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Page 1
Linkage and association analysis of CACNG3 in childhood absence epilepsy.
Everett KV, Chioza B, Aicardi J, Aschauer H, Brouwer O, Callenbach P, Covanis A, Dulac O, Eeg-Olofsson O, Feucht M, Friis M, Goutieres F, Guerrini R, Heils A, Kjeldsen M, Lehesjoki AE, Makoff A, Nabbout R, Olsson I, Sander T, Sirén A, McKeigue P, Robinson R, Taske N, Rees M, Gardiner M. Everett KV, et al. Among authors: goutieres f. Eur J Hum Genet. 2007 Apr;15(4):463-72. doi: 10.1038/sj.ejhg.5201783. Epub 2007 Jan 31. Eur J Hum Genet. 2007. PMID: 17264864 Free PMC article.
Linkage analysis between childhood absence epilepsy and genes encoding GABAA and GABAB receptors, voltage-dependent calcium channels, and the ECA1 region on chromosome 8q.
Robinson R, Taske N, Sander T, Heils A, Whitehouse W, Goutières F, Aicardi J, Lehesjoki AE, Siren A, Laue Friis M, Kjeldsen MJ, Panayiotopoulos C, Kennedy C, Ferrie C, Rees M, Gardiner RM. Robinson R, et al. Among authors: goutieres f. Epilepsy Res. 2002 Feb;48(3):169-79. doi: 10.1016/s0920-1211(01)00335-7. Epilepsy Res. 2002. PMID: 11904235
Paroxysmal extreme pain disorder (previously familial rectal pain syndrome).
Fertleman CR, Ferrie CD, Aicardi J, Bednarek NA, Eeg-Olofsson O, Elmslie FV, Griesemer DA, Goutières F, Kirkpatrick M, Malmros IN, Pollitzer M, Rossiter M, Roulet-Perez E, Schubert R, Smith VV, Testard H, Wong V, Stephenson JB. Fertleman CR, et al. Among authors: goutieres f. Neurology. 2007 Aug 7;69(6):586-95. doi: 10.1212/01.wnl.0000268065.16865.5f. Neurology. 2007. PMID: 17679678
Atypical forms of Rett syndrome.
Goutières F, Aicardi J. Goutières F, et al. Am J Med Genet Suppl. 1986;1:183-94. doi: 10.1002/ajmg.1320250521. Am J Med Genet Suppl. 1986. PMID: 3087180
[Neonatal myoclonic encephalopathy (author's transl)].
Aicardi J, Goutieres F. Aicardi J, et al. Among authors: goutieres f. Rev Electroencephalogr Neurophysiol Clin. 1978 Jan-Mar;8(1):99-101. doi: 10.1016/s0370-4475(78)80124-5. Rev Electroencephalogr Neurophysiol Clin. 1978. PMID: 663355 French.
88 results