
, vol.79
, pp. 252-263
-
-
Kawashima, M.1
Tamiya, G.2
Oka, A.3
Hohjoh, H.4
Juji, T.5
Ebisawa, T.6
-
19
-
-
38049174218
-
Homer1a is a core brain molecular correlate of sleep loss
-
Maret S, Dorsaz S, Gurcel L, Pradervand S, Petit B, Pfister C, et al. Homer1a is a core brain molecular correlate of sleep loss. Proc Natl Acad Sci USA. 2007;104:20090-5.
-
(2007)
Proc Natl Acad Sci USA
, vol.104
, pp. 20090-20095
-
-
Maret, S.1
Dorsaz, S.2
Gurcel, L.3
Pradervand, S.4
Petit, B.5
Pfister, C.6
-
20
-
-
0004452705
-
Circadian disorders of the sleep-wake cycle
-
Kryger MH, Roth T, Dement C, editors, Philadelphia: WB Saunders;
-
Baker SK, Zee PC. Circadian disorders of the sleep-wake cycle. In: Kryger MH, Roth T, Dement C, editors. Principles and practice of sleep medicine. Philadelphia: WB Saunders; 2000. p. 606-14.
-
(2000)
Principles and practice of sleep medicine
, pp. 606-614
-
-
Baker, S.K.1
Zee, P.C.2
-
21
-
-
33748452422
-
Genetics of the sleep-wake cycle and its disorders
-
Hamet P, Tremblay J. Genetics of the sleep-wake cycle and its disorders. Metabolism. 2006;55:S7-12.
-
(2006)
Metabolism
, vol.55
-
-
Hamet, P.1
Tremblay, J.2
-
22
-
-
28244474084
-
Clinical evaluation and treatment of insomnia in childhood
-
Nunes ML, Cavalcante V. Clinical evaluation and treatment of insomnia in childhood. J Pediatr (Rio J). 2005;81:277-86.
-
(2005)
J Pediatr (Rio J)
, vol.81
, pp. 277-286
-
-
Nunes, M.L.1
Cavalcante, V.2
-
24
-
-
34247645396
-
Reduced NREM sleep instability in children with sleep disordered breathing
-
Kheirandish-Gozal L, Miano S, Bruni O, Ferri R, Pagani J, Villa MP, et al. Reduced NREM sleep instability in children with sleep disordered breathing. Sleep. 2007;30:450-7.
-
(2007)
Sleep
, vol.30
, pp. 450-457
-
-
Kheirandish-Gozal, L.1
Miano, S.2
Bruni, O.3
Ferri, R.4
Pagani, J.5
Villa, M.P.6
-
25
-
-
33846828395
-
Genetic susceptibility to obstructive sleep apnea in the obese children
-
Kalra M, Chakraborty R. Genetic susceptibility to obstructive sleep apnea in the obese children. Sleep Med. 2007;8:169-75.
-
(2007)
Sleep Med
, vol.8
, pp. 169-175
-
-
Kalra, M.1
Chakraborty, R.2
-
26
-
-
23444441294
-
Genetic determinants of upper airway structures that predispose to obstructive sleep apnea
-
Schwab RJ. Genetic determinants of upper airway structures that predispose to obstructive sleep apnea. Respir Physiol Neurobiol. 2005;147:289-98.
-
(2005)
Respir Physiol Neurobiol
, vol.147
, pp. 289-298
-
-
Schwab, R.J.1
-
27
-
-
22144463801
-
The biology and genetics of obesity and obstructive sleep apnea
-
Tung A. The biology and genetics of obesity and obstructive sleep apnea. Anesthesiol Clin North America. 2005;23:445-61.
-
(2005)
Anesthesiol Clin North America
, vol.23
, pp. 445-461
-
-
Tung, A.1
-
29
-
-
35148843376
-
Sleep apneas are increased in mice lacking monoamine oxidase A
-
Real C, Popa D, Seif I, Callebert J, Launay JM, Adrien J, et al. Sleep apneas are increased in mice lacking monoamine oxidase A. Sleep. 2007;30:1295-302.
