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La ricerca find articoli where authors phrase all words ' HURKO O' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 40 riferimenti
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    1. McGinnis, RE; Fox, H; Yates, P; Cameron, LA; Barnes, MR; Gray, IC; Spurr, NK; Hurko, O; St Clair, D
      Failure to confirm NOTCH4 association with schizophrenia in a large population-based sample from Scotland

      NATURE GENETICS
    2. Hurko, O
      Genetics and genomics in neuropsychopharmacology: the impact on drug discovery and development

      EUROPEAN NEUROPSYCHOPHARMACOLOGY
    3. Elmaci, I; Ain, MC; Wright, MJ; Lee, RR; Sheppard, JME; Rigomonti, D; Hurko, O
      Perioperative intracranial hemorrhage in achondroplasia (vol 12, pg 217, 2000)

      JOURNAL OF NEUROSURGICAL ANESTHESIOLOGY
    4. Elmaci, I; Ain, MC; Wright, MJ; Lee, RR; Sheppard, JME; Rigamonti, D; Hurko, O
      Perioperative intracranial hemorrhage in achondroplasia - A case report

      JOURNAL OF NEUROSURGICAL ANESTHESIOLOGY
    5. Ain, MC; Elmaci, I; Hurko, O; Clatterbuck, RE; Lee, RR; Rigamonti, D
      Reoperation for spinal restenosis in achondroplasia

      JOURNAL OF SPINAL DISORDERS
    6. Crockett, MM; Carten, MF; Hurko, O; Sponseller, PD
      Motor milestones in children with diastrophic dysplasia

      JOURNAL OF PEDIATRIC ORTHOPAEDICS
    7. Hurko, O; Walsh, FS
      Novel drug development for amyotrophic lateral sclerosis

      JOURNAL OF THE NEUROLOGICAL SCIENCES
    8. Crawford, TO; Sladky, JT; Hurko, O; Besner-Johnston, A; Kelley, RI
      Abnormal fatty acid metabolism in childhood spinal muscular atrophy

      ANNALS OF NEUROLOGY
    9. Bellus, GA; Bamshad, MJ; Przylepa, KA; Dorst, J; Lee, RR; Hurko, O; Jabs, EW; Curry, CJR; Wilcox, WR; Lachman, RS; Rimoin, DL; Francomano, CA
      Severe achondroplasia with developmental delay and acanthosis nigricans (SADDAN): Phenotypic analysis of a new skeletal dysplasia caused by a Lys650Met mutation in fibroblast growth factor receptor 3

      AMERICAN JOURNAL OF MEDICAL GENETICS
    10. Becher, MW; Wills, ML; Noll, WM; Hurko, O; Price, DL
      Kearns-Sayre syndrome with features of Pearson's marrow-pancreas syndrome and a novel 2905-base pair mitochondrial DNA deletion

      HUMAN PATHOLOGY
    11. Hurko, O; Provost, TT
      Neurology and the skin

      JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
    12. ZANFERRARI C; LAVADOS PM; HURKO O; OPPENHEIMER SM; WITYK RJ
      CEREBROVASCULAR DISEASES IN PATIENTS WITH MARFAN-SYNDROME - A RETROSPECTIVE STUDY

      Stroke
    13. MOGAYZEL PJ; CARROLL JL; LOUGHLIN GM; HURKO O; FRANCOMANO CA; MARCUS CL
      SLEEP-DISORDERED BREATHING IN CHILDREN WITH ACHONDROPLASIA

      The Journal of pediatrics
    14. HURKO O
      THE EXPLOSION OF NEUROGENETICS

      Current opinion in neurology
    15. HURKO O
      RECENT ADVANCES IN HERITABLE ATAXIAS

      Annals of neurology
    16. POLYMEROPOULOS MH; HURKO O; HSU F; RUBENSTEIN J; BASNET S; LANE K; DIETZ H; SPETZLER RF; RIGAMONTI D
      LINKAGE OF THE LOCUS FOR CEREBRAL CAVERNOUS HEMANGIOMAS TO HUMAN-CHROMOSOME-7Q IN 4 FAMILIES OF MEXICAN-AMERICAN DESCENT

      Neurology
    17. CAMACHO JA; GOODMAN BK; HAMOSH A; HURKO O; THOMAS GH
      MIDAS SYNDROME IN A 46,XX NEWBORN WITH AMBIGUOUS GENITALIA AND A CRYPTIC, DE-NOVO X-Y TRANSLOCATION

      American journal of human genetics
    18. HURKO O
      MITOCHONDRIAL-DNA AND LEUKOENCEPHALOPATHIES

      Molecular and chemical neuropathology
    19. HURKO O; POLYMEROPOULOS MH; HSU F; RUBENSTEIN J; BASNET S; LANE K; DIETZ H; SPETZLER F; RIGAMONTI D
      LINKAGE AND HAPLOTYPE ANALYSIS OF AUTOSOMAL-DOMINANT CAVERNOUS HEMANGIOMAS OF THE BRAIN IN 4 MEXICAN-AMERICAN FAMILIES

      Neurology
    20. ZEE DS; VERSINO M; HURKO O
      CEREBELLAR PATIENTS HAVE OCULAR MISALIGNMENT DURING BOTH FIXATION ANDSACCADES

      Neurology
    21. HOFHAUS G; JOHNS DR; HURKO O; ATTARDI G; CHOMYN A
      RESPIRATION AND GROWTH DEFECTS IN TRANSMITOCHONDRIAL CELL-LINES CARRYING THE 11778-MUTATION ASSOCIATED WITH LEBERS HEREDITARY OPTIC NEUROPATHY

      The Journal of biological chemistry
    22. VERSINO M; HURKO O; ZEE DS
      DISORDERS OF BINOCULAR CONTROL OF EYE-MOVEMENTS IN PATIENTS WITH CEREBELLAR DYSFUNCTION

      Brain
    23. WALKUP JT; LABUDA MC; SINGER HS; BROWN J; RIDDLE MA; HURKO O
      FAMILY STUDY AND SEGREGATION ANALYSIS OF TOURETTE SYNDROME - EVIDENCEFOR A MIXED-MODEL OF INHERITANCE

      American journal of human genetics
    24. SINGER HS; LABUDA M; WALKUP J; RIDDLE M; HURKO O
      FAMILY STUDY AND SEGREGATION ANALYSIS OF TOURETTES-SYNDROME - EVIDENCE FOR A MAJOR ADDITIVE LOCUS AND MULTIFACTORIAL BACKGROUND

      Annals of neurology
    25. CRAWFORD TO; SLADKY JT; HURKO O; KELLEY RI
      ABNORMALITIES IN FATTY-ACID METABOLISM IN INFANTS WITH TYPE-1 SPINAL MUSCULAR-ATROPHY

      Annals of neurology
    26. ZEIDMAN SM; MONSEIN LH; AROSARENA O; ALETICH V; BIAFORE JAM; DAWSON RC; DEBRUN GM; HURKO O
      REVERSIBILITY OF WHITE-MATTER CHANGES AND DEMENTIA AFTER TREATMENT OFDURAL FISTULAS

      American journal of neuroradiology
    27. BECHER MW; NOLL WW; HURKO O; PRICE DL
      NOVEL 2905-BP MITOCHONDRIAL-DNA DELETION IN KEARNS-SAYRE SYNDROME

      Journal of neuropathology and experimental neurology
    28. WALKUP JT; LABUDA MC; HURKO O; RIDDLE MA; SINGER HS
      A FAMILY STUDY AND SEGREGATION ANALYSIS OF TOURETTES-SYNDROME - EVIDENCE FOR A MIXED-MODEL OF INHERITANCE

      American journal of human genetics
    29. SPENCER F; HUGERAT Y; SIMCHEN G; HURKO O; CONNELLY C; HIETER P
      YEAST KAR1 MUTANTS PROVIDE AN EFFECTIVE METHOD FOR YAC TRANSFER TO NEW HOSTS

