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La ricerca find articoli where soggetti phrase all words 'neurogenetics' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 63 riferimenti
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    1. Finnila, S; Tuisku, S; Herva, R; Majamaa, K
      A novel mitochondrial DNA mutation and a mutation in the Notch3 gene in a patient with myopathy and CADASIL

      JOURNAL OF MOLECULAR MEDICINE-JMM
    2. Sciacco, M; Prelle, A; Comi, GP; Napoli, L; Battistel, A; Bresolin, N; Tancredi, L; Lamperti, C; Bordoni, A; Fagiolari, G; Ciscato, P; Chiveri, L; Perini, MP; Fortunato, F; Adobbati, L; Messina, S; Toscano, A; Martinelli-Boneschi, F; Papadimitriou, A; Scarlato, G; Moggio, M
      Retrospective study of patients affected of a large population with mitochondrial disorders: clinical, morphological and molecular genetic evaluation

      JOURNAL OF NEUROLOGY
    3. Kuhlenbaumer, G; Meuleman, J; De Jonghe, P; Falck, B; Young, P; Hunermund, G; Van Broeckhoven, C; Timmerman, V; Stogbauer, F
      Hereditary neuralgic amyotrophy (HNA) is genetically heterogeneous

      JOURNAL OF NEUROLOGY
    4. Rogers, DC; Peters, J; Martin, JE; Ball, S; Nicholson, SJ; Witherden, AS; Hafezparast, M; Latcham, J; Robinson, TL; Quilter, CA; Fisher, EMC
      SHIRPA, a protocol for behavioral assessment: validation for longitudinal study of neurological dysfunction in mice

      NEUROSCIENCE LETTERS
    5. Zink, M; Grimm, L; Wszolek, ZK; Gasser, T
      Autosomal-dominant Parkinson's disease linked to 2p13 is not caused by mutations in transforming growth factor alpha (TGF alpha)

      JOURNAL OF NEURAL TRANSMISSION
    6. Airey, DC; Lu, L; Williams, RW
      Genetic control of the mouse cerebellum: Identification of quantitative trait loci modulating size and architecture

      JOURNAL OF NEUROSCIENCE
    7. Weinshenker, BG; Hebrink, D; Kantarci, OH; Schaefer-Klein, J; Atkinson, E; Schaid, D; McMurray, CM
      Genetic variation in the transforming growth factor beta 1 gene in multiple sclerosis

      JOURNAL OF NEUROIMMUNOLOGY
    8. Modin, H; Dai, Y; Masterman, T; Svejgaard, A; Sorensen, PS; Oturai, A; Ryder, LP; Spurkland, A; Vartdal, F; Laaksonen, M; Sandberg-Wollheim, M; Myhr, KM; Nyland, H; Hillert, J
      No linkage or association of the nitric oxide synthase genes to multiple sclerosis

      JOURNAL OF NEUROIMMUNOLOGY
    9. Ross, ME; Walsh, CA
      Human brain malformations and their lessons for neuronal migration

      ANNUAL REVIEW OF NEUROSCIENCE
    10. Schmitt, JE; Eliez, S; Warsofsky, IS; Bellugi, U; Reiss, AL
      Enlarged cerebellar vermis in Williams syndrome

      JOURNAL OF PSYCHIATRIC RESEARCH
    11. Narayanan, R; Ramaswami, M
      Endocytosis in Drosophila: Progress, possibilities, prognostications

      EXPERIMENTAL CELL RESEARCH
    12. Sedelis, M; Hofele, K; Auburger, GW; Morgan, S; Huston, JP; Schwarting, RKW
      Evidence for resistance to MPTP in C57BL/6 x BALB/c FI hybrids as comparedwith their progenitor strains

      NEUROREPORT
    13. Sun, Q; Bahri, S; Schmid, A; Chia, W; Zinn, K
      Receptor tyrosine phosphatases regulate axon guidance across the midline of the Drosophila embryo

      DEVELOPMENT
    14. Gardiner, RM
      Impact of our understanding of the genetic aetiology of epilepsy

      JOURNAL OF NEUROLOGY
    15. Visser, JE; Bar, PR; Jinnah, HA
      Lesch-Nyhan disease and the basal ganglia