-
(2007)
Sleep
, vol.30
, pp. 1295-1302
-
-
Real, C.1
Popa, D.2
Seif, I.3
Callebert, J.4
Launay, J.M.5
Adrien, J.6
-
30
-
-
57149112124
-
Genome-wide gene expression profiling in children with non-obese obstructive sleep apnea
-
In press
-
Khalyfa A, Capdevila OS, Buazza MO, Serpero LD, Kheirandish-Gozal L, Gozal D. Genome-wide gene expression profiling in children with non-obese obstructive sleep apnea. Sleep Med. In press 2008.
-
(2008)
Sleep Med
-
-
Khalyfa, A.1
Capdevila, O.S.2
Buazza, M.O.3
Serpero, L.D.4
Kheirandish-Gozal, L.5
Gozal, D.6
-
31
-
-
34547610061
-
APOE epsilon 4 allele, cognitive dysfunction, and obstructive sleep apnea in children
-
Gozal D, Capdevila OS, Kheirandish-Gozal L, Crabtree VM. APOE epsilon 4 allele, cognitive dysfunction, and obstructive sleep apnea in children. Neurology. 2007;69:243-9.
-
(2007)
Neurology
, vol.69
, pp. 243-249
-
-
Gozal, D.1
Capdevila, O.S.2
Kheirandish-Gozal, L.3
Crabtree, V.M.4
-
32
-
-
33750308030
-
Genetic basis for sleep regulation and sleep disorders
-
Raizen DM, Mason TB, Pack AI. Genetic basis for sleep regulation and sleep disorders. Semin Neurol. 2006;26:467-83.
-
(2006)
Semin Neurol
, vol.26
, pp. 467-483
-
-
Raizen, D.M.1
Mason, T.B.2
Pack, A.I.3
-
34
-
-
0002737208
-
Association of misoprostol, Moebius syndrome and congenital central alveolar hypoventilation. Case report
-
Nunes ML, Friedrich MG, Loch LF. Association of misoprostol, Moebius syndrome and congenital central alveolar hypoventilation. Case report. Arq Neuropsiquiatr. 1999;57:88-91.
-
(1999)
Arq Neuropsiquiatr
, vol.57
, pp. 88-91
-
-
Nunes, M.L.1
Friedrich, M.G.2
Loch, L.F.3
-
35
-
-
0040160505
-
-
Nunes ML, Fiori HH, Holzhey C. Neurochristopathy in the differential diagnosis of newborn's apnea: case report. Arq Neuropsiquiatr. 2001;59:968-71.
-
Nunes ML, Fiori HH, Holzhey C. Neurochristopathy in the differential diagnosis of newborn's apnea: case report. Arq Neuropsiquiatr. 2001;59:968-71.
-
-
-
-
36
-
-
38849088791
-
Parental origin and somatic mosaicism of PHOX2B mutations in congenital central hypoventilation syndrome
-
Parodi S, Bachetti T, Lantieri F, Di Duca M, Santamaria G, Ottonello G, et al. Parental origin and somatic mosaicism of PHOX2B mutations in congenital central hypoventilation syndrome. Hum Mutat. 2008;29:206.
-
(2008)
Hum Mutat
, vol.29
, pp. 206
-
-
Parodi, S.1
Bachetti, T.2
Lantieri, F.3
Di Duca, M.4
Santamaria, G.5
Ottonello, G.6
-
37
-
-
0018165812
-
Congenital failure of automatic control of ventilation, gastrointestinal motility and heart rate
-
Haddad GG, Mezza NM, Defendini R, Blanc WA, Driscoll JM, Epstein MA, et al. Congenital failure of automatic control of ventilation, gastrointestinal motility and heart rate. Medicine (Baltimore). 1978;57:517-26.
-
(1978)
Medicine (Baltimore)
, vol.57
, pp. 517-526
-
-
Haddad, G.G.1
Mezza, N.M.2
Defendini, R.3
Blanc, W.A.4
Driscoll, J.M.5
Epstein, M.A.6
-
39
-
-
22044438226
-
Pediatric disorders with autonomic dysfunction: What role for PHOX2B?
-
Gaultier C, Trang H, Dauger S, Gallego J. Pediatric disorders with autonomic dysfunction: what role for PHOX2B? Pediatr Res. 2005;58:1-6.
