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1. Barthelemy, C; de Baulny, HO; Diaz, J; Cheval, MA; Frachon, P; Romero, N; Goutieres, F; Fardeau, M; Lombes, A
   Late-onset mitochondrial DNA depletion: DNA copy number, multiple deletions, and compensation
   ANNALS OF NEUROLOGY
   
   C. Barthelemy et al., "Late-onset mitochondrial DNA depletion: DNA copy number, multiple deletions, and compensation", ANN NEUROL, 49(5), 2001, pp. 607-617
2. Aicardi, J; Goutieres, F
   Systemic lupus erythematosus or Aicardi-Goutieres syndrome?
   NEUROPEDIATRICS
   
   J. Aicardi e F. Goutieres, "Systemic lupus erythematosus or Aicardi-Goutieres syndrome?", NEUROPEDIAT, 31(3), 2000, pp. 113-113
3. Arzimanoglou, AA; Salefranque, F; Goutieres, F; Aicardi, J
   Hemifacial spasm or subcortical epilepsy?
   EPILEPTIC DISORDERS
   
   A.A. Arzimanoglou et al., "Hemifacial spasm or subcortical epilepsy?", EPILEPT DIS, 1(2), 1999, pp. 121-125
4. Sermet-Gaudelus, I; Stambouli, F; Abadie, V; Goutieres, F; Lenoir, G; Gendrel, D; Gaillard, JL
   Rapid improvement of intracranial tuberculomas after addition of ofloxacinto first-line antituberculosis treatment
   EUROPEAN JOURNAL OF CLINICAL MICROBIOLOGY & INFECTIOUS DISEASES
   
   I. Sermet-Gaudelus et al., "Rapid improvement of intracranial tuberculomas after addition of ofloxacinto first-line antituberculosis treatment", EUR J CL M, 18(10), 1999, pp. 726-728
5. Goutieres, F; Dollfus, H; Becquet, F; Dufier, JL
   Extensive brain calcification in two children with bilateral Coats' disease
   NEUROPEDIATRICS
   
   F. Goutieres et al., "Extensive brain calcification in two children with bilateral Coats' disease", NEUROPEDIAT, 30(1), 1999, pp. 19-21
6. Bourgeois, M; Sainte-Rose, C; Lellouch-Tubiana, A; Malucci, C; Brunelle, F; Maixner, W; Cinalli, G; Pierre-Kahn, A; Renier, D; Zerah, M; Hirsch, JF; Goutieres, F; Aicardi, J
   Surgery of epilepsy associated with focal lesions in childhood
   JOURNAL OF NEUROSURGERY
   
   M. Bourgeois et al., "Surgery of epilepsy associated with focal lesions in childhood", J NEUROSURG, 90(5), 1999, pp. 833-842
7. Faure, S; Bordelais, I; Marquette, C; Rittey, C; Campos-Castello, J; Goutieres, F; Ponsot, G; Weissenbach, J; Lebon, P
   Aicardi-Goutieres syndrome: monogenic recessive disease, genetically heterogeneous disease, or multifactorial disease?
   CLINICAL GENETICS
   
   S. Faure et al., "Aicardi-Goutieres syndrome: monogenic recessive disease, genetically heterogeneous disease, or multifactorial disease?", CLIN GENET, 56(2), 1999, pp. 149-153
8. Goutieres, F; Aicardi, J; Barth, PG; Lebon, P
   Aicardi-Goutieres syndrome: An update and results of interferon-alpha studies
   ANNALS OF NEUROLOGY
   
   F. Goutieres et al., "Aicardi-Goutieres syndrome: An update and results of interferon-alpha studies", ANN NEUROL, 44(6), 1998, pp. 900-907
9. Bourgeois, M; Sainte-Rose, C; Lellouch-Tubiana, A; Brunelle, F; Charron, B; Laroussinie, F; Salefranque, F; Hertz-Pannier, L; Pierre-Kahn, A; Renier, D; Cinalli, G; Zerah, M; Hoppe-Hirsch, E; Goutieres, F; Aicardi, J; Hirsch, JF
   Epilepsy and focal lesions in children: The significance of lesion removal
   DRUG-RESISTANT SEVERE PARTIAL EPILEPSY IN CHILDREN: DIAGNOSTIC STRATEGIES AND SURGICAL TREATMENTS
   