      BRAIN RESEARCH REVIEWS
    16. Gonzalez-Lima, F; Sadile, AG
      Network operations revealed by brain metabolic mapping in a genetic model of hyperactivity and attention deficit: the Naples high- and low-excitability rats

      NEUROSCIENCE AND BIOBEHAVIORAL REVIEWS
    17. Cowan, WM; Harter, DH; Kandel, ER
      The emergence of modern neuroscience: Some implications for neurology and psychiatry

      ANNUAL REVIEW OF NEUROSCIENCE
    18. Ganetzky, B
      Genetic analysis of ion channel dysfunction in Drosophila

      KIDNEY INTERNATIONAL
    19. Suaudeau, C; Rinaldi, D; Lepicard, E; Venault, P; Crusio, WE; Costentin, J; Chapouthier, G
      Divergent levels of anxiety in mice selected for differences in sensitivity to a convulsant agent

      PHYSIOLOGY & BEHAVIOR
    20. McCormack, ML; Guttmann, RP; Schumann, M; Farmer, JM; Stolle, CA; Campuzano, V; Koenig, M; Lynch, DR
      Frataxin point mutations in two patients with Friedreich's ataxia and unusual clinical features

      JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
    21. Skuse, DH
      Behavioural neuroscience and child psychopathology: Insights from model systems

      JOURNAL OF CHILD PSYCHOLOGY AND PSYCHIATRY AND ALLIED DISCIPLINES
    22. Bate, L; Gardiner, M
      Genetics of inherited epilepsies

      EPILEPTIC DISORDERS
    23. Keverne, EB
      GABA-ergic neurons and the neurobiology of schizophrenia and other psychoses

      BRAIN RESEARCH BULLETIN
    24. Pandolfo, M
      Friedreich's ataxia: Clinical aspects and pathogenesis

      SEMINARS IN NEUROLOGY
    25. DeZazzo, J; Xia, SZ; Christensen, J; Velinzon, K; Tully, T
      Developmental expression of an amn(+) transgene rescues the mutant memory defect of amnesiac adults

      JOURNAL OF NEUROSCIENCE
    26. Rose, S
      Precis of lifelines: Biology, freedom, determinism

      BEHAVIORAL AND BRAIN SCIENCES
    27. Dichgans, J; Schulz, JB
      Focal aging: Clues from neurodegenerative diseases

      NERVENARZT
    28. Mole, S; Gardiner, M
      Molecular genetics of the neuronal ceroid lipofuscinoses

      EPILEPSIA
    29. Hamre, K; Tharp, R; Poon, K; Xiong, XP; Smeyne, RJ
      Differential strain susceptibility following 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) administration acts in an autosomal dominant fashion: quantitative analysis in seven strains of Mus musculus

      BRAIN RESEARCH
    30. RESTIFO LL; HAUGLUM W
      PARALLEL MOLECULAR-GENETIC PATHWAYS OPERATE DURING CNS METAMORPHOSIS IN DROSOPHILA

      Molecular and cellular neurosciences (Print)
    31. STIMSON DT; ESTES PS; SMITH M; KELLY LE; RAMASWAMI M
      A PRODUCT OF THE DROSOPHILA STONED LOCUS REGULATES NEUROTRANSMITTER RELEASE

      The Journal of neuroscience
    32. POTTER NT; TARLETON J
      NEUROGENETICS IN DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS - ADVANCES IN MOLECULAR DIAGNOSIS

      Journal of developmental and behavioral pediatrics
    33. PFLUGFELDER GO
      GENETIC LESIONS IN DROSOPHILA BEHAVIORAL MUTANTS

      Behavioural brain research
    34. FEINSTEIN C; REISS AL
      AUTISM - THE POINT-OF-VIEW FROM FRAGILE-X STUDIES

      Journal of autism and developmental disorders
    35. SRIVASTAVA AK; SHUKLA KK; SRIVASTAVA SK
      EXPLORING NEURO-GENETIC PROCESSING OF ELECTRONIC NOSE DATA

      Microelectronics
    36. CHAPOUTHIER G; LAUNAY JM; VENAULT P; BRETON C; ROUBERTOUX PL; CRUSIO WE
      GENETIC SELECTION OF MOUSE LINES DIFFERING IN SENSITIVITY TO A BENZODIAZEPINE RECEPTOR INVERSE AGONIST