      Genomics
    30. HURKO O
      MITOCHONDRIAL-DNA MUTATIONS IN LEBERS OPTIC NEUROPATHY

      Annals of neurology
    31. BURGHES AHM; INGRAHAM SE; KOTEJARAI Z; ROSENFELD S; HERTA N; NADKARNI N; DIDONATO CJ; CARPTEN J; HURKO O; FLORENCE J; MOXLEY RT; COBBEN JM; MENDELL JR
      LINKAGE MAPPING OF THE SPINAL MUSCULAR-ATROPHY GENE

      Human genetics
    32. UEMATSU S; WANG H; KOPITS SE; HURKO O
      TOTAL CRANIOSPINAL DECOMPRESSION IN ACHONDROPLASTIC STENOSIS

      Neurosurgery
    33. DIDONATO CJ; MORGAN K; CARPTEN JD; FUERST P; INGRAHAM SE; PRESCOTT G; MCPHERSON JD; WIRTH B; ZERRES K; HURKO O; WASMUTH JJ; MENDELL JR; BURGHES AHM; SIMARD LR
      ASSOCIATION BETWEEN AG1-CA ALLELES AND SEVERITY OF AUTOSOMAL RECESSIVE PROXIMAL SPINAL MUSCULAR-ATROPHY

      American journal of human genetics
    34. LEBO RV; CHANCE PF; DYCK PJ; REDILAFLORES MT; LYNCH ED; GOLBUS MS; BIRD TD; KING MC; ANDERSON LA; HALL J; WIEGANT J; JIANG ZR; DAZIN PF; PUNNETT HH; SCHONBERG SA; MOORE K; SHULL MM; GENDLER S; HURKO O; LOVELACE RE; LATOV N; TROFATTER J; CONNEALLY PM
      CHROMOSOME 1 CHARCOT-MARIE-TOOTH DISEASE (CMT1B) LOCUS IN THE FC-GAMMA RECEPTOR GENE REGION (VOL 88, PG 1, 1991)

      Human genetics
    35. LEBO RV; MARTELLI L; SU Y; LI LY; LYNCH E; MANSFIELD E; PUA KH; WATSON DF; CHUEH J; HURKO O
      PRENATAL-DIAGNOSIS OF CHARCOT-MARIE-TOOTH DISEASE TYPE-1A BY MULTICOLOR IN-SITU HYBRIDIZATION

      American journal of medical genetics
    36. NADKARNI N; INGRAHAM S; KOLE J; DIDONATO C; ROSENFELD S; HERTA N; HURKO O; HYSER C; FLORENCE J; FISCHBECK K; MENDELL JR; BURGHES AHM
      LINKAGE ANALYSIS OF SPINAL MUSCULAR-ATROPHY

      Neurology
    37. YONEDA M; CHOMYN A; MARTINUZZI A; HURKO O; ATTARDI G
      MARKED REPLICATIVE ADVANTAGE OF MTDNA CARRYING A POINT MUTATION THAT CAUSES THE MELAS SYNDROME

      Neurology
    38. FRANCOMANO CA; CARSON B; SEIDLER A; JAMES C; MATTHEWS C; MILLER D; ROIG C; HURKO O
      MORBIDITY AND MORTALITY IN ACHONDROPLASIA - EFFICACY OF PROSPECTIVE EVALUATION AND SURGICAL INTERVENTION

      American journal of human genetics
    39. LI LY; SU Y; SU X; MARTELLI L; HURKO O; SHAPIRO L; CHUEH J; LEBO RV
      IN-SITU HYBRIDIZATION WITH DIFFERENT COLOR CONTROL PROBE DETERMINES GENE ANEUPLOIDY RELIABLY

      American journal of human genetics
    40. THRELKELD A; MILLER NR; GOLNIK K; GRIFFIN J; KUNCL R; JOHNS D; HURKO O
      MYO-NEURO-GASTROINTESTINAL ENCEPHALOPATHY (MNGIE) SYNDROME - HISTOPATHOLOGICAL CHARACTERIZATION AND CLINICAL DESCRIPTION OF A MITOCHONDRIOPATHY ASSOCIATED WITH PTOSIS AND OPHTHALMOPARESIS

      Investigative ophthalmology & visual science


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Documento generato il 21/01/21 alle ore 21:51:53