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La ricerca find articoli where authors phrase all words ' DESNUELLE C' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 36 riferimenti
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    1. Desnuelle, C; Dib, M; Garrel, C; Favier, A
      A double-blind, placebo-controlled randomized clinical trial of alpha-tocopherol (vitamin E) in the treatment of amyotrophic lateral sclerosis

      AMYOTROPHIC LATERAL SCLEROSIS AND OTHER MOTOR NEURON DISORDERS
    2. Narbonne, H; Perucca-Lostanlen, D; Desnuelle, C; Vialettes, B; Saunieres, A; Paquis-Flucklinger, W
      Searching for A3243G mitochondrial DNA mutation in buccal mucosa in order to improve the screening of patients with mitochondrial diabetes

      EUROPEAN JOURNAL OF ENDOCRINOLOGY
    3. Paul, R; Desnuelle, C; Pouget, J; Pellissier, JF; Richelme, C; Monfort, MF; Butori, C; Saunieres, A; Paquis-Flucklinger, V
      Importance of searching for associated mitochondrial DNA alterations in patients with multiple deletions

      EUROPEAN JOURNAL OF HUMAN GENETICS
    4. Santucci-Darmanin, S; Walpita, D; Lespinasse, F; Desnuelle, C; Ashley, T; Paquis-Flucklinger, V
      MSH4 acts in conjunction with MLH1 during mammalian meiosis

      FASEB JOURNAL
    5. Perucca-Lostanlen, D; Narbonne, H; Hernandez, JB; Staccini, P; Saunieres, A; Paquis-Flucklinger, V; Vialettes, B; Desnuelle, C
      Mitochondrial DNA variations in patients with maternally inherited diabetes and deafness syndrome

      BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
    6. Santucci-Darmanin, S; Paul, R; Michiels, JF; Saunieres, A; Desnuelle, C; Paquis-Flucklinger, V
      Alternative splicing of hMSH4: two isoforms in testis and abnormal transcripts in somatic tissues

      MAMMALIAN GENOME
    7. Boileau, P; Remi, M; Lemaire, M; Rousseau, P; Desnuelle, C; Argenson, C
      A plea for accelerated rehabilitation progam after ACL repair with bone-tendon-bone graft

      REVUE DE CHIRURGIE ORTHOPEDIQUE ET REPARATRICE DE L APPAREIL MOTEUR
    8. PAQUISFLUCKLINGER V; VIALETTES B; VAGUE P; CANIVET B; HIERONIMUS S; OLIVER C; PELLISSIER JF; SAUNIERES A; DESNUELLE C
      IMPORTANCE OF SEARCHING FOR MTDNA DEFECTS IN PATIENTS WITH DIABETES AND HEARING DEFICIT

      Diabetologia
    9. PAQUISFLUCKLINGER V; SANTUCCIDARMANIN S; PAUL R; SAUNIERES A; TURCCAREL C; DESNUELLE C
      CLONING AND EXPRESSION ANALYSIS OF A MEIOSIS-SPECIFIC MUTS HOMOLOG - THE HUMAN MSH4 GENE

      Genomics
    10. HYVERNAT H; GAID H; CASSUTOVIGUIER E; DESNUELLE C; BRACCO J
      ACUTE-RENAL-FAILURE REVEALING MCARDLES-DI SEASE

      La Presse medicale
    11. VIALETTES BH; PAQUISFLUCKLINGER V; PELISSIER JF; BENDAHAN D; NARBONNE H; SILVESTREAILLAUD P; MONTFORT MF; RIGHINICHOSSEGROS M; POUGET J; COZZONE PJ; DESNUELLE C
      PHENOTYPIC-EXPRESSION OF DIABETES SECONDARY TO A T14709C MUTATION OF MITOCHONDRIAL-DNA - COMPARISON WITH MIDD SYNDROME (A3243G MUTATION) - A CASE-REPORT

      Diabetes care
    12. LEBRUN C; BOUCRAUT J; ESCANDE N; BRUNETTO JL; DELPONT E; CHATEL M; DESNUELLE C
      SERUM IGG ANTIBODIES AGAINST GQ1B AND GM1 GANGLIOSIDES ANALYSIS IN PATIENTS WITH ACUTE INFLAMMATORY DEMYELINATING POLYRADICULOPATHY AND OPHTHALMOPLEGIA

      Neurology
    13. VIALETTES B; NARBONNE H; PAQUISFLUCKLINGER V; BENDAHAN D; PELISSIER JF; MONFORT MF; SILVESTREAILLAUD P; DESNUELLE C
      PREVALENCE OF BLOOD AND MUSCLE MT DNA ANOMALY IN A HIGHLY SELECTED DIABETIC POPULATION AT RISK OF MITOCHONDRIAL CYTOPATHY

