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La ricerca find articoli where authors phrase all words ' Goutieres, F' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 22 riferimenti
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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
    2. Aicardi, J; Goutieres, F
      Systemic lupus erythematosus or Aicardi-Goutieres syndrome?

      NEUROPEDIATRICS
    3. Arzimanoglou, AA; Salefranque, F; Goutieres, F; Aicardi, J
      Hemifacial spasm or subcortical epilepsy?

      EPILEPTIC DISORDERS
    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
    5. Goutieres, F; Dollfus, H; Becquet, F; Dufier, JL
      Extensive brain calcification in two children with bilateral Coats' disease

      NEUROPEDIATRICS
    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
    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
    8. Goutieres, F; Aicardi, J; Barth, PG; Lebon, P
      Aicardi-Goutieres syndrome: An update and results of interferon-alpha studies

      ANNALS OF NEUROLOGY
    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
    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
    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
    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
    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
    14. GOUTIERES F
      BOURNEVILLE TUBEROUS SCLEROSIS

      Archives de pediatrie
    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
    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
    17. ARZIMANOGLOU AA; BOURGEOIS M; GOUTIERES F; SALEFRANQUE F; AICARDI J
      EPILEPSY IN RETT-SYNDROME

      Epilepsia
    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
    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
    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
    21. GOUTIERES F
      FAMILIAL ENCEPHALOPATHIES WITH CALCIFICAT IONS OF THE BASAL GANGLIA

      La Presse medicale
    22. BOURGEOIS M; AICARDI J; GOUTIERES F
      ALTERNATING HEMIPLEGIA OF CHILDHOOD

      The Journal of pediatrics


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 18/01/21 alle ore 17:55:16