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Volumn 49, Issue 6, 2001, Pages 786-792

Evidence for digenic inheritance in a family with both febrile convulsions and temporal lobe epilepsy implicating chromosomes 18qter and 1q25-q31

(10) Baulac, Stéphanie a Picard, Fabienne a Herman, Alexandra b Feingold, Josué a Genin, Emmanuelle a Hirsch, Edouard a Prud'Homme, Jean François c Baulac, Michel d Brice, Alexis e Leguern, Eric a

a PITIÉ SALPÊTRIÈRE HOSPITAL (France)

b INSERM (France)

c GENEVA UNIVERSITY HOSPITALS (Switzerland)

d BICÊTRE HOSPITAL (France)

e GÉNÉTHON (France)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CHROMOSOME 18Q; CHROMOSOME 1Q; CLINICAL ARTICLE; FAMILIAL DISEASE; FEBRILE CONVULSION; GENE LOCUS; GENETIC LINKAGE; GENETIC PREDISPOSITION; HAPLOTYPE; HUMAN; INHERITANCE; PHENOTYPE; PRIORITY JOURNAL; TEMPORAL LOBE EPILEPSY;

ADOLESCENT; ADULT; AGE OF ONSET; CHILD; CHILD, PRESCHOOL; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 1; CHROMOSOMES, HUMAN, PAIR 18; EPILEPSY, TEMPORAL LOBE; FEMALE; FRANCE; GENETIC MARKERS; HAPLOTYPES; HIPPOCAMPUS; HUMANS; INFANT; LOD SCORE; MAGNETIC RESONANCE IMAGING; MALE; PEDIGREE; PENETRANCE; SEIZURES, FEBRILE;

EID: 0034985911 PISSN: 03645134 EISSN: None Source Type: Journal
DOI: 10.1002/ana.1014 Document Type: Article

Times cited : (89)

References (34)

1
- 0026302331
- Genetic studies of febrile convulsions: Analysis of twin and family data
- (1991) Epilepsy Res , vol.4 , Issue.SUPPL. , pp. 119-128
- Tsuboi, T.¹ Endo, S.²

2
- 0023242310
- Complex segregation analysis of febrile convulsions
- (1987) Am J Hum Genet , vol.41 , pp. 249-257
- Rich, S.S.¹ Annegers, J.F.² Hauser, W.A.³

3
- 0030044668
- Pedigree analysis in families with febrile seizures
- (1996) Am J Med Genet , vol.61 , pp. 345-352
- Johnson, W.G.¹ Kugler, S.L.² Stenroos, E.S.³

4
- 0029881889
- Suggestion of a major gene for familial febrile convulsions mapping to 8q13-21
- (1996) J Med Genet , vol.33 , pp. 308-312
- Wallace, R.H.¹ Berkovic, S.F.² Howell, R.A.³

5
- 6844240853
- Evidence for a novel gene for familial febrile convulsions, FEB2, linked to chromosome 19p in an extended family from the Midwest
- (1998) Hum Mol Genet , vol.7 , pp. 63-67
- Johnson, E.W.¹ Dubovsky, J.² Rich, S.S.³

6
- 0032511770
- Hereditary febrile seizures: Phenotype and evidence for a chromosome 19p locus
- (1998) Am J Med Genet , vol.79 , pp. 354-361
- Kugler, S.L.¹ Stenroos, E.S.² Mandelbaum, D.E.³

7
- 0029620481
- Febrile convulsions. Is seizure duration the most important predictor of temporal lobe epilepsy?
- (1995) Brain , vol.118 , pp. 1521-1528
- Maher, J.¹ McLachlan, R.S.²

8
- 0029396762
- Frequency and characteristics of dual pathology in patients with lesional epilepsy
- (1995) Neurology , vol.45 , pp. 2058-2064
- Cendes, F.¹ Cook, M.J.² Watson, C.³

9
- 0030943313
- Generalized epilepsy with febrile seizures plus. A genetic disorder with heterogeneous clinical phenotypes
- (1997) Brain , vol.120 , pp. 479-490
- Scheffer, I.E.¹ Berkovic, S.F.²

10
- 17344367657
- +-channel beta1 subunit gene SCN1B
- (1998) Nat Genet , vol.19 , pp. 366-370
- Wallace, R.H.¹ Wang, D.W.² Singh, R.³

11
- 0033364824
- A second locus for familial generalized epilepsy with febrile seizures plus maps to chromosome 2q21-q33
- (1999) Am J Hum Genet , vol.65 , pp. 1078-1085
- Baulac, S.¹ Gourfinkel-An, I.² Picard, F.³

12
- 0033361895
- Identification of a new locus for generalized epilepsy with febrile seizures plus (GEFS+) on chromosome 2q24-q33
- (1999) Am J Hum Genet , vol.65 , pp. 1396-1400
- Moulard, B.¹ Guipponi, M.² Chaigne, D.³

13
- 0033912108
- A new locus for generalized epilepsy with febrile seizures plus maps to chromosome 2
- (2000) Am J Hum Genet , vol.66 , pp. 698-701
- Lopes-Cendes, I.¹ Scheffer, I.E.² Berkovic, S.F.³

14
- 0032834017
- A locus for febrile seizures (FEB3) maps to chromosome 2q23-24
- (1999) Ann Neurol , vol.46 , pp. 671-678
- Peiffer, A.¹ Thompson, J.² Charlier, C.³

15
- 0034069651
- Mutations of SCN1A, encoding a neuronal sodium channel, in two families with GEFS+2
- (2000) Nat Genet , vol.24 , pp. 343-345
- Escayg, A.¹ MacDonald, B.T.² Meisler, M.H.³

16
- 0029834204
- Familial temporal lobe epilepsy: A common disorder identified in twins
- (1996) Ann Neurol , vol.40 , pp. 227-235
- Berkovic, S.F.¹ McIntosh, A.² Howell, R.A.³

17
- 0029059069
- Localization of a gene for partial epilepsy to chromosome 10q
- (1995) Nat Genet , vol.10 , pp. 56-60
- Ottman, R.¹ Risch, N.² Hauser, W.A.³

18
- 0345003726
- Autosomal dominant lateral temporal epilepsy: Clinical and genetic study of a large Basque pedigree linked to chromosome 10q
- (1999) Ann Neurol , vol.45 , pp. 182-188
- Poza, J.J.¹ Saenz, A.² Martinez-Gil, A.³

19
- 4243890651
- The genetics of febrile convulsions and temporal lobe epilepsy
- Berkovic SF, Genton P, Hirsch E, Picard F, editors. Genetics of focal epilepsies. London: John Libbey
- (1999) , pp. 149-158
- Mc Lachlan, R.S.¹ Bulman, D.E.²

20
- 0031948473
- Epilepsy diagnosis and localization in patients with antecedent childhood febrile convulsions
- (1998) Neurology , vol.50 , pp. 917-922
- Hamati-Haddad, A.¹ Abou-Khalil, B.²

21
- 0027430322
- Characteristics of medial temporal lobe epilepsy: I. Results of history and physical examination
- (1993) Ann Neurol , vol.34 , pp. 774-780
- French, J.A.¹ Williamson, P.D.² Thadani, V.M.³

22
- 0344765463
- Hippocampal malformation as a cause of familial febrile convulsions and subsequent hippocampal sclerosis
- (1998) Neurology , vol.50 , pp. 909-917
- Fernandez, G.¹ Effenberger, O.² Vinz, B.³

23
- 17344377862
- Dominant partial epilepsies: A clinical, electrophysiological and genetic study of 19 European families
- (2000) Brain , vol.123 , pp. 1247-1262
- Picard, F.¹ Baulac, S.² Kahane, P.³

24
- 8944231154
- MR determination of hippocampal volume: Comparison of three methods
- (1996) Am J Neuroradiol , vol.17 , pp. 1091-1098
- Hasboun, D.¹ Chantome, M.² Zouaoui, A.³

25
- 15444351738
- Hippocampal developmental changes in patients with partial epilepsy: Magnetic resonance imaging and clinical aspects
- (1998) Ann Neurol , vol.44 , pp. 223-233
- Baulac, M.¹ De Grissac, N.² Hasboun, D.³

26
- 0028906389
- Posterior probability, of linkage and maximal lod score
- (1995) Ann Hum Genet , vol.59 , pp. 123-132
- Genin, E.¹ Martinez, M.² Clerget-Darpoux, F.³

27
- 0030851777
- True and false positive peaks in genomewide scans: Applications of length-biased sampling to linkage mapping
- (1997) Am J Hum Genet , vol.61 , pp. 430-438
- Terwilliger, J.D.¹ Shannon, W.D.² Lathrop, G.M.³

28
- 0031744007
- Is the underlying cause of epilepsy a major prognostic factor for recurrence?
- (1998) Neurology , vol.51 , pp. 1256-1262
- Semah, F.¹ Picot, M.C.² Adam, C.³

29
- 0028245437
- Digenic retinitis pigmentosa due to mutations at the unlinked peripherin/RDS and ROM1 loci
- (1994) Science , vol.264 , pp. 1604-1608
- Kajiwara, K.¹ Berson, E.L.² Dryja, T.P.³

30
- 0032231413
- Evidence for digenic inheritance of nonsyndromic hereditary hearing loss in a Swedish family
- (1998) Am J Hum Genet , vol.63 , pp. 786-793
- Balciuniene, J.¹ Dahl, N.² Borg, E.³

31
- 0033365218
- Possible interaction between USH1B and USH3 gene products as implied by apparent digenic deafness inheritance
- (1999) Am J Hum Genet , vol.65 , pp. 261-265
- Adato, A.¹ Kalinski, H.² Weil, D.³

32
- 0033365396
- Digenic junctional epidermolysis bullosa: Mutations in COL17A1 and LAMB3 genes
- (1999) Am J Hum Genet , vol.65 , pp. 1530-1537
- Floeth, M.¹ Bruckner-Tuderman, L.²

33
- 0030979154
- Apparent digenic inheritance of Waardenburg syndrome type 2 (WS2) and autosomal recessive ocular albinism (AROA)
- (1997) Hum Mol Genet , vol.6 , pp. 659-664
- Morell, R.¹ Spritz, R.A.² Ho, L.³

34
- 0033601867
- Expression of mRNA encoding alpha1 E and alpha1 G subunit in the brain of a rat model of absence epilepsy
- (1999) Neuroreport , vol.10 , pp. 569-574
- De Borman, B.¹ Lakaye, B.² Minet, A.³

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