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La ricerca find articoli where soggetti phrase all words 'heterotopia' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 247 riferimenti
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    1. Barkovich, AJ; Kuzniecky, RI; Dobyns, WB
      Radiologic classification of malformations of cortical development

      CURRENT OPINION IN NEUROLOGY
    2. Chang, AH; Kaufmann, WE; Brat, DJ
      Ectopic cerebellum presenting as a suprasellar mass in infancy: Implications for cerebellar development

      PEDIATRIC AND DEVELOPMENTAL PATHOLOGY
    3. Gleeson, JG
      Neuronal migration disorders

      MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS
    4. Spreer, J; Martin, P; Greenlee, MW; Wohlfarth, R; Hammen, A; Arnold, SM; Schumacher, M
      Functional MRI in patients with band heterotopia

      NEUROIMAGE
    5. Friocourt, G; Chafey, P; Billuart, P; Koulakoff, A; Vine, MC; Schaar, BT; McConnell, SK; Francis, F; Chelly, J
      Doublecortin interacts with mu subunits of clathrin adaptor complexes in the developing nervous system

      MOLECULAR AND CELLULAR NEUROSCIENCE
    6. Matsumoto, N; Leventer, RJ; Kuc, JA; Mewborn, SK; Dudlicek, LL; Ramocki, MB; Pilz, DT; Mills, PL; Das, S; Ross, ME; Ledbetter, DH; Dobyns, WB
      Mutation analysis of the DCX gene and genotype/phenotype correlation in subcortical band heterotopia

      EUROPEAN JOURNAL OF HUMAN GENETICS
    7. Shmueli, O; Gdalyahu, A; Sorokina, K; Nevo, E; Avivi, A; Reiner, O
      DCX in PC12 cells: CREB-mediated transcription and neurite outgrowth

      HUMAN MOLECULAR GENETICS
    8. Winter, RM
      Editorial comment - Cerebro-fronto-facial syndrome: three types?

      CLINICAL DYSMORPHOLOGY
    9. Guion-Almeida, ML; Richieri-Costa, A
      Frontonasal dysplasia, macroblepharon, eyelid colobomas, ear anomalies, macrostomia, mental retardation and CNS structural anomalies: defining the phenotype

      CLINICAL DYSMORPHOLOGY
    10. Der Kaloustian, VM; Pelletier, M; Costa, T; Blackston, DR; Oudjhane, K
      A new syndrome with craniofacial and skeletal dysmorphisms and developmental delay

      CLINICAL DYSMORPHOLOGY
    11. Taege, C; Musil, A; Klohs, G; Rath, FW
      Cerebral heterotopia appearing as an extranasal polyp

      EUROPEAN JOURNAL OF PEDIATRIC SURGERY
    12. de Rouvroit, CL; Goffinet, AM
      Neuronal migration

      MECHANISMS OF DEVELOPMENT
    13. Iannetti, P; Spalice, A; Raucci, U; Perla, FM
      Functional neuroradiologic investigations in band heterotopia

      PEDIATRIC NEUROLOGY
    14. Rafalowska, J; Dziewulska, D; Podlecka, A; Maslinska, D
      Early ontogenic disturbances in cell migration in mentally disabled adult

      CLINICAL NEUROPATHOLOGY
    15. Kuzniecky, RI; Barkovich, AJ
      Malformations of cortical development and epilepsy

      BRAIN & DEVELOPMENT
    16. Kato, M; Kanai, M; Soma, O; Takusa, Y; Kimura, T; Numakura, C; Matsuki, T; Nakamura, S; Hayasaka, L
      Mutation of the doublecortin gene in male patients with double cortex syndrome: Somatic mosaicism detected by hair root analysis

      ANNALS OF NEUROLOGY
    17. Briellmann, RS; Jackson, GD; Torn-Broers, Y; Berkovic, SF
      Causes of epilepsies: Insights from discordant monozygous twins

      ANNALS OF NEUROLOGY
    18. Golden, JA
      Cell migration and cerebral cortical development

      NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY
    19. Wenzel, HJ; Robbins, CA; Tsai, LH; Schwartzkroin, PA
      Abnormal morphological and functional organization of the hippocampus in ap35 mutant model of cortical dysplasia associated with spontaneous seizures

      JOURNAL OF NEUROSCIENCE
    20. Castro, PA; Cooper, EC; Lowenstein, DH; Baraban, SC
      Hippocampal heterotopia lack functional kv4.2 potassium channels in the methylazoxymethanol model of cortical malformations and epilepsy

      JOURNAL OF NEUROSCIENCE
    21. Klisch, J; Juengling, F; Spreer, J; Koch, D; Thiel, T; Buchert, M; Arnold, S; Feuerhake, F; Schumacher, M
      Lhermitte-Duclos disease: Assessment with MR imaging, positron emission tomography, singe-photon emission CT, and MR spectroscopy

      AMERICAN JOURNAL OF NEURORADIOLOGY
    22. Vreugdenhil, E; Engels, B; Middelburg, R; van Koningsbruggen, S; Knol, J; Veldhuisen, B; de Kloet, ER
      Multiple transcripts generated by the DCAMKL gene are expressed in the rathippocampus

      MOLECULAR BRAIN RESEARCH
    23. van der Flier, A; Sonnenberg, A
      Structural and functional aspects of filamins

      BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH
    24. Guerrini, R; Carrozzo, R
      Epilepsy and genetic malformations of the cerebral cortex

      AMERICAN JOURNAL OF MEDICAL GENETICS
    25. Priolo, M; De Toni, T; Baffico, M; Cama, A; Seri, M; Cusano, R; Costabello, L; Fondelli, P; Capra, V; Silengo, M; Ravazzolo, R; Lerone, M
      Fontaine-Farriaux craniosynostosis: Second report in the literature

      AMERICAN JOURNAL OF MEDICAL GENETICS
    26. Ross, ME; Walsh, CA
      Human brain malformations and their lessons for neuronal migration

      ANNUAL REVIEW OF NEUROSCIENCE
    27. Kashani, AH; Hutchins, GM
      Meningeal-cutaneous relationships in anencephaly: Evidence for a primary mesenchymal abnormality

      HUMAN PATHOLOGY
    28. Duncan, JS
      Epileptogenic networks: cerebral dysplasias and cerebral ectopias - Functional neuroimaging

      REVUE NEUROLOGIQUE
    29. Leventer, RJ; Cardoso, C; Ledbetter, DH; Dobyns, WB
      LIS1 missense mutations cause milder lissencephaly phenotypes including a child with normal IQ

      NEUROLOGY
    30. Demelas, L; Serra, G; Conti, M; Achene, A; Mastropaolo, C; Matsumoto, N; Dudlicek, LL; Mills, PL; Dobyns, WB; Ledbetter, DH; Das, S
      Incomplete penetrance with normal MRI in a woman with germline mutation ofthe DCX gene

      NEUROLOGY
    31. Kathuria, MK; