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La ricerca find articoli where authors phrase all words ' LANDRIEU P' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 51 riferimenti
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    1. Houten, SM; Koster, J; Romeijn, GJ; Frenkel, J; Di Rocco, M; Caruso, U; Landrieu, P; Kelley, RI; Kuis, W; Poll-The, BT; Gibson, KM; Wanders, RJA; Waterham, HR
      Organization of the mevalonate kinase (MVK) gene and identification of novel mutations causing mevalonic aciduria and hyperimmunoglobulinaemia D and periodic fever syndrome (vol 9, pg 253, 2001)

      EUROPEAN JOURNAL OF HUMAN GENETICS
    2. Houten, SM; Koster, J; Romeijn, GJ; Frenkel, J; Di Rocco, M; Caruso, U; Landrieu, P; Kelley, RI; Kuis, W; Poll-The, BT; Gibson, KM; Wanders, RJA; Waterham, HR
      Organization of the mevalonate kinase (MVK) gene and identification of novel mutations causing mevalonic aciduria and hyperimmunoglobulinaemia D and periodic fever syndrome

      EUROPEAN JOURNAL OF HUMAN GENETICS
    3. Monnier, N; Romero, NB; Lerale, J; Landrieu, P; Nivoche, Y; Fardeau, M; Lunardi, J
      Familial and sporadic forms of central core disease are associated with mutations in the C-terminal domain of the skeletal muscle ryanodine receptor

      HUMAN MOLECULAR GENETICS
    4. Landrieu, P
      Fetal immobility syndrome - Warning sings in etiopathogenic diagnosis

      ARCHIVES DE PEDIATRIE
    5. Gauthier-Villars, M; Landrieu, P; Cormier-Daire, V; Jacquemin, E; Chretien, D; Rotig, A; Rustin, P; Munnich, A; de Lonlay, P
      Respiratory chain deficiency in Alpers syndrome

      NEUROPEDIATRICS
    6. Charollais, A; Lacroix, C; Nouyrigat, V; Devictor, D; Landrieu, P
      Arthrogryposis and multicystic encephalopathy after acute fetal distress in the end stage of gestation

      NEUROPEDIATRICS
    7. Defresne, P; Meyer, L; Tardieu, M; Scalais, E; Nuttin, C; De Bont, B; Loftus, G; Landrieu, P; Kadhim, H; Sebire, G
      Efficacy of high dose steroid therapy in children with severe acute transverse myelitis

      JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
    8. Bomont, P; Cavalier, L; Blondeau, F; Hamida, CB; Belal, S; Tazir, M; Demir, E; Topaloglu, H; Korinthenberg, R; Tuysuz, B; Landrieu, P; Hentati, F; Koenig, M
      The gene encoding gigaxonin, a new member of the cytoskeletal BTB/kelch repeat family, is mutated in giant axonal neuropathy

      NATURE GENETICS
    9. Cavalier, L; BenHamida, C; Amouri, R; Belal, S; Bomont, P; Lagarde, N; Gressin, L; Callen, D; Demir, E; Topaloglu, H; Landrieu, P; Ioos, C; Ben Hamida, M; Koenig, M; Hentati, F
      Giant axonal neuropathy locus refinement to a < 590 kb critical interval

      EUROPEAN JOURNAL OF HUMAN GENETICS
    10. Heissessen, L; Dusser, A; Nouirygat, V; Navelet, Y; Charollais, A; Husson, B; Landrieu, P
      Epilepsy presenting as life-threatening events in infants

      ARCHIVES DE PEDIATRIE
    11. Landrieu, P
      Advances in pediatric neurology?