      Diabetologia
    14. PAQUISFLUCKLINGER V; SANTUCCIDARMANIN S; PAUL R; SAUNIERES A; TURCCAREL C; DESNUELLE C
      IDENTIFICATION OF THE HUMAN MSH4 GENE - A MEIOSIS-SPECIFIC MUTS HOMOLOG

      American journal of human genetics
    15. BLIN O; AZULAY JP; DESNUELLE C; BILLETURC F; BRAGUER D; BESSE D; BRANGER E; CREVAT A; SERRATRICE G; POUGET JY
      A CONTROLLED ONE-YEAR TRIAL OF DEXTROMETHORPHAN IN AMYOTROPHIC-LATERAL-SCLEROSIS

      Clinical neuropharmacology
    16. PAUL R; SANTUCCI S; SAUNIERES A; DESNUELLE C; PAQUISFLUCKLINGER V
      RAPID MAPPING OF MITOCHONDRIAL-DNA DELETIONS BY LARGE-FRAGMENT PCR

      Trends in genetics
    17. LANTERIMINET M; DESNUELLE C
      MIGRAINE WITH MITOCHONDRIAL DYSFUNCTION

      Revue neurologique
    18. PISANO P; DURAND A; AUTRET E; DESNUELLE C; PINSARD N; SERRATRICE G; LEGOUT V; JOUBERT M; BLIN O
      PLASMA-CONCENTRATIONS AND PHARMACOKINETICS OF IDEBENONE AND ITS METABOLITES FOLLOWING SINGLE AND REPEATED DOSES IN YOUNG-PATIENTS WITH MITOCHONDRIAL ENCEPHALOMYOPATHY

      European Journal of Clinical Pharmacology
    19. LACOMBLEZ L; BENSIMON G; LEIGH PN; GUILLET P; POWE L; DURRLEMAN S; DELUMEAU JC; MEININGER V; PUECH AJ; WHITEHEAD J; ASSELAIN B; CESARO P; LARREY D; ROSSOR M; ZIMMERMAN HJ; SALZMAN P; DOPPLER V; LLOYD CM; MALOTEAUX JM; DELWAIDE C; LATERRE EC; BOUCHARD JP; DUQUETTE P; GIRARD M; MASSE C; EISEN A; BLIN O; AZULAY JP; BILLETURC F; POUGET J; BOUCHE P; CAMU M; CARLANDER B; BILLIARD M; CLANET M; ANGIBAUD G; ARNEBES MC; BENAZET M; COURATIER P; VALLAT JM; DESNUELLE C; LAGUENY A; ELLIE E; DIB M; ROZIER A; SALACHAS F; VIADER F; DELAUNAY D; DENGLER R; KUTHER G; TROGER M; LUDOLPH A; BACHUS R; GERICKE C; PRZUNTEK H; LANGKAFEL M; SCHIMRIGK K; JOST WH; OSTERHAGE J; PRUDLO J; MORA J; CHAVERRI D; SAENZ E; JEFFERSON D; ORPE V; LANE RJM; ORRELL RW; BARBIE T; MITCHELL JD; KILSHAW J; PALL HS; GOODWIN M; SCHADY W; DUNCAN S; MOORE C; RICHARDS C; SHAW PJ; CHARI G; PICKERING B; SWASH M; HARATI Y; GOOCH CL; ECHOLS CW; MILLER RG; GELINAS DF; QUIEN A; MUNSTAT TL; THORNELL B; ROTHSTEIN JD; CLAWSON L; SUFIT R; CASEY P; DELUMEAU J; TRUFFINET P; DEBOVE C; ENFRIN P; HAMPTON G; MULLER F; NGUYEN T; ROTHFUSS D; SENECHAL A; SHU C; LESWELL P; WHITWORTH P; DEBOE M; DEBRUYCKERE M; FISHER W; KONIG M; VERDUGO L; DELOSTERREROS MS; DEAKIN D; GIGUERE M; ADAIR K; FRANCO M; SKARINSKY D; WEXLER M; PIZZATO M; LEDOUX L; CAMPAGNES E; HARTNETT M; BASTIEN P; BEJUIT R; KIM Y; LELANN L; LEROY F; PAPILLON C; ORVOENFRIJA E
      A CONFIRMATORY DOSE-RANGING STUDY OF RILUZOLE IN ALS