      Brain research
    37. LIVY DJ; WAHLSTEN D
      RETARDED FORMATION OF THE HIPPOCAMPAL COMMISSURE IN EMBRYOS FROM MOUSE STRAINS LACKING A CORPUS-CALLOSUM

      Hippocampus
    38. DESAI CJ; KRUEGER NX; SAITO H; ZINN K
      COMPETITION AND COOPERATION AMONG RECEPTOR TYROSINE PHOSPHATASES CONTROL MOTONEURON GROWTH CONE GUIDANCE IN DROSOPHILA

      Development
    39. MULLER U
      MOLECULAR ANALYSIS OF THE NEUROGENETIC DI SORDERS HUNTINGTONS-DISEASE, AMYOTROPHIC-LATERAL-SCLEROSIS AND ALZHEIMERS-DISEASE

      Nervenheilkunde
    40. TITUS SA; WARMKE JW; GANETZKY B
      THE DROSOPHILA ERG K+ CHANNEL POLYPEPTIDE IS ENCODED BY THE SEIZURE LOCUS

      The Journal of neuroscience
    41. BALLANTYNE AO; SCARVIE KM; TRAUNER DA
      ACADEMIC-ACHIEVEMENT IN INDIVIDUALS WITH INFANTILE NEPHROPATHIC CYSTINOSIS

      American journal of medical genetics
    42. BACHUS R; CLAUS A; MEYER T; RIEPE M; LUDOLPH AC
      MOLECULAR-GENETICS OF AMYOTROPHIC-LATERAL -SCLEROSIS

      Nervenarzt
    43. BARONDES SH; ALBERTS BM; ANDREASEN NC; BARGMANN C; BENES F; GOLDMANRAKIC P; GOTTESMAN I; HEINEMANN SF; JONES EG; KIRSCHNER M; LEWIS D; RAFF M; ROSES A; RUBENSTEIN J; SNYDER S; WATSON SJ; WEINBERGER DR; YOLKEN RH
      WORKSHOP ON SCHIZOPHRENIA

      Proceedings of the National Academy of Sciences of the United Statesof America
    44. ESTES PS; ROOS J; VANDERBLIEK A; KELLY RB; KRISHNAN KS; RAMASWAMI M
      TRAFFIC OF DYNAMIN WITHIN INDIVIDUAL DROSOPHILA SYNAPTIC BOUTONS RELATIVE TO COMPARTMENT-SPECIFIC MARKERS

      The Journal of neuroscience
    45. MONASTIRIOTI M; LINN CE; WHITE K
      CHARACTERIZATION OF DROSOPHILA TYRAMINE BETA-HYDROXYLASE GENE AND ISOLATION OF MUTANT FLIES LACKING OCTOPAMINE

      The Journal of neuroscience
    46. YAPIJAKIS C; KAPAKI E; BOUSSIOU M; VASSILOPOULOS D; PAPAGEORGIOU C
      PRENATAL-DIAGNOSIS OF X-LINKED SPINAL AND BULBAR MUSCULAR-ATROPHY IN A GREEK FAMILY

      Prenatal diagnosis
    47. GOLDSTEIN DS; LENDERS JWM; KALER SG; EISENHOFER G
      CATECHOLAMINE PHENOTYPING - CLUES TO THE DIAGNOSIS, TREATMENT, AND PATHOPHYSIOLOGY OF NEUROGENETIC DISORDERS

      Journal of neurochemistry
    48. SUN YA; WYMAN RJ
      PASSOVER ELIMINATES GAP JUNCTIONAL COMMUNICATION BETWEEN NEURONS OF THE GIANT FIBER SYSTEM IN DROSOPHILA

      Journal of neurobiology
    49. RESTIFO LL; ESTES PS; DELLORUSSO C
      GENETICS OF ECDYSTEROID-REGULATED CENTRAL-NERVOUS-SYSTEM METAMORPHOSIS IN DROSOPHILA (DIPTERA, DROSOPHILIDAE)

      European journal of entomology
    50. PFLUGFELDER GO; HEISENBERG M
      OPTOMOTOR-BLIND OF DROSOPHILA-MELANOGASTER - A NEUROGENETIC APPROACH TO OPTIC LOBE DEVELOPMENT AND OPTOMOTOR BEHAVIOR

      Comparative biochemistry and physiology. Part A, Physiology
    51. LANG C; ROTT HD
      GENETICALLY-DETERMINED DISEASES OF EXTRAP YRAMIDAL SYSTEM