      ARCHIVES DE PEDIATRIE
    12. Chabrier, S; Husson, B; Lasjaunias, P; Landrieu, P; Tardieu, M
      Stroke in childhood: Outcome and recurrence risk by mechanism in 59 patients

      JOURNAL OF CHILD NEUROLOGY
    13. Pingault, V; Guiochon-Mantel, A; Bondurand, N; Faure, C; Lacroix, C; Lyonnet, S; Goosens, M; Landrieu, P
      Peripheral neuropathy with hypomyelination, chronic intestinal pseudo-obstruction and deafness: A developmental "neural crest syndrome" related to a SOX10 mutation

      ANNALS OF NEUROLOGY
    14. Landrieu, P
      Progress in pediatric neurology.

      REVUE NEUROLOGIQUE
    15. Thebaud, B; Husson, B; Navelet, Y; Huault, G; Landrieu, P; Devictor, D; Sebire, G
      Haemorrhagic shock and encephalopathy syndrome: neurological course and predictors of outcome

      INTENSIVE CARE MEDICINE
    16. Bader-Meunier, B; Mielot, F; Breton-Gorius, J; Cramer, E; Guichard, J; Landrieu, P; Dommergues, JP; Tchernia, G
      Hematologic involvement in mitochondrial cytopathies in childhood: A retrospective study of bone marrow smears

      PEDIATRIC RESEARCH
    17. LEROYMALHERBE V; SEBIRE G; HOLLENBERG H; TARDIEU M; LANDRIEU P
      NEUROGENIC BLADDER IN CHILDREN WITH ACUTE TRANSVERSE MYELOPATHY

      Archives de pediatrie
    18. TABARKI B; HUSSON B; LANDRIEU P
      ACUTE CEREBELLAR ATROPHY IN ENCEPHALITIS

      Journal of child neurology
    19. CHABRIER S; RODESCH G; LASJAUNIAS P; TARDIEU M; LANDRIEU P; SEBIRE G
      TRANSIENT CEREBRAL ARTERIOPATHY - A DISORDER RECOGNIZED BY SERIAL ANGIOGRAMS IN CHILDREN WITH STROKE

      Journal of child neurology
    20. DELANOE C; SEBIRE G; LANDRIEU P; HUAULT G; METRAL S
      ACUTE INFLAMMATORY DEMYELINATING POLYRADICULOPATHY IN CHILDREN - CLINICAL AND ELECTRODIAGNOSTIC STUDIES

      Annals of neurology
    21. LANDRIEU P; HUSSON B; PARIENTE D; LACROIX C
      MRI-NEUROPATHOLOGICAL CORRELATIONS IN TYPE-1 LISSENCEPHALY

      Neuroradiology
    22. LANDRIEU P; BLANCHE S; VANIER MT; METRAL S; HUSSON B; SANDHOFF K; FISCHER A
      BONE-MARROW TRANSPLANTATION IN METACHROMATIC LEUKODYSTROPHY CAUSED BYSAPOSIN-B DEFICIENCY - A CASE-REPORT WITH A 3-YEAR FOLLOW-UP PERIOD

      The Journal of pediatrics
    23. TABARKI B; ELMADANI A; ALVAREZ H; HUSSON B; LASJAUNIAS P; LANDRIEU P; TARDIEU M; SEBIRE G
      CHILDHOOD STROKE DUE TO A TRAUMATIC VERTE BRAL ARTERY DISSECTION

      Archives de pediatrie
    24. FERLIN T; LANDRIEU P; RAMBAUD C; FERNANDEZ H; DUMOULIN R; RUSTIN P; MOUSSON B
      SEGREGATION OF THE GB993 MUTANT MITOCHONDRIAL-DNA THROUGH GENERATIONSAND EMBRYONIC-TISSUES IN A FAMILY AT RISK OF LEIGH-SYNDROME

      The Journal of pediatrics
    25. SEBIRE G; HOLLENBERG H; MEYER L; HUAULT G; LANDRIEU P; TARDIEU M
      HIGH-DOSE METHYLPREDNISOLONE IN SEVERE ACUTE TRANSVERSE MYELOPATHY