      Neurology
    20. MILLER RG; BOUCHARD JP; DUQUETTE P; EISEN A; GELINAS DF; HARATI Y; MUNSAT TL; POWE L; ROTHSTEIN J; SALZMAN P; SUFIT RL; GUILLET P; BENSIMON G; DELUMEAU JC; DURRLEMAN S; LACOMBLEZ L; LEIGH PN; MEININGER V; MALOTEAUX JM; DELWAIDE C; GIRARD M; MASSE C; BLIN O; AZULAY JP; BILLETURC F; POUGET J; BOUCHE P; CAMU W; CARLANDER B; CLANET M; ANGIBAUD G; ARNEBES MC; BENAZET M; COURATIER P; DESNUELLE C; LAGUENY A; ELLIE E; DIB M; ROZIER A; SALACHAS F; VIADER F; DELAUNAY D; DENGLER R; GUTHER G; TROGER M; LUDOLPH A; BACHUS R; GERICKE C; PRZUNTEK H; LANGKAFEL M; SCHIMRIGK K; JOST WH; OSTERHAGE J; PRUDLO J; MORA J; CHAVERRI D; SAENZ E; JEFFERSON D; ORPE V; LANE RJM; ORRELL RW; LLOYD CM; BARBIE T; MITCHELL JD; KILSHAW J; PALL HS; GOODWIN M; SCHADY W; DUNCAN S; MOORE C; RICKARDS C; SHAW PJ; PICKERING CB; SWASH M; GOOCH CL; ECHOLS CW; QUIEN A; THORNELL B; ROTHSTEIN JD; CLAWSON L; SUFIT R; CASEY P
      CLINICAL-TRIALS OF RILUZOLE IN PATIENTS WITH ALS

      Neurology
    21. VIALETTES B; PAQUISFLUCKINGER V; SILVESTREAILLAUD P; PELISSIER JF; NARBONNE H; BENDAHAN D; COZZONE P; DESNUELLE C
      FAMILIAL DIABETES SECONDARY TO A NOVEL-POINT-MUTATION(14709) OF MT-DNA IN THE REGION CODING FOR TRNA(GLU)

      Diabetologia
    22. LOPES J; LEGUERN E; GOUIDER R; TARDIEU S; ABBAS N; BIROUK N; GUGENHEIM M; BOUCHE P; AGID Y; BRICE A; ARNEBES MC; BRICHET B; CHAPON F; CHAZOT G; CLAVELOU P; DESNUELLE C; DIRAISON P; DUBAS F; GONNAUD PM; HURTEVENT JF; KUNTZER T; LAGUENY A; MABIN D; MAYER M; OCHSNER F; OLLAGNONROMAN E; POUGET J; TABARAUD F; VALLAT JM; VANDENBERGHE A
      RECOMBINATION HOT-SPOT IN A 3.2-KB REGION OF THE CHARCOT-MARIE-TOOTH TYPE 1A REPEAT SEQUENCES - NEW TOOLS FOR MOLECULAR DIAGNOSIS OF HEREDITARY NEUROPATHY WITH LIABILITY TO PRESSURE PALSIES AND OF CHARCOT-MARIE-TOOTH TYPE 1A

      American journal of human genetics
    23. LEGUERN E; GOUIDER R; LOPES J; ABBAS N; GUGENHEIM M; TARDIEU S; RAVISE N; LEGER JM; VALLAT JM; BOUCHE P; AGID Y; BRICE A; ARNEBES MC; BRICHET B; BIROUK N; CHAPON F; CHAZOT G; CLAVELOU P; DESNUELLE C; DIRAISON P; DUBAS F; GONNAUD PM; HURTEVENT JF; KUNTZER T; LAGUENY A; MABIN D; OSHSNER F; OLLAGNONROMAN E; POUGET J; TABERAUD F; VANDENBERGHE A
      CONSTANT REARRANGEMENT OF THE CMT1A-REP SEQUENCES IN HNPP PATIENTS WITH A DELETION IN CHROMOSOME 17P11.2 - A STUDY OF 30 UNRELATED CASES

      Human molecular genetics
    24. PAQUISFLUCKLINGER V; PELLISSIER JF; CAMBOULIVES J; CHABROL B; SAUNIERES A; MONFORT MF; GIUDICELLI H; DESNUELLE C
      EARLY-ONSET FATAL ENCEPHALOMYOPATHY ASSOCIATED WITH SEVERE MTDNA DEPLETION

      European journal of pediatrics
    25. BUTORI C; DESNUELLE C; HOFMAN P; PAQUIS V; DURANT J; CARLES M; PESCE A; MICHIELS JF
      THE MUSCULAR DISORDERS IN AIDS PATIENTS - A REPORT OF 17 CASES

