F. Goutières

发表

Deficiency in complex II of the respiratory chain, presenting as a leukodystrophy in two sisters with leigh syndrome

A. Munnich, J. Aicardi, P. Rustin, 1992, Brain and Development.

Does Migraine‐related Stroke Occur in Childhood?

T. Deonna, J. Penzien, F. Vassella, 1990, Developmental medicine and child neurology.

Three new cases of the Schinzel-Giedion syndrome and review of the literature.

S. Lyonnet, M. le Merrer, V. Zupan, 1994, American journal of medical genetics.

Extensive brain calcifications, leukodystrophy, and formation of parenchymal cysts

C. Lacroix, P. Landrieu, M. Zérah, 1996, Neurology.

Creutzfeldt-Jakob disease with unusually extensive neuropathology in a child treated with native human growth hormone

H. Budka, P. Brown, J. Mikol, 2012, Clinical neuropathology.

Anterior horn cell disease associated with pontocerebellar hypoplasia in infants.

J. Aicardi, F. Goutières, É. Farkas, 1977, Journal of neurology, neurosurgery, and psychiatry.

Moyamoya, a nonspecific radiological syndrome

J. Aicardi, G. Debrun, J. Sauvegrain, 2004, Neuroradiology.

Early intrathecal synthesis of interferon in herpes encephalitis.

J. Aicardi, G. Ponsot, P. Lebon, 1979, Biomedicine / [publiee pour l'A.A.I.C.I.G.].

Will to live in the terminally ill

G. Sutherland, J. Aicardi, P. Griffiths, 1999 .

Aicardi–Goutières syndrome

F. Goutières, 2005, Brain and Development.

Late‐onset mitochondrial DNA depletion: DNA copy number, multiple deletions, and compensation

N. Romero, M. Fardeau, P. Frachon, 2001, Annals of neurology.

Aicardi‐Goutières syndrome: An update and results of interferon‐α studies

J. Aicardi, P. Lebon, P. Barth, 1998, Annals of neurology.

Aicardi–Goutières syndrome: monogenic recessive disease, genetically heterogeneous disease, or multifactorial disease?

J. Weissenbach, G. Ponsot, P. Lebon, 1999, Clinical genetics.

Paroxysmal extreme pain disorder (previously familial rectal pain syndrome)

C. Fertleman, J. Aicardi, V. Wong, 2007, Neurology.

Rett syndrome: Criteria for inclusion and exclusion

F. Hanefeld, B. Hagberg, A. Rett, 1985, Brain and Development.

Linkage analysis between childhood absence epilepsy and genes encoding GABAA and GABAB receptors, voltage-dependent calcium channels, and the ECA1 region on chromosome 8q.

J. Aicardi, A. Heils, C. Panayiotopoulos, 2002, Epilepsy research.

Late-onset mitochondrial DNA depletion: DNA copy number, multiple deletions, and compensation.

N. Romero, M. Fardeau, P. Frachon, 2001 .

The juvenile and chronic forms of GM2 gangliosidosis

J. Aicardi, J. Mikol, M. Vanier, 1990, Neurology.

[An unusual cerebral malformation associated with thanatophoric dwarfism].

J. Aicardi, F. Goutières, E. Farkas‐Bargeton, 1971, Revue neurologique (Paris).

Extensive brain calcification in two children with bilateral Coats' disease.

H. Dollfus, J. Dufier, F. Goutières, 1999, Neuropediatrics.

Ischemic Strokes in Children

J. Aicardi, F. Goutières, A. Dusser, 1986, Journal of child neurology.

Clinical and molecular phenotype of Aicardi-Goutieres syndrome.

A. Green, D. Bonthron, E. Bertini, 2007, American journal of human genetics.

Systemic Lupus Erythematosus or Aicardi-Goutières Syndrome?

J. Aicardi, F. Goutières, 2000, Neuropediatrics.

Intrathecal synthesis of interferon-alpha in infants with progressive familial encephalopathy

J. Aicardi, G. Ponsot, P. Lebon, 1988, Journal of the Neurological Sciences.

A Progressive familial encephalopathy in infancy with calcifications of the basal ganglia and chronic cerebrospinal fluid lymphocytosis

J. Aicardi, F. Goutières, 1984, Annals of neurology.

Atypical presentations of pyridoxine‐dependent seizures: A treatable cause of intractable epilepsy in infants

J. Aicardi, F. Goutières, 1985, Annals of neurology.

Multicystic encephalomalacia of infants and its relation to abnormal gestation and hydranencephaly.

