-
1
-
-
84882368341
-
Restless legs syndrome
-
Ekbom KA. Restless legs syndrome. Neurology. 1960;10:868.
-
(1960)
Neurology
, vol.10
, pp. 868
-
-
Ekbom, K.A.1
-
2
-
-
0028631901
-
Restless legs syndrome and sleep bruxism: Prevalence and association among Canadians
-
Lavigne GJ, Montplaisir JY. Restless legs syndrome and sleep bruxism: prevalence and association among Canadians. Sleep. 1994;17:739-743.
-
(1994)
Sleep
, vol.17
, pp. 739-743
-
-
Lavigne, G.J.1
Montplaisir, J.Y.2
-
3
-
-
0034710292
-
Epidemiology of restless legs symptoms in adults
-
Phillips B, Young T, Finn L, Asher K, Hening WA, Purvis C. Epidemiology of restless legs symptoms in adults. Arch Intern Med. 2000;160:2137-2141.
-
(2000)
Arch Intern Med
, vol.160
, pp. 2137-2141
-
-
Phillips, B.1
Young, T.2
Finn, L.3
Asher, K.4
Hening, W.A.5
Purvis, C.6
-
4
-
-
0034646434
-
Memory and Morbidity in Augsburg Elderly. Prevalence and risk factors of RLS in an elderly population: The MEMO study
-
Rothdach AJ, Trenkwalder C, Haberstock J, Keil U, Berger K. Memory and Morbidity in Augsburg Elderly. Prevalence and risk factors of RLS in an elderly population: the MEMO study. Neurology. 2000;54:1064-1068.
-
(2000)
Neurology
, vol.54
, pp. 1064-1068
-
-
Rothdach, A.J.1
Trenkwalder, C.2
Haberstock, J.3
Keil, U.4
Berger, K.5
-
5
-
-
0030059442
-
Clinical symptoms and possible anticipation in a large kindred of familial restless legs syndrome
-
Trenkwalder C, Seidel VC, Gasser T, Oertel WH. Clinical symptoms and possible anticipation in a large kindred of familial restless legs syndrome. Mov Disord. 1996;11:389-394.
-
(1996)
Mov Disord
, vol.11
, pp. 389-394
-
-
Trenkwalder, C.1
Seidel, V.C.2
Gasser, T.3
Oertel, W.H.4
-
6
-
-
0032904427
-
Studies of penetrance and anticipation in five autosomal-dominant restless legs syndrome pedigrees
-
Lazzarini A, Walters AS, Hickey K, et al. Studies of penetrance and anticipation in five autosomal-dominant restless legs syndrome pedigrees. Mov Disord. 1999;14:111-116.
-
(1999)
Mov Disord
, vol.14
, pp. 111-116
-
-
Lazzarini, A.1
Walters, A.S.2
Hickey, K.3
-
7
-
-
0034649387
-
Restless legs syndrome in monozygotic twins: Clinical correlates
-
Ondo WG, Vuong KD, Wang Q. Restless legs syndrome in monozygotic twins: clinical correlates. Neurology. 2000;55:1404-1406.
-
(2000)
Neurology
, vol.55
, pp. 1404-1406
-
-
Ondo, W.G.1
Vuong, K.D.2
Wang, Q.3
-
8
-
-
0029938217
-
A questionnaire study of 138 patients with restless legs syndrome: The "Night-Walkers" survey
-
Walters AS, Hickey K, Maltzman J, et al. A questionnaire study of 138 patients with restless legs syndrome: the "Night-Walkers" survey. Neurology. 1996;46:92-95.
-
(1996)
Neurology
, vol.46
, pp. 92-95
-
-
Walters, A.S.1
Hickey, K.2
Maltzman, J.3
-
9
-
-
0031027378
-
Clinical, polysomnographic, and genetic characteristics of restless legs syndrome: A study of 133 patients diagnosed with new standard criteria
-
Montplaisir J, Boucher S, Poirier G, Lavigne G, Lapierre O, Lesperance P. Clinical, polysomnographic, and genetic characteristics of restless legs syndrome: a study of 133 patients diagnosed with new standard criteria. Mov Disord. 1997;12:61-65.
-
(1997)
Mov Disord
, vol.12
, pp. 61-65
-
-
Montplaisir, J.1
Boucher, S.2
Poirier, G.3
Lavigne, G.4
Lapierre, O.5
Lesperance, P.6
-
10
-
-
0036714378
-
Complex segregation analysis of restless legs syndrome provides evidence for an autosomal dominant mode of inheritance in early age at onset families
-
Winkelmann J, Muller-Myhsok B, Wittchen HU, et al. Complex segregation analysis of restless legs syndrome provides evidence for an autosomal dominant mode of inheritance in early age at onset families. Ann Neurol. 2002;52:297-302.
-
(2002)
Ann Neurol
, vol.52
, pp. 297-302
-
-
Winkelmann, J.1
Muller-Myhsok, B.2
Wittchen, H.U.3
-
11
-
-
16844384404
-
RLS patients with a younger age of onset have a higher frequency of affected relatives
-
Hening WA, Washburn T, Somel D, LeSage S, Allen RP, Earley CJ. RLS patients with a younger age of onset have a higher frequency of affected relatives [abstract]. Neurology. 2003;60(suppl 1):S05.004.
-
(2003)
Neurology
, vol.60
, Issue.SUPPL. 1
-
-
Hening, W.A.1
Washburn, T.2
Somel, D.3
LeSage, S.4
Allen, R.P.5
Earley, C.J.6
-
13
-
-
0035208888
-
Identification of a major susceptibility locus for restless legs syndrome on chromosome 12q
-
Desautels A, Turecki G, Montplaisir J, Sequeira A, Verner A, Rouleau GA. Identification of a major susceptibility locus for restless legs syndrome on chromosome 12q. Am J Hum Genet. 2001;69:1266-1270.
-
(2001)
Am J Hum Genet
, vol.69
, pp. 1266-1270
-
-
Desautels, A.1
Turecki, G.2
Montplaisir, J.3
Sequeira, A.4
Verner, A.5
Rouleau, G.A.6
-
14
-
-
0028940272
-
Variability of the genetic contribution of Quebec population founders associated to some deleterious genes
-
Heyer E, Tremblay M. Variability of the genetic contribution of Quebec population founders associated to some deleterious genes. Am J Hum Genet. 1995;56:970-978.
-
(1995)
Am J Hum Genet
, vol.56
, pp. 970-978
-
-
Heyer, E.1
Tremblay, M.2
-
15
-
-
0028296815
-
Linkage disequilibrium analysis of childhood-onset spinal muscular atrophy (SMA) in the French-Canadian population
-
Simard LR, Prescott G, Rochette C. et al. Linkage disequilibrium analysis of childhood-onset spinal muscular atrophy (SMA) in the French-Canadian population. Hum Mol Genet. 1994;3:459-463.
-
(1994)
Hum Mol Genet
, vol.3
, pp. 459-463
-
-
Simard, L.R.1
Prescott, G.2
Rochette, C.3
-
16
-
-
0029129647
-
Toward a better definition of the restless legs syndrome: The International Restless Legs Syndrome Study Group
-
Walters AS. Toward a better definition of the restless legs syndrome: the International Restless Legs Syndrome Study Group. Mov Disord. 1995;10:634-642.
-
(1995)
Mov Disord
, vol.10
, pp. 634-642
-
-
Walters, A.S.1
-
17
-
-
0036460935
-
Effects of immobility on sensory and motor symptoms of restless legs syndrome
-
Michaud M, Lavigne G, Desautels A, Poirier G, Montplaisir J. Effects of immobility on sensory and motor symptoms of restless legs syndrome. Mov Disord. 2002;17:112-115.
-
(2002)
Mov Disord
, vol.17
, pp. 112-115
-
-
Michaud, M.1
Lavigne, G.2
Desautels, A.3
Poirier, G.4
Montplaisir, J.5
-
21
-
-
0029946879
-
Faster linkage analysis computations for pedigrees with loops or unused alleles
-
Schaffer AA. Faster linkage analysis computations for pedigrees with loops or unused alleles. Hum Hered. 1996;46:226-235.
-
(1996)
Hum Hered
, vol.46
, pp. 226-235
-
-
Schaffer, A.A.1
-
22
-
-
0039513062
-
Computer-simulation methods in human linkage analysis
-
Ott J. Computer-simulation methods in human linkage analysis. Proc Natl Acad Sci U S A 1989;86:4175-4178.
-
(1989)
Proc Natl Acad Sci U S A
, vol.86
, pp. 4175-4178
-
-
Ott, J.1
-
23
-
-
0025008255
-
Measuring the inflation of the lod score due to its maximization over model parameter values in human linkage analysis
-
Weeks DE, Lehner T, Squires-Wheeler E, Kaufmann C, Ott J. Measuring the inflation of the lod score due to its maximization over model parameter values in human linkage analysis. Genet Epidemiol. 1990;7:237-243.
-
(1990)
Genet Epidemiol
, vol.7
, pp. 237-243
-
-
Weeks, D.E.1
Lehner, T.2
Squires-Wheeler, E.3
Kaufmann, C.4
Ott, J.5
-
24
-
-
0029945706
-
Descent graphs in pedigree analysis: Applications to haplotyping, location scores, and marker-sharing statistics
-
Sobel E, Lange K. Descent graphs in pedigree analysis: applications to haplotyping, location scores, and marker-sharing statistics. Am J Hum Genet. 1996;58:1323-1337.
-
(1996)
Am J Hum Genet
, vol.58
, pp. 1323-1337
-
-
Sobel, E.1
Lange, K.2
-
26
-
-
0028877463
-
Genetic dissection of complex traits: Guidelines for interpreting and reporting linkage results
-
Lander E, Kruglyak L. Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results. Nat Genet. 1995;11:241-247.
-
(1995)
Nat Genet
, vol.11
, pp. 241-247
-
-
Lander, E.1
Kruglyak, L.2
-
27
-
-
18444418887
-
Mode of inheritance and susceptibility locus for restless legs syndrome on chromosome 12q
-
Kock N, Culjkovic B, Maniak S, et al. Mode of inheritance and susceptibility locus for restless legs syndrome on chromosome 12q. Am J Hum Genet, 2002;71:205-208.
-
(2002)
Am J Hum Genet
, vol.71
, pp. 205-208
-
-
Kock, N.1
Culjkovic, B.2
Maniak, S.3
-
28
-
-
0038691989
-
Autosomal dominant restless legs syndrome maps on chromosome 14q
-
Bonati MT, Ferini-Strambi L, Aridon P, Oldani A, Zucconi M, Casari G. Autosomal dominant restless legs syndrome maps on chromosome 14q. Brain. 2003;126:1485-1492.
-
(2003)
Brain
, vol.126
, pp. 1485-1492
-
-
Bonati, M.T.1
Ferini-Strambi, L.2
Aridon, P.3
Oldani, A.4
Zucconi, M.5
Casari, G.6
-
29
-
-
2342527865
-
Genomewide linkage scan identifies a novel susceptibility locus for restless legs syndrome on chromosome 9p
-
Chen S, Ondo WG, Rao S, Li L, Chen Q, Wang Q. Genomewide linkage scan identifies a novel susceptibility locus for restless legs syndrome on chromosome 9p. Am J Hum Genet. 2004;74:876-885.
-
(2004)
Am J Hum Genet
, vol.74
, pp. 876-885
-
-
Chen, S.1
Ondo, W.G.2
Rao, S.3
Li, L.4
Chen, Q.5
Wang, Q.6
-
30
-
-
0032499264
-
Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism
-
Kitada T, Asakawa S, Hattori N, et al. Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism. Nature. 1998;392:605-608.
-
(1998)
Nature
, vol.392
, pp. 605-608
-
-
Kitada, T.1
Asakawa, S.2
Hattori, N.3
-
31
-
-
0033868381
-
Novel mutations, pseudo-dominant inheritance, and possible familial affects in patients with autosomal recessive juvenile parkinsonism
-
Maruyama M, Ikeuchi T, Saito M, et al. Novel mutations, pseudo-dominant inheritance, and possible familial affects in patients with autosomal recessive juvenile parkinsonism. Ann Neurol. 2000;48:245-250.
-
(2000)
Ann Neurol
, vol.48
, pp. 245-250
-
-
Maruyama, M.1
Ikeuchi, T.2
Saito, M.3
-
32
-
-
0035845715
-
Pseudodominant inheritance and exon 2 triplication in a family with parkin gene mutations
-
Lucking CB, Bonifati V, Periquet M, Vanacore N, Brice A, Meco G. Pseudodominant inheritance and exon 2 triplication in a family with parkin gene mutations. Neurology. 2001;57:924-927.
-
(2001)
Neurology
, vol.57
, pp. 924-927
-
-
Lucking, C.B.1
Bonifati, V.2
Periquet, M.3
Vanacore, N.4
Brice, A.5
Meco, G.6
-
33
-
-
12244283716
-
Pseudoautosomal dominant inheritance of PARK2: Two families with parkin gene mutations
-
Kobayashi T, Matsumine H, Zhang J, Imamichi Y, Mizuno Y, Hattori N. Pseudoautosomal dominant inheritance of PARK2: two families with parkin gene mutations. J Neurol Sci. 2003;207:11-17.
-
(2003)
J Neurol Sci
, vol.207
, pp. 11-17
-
-
Kobayashi, T.1
Matsumine, H.2
Zhang, J.3
Imamichi, Y.4
Mizuno, Y.5
Hattori, N.6
-
34
-
-
0038754178
-
Parkin mutations and susceptibility alleles in late-onset Parkinson's disease
-
Oliveira SA, Scott WK, Martin ER, et al. Parkin mutations and susceptibility alleles in late-onset Parkinson's disease. Ann Neurol. 2003;53:624-629.
-
(2003)
Ann Neurol
, vol.53
, pp. 624-629
-
-
Oliveira, S.A.1
Scott, W.K.2
Martin, E.R.3
-
35
-
-
12244262766
-
Heterozygosity for a mutation in the parkin gene leads to later onset Parkinson disease
-
Foroud T, Uniacke SK, Liu L, et al. Heterozygosity for a mutation in the parkin gene leads to later onset Parkinson disease. Neurology. 2003;60:796-801.
-
(2003)
Neurology
, vol.60
, pp. 796-801
-
-
Foroud, T.1
Uniacke, S.K.2
Liu, L.3
-
36
-
-
0027194791
-
Gene dose of apolipoprotein E type 4 allele and the risk of Alzheimer's disease in late onset families
-
Corder EH, Saunders AM, Strittmatter WJ, et al. Gene dose of apolipoprotein E type 4 allele and the risk of Alzheimer's disease in late onset families. Science. 1993;261:921-923.
-
(1993)
Science
, vol.261
, pp. 921-923
-
-
Corder, E.H.1
Saunders, A.M.2
Strittmatter, W.J.3
-
37
-
-
0028148889
-
Mutations in the BRCA1 gene in families with early-onset breast and ovarian cancer
-
Castilla LH, Couch FJ, Erdos MR, et al. Mutations in the BRCA1 gene in families with early-onset breast and ovarian cancer. Nat Genet. 1994;8:387-391.
-
(1994)
Nat Genet
, vol.8
, pp. 387-391
-
-
Castilla, L.H.1
Couch, F.J.2
Erdos, M.R.3
-
38
-
-
2342429206
-
Mutational analysis of neurotensin in familial restless legs syndrome
-
Desautels A, Turecki G, Xiong L, Rochefort D, Montplaisir J, Rouleau GA. Mutational analysis of neurotensin in familial restless legs syndrome. Mov Disord. 2004;19:90-94.
-
(2004)
Mov Disord
, vol.19
, pp. 90-94
-
-
Desautels, A.1
Turecki, G.2
Xiong, L.3
Rochefort, D.4
Montplaisir, J.5
Rouleau, G.A.6
-
39
-
-
0034102395
-
Abnormalities in CSF concentrations of ferritin and transferrin in restless legs syndrome
-
Earley CJ, Connor JR, Beard JL, Malecki EA, Epstein DK, Allen RP. Abnormalities in CSF concentrations of ferritin and transferrin in restless legs syndrome. Neurology. 2000;54:1698-1700.
-
(2000)
Neurology
, vol.54
, pp. 1698-1700
-
-
Earley, C.J.1
Connor, J.R.2
Beard, J.L.3
Malecki, E.A.4
Epstein, D.K.5
Allen, R.P.6
-
40
-
-
0035936633
-
MR1 measurement of brain iron in patients with restless legs syndrome
-
Allen RP, Barker PB, Wehrl F, Song HK, Earley CJ. MR1 measurement of brain iron in patients with restless legs syndrome. Neurology. 2001;56:263-265.
-
(2001)
Neurology
, vol.56
, pp. 263-265
-
-
Allen, R.P.1
Barker, P.B.2
Wehrl, F.3
Song, H.K.4
Earley, C.J.5
-
41
-
-
0028239363
-
Iron status and restless legs syndrome in the elderly
-
O'Keeffe ST, Gavin K, Lavan JN. Iron status and restless legs syndrome in the elderly. Age Ageing. 1994;23:200-203.
-
(1994)
Age Ageing
, vol.23
, pp. 200-203
-
-
O'Keeffe, S.T.1
Gavin, K.2
Lavan, J.N.3
-
42
-
-
0035049699
-
Restless legs syndrome in spinocerebellar ataxia types 1,2, and 3
-
Abele M, Burk K, Laccone F, Dichgans J, Klockgether T. Restless legs syndrome in spinocerebellar ataxia types 1,2, and 3. J Neurol. 2001;248:311-314.
-
(2001)
J Neurol
, vol.248
, pp. 311-314
-
-
Abele, M.1
Burk, K.2
Laccone, F.3
Dichgans, J.4
Klockgether, T.5
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