      Archives of Disease in Childhood
    26. THIBAUD D; THIBAUD E; LANDRIEU P; ZERAH M
      PRIMARY AMENORRHEA AS THE FIRST MANIFESTA TION OF A CONGENITAL HYDROCEPHALUS

      Archives de pediatrie
    27. BOUSQUET O; BASSEVILLE M; VILAPORCILE E; DEVILLEMEUR TB; HAUW JJ; LANDRIEU P; PORTIER MM
      AGGREGATION OF A SUBPOPULATION OF VIMENTIN FILAMENTS IN CULTURED HUMAN SKIN FIBROBLASTS DERIVED FROM PATIENTS WITH GIANT AXONAL NEUROPATHY

      Cell motility and the cytoskeleton
    28. VENENCIE PY; DUSSER A; FABRE M; AITKEN G; LANDRIEU P
      DARIER DISEASE AND PROGRESSIVE ENCEPHALOP ATHY - A FAMILIAL CASE

      Annales de pediatrie
    29. 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
    30. SEBIRE G; HUSSON B; DUSSER A; NAVELET Y; TARDIEU M; LANDRIEU P
      CONGENITAL UNILATERAL PERISYLVIAN SYNDROME - RADIOLOGICAL BASIS AND CLINICAL CORRELATIONS

      Journal of Neurology, Neurosurgery and Psychiatry
    31. BURGLEN L; AMIEL J; VIOLLET L; LEFEBVRE S; BURLET P; CLERMONT O; RACLIN V; LANDRIEU P; VERLOES A; MUNNICH A; MELKI J
      SURVIVAL MOTOR-NEURON GENE DELETION IN THE ARTHROGRYPOSIS MULTIPLEX CONGENITA-SPINAL MUSCULAR-ATROPHY ASSOCIATION

      The Journal of clinical investigation
    32. EPELBAUM C; TARDIEU M; LANDRIEU P; FERRARI P
      CONSEQUENCES OF THE ANNOUNCEMENT OF EARLY HANDICAP ON THE PARENTS CHILD RELATION - A RESEARCH/

      Annales medico-psychologiques
    33. HENSELER M; KLEIN A; REBER M; VANIER MT; LANDRIEU P; SANDHOFF K
      ANALYSIS OF A SPLICE-SITE MUTATION IN THE SAP-PRECURSOR GENE OF A PATIENT WITH METACHROMATIC LEUKODYSTROPHY

      American journal of human genetics
    34. SEBIRE G; HUSSON B; LASSER C; TARDIEU M; DOMMERGUES JP; LANDRIEU P
      HYPERTENSIVE ENCEPHALOPATHY - CLINICORADI OLOGICAL ASPECTS AND TREATMENT

      Archives de pediatrie
    35. VENENCIE PY; PAUWELS C; MALHERBE V; PERIE G; LANDRIEU P
      FUCOSIDOSIS WITH ANGIOKERATOMA - IMMUNOHI STOCHEMICAL AND ULTRASTRUCTURAL STUDIES

      Annales de dermatologie et de venereologie
    36. AMIEL J; MAZIERE JC; BEUCLER I; KOENIG M; REUTENAUER L; LOUX N; BONNEFONT D; FEO C; LANDRIEU P
      FAMILIAL ISOLATED VITAMIN-E-DEFICIENCY - EXTENSIVE STUDY OF A LARGE FAMILY WITH A 5-YEAR THERAPEUTIC FOLLOW-UP

      Journal of inherited metabolic disease
    37. BURGLEN L; SPIEGEL R; IGNATIUS J; COBBEN JM; LANDRIEU P; LEFEBVRE S; MUNNICH A; MELKI J
      SMN GENE DELETION IN VARIANT OF INFANTILE SPINAL MUSCULAR-ATROPHY

      Lancet
    38. 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
    39. 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
    40. LEROYMALHERBE V; HUSSON B; LANDRIEU P; TARDIEU M
      LATE MATURATION OF SUCKING AND SWALLOWING