J. Aicardi, F. Goutières, A. H. De Verbois, 1972, Journal of the neurological sciences.

Absence of the septum pellucidum with porencephalia. A neuroradiologic syndrome with variable clinical expression.

J. Aicardi, F. Goutières, L. Menezes, 1988, Archives of neurology.

THE SYNDROME OF ABSENCE OF THE SEPTUM PELLUCIDUM WITH PORENCEPHALIES AND OTHER DEVELOPMENTAL DEFECTS

J. Aicardi, F. Goutières, 1981, Neuropediatrics.

An ultramicroscopic study of skin and conjunctival biopsies in chronic neurological disorders of childhood

J. Aicardi, F. Goutières, M. L. Arsénio-Nunes, 1981, Annals of neurology.

An ultramicroscopic study of the skin in the diagnosis of the infantile and late infantile types of ceroid-lipofuscinosis.

F. Goutières, M. L. Arsénio-Nunes, M. Arsénio-Nunes, 1975, Journal of neurology, neurosurgery, and psychiatry.

Intrachromosomal insertion mimicking a pericentric inversion: Molecular cytogenetic characterization of a three break rearrangement of chromosome 20

M. Prieur, C. Turleau, F. Goutières, 2005, American journal of medical genetics. Part A.

Anultramicroscopic study oftheskin inthe diagnosis oftheinfantile andlate infantile types ofceroid-lipofusci nosis1

F. Goutières, M. L. Arsénio-Nunes, 1975 .

Diagnosis of infantile neuroaxonal dystrophy by conjunctival biopsy.

F. Goutières, M. L. Arsénio-Nunes, 1978, Journal of neurology, neurosurgery, and psychiatry.

Linkage analysis between childhood absence epilepsy and genes encoding GABAA and GABAB receptors, voltage-dependent calcium channels, and the ECA1 region on chromosome 8q

J. Aicardi, A. Heils, C. Panayiotopoulos, 2002, Epilepsy Research.

Accidental percutaneous hexachlorophane intoxication in children.

J. Aicardi, F. Goutières, 1977, British medical journal.

Alternating hemiplegia of childhood.

J. Aicardi, M. Bourgeois, F Goutières, 1993, The Journal of pediatrics.

Ullrich's congenital atonic sclerotic muscular dystrophy

J. Aicardi, F. Goutières, L. D. Paillette, 1989, Journal of Neurology.

Schilder's myelinoclastic diffuse sclerosis.

J. Aicardi, C. Poser, F. Goutières, 1986, Pediatrics.

Acute measles encephalitis in children with immunosuppression.

J. Aicardi, P. Lebon, F. Goutières, 1977, Pediatrics.

Linkage and association analysis of CACNG 3 in childhood absence epilepsy

P. McKeigue, J. Aicardi, A. Heils, 2008 .

Linkage and association analysis of CACNG3 in childhood absence epilepsy

P. McKeigue, J. Aicardi, A. Heils, 2007, European Journal of Human Genetics.

Hereditary infantile hemiparesis, retinal arteriolar tortuosity, and leukoencephalopathy

P. Massin, F. Chapon, A. Gaudric, 2003, Neurology.

Leucoencéphalopathie familiale associée à une acidose lactique congénitale

F. Goutières, S. Thieffry, E. Farkas‐Bargeton, 1971, Acta Neuropathologica.

[Familial leukoencephalopathy associated with congenital lactic acidosis].

F. Goutières, S. Thieffry, E. Farkas‐Bargeton, 1971, Acta neuropathologica.

Acute neurological dysfunction associated with destructive lesions of the basal ganglia in children

J. Aicardi, F Goutières, J Aicardi, 1982, Annals of neurology.

Subacute sclerosing panencephalitis: detection of measles virus RNA in appendix lymphoid tissue before clinical signs.

P. Lebon, S. Rozenblatt, J. Fournier, 1986, British medical journal.

Aicardi-Goutières syndrome: an update and results of interferon-alpha studies.

J. Aicardi, P. Lebon, P. Barth, 1998, Annals of neurology.

Extensive macrogyri or no visible gyri

J. Aicardi, M. Tardieu, P. Landrieu, 1995, Neurology.

[Dopa-sensitive dystonia].

J. Aicardi, P. Rondot, M. Ziégler, 1992, Revue neurologique.

Absorption of phenobarbital after the intramuscular administration of single doses in infants.

J. Aicardi, F. Goutières, A. Brachet-Liermain, 1975, The Journal of pediatrics.

Surgery of epilepsy associated with focal lesions in childhood.

J. Hirsch, W. Maixner, J. Aicardi, 1999, Journal of neurosurgery.

CT Scans of Infants with Glutaric Aciduria

J. Aicardi, F. Goutières, H. Ogier, 1985, Developmental medicine and child neurology.

[Neonatal myoclonic encephalopathy (author's transl)].

J. Aicardi, F. Goutières, 1978, Revue d'electroencephalographie et de neurophysiologie clinique.

Congenital hydrocephalus and eye abnormalities with severe developmental brain defects: Warburg's syndrome

J. Aicardi, C. Bordarier, F. Goutières, 1984, Annals of neurology.

A peculiar case of acquired aphasia with epilepsy in childhood

J. Aicardi, C. Chevrie-Muller, J. Chevrie, 1991, Journal of Neurolinguistics.

Neuronal intranuclear inclusion disease in a child: Diagnosis by rectal biopsy

J. Aicardi, J. Mikol, F. Goutières, 1990, Annals of neurology.

Digito‐reno‐cerebral syndrome: confirmation of Eronen syndrome

A. David, M. Merrer, F. Goutières, 1992, Clinical genetics.

Atypical forms of Rett syndrome.

J. Aicardi, F. Goutières, 1986, American journal of medical genetics. Supplement.

New experience with rett syndrome in france: The problem of atypical cases

J. Aicardi, F. Goutières, 1987, Brain and Development.

A predominantly cervical form of spinal muscular atrophy.

J. Aicardi, D. Bogićević, F. Goutières, 1991, Journal of neurology, neurosurgery, and psychiatry.

Surgery in epilepsy associated with focal lesions in childhood

J. Hirsch, J. Aicardi, F. Brunelle, 1999 .

Deletion of mitochondrial DNA in patient with chronic tubulointerstitial nephritis.

A. Munnich, P. Rustin, A. Rötig, 1995, The Journal of pediatrics.

Hemifacial spasm or subcortical epilepsy?

J. Aicardi, A. Arzimanoglou, F. Salefranque, 1999, Epileptic disorders : international epilepsy journal with videotape.

Glycine Encephalopathy1

J. Aicardi, P. Plouin, B. dalla Bernardina, 1979, Neuropadiatrie.

Rapid Improvement of Intracranial Tuberculomas After Addition of Ofloxacin to First-Line Antituberculosis Treatment

I. Sermet-Gaudelus, J. Gaillard, G. Lenoir, 1999, European Journal of Clinical Microbiology and Infectious Diseases.

The Syndrome of Myoclonic Epilepsy with Ragged-Red Fibers. Report of a Case and Review of the Literature

J. Aicardi, J. Chevrie, F. Goutières, 1987, Neuropediatrics.

Moyamoya disease in a child with glycogen storage disease type Ia.

M. Bourgeois, M. Odiévre, P. Labrune, 1997, Neuropediatrics.

Diffuse cortical dysplasia, or the 'double cortex' syndrome

F. Andermann, J. Aicardi, A. Palmini, 1991, Neurology.

Alternating Hemiplegia of Childhood

J. Aicardi, F. Goutières, M. Mikati, 2010 .

Morphological diagnosis of Niemann-Pick disease type C by skin and conjunctival biopsies.

F. Goutières, M. Arsénio-Nunes, 1981, Acta neuropathologica. Supplementum.

Leukoencephalopathy, Megalencephaly, and Mild Clinical Course. A Recently Individualized Familial Leukodystrophy. Report on Five New Cases

J. Aicardi, M. Bourgeois, J. Boulloche, 1996, Journal of child neurology.

Congenital Hydrocephalus and Eye Abnormdties

C. Bordarier, F. Goutières, Aicardi, 2004 .

Alternating hemiplegia of childhood.

F. Goutières, Marle Bourgeois, Jean Aicardi, 1993, The Journal of pediatrics.

[Neonatal forms of Steinert's mytonic dystrophy].

J. Aicardi, D. Conti, F. Goutières, 1974, Journal of the neurological sciences.