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Atypical presentations of pyridoxine-dependent seizures: a treatable cause of intractable epilepsy in infants.
Goutières F, Aicardi J. Goutières F, et al. Ann Neurol. 1985 Feb;17(2):117-20. doi: 10.1002/ana.410170203. Ann Neurol. 1985. PMID: 3977296
Late-onset mitochondrial DNA depletion: DNA copy number, multiple deletions, and compensation.
Barthélémy C, Ogier de Baulny H, Diaz J, Cheval MA, Frachon P, Romero N, Goutieres F, Fardeau M, Lombès A. Barthélémy C, et al. Among authors: goutieres f. Ann Neurol. 2001 May;49(5):607-17. Ann Neurol. 2001. PMID: 11357951
Acute neurological dysfunction associated with destructive lesions of the basal ganglia in children.
Goutières F, Aicardi J. Goutières F, et al. Ann Neurol. 1982 Oct;12(4):328-32. doi: 10.1002/ana.410120403. Ann Neurol. 1982. PMID: 7149658
Congenital hydrocephalus and eye abnormalities with severe developmental brain defects: Warburg's syndrome.
Bordarier C, Aicardi J, Goutieres F. Bordarier C, et al. Among authors: goutieres f. Ann Neurol. 1984 Jul;16(1):60-5. doi: 10.1002/ana.410160112. Ann Neurol. 1984. PMID: 6431899
An ultramicroscopic study of skin and conjunctival biopsies in chronic neurological disorders of childhood.
Arsenio-Nunes ML, Goutières F, Aicardi J. Arsenio-Nunes ML, et al. Among authors: goutieres f. Ann Neurol. 1981 Feb;9(2):163-73. doi: 10.1002/ana.410090210. Ann Neurol. 1981. PMID: 7235631
Hereditary infantile hemiparesis, retinal arteriolar tortuosity, and leukoencephalopathy.
Vahedi K, Massin P, Guichard JP, Miocque S, Polivka M, Goutières F, Dress D, Chapon F, Ruchoux MM, Riant F, Joutel A, Gaudric A, Bousser MG, Tournier-Lasserve E. Vahedi K, et al. Among authors: goutieres f. Neurology. 2003 Jan 14;60(1):57-63. doi: 10.1212/wnl.60.1.57. Neurology. 2003. PMID: 12525718
The juvenile and chronic forms of GM2 gangliosidosis: clinical and enzymatic heterogeneity.
Specola N, Vanier MT, Goutières F, Mikol J, Aicardi J. Specola N, et al. Among authors: goutieres f. Neurology. 1990 Jan;40(1):145-50. doi: 10.1212/wnl.40.1.145. Neurology. 1990. PMID: 2136940
Deletion of mitochondrial DNA in patient with chronic tubulointerstitial nephritis.
Rötig A, Goutières F, Niaudet P, Rustin P, Chretien D, Guest G, Mikol J, Gubler MC, Munnich A. Rötig A, et al. Among authors: goutieres f. J Pediatr. 1995 Apr;126(4):597-601. doi: 10.1016/s0022-3476(95)70359-4. J Pediatr. 1995. PMID: 7699541
Ullrich's congenital atonic sclerotic muscular dystrophy. A case report.
De Paillette L, Aicardi J, Goutières F. De Paillette L, et al. Among authors: goutieres f. J Neurol. 1989 Feb;236(2):108-10. doi: 10.1007/BF00314406. J Neurol. 1989. PMID: 2651568 Review.
A progressive familial encephalopathy in infancy with calcifications of the basal ganglia and chronic cerebrospinal fluid lymphocytosis.
Aicardi J, Goutières F. Aicardi J, et al. Among authors: goutieres f. Ann Neurol. 1984 Jan;15(1):49-54. doi: 10.1002/ana.410150109. Ann Neurol. 1984. PMID: 6712192
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