      Archives de pediatrie
    41. LANDRIEU P; LACROIX C
      SCHIZENCEPHALY, CONSEQUENCE OF A DEVELOPMENTAL VASCULOPATHY - A CLINICOPATHOLOGICAL REPORT

      Clinical neuropathology
    42. MANTEL A; LEONARD C; HUSSON B; MILADI N; TARDIEU M; LANDRIEU P
      SUBMICROSCOPIC DELETIONS OF 17P13.3 IN TYPE-1 LISSENCEPHALY

      Human genetics
    43. DEMERSAY AC; BENICHOU JJ; LANDRIEU P; LABRUNE B
      TRANSIENT BENIGN CORTICAL BLINDNESS AFTER HEAD-INJURY - 2 CASE-REPORTS

      Annales de pediatrie
    44. BOURGERON T; CHRETIEN D; POGGIBACH J; DOONAN S; RABIER D; LETOUZE P; MUNNICH A; ROTIG A; LANDRIEU P; RUSTIN P
      MUTATION OF THE FUMARASE GENE IN 2 SIBLINGS WITH PROGRESSIVE ENCEPHALOPATHY AND FUMARASE DEFICIENCY

      The Journal of clinical investigation
    45. BADERMEUNIER B; ROTIG A; MIELOT F; LAVERGNE JM; CROISILLE L; RUSTIN P; LANDRIEU P; DOMMERGUES JP; MUNNICH A; TCHERNIA G
      REFRACTORY-ANEMIA AND MITOCHONDRIAL CYTOPATHY IN CHILDHOOD

      British Journal of Haematology
    46. BOESPFLUGTANGUY O; MIMAULT C; MELKI J; CAVAGNA A; GIRAUD G; DINH DP; DASTUGUE B; DAUTIGNY A; AICARDI J; GOUTTIERES F; BAUMANN N; BERTINI E; DAVID A; HENOCQ A; LANDRIEU P; TARDIEU M; LEBERRE C; LEMAREC B; LYON G; MAYER M; PINARD JM; PONSOT G; MATHIEU M; SAINTIVE JP; SAURA R; VALLEE L
      GENETIC HOMOGENEITY OF PELIZAEUS-MERZBACHER-DISEASE - TIGHT LINKAGE TO THE PROTEOLIPOPROTEIN LOCUS IN 16 AFFECTED FAMILIES

      American journal of human genetics
    47. ROUSSEAU S; METRAL S; LACROIX C; CAHUSAC C; NOCTON F; LANDRIEU P
      ANTERIOR SPINAL ARTERY SYNDROME MIMICKING INFANTILE SPINAL MUSCULAR-ATROPHY

      American journal of perinatology
    48. PEUDENIER S; DELEUZE JF; PHAMDINH D; LACROIX C; BOULLOCHE J; LANDRIEU P
      INFANTILE NEUROPATHY WITH UNSTABLE MYELIN - STUDY OF THE PO PROTEIN

      Journal of neurology
    49. MALHERBE V; PARIENTE D; TARDIEU M; LACROIX C; VENENCIE PY; HIBON D; VEDRENNE J; LANDRIEU P
      CENTRAL-NERVOUS-SYSTEM LESIONS IN HYPOMELANOSIS OF ITO - AN MRI AND PATHOLOGICAL-STUDY

      Journal of neurology
    50. LANDRIEU P
      APPROACHES TO CHRONIC CEREBELLAR PATHOLOG Y IN INFANTS

      Revue neurologique
    51. BOURGERON T; CHRETIEN D; ROTIG A; MUNNICH A; LANDRIEU P; RUSTIN P
      MOLECULAR CHARACTERIZATION OF FUMARASE DEFICIENCY IN 2 CHILDREN WITH PROGRESSIVE ENCEPHALOPATHY

      American journal of human genetics


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 04/06/20 alle ore 20:28:51