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La ricerca find articoli where authors phrase all words ' Chabrol, B' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 48 riferimenti
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    1. Chabrol, B; Figarella-Branger, D; Coquet, M; Mancini, J; Fontan, D; Pedespan, JM; Francannet, C; Pouget, J; Beaufrere, AM; Pellilssier, JF
      X-linked myopathy with excessive autophagy: a clinicopathological study offive new families

      NEUROMUSCULAR DISORDERS
    2. Chabrol, B; Mely, L; Lethel, V; Hugonenc, C; Dubus, JC; Mancini, J
      Neurological complications linked to antalgesics and anti-inflammatory agents

      ARCHIVES DE PEDIATRIE
    3. Tsimaratos, M; Kone-Paut, I; Divry, P; Philip, N; Chabrol, B
      Mevalonic aciduria and hyper-IgD syndrome: Two sides of the same coin?

      JOURNAL OF INHERITED METABOLIC DISEASE
    4. de Lonlay, P; Seta, N; Barrot, S; Chabrol, B; Drouin, V; Gabriel, BM; Journel, H; Kretz, M; Laurent, J; Le Merrer, M; Leroy, A; Pedespan, D; Sarda, P; Villeneuve, N; Schmitz, J; van Schaftingen, E; Matthijs, G; Jaeken, J; Korner, C; Munnich, A; Saudubray, JM; Cormier-Daire, V
      A broad spectrum of clinical presentations in congenital disorders of glycosylation I: a series of 26 cases

      JOURNAL OF MEDICAL GENETICS
    5. Mancini, J; Lethel, V; Hugonenq, C; Chabrol, B
      Brain injuries in early foetal life: consequences for brain development

      DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY
    6. Villard, L; des Portes, V; Levy, N; Louboutin, JP; Recan, D; Coquet, M; Chabrol, B; Figarella-Branger, D; Chelly, J; Pellissier, JF; Fontes, M
      Linkage of X-linked myopathy with excessive autophagy (XMEA) to Xq28

      EUROPEAN JOURNAL OF HUMAN GENETICS
    7. Chandler, D; Angelicheva, D; Heather, L; Gooding, R; Gresham, D; Yanakiev, P; de Jonge, R; Baas, F; Dye, D; Karagyozov, L; Savov, A; Blechschmidt, K; Keats, B; Thomas, PK; King, RHM; Starr, A; Nikolova, A; Colomer, J; Ishpekova, B; Tournev, I; Urtizberea, JA; Merlini, L; Butinar, D; Chabrol, B; Voit, T; Baethmann, M; Nedkova, V; Corches, A; Kalaydjieva, L
      Hereditary motor and sensory neuropathy Lom (HMSNL): refined genetic mapping in Romani (Gypsy) families from several European countries

      NEUROMUSCULAR DISORDERS
    8. Tsimaratos, M; Cloarec, S; Roquelaure, B; Retornaz, K; Picon, G; Chabrol, B; Guys, JM; Sarles, J; Nivet, H
      Chronic renal failure and portal hypertension - is portosystemic shunt indicated?

      PEDIATRIC NEPHROLOGY
    9. Lethel, V; Chabrol, B; Livet, MO; Mancini, J
      Lamotrigine therapy in children: retrospective study of 32 patients.

      ARCHIVES DE PEDIATRIE
    10. Camoin-Jau, L; Kone-Paut, I; Chabrol, B; Sampol, J; Dignat-George, F
      Circulating endothelial cells in Behcet's disease with cerebral thrombophlebitis

      THROMBOSIS AND HAEMOSTASIS
    11. Serratrice, J; Chabrol, B; Attarrian, S; Figarella-Branger, D
      Pseudometabolic dystrophinopathy without immunohistochemical anomaly

      REVUE NEUROLOGIQUE
    12. Salvan, AM; Confort-Gouny, S; Chabrol, B; Cozzone, PJ; Vion-Dury, J
      Brain metabolic impairment in non-cerebral and cerebral forms of X-linked adrenoleukodystrophy by proton MRS: Identification of metabolic patterns bydiscriminant analysis

      MAGNETIC RESONANCE IN MEDICINE
    13. Salvan, AM; Chabrol, B; Lamoureux, S; Confort-Gouny, S; Cozzone, PJ; Vion-Dury, J
      In vivo brain proton MR spectroscopy in a case of molybdenum cofactor deficiency

      PEDIATRIC RADIOLOGY
    14. Chabrol, B; Decarie, JC; Fortin, G
      The role of cranial MRI in identifying patients suffering from child abuseand presenting with unexplained neurological findings

      CHILD ABUSE & NEGLECT
    15. Livet, NO; Moncla, A; Philip, N; Chabrol, B; Mancini, J
      Clinical approach to gene-dependant mental deficiencies.