   M. Bourgeois et al., "Epilepsy and focal lesions in children: The significance of lesion removal", DRUG-RESISTANT SEVERE PARTIAL EPILEPSY IN CHILDREN: DIAGNOSTIC STRATEGIES AND SURGICAL TREATMENTS, 1998, pp. 212-226
10. MIKOL J; LAVERGNESLOVE A; LECOZ P; GOUTIERES F; VANIER MT
    B1 VARIANT OF GM2 GANGLIOSIDOSIS - PATHOLOGICAL AND BIOCHEMICAL-STUDYOF A LATE-ONSET FORM
    Brain pathology
    
    J. Mikol et al., "B1 VARIANT OF GM2 GANGLIOSIDOSIS - PATHOLOGICAL AND BIOCHEMICAL-STUDYOF A LATE-ONSET FORM", Brain pathology, 7(4), 1997, pp. 1062-1062
11. GOUTIERES F; BOURGEOIS M; TRIOCHE P; DEMELIER JF; ODIEVRE M; LABRUNE P
    MOYAMOYA DISEASE IN A CHILD WITH GLYCOGEN-STORAGE-DISEASE TYPE IA
    Neuropediatrics
    
    F. Goutieres et al., "MOYAMOYA DISEASE IN A CHILD WITH GLYCOGEN-STORAGE-DISEASE TYPE IA", Neuropediatrics, 28(2), 1997, pp. 133-134
12. GOUTIERES F; BOULLOCHE J; BOURGEOIS M; AICARDI J
    LEUKOENCEPHALOPATHY, MEGALENCEPHALY, AND MILD CLINICAL COURSE - A RECENTLY INDIVIDUALIZED FAMILIAL LEUKODYSTROPHY - REPORT ON 5 NEW CASES
    Journal of child neurology
    
    F. Goutieres et al., "LEUKOENCEPHALOPATHY, MEGALENCEPHALY, AND MILD CLINICAL COURSE - A RECENTLY INDIVIDUALIZED FAMILIAL LEUKODYSTROPHY - REPORT ON 5 NEW CASES", Journal of child neurology, 11(6), 1996, pp. 439-444
13. LABRUNE P; LACROIX C; GOUTIERES F; DELAVEAUCOUPET J; CHEVALIER P; ZERAH M; HUSSON B; LANDRIEU P
    EXTENSIVE BRAIN CALCIFICATIONS LEUKODYSTROPHY, AND FORMATION OF PARENCHYMAL CYSTS - A NEW PROGRESSIVE DISORDER DUE TO DIFFUSE CEREBRAL MICROANGIOPATHY
    Neurology
    
    P. Labrune et al., "EXTENSIVE BRAIN CALCIFICATIONS LEUKODYSTROPHY, AND FORMATION OF PARENCHYMAL CYSTS - A NEW PROGRESSIVE DISORDER DUE TO DIFFUSE CEREBRAL MICROANGIOPATHY", Neurology, 46(5), 1996, pp. 1297-1301
14. GOUTIERES F
    BOURNEVILLE TUBEROUS SCLEROSIS
    Archives de pediatrie
    
    F. Goutieres, "BOURNEVILLE TUBEROUS SCLEROSIS", Archives de pediatrie, 2, 1995, pp. 82-83
15. SEBIRE G; GOUTIERES F; TARDIEU M; LANDRIEU P; AICARDI J
    EXTENSIVE MACROGYRI OR NO VISIBLE GYRI - DISTINCT CLINICAL, ELECTROENCEPHALOGRAPHIC, AND GENETIC FEATURES ACCORDING TO DIFFERENT IMAGING PATTERNS
    Neurology
    
    G. Sebire et al., "EXTENSIVE MACROGYRI OR NO VISIBLE GYRI - DISTINCT CLINICAL, ELECTROENCEPHALOGRAPHIC, AND GENETIC FEATURES ACCORDING TO DIFFERENT IMAGING PATTERNS", Neurology, 45(6), 1995, pp. 1105-1111
16. ROTIG A; GOUTIERES F; NIAUDET P; RUSTIN P; CHRETIEN D; GUEST G; MIKOL J; GUBLER MC; MUNNICH A
    DELETION OF MITOCHONDRIAL-DNA IN PATIENT WITH CHRONIC TUBULOINTERSTITIAL NEPHRITIS
    The Journal of pediatrics
    
    A. Rotig et al., "DELETION OF MITOCHONDRIAL-DNA IN PATIENT WITH CHRONIC TUBULOINTERSTITIAL NEPHRITIS", The Journal of pediatrics, 126(4), 1995, pp. 597-601
17. ARZIMANOGLOU AA; BOURGEOIS M; GOUTIERES F; SALEFRANQUE F; AICARDI J
    EPILEPSY IN RETT-SYNDROME
    Epilepsia
    
    A.A. Arzimanoglou et al., "EPILEPSY IN RETT-SYNDROME", Epilepsia, 36, 1995, pp. 238-239
18. DOERFLINGER N; LINDER C; OUAHCHI K; GYAPAY G; WEISSENBACH J; LEPASLIER D; RIGAULT P; BELAL S; BENHAMIDA C; HENTATI F; BENHAMIDA M; PANDOLFO M; DIDONATO S; SOKOL R; KAYDEN H; LANDRIEU P; DURR A; BRICE A; GOUTIERES F; KOHLSCHUTTER A; SABOURAUD P; BENOMAR A; YAHYAOUI M; MANDEL JL; KOENIG M
    ATAXIA WITH VITAMIN-E-DEFICIENCY - REFINEMENT OF GENETIC LOCALIZATIONAND ANALYSIS OF LINKAGE DISEQUILIBRIUM BY USING NEW MARKERS IN 14 FAMILIES
    American journal of human genetics
    
    N. Doerflinger et al., "ATAXIA WITH VITAMIN-E-DEFICIENCY - REFINEMENT OF GENETIC LOCALIZATIONAND ANALYSIS OF LINKAGE DISEQUILIBRIUM BY USING NEW MARKERS IN 14 FAMILIES", American journal of human genetics, 56(5), 1995, pp. 1116-1124
19. LABRUNE P; LYONNET S; ZUPAN V; IMBERT MC; GOUTIERES F; HUBERT P; LEMERRER M
    3 NEW CASES OF THE SCHINZEL-GIEDION SYNDROME AND REVIEW OF THE LITERATURE
    American journal of medical genetics
    
    P. Labrune et al., "3 NEW CASES OF THE SCHINZEL-GIEDION SYNDROME AND REVIEW OF THE LITERATURE", American journal of medical genetics, 50(1), 1994, pp. 90-93
20. LECOZ P; ASSOULINE E; VANIER MT; GOUTIERES F; MIKOL J; WOIMANT F; PINARD JM; AICARDI J; HAGUENAU M
    GM2-GANGLIOSIDOSIS VARIANT B1 - A FAMILY WITH LATE JUVENILE-ONSET
    Revue neurologique
    
    P. Lecoz et al., "GM2-GANGLIOSIDOSIS VARIANT B1 - A FAMILY WITH LATE JUVENILE-ONSET", Revue neurologique, 150(1), 1994, pp. 61-66
21. GOUTIERES F
    FAMILIAL ENCEPHALOPATHIES WITH CALCIFICAT IONS OF THE BASAL GANGLIA
    La Presse medicale
    
    F. Goutieres, "FAMILIAL ENCEPHALOPATHIES WITH CALCIFICAT IONS OF THE BASAL GANGLIA", La Presse medicale, 22(39), 1993, pp. 1948-1950
22. BOURGEOIS M; AICARDI J; GOUTIERES F
    ALTERNATING HEMIPLEGIA OF CHILDHOOD
    The Journal of pediatrics
    
    M. Bourgeois et al., "ALTERNATING HEMIPLEGIA OF CHILDHOOD", The Journal of pediatrics, 122(5), 1993, pp. 673-679