      Annales de pathologie
    26. VIALETTES B; PAQUISFLUCKINGER V; SILVESTREAILLAUD P; BENDAHAN D; PELISSIER JF; ETCHARYBOUYX F; RACCAH D; GIN H; GUILLAUSSEAU PJ; VANUXEN D; ORSINI F; POUGET J; COZZONE P; DESNUELLE C
      EXTRA-PANCREATIC MANIFESTATIONS IN DIABETES SECONDARY TO MITOCHONDRIAL-DNA POINT MUTATION WITHIN THE TRNA(LEU(UUR)) GENE

      Diabetes care
    27. PAQUIS V; PAUL R; ASKANAS V; ENGEL WK; DESNUELLE C
      MTDNA DELETIONS IN MUSCLE OF SPORADIC INCLUSION-BODY MYOSITIS (S-IBM)AND HEREDITARY INCLUSION-BODY MHYOPATHY (H-IBM)

      Neurology
    28. SILVESTREAILLAUD P; BENDAHAN D; PAQUISFLUCKINGER V; POUGET J; PELISSIER JF; DESNUELLE C; COZZONE PJ; VIALLETTES B
      COULD COENZYME-Q10 AND L-CARNITINE BE A TREATMENT FOR DIABETES SECONDARY TO 3243 MUTATION OF MTDNA

      Diabetologia
    29. TROUILLAS P; SERRATRICE G; LAPLANE D; RASCOL A; AUGUSTIN P; BARROCHE G; CLANET M; DEGOS CF; DESNUELLE C; DUMAS R; MICHEL D; VIALLET F; WARTER JM; ADELEINE P
      LEVOROTATORY FORM OF 5-HYDROXYTRYPTOPHAN IN FRIEDREICHS ATAXIA - RESULTS OF A DOUBLE-BLIND DRUG-PLACEBO COOPERATIVE STUDY

      Archives of neurology
    30. DESNUELLE C
      LESSONS LEARNED FROM DYSTROPHIN

      La Presse medicale
    31. HARLE JR; DISDIER P; BOLLA G; COULOM F; FIGARELLABRANGER D; DESNUELLE C; PELLISSIER JF; WEILLER PJ
      RELATIONSHIPS BETWEEN POLYMYALGIA-RHEUMAT ICA AND MITOCHONDRIAL MYOPATHY - 24 CASES

      La Presse medicale
    32. DELPONT E; MARTINMOUTOT N; BRUNETTO JL; DESNUELLE C
      LAMBERT-EATON SYNDROME WITHOUT CALCIUM-CH ANNEL AUTOANTIBODIES

      Revue neurologique
    33. DROUET A; PELLISSIER JF; DESNUELLE C; VALANCE J
      LATE-ONSET MITOCHONDRIAL ENCEPHALOMYOPATH IES AFFECTING PREDOMINANTLYTHE CENTRAL-NERVOUS-SYSTEM

      Revue neurologique
    34. BLIN O; DESNUELLE C; RASCOL O; BORG M; SAINTPAUL HP; AZULAY JP; BILLE F; FIGARELLA D; COULOM F; PELLISSIER JF; MONTASTRUC JL; CHATEL M; SERRATRICE G
      MITOCHONDRIAL RESPIRATORY-FAILURE IN SKELETAL-MUSCLE FROM PATIENTS WITH PARKINSONS-DISEASE AND MULTIPLE SYSTEM ATROPHY

      Journal of the neurological sciences
    35. SOUBRIER MJ; DUBOST JJ; SAUVEZIE BJM; ARFI S; AUDHUY B; AUMAITRE O; BATAILLE R; BLOTMANN F; BROUSSOLLE E; CAMUS JP; CHAPMAN A; CHRISTOFOROV B; CLAVELOU P; DESNUELLE C; FLORI B; GROSBOIS B; MAILLOT F; MALAPERT D; MAIHEUX F; MENKES C; PIETTE JC; ROULLET E; RISTORI JM; SORS C; STURTZ F; VIGHETTO A; WOIMANT F; WESCHLER B
      POEMS-SYNDROME - A STUDY OF 25 CASES AND A REVIEW OF THE LITERATURE

      The American journal of medicine
    36. AZULAY JP; PELLISSIER JF; DESNUELLE C; POUGET J; SERRATRICE G
      AUTOSOMAL DOMINANT CEREBELLAR-ATAXIA WITH MITOCHONDRIAL MYOPATHY - REPORT OF A FAMILY

      Neurology


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Documento generato il 20/10/20 alle ore 22:45:59