      Nervenheilkunde
    52. LASSALLE JM
      NEUROGENETIC BASIS OF COGNITION - FACTS AND HYPOTHESES

      Behavioural processes
    53. REES M; ELMSLIE F; WHITEHOUSE W; SUNDQVIST A; GARDINER M
      ANALYSIS OF A HUMAN BRAIN VOLTAGE-GATED POTASSIUM CHANNEL GENE, KCNA6(HBK2), IN PATIENTS WITH JUVENILE MYOCLONIC EPILEPSY

      Neuropediatrics
    54. TAKAHASHI JS
      MOLECULAR NEUROBIOLOGY AND GENETICS OF CIRCADIAN-RHYTHMS IN MAMMALS

      Annual review of neuroscience
    55. KRISHNAN SN; FREI E; SCHALET AP; WYMAN RJ
      MOLECULAR-BASIS OF INTRACISTRONIC COMPLEMENTATION IN THE PASSOVER LOCUS OF DROSOPHILA

      Proceedings of the National Academy of Sciences of the United Statesof America
    56. RAUTENSTRAUSS B; GREHL H
      THE APPLICATION OF METHODS OF MOLECULAR-B IOLOGY GIVES NEW INSIGHTS IN CAUSE AND PROGRESS OF NEUROGENETIC DISEASES

      Monatsschrift fur Kinderheilkunde
    57. THACKERAY JR; GANETZKY B
      DEVELOPMENTALLY-REGULATED ALTERNATIVE SPLICING GENERATES A COMPLEX ARRAY OF DROSOPHILA-PARA SODIUM-CHANNEL ISOFORMS

      The Journal of neuroscience
    58. JINNAH HA; WOJCIK BE; HUNT M; NARANG N; LEE KY; GOLDSTEIN M; WAMSLEY JK; LANGLAIS PJ; FRIEDMANN T
      DOPAMINE DEFICIENCY IN A GENETIC MOUSE MODEL OF LESCH-NYHAN DISEASE

      The Journal of neuroscience
    59. REES M; CURTIS D; PARKER K; SUNDQVIST A; BARALLE D; BESPALOVA IN; BURMEISTER M; CHUNG E; GARDINER RM; WHITEHOUSE WP
      LINKAGE ANALYSIS OF IDIOPATHIC GENERALIZED EPILEPSY IN FAMILIES OF PROBANDS WITH JUVENILE MYOCLONIC EPILEPSY AND MARKER LOCI THE REGION OF EPM-1 ON CHROMOSOME 21Q - UNVERRICHT-LUNDBORG DISEASE AND JME ARE NOT ALLELIC VARIANTS

      Neuropediatrics
    60. ORDWAY RW; PALLANCK L; GANETZKY B
      NEURALLY EXPRESSED DROSOPHILA GENES ENCODING HOMOLOGS OF THE NSF AND SNAP SECRETORY PROTEINS

      Proceedings of the National Academy of Sciences of the United Statesof America
    61. COOLS AR; ROTS NY; ELLENBROEK B; DEKLOET ER
      BIMODAL SHAPE OF INDIVIDUAL VARIATION IN BEHAVIOR OF WISTAR RATS - THE OVERALL OUTCOME OF A FUNDAMENTALLY DIFFERENT MAKE-UP AND REACTIVITY OF THE BRAIN, THE ENDOCRINOLOGIC AND THE IMMUNOLOGICAL SYSTEM

      Neuropsychobiology
    62. WHITEHOUSE W; DIEBOLD U; REES M; PARKER K; DOOSE H; GARDINER RM
      EXCLUSION OF LINKAGE OF GENETIC FOCAL SHARP WAVES TO THE HLA REGION ON CHROMOSOME-6P IN FAMILIES WITH BENIGN PARTIAL EPILEPSY WITH CENTROTEMPORAL SHARP WAVES

      Neuropediatrics
    63. WSZOLEK ZK; CORDES M; CALNE DB; MUNTER MD; CORDES I; PFEIFER RF
      HEREDITARY PARKINSONS-DISEASE - REPORT ON 3 FAMILIES WITH AUTOSOMAL-DOMINANT INHERITANCE PATTERN

      Nervenarzt


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 15/07/19 alle ore 19:59:59