-
(2005)
Pediatr Res
, vol.58
, pp. 1-6
-
-
Gaultier, C.1
Trang, H.2
Dauger, S.3
Gallego, J.4
-
41
-
-
33846933516
-
Late-onset central hypoventilation syndrome : A family genetic study
-
Doherty LS, Kiely JL, Deegan PC, Nolan G, McCabe S, Green AJ, et al. Late-onset central hypoventilation syndrome : a family genetic study. Eur Respir J. 2007;29:312-6.
-
(2007)
Eur Respir J
, vol.29
, pp. 312-316
-
-
Doherty, L.S.1
Kiely, J.L.2
Deegan, P.C.3
Nolan, G.4
McCabe, S.5
Green, A.J.6
-
42
-
-
0025996125
-
Defining the sudden death syndrome (SIDS): Deliberations of an expert panel convened by the National Institute of child Health and Human Development
-
Willinger M, James LS, Catz C. Defining the sudden death syndrome (SIDS): deliberations of an expert panel convened by the National Institute of child Health and Human Development. Pediatr Pathol. 1991;11:677-84.
-
(1991)
Pediatr Pathol
, vol.11
, pp. 677-684
-
-
Willinger, M.1
James, L.S.2
Catz, C.3
-
43
-
-
33750010853
-
Sleep practices and sudden death syndrome: A new proposal for scoring risk factors
-
Geib LT, Aerts D, Nunes ML. Sleep practices and sudden death syndrome: a new proposal for scoring risk factors. Sleep. 2006;29:1288-94.
-
(2006)
Sleep
, vol.29
, pp. 1288-1294
-
-
Geib, L.T.1
Aerts, D.2
Nunes, M.L.3
-
44
-
-
33646001749
-
The incidence of sudden infant death syndrome in a cohort of infants
-
Geib LT, Nunes ML. The incidence of sudden infant death syndrome in a cohort of infants. J Pediatr (Rio J). 2006;82:21-6
-
(2006)
J Pediatr (Rio J)
, vol.82
, pp. 21-26
-
-
Geib, L.T.1
Nunes, M.L.2
-
45
-
-
33646235382
-
Sleeping habits related to sudden infant death syndrome: A population based study
-
Geib LT, Nunes ML. Sleeping habits related to sudden infant death syndrome: a population based study. Cad Saude Publica. 2006;22:415-23.
-
(2006)
Cad Saude Publica
, vol.22
, pp. 415-423
-
-
Geib, L.T.1
Nunes, M.L.2
-
47
-
-
33644512784
-
International Restless Legs Syndrome Study Group (IRLSSG). The official World Association of Sleep Medicine (WASM) standards for recording and scoring periodic leg movements in sleep (PLMS) and wakefulness (PLMW) developed in collaboration with a task force from the International Restless Legs Syndrome Study Group (IRLSSG)
-
Zucconi M, Ferri R, Allen R, Baier PC, Bruni O, Chokroverty S, et al.; International Restless Legs Syndrome Study Group (IRLSSG). The official World Association of Sleep Medicine (WASM) standards for recording and scoring periodic leg movements in sleep (PLMS) and wakefulness (PLMW) developed in collaboration with a task force from the International Restless Legs Syndrome Study Group (IRLSSG). Sleep Med. 2006;7:175-83.
-
(2006)
Sleep Med
, vol.7
, pp. 175-183
-
-
Zucconi, M.1
Ferri, R.2
Allen, R.3
Baier, P.C.4
Bruni, O.5
Chokroverty, S.6
-
48
-
-
33745122229
-
New approaches to the study of periodic leg movements during sleep in restless legs syndrome
-
Ferri R, Zucconi M, Manconi M, Plazzi G, Bruni O, Ferini-Strambi L. New approaches to the study of periodic leg movements during sleep in restless legs syndrome. Sleep. 2006;29:759-69.
-
(2006)
Sleep
, vol.29
, pp. 759-769
-
-
Ferri, R.1
Zucconi, M.2
Manconi, M.3
Plazzi, G.4
Bruni, O.5
Ferini-Strambi, L.6
-
49
-
-
57349132638
-
Age-related changes in periodic legs movements during sleep in patients with restless legs syndrome
-
In press
-
Ferri R, Manconi M, Lanuzza B, Cosentino FI, Bruni O, Ferini-Strambi L, et al. Age-related changes in periodic legs movements during sleep in patients with restless legs syndrome. Sleep Med. In press 2007.
-
(2007)
Sleep Med
-
-
Ferri, R.1
Manconi, M.2
Lanuzza, B.3
Cosentino, F.I.4
Bruni, O.5
Ferini-Strambi, L.6
-
50
-
-
33845597581
-
Different periodicity and time structure of leg movements during sleep in narcolepsy/cataplexy and restless legs syndrome
-
Ferri R, Zucconi M, Manconi M, Bruni O, Ferini-Strambi L, Vandi S, et al. Different periodicity and time structure of leg movements during sleep in narcolepsy/cataplexy and restless legs syndrome. Sleep. 2006;29:1587-94.
-
(2006)
Sleep
, vol.29
, pp. 1587-1594
-
-
Ferri, R.1
Zucconi, M.2
Manconi, M.3
Bruni, O.4
Ferini-Strambi, L.5
Vandi, S.6
-
51
-
-
0036838255
-
Restless legs syndrome and periodic limb movements of sleep: Fact, fad, and fiction
-
Patel S. Restless legs syndrome and periodic limb movements of sleep: fact, fad, and fiction. Curr Opin Pulm Med. 2002;8:498-501.
-
(2002)
Curr Opin Pulm Med
, vol.8
, pp. 498-501
-
-
Patel, S.1
-
52
-
-
34547926806
-
A genetic risk factor for periodic limb movement
-
Stefansson H, Rye DB, Hicks A, Petursson H, Ingason A, Thorgeirsson TE, et al. A genetic risk factor for periodic limb movement. N Engl J Med. 2007;357:639-47.
-
(2007)
N Engl J Med
, vol.357
, pp. 639-647
-
-
Stefansson, H.1
Rye, D.B.2
Hicks, A.3
Petursson, H.4
Ingason, A.5
Thorgeirsson, T.E.6
-
53
-
-
34547497308
-
Genome-wide association study of restless legs syndrome identifies common variants in three genomic regions
-
Winkelmann J, Schormair B, Lichtner P, Ripke S, Xiong L, Jalilzadeh S, et al. Genome-wide association study of restless legs syndrome identifies common variants in three genomic regions. Nat Genet. 2007;39:1000-6.
-
(2007)
Nat Genet
, vol.39
, pp. 1000-1006
-
-
Winkelmann, J.1
Schormair, B.2
Lichtner, P.3
Ripke, S.4
Xiong, L.5
Jalilzadeh, S.6
-
54
-
-
0037275638
-
HLA and genetic susceptibility of sleep walking
-
Lecendreux M, Bassetti C, Dauvilliers Y, Mayer G, Neidhart E, Tafti M. HLA and genetic susceptibility of sleep walking. Mol Psychiatr. 2003;8:114-7.
-
(2003)
Mol Psychiatr
, vol.8
, pp. 114-117
-
-
Lecendreux, M.1
Bassetti, C.2
Dauvilliers, Y.3
Mayer, G.4
Neidhart, E.5
Tafti, M.6
-
55
-
-
0031436567
-
A parasomnia overlap disorders involving sleepwalking, sleep terrors and REM sleep behavior disorder in 33 polysomnographically confirmed cases
-
Schenck CH, Boyd JL, Mahowald MV. A parasomnia overlap disorders involving sleepwalking, sleep terrors and REM sleep behavior disorder in 33 polysomnographically confirmed cases. Sleep. 1997;20:972-81.
-
(1997)
Sleep
, vol.20
, pp. 972-981
-
-
Schenck, C.H.1
Boyd, J.L.2
Mahowald, M.V.3
-
56
-
-
14644408095
-
Genetics of normal and pathological sleep in humans
-
Dauvilliers Y, Maret S, Tafti M. Genetics of normal and pathological sleep in humans. Sleep Med Rev. 2005;9:91-100.
-
(2005)
Sleep Med Rev
, vol.9
, pp. 91-100
-
-
Dauvilliers, Y.1
Maret, S.2
Tafti, M.3
|