      REVUE NEUROLOGIQUE
    16. Salvan, AM; Confort-Gouny, S; Cozzone, PJ; Vion-Dury, J; Chabrol, B; Mancini, J
      In vivo cerebral proton MRS in a case of subacute sclerosing panencephalitis

      JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
    17. Chabrol, B; Fortin, G; Bernard-Bonnin, AC; Allard-Dansereau, C; Chabot, G; Methot, B
      Child abuse and neglect in Quebec: program of the child protection clinic of Sainte-Justine Hospital, Montreal

      ARCHIVES DE PEDIATRIE
    18. PHILIP N; CHABROL B; LETHEL V
      GENETICS OF AGENESIS OF THE CORPUS-CALLOS UM

      Neuro-chirurgie
    19. CHABROL B
      NEURONAL CEROID-LIPOFUSCINOSIS - RECENT A DVANCES

      Archives de pediatrie
    20. PHILIP N; SIGAUDY S; CHABROL B
      BEHAVIORAL PHENOTYPES

      Archives de pediatrie
    21. KONEPAUT I; CHABROL B; RISS JM; MANCINI J; RAYBAUD C; GARNIER JM
      NEUROLOGIC ONSET OF BEHCETS-DISEASE - A DIAGNOSTIC ENIGMA IN CHILDHOOD

      Journal of child neurology
    22. MANCINI J; GIRARD N; CHABROL B; LAMOUREUX S; LIVET MO; THURET I; PINSARD N
      ISCHEMIC CEREBROVASCULAR-DISEASE IN CHILDREN - RETROSPECTIVE STUDY OF35 PATIENTS

      Journal of child neurology
    23. CHABROL B; SIGAUDY S; PAQUIS V; MONTFORT MF; GIUDICELLI H; PELLISSIER JF; MILLET V; MANCINI J; PHILIP N
      STUVE-WIEDEMANN SYNDROME AND DEFECTS OF THE MITOCHONDRIAL RESPIRATORY-CHAIN

      American journal of medical genetics
    24. GIRE C; PEREZ N; LAMOUREUX S; MANCINI J; PINSARD N; CHABROL B
      GUILLAIN-BARRE-SYNDROME IN CHILDHOOD - A RETROSPECTIVE STUDY OF 31 CASES

      Annales de pediatrie
    25. MANCINI J; CHABROL B; COSTE D
      NUTRITIONAL FACTORS THAT AFFECT CENTRAL-N ERVOUS-SYSTEM DEVELOPMENT

      Annales de pediatrie
    26. CHABROL B; CARRELET P; DUBUS JC; BOLLINI G; PELLISSIER JF; LAMOUREUX S; PHILIP N; MANCINI J
      INFANTILE SPINAL MUSCULAR-ATROPHY - CURRE NT ASPECTS

      Annales de pediatrie
    27. LIVET MO; MONCLA A; COURNELLE MA; CHABROL B; MANCINI J
      THE BEHAVIORAL-PHENOTYPE - CONTRIBUTION T O THE DIAGNOSIS AND MANAGEMENT OF INHERITED DISEASES

      Annales de pediatrie
    28. GIRE C; LAMOUREUX S; GHODBANE D; YVORRA S; MANCINI J; CHABROL B
      RUPTURE OF A CEREBRAL ANEURYSM ASSOCIATED WITH COARCTATION OF THE AORTA

      Revue neurologique
    29. CHABROL B; PAQUIS V
      CEREBRAL INFARCTION ASSOCIATED WITH KEARNS-SAYRE-SYNDROME

      Neurology
    30. MANCINI J; CHABROL B; PINSARD N
      PREVENTION OF RECURRENT FEBRILE SEIZURES

      Archives de pediatrie
    31. MANCINI J; CHABROL B; MOULENE E; PINSARD N
      RELAPSING ACUTE ENCEPHALOPATHY - A COMPLICATION OF DIPHTHERIA-TETANUS-POLIOMYELITIS IMMUNIZATION IN A YOUNG BOY

      European journal of pediatrics
    32. SIGAUDY S; PHILIP N; GIRE C; CHABROL B
      ORAL-FACIAL-DIGITAL SYNDROME WITH RETINAL ABNORMALITIES - REPORT OF ANEW CASE

      American journal of medical genetics
    33. AICARDI J; HAUSER E; STEINBOCK H; SZYPER M; HOLSTEEN V; OSTERGAARD J; PEDERSEN SA; TAUDORF K; BARTHEZCARPENTIER MA; BADINANDHUBERT N; BERQUIN P; BOULLOCHE J; BOURGEOIS M; CARRIERE JP; CHABROL B; CHIRON C; CLARIS O; ECHENNE B; GAUTHIERMOREL D; LIVET MO; LOPEZ N; MANCINI J; NETTER JC; QUILLEROU D; RICHELME CH; ROUSSELLE C; DESTMARTIN A; DESWARTE M; AUERSWALD G; BRANDL U; KURLEMANN G; SIEMES H; SPOHR HL; AARTS WFM; BEGEER JH; HEERSMA DJ; LAAN LAEM; PETERS ACB; CAVAZZUTTI GB; CURATOLO P; FOIS A; FRANZONI E; GOBBI G; INCORPORA G; VIGEVANO F; CAMPISTOL J; CAMPOS J; CASAS C; HERRANZ JL; NIETO M; PRATS JM; AMARK P; BLENNOW G; THEORELL K; TONNBY B; HAENGGELI CA; WEISSERT M; APPLETON UKR; ROBINSON R; DESOUSA C; THOMAS N; ANDERMANN F; APPLETON R; ARZIMANOGLOU; BOYD S; BRANDT W; BUTI D; DULAC O; FARRELL K; MOSHE S; MOTTE J; PLOUIN P; SHIELDS WD; MUMFORD JP; DUMAS C; WOOD S
      VIGABATRIN AS INITIAL THERAPY FOR INFANTILE SPASMS - A EUROPEAN RETROSPECTIVE SURVEY

      Epilepsia
    34. CHABROL B; VIONDURY J; CONFORTGOUNY S; COZZONE PJ
      MAGNETIC-RESONANCE SPECTROSCOPY - A NEW T ECHNIQUE FOR BRAIN METABOLISM EXPLORATION IN CHILDREN

      Archives de pediatrie
    35. MANCINI J; CHABROL B; LIVET MO; PHILIP N; PINSARD N
      PRAGMATIC DIAGNOSTIC-APPROACH TO MENTAL D EFICIENCY

      Archives de pediatrie
    36. CHABROL B; SALVAN AM; CONFORTGOUNY S; VIONDURY J; COZZONE PJ
      LOCALIZED PROTON MAGNETIC-RESONANCE SPECTROSCOPY OF THE BRAIN DIFFERENTIATES THE INBORN METABOLIC ENCEPHALOPATHIES IN CHILDREN

      Comptes rendus de l'Academie des sciences. Serie 3, Sciences de la vie
    37. 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
    38. CONFORTGOUNY S; VIONDURY J; CHABROL B; NICOLI F; COZZONE PJ
      LOCALIZED PROTON MAGNETIC-RESONANCE SPECTROSCOPY IN X-LINKED ADRENOLEUKODYSTROPHY

      Neuroradiology
    39. MANCINI J; GIRARD N; LIVET MO; CHABROL B; GAMBARELLI D; LENA G; PINSARD N
      EPILEPSY AND TUBEROUS SCLEROSIS - A RETROSPECTIVE STUDY IN 50 CHILDREN

      Epilepsia
    40. CHABROL B; CHAPUIS Y; DEBURGE JP; EURIN B; FUZELLIER G; HABERER JP; MARESCAUX J; MARTY J; OURABAH R; SAMII K; BLERY C
      INDICATION FOR PREOPERATIVE EXAMINATIONS

      Annales de chirurgie
    41. CHABROL B; MANCINI J; BENELLI C; GIRE C; MUNNICH A
      LEIGH-SYNDROME - PYRUVATE-DEHYDROGENASE DEFECT - A CASE WITH PERIPHERAL NEUROPATHY

      Journal of child neurology
    42. CHABROL B; MANCINI J; CHRETIEN D; RUSTIN P; MUNNICH A; PINSARD N
      VALPROATE-INDUCED HEPATIC-FAILURE IN A CASE OF CYTOCHROME-C-OXIDASE DEFICIENCY

      European journal of pediatrics
    43. LENA G; DUFOUR T; GAMBARELLI D; CHABROL B; MANCINI J
      CHORISTOMA OF THE INTRACRANIAL MAXILLARY NERVE IN A CHILD - CASE-REPORT

      Journal of neurosurgery
    44. MANCINI J; PHILIP N; CHABROL B; DIVRY P; ROLLAND MO; PINSARD N
      MEVALONIC ACIDURIA IN 3 SIBLINGS - A NEW RECOGNIZABLE METABOLIC ENCEPHALOPATHY

      Pediatric neurology
    45. DIVRY P; JAKOBS C; VIANEYSABAN C; GIBSON KM; MICHELAKAKIS H; PAPADIMITRIOU A; DIVARI R; CHABROL B; COURNELLE MA; LIVET MO
      L-2-HYDROXYGLUTARIC ACIDURIA - 2 FURTHER CASES

      Journal of inherited metabolic disease
    46. HABIB M; DUBROCARD S; CHABROL B
      BRAIN LATERALIZATION AND CALLOSAL FUNCTION IN DEVELOPMENTAL DYSPHASIA

      Brain and language
    47. DESNUELLE CJ; LUNARDI J; FIGARELLABRANGER D; COULOM F; CHABROL B; SERRATRICE G; PELLISSIER JF
      POINT MUTATIONS IN MITOCHONDRIAL-DNA DESCRIBED IN LEBER HEREDITARY OPTIC NEUROPATHY DETECTED IN A 2-YEAR-OLD GIRL PRESENTING AS LEBER CONGENITAL AMAUROSIS (LCA)

      Neurology
    48. CHABROL B; MANCINI J; BERTRAND C; VIANEYSABAN C; DIVRY P; LIVET MO; PINSARD N
      MEDIUM-CHAIN ACYL-COA DEHYDROGENASE-DEFIC IENCY REVEALED BY GENERALIZED SEIZURES

      Archives francaises de pediatrie


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 15/01/21 alle ore 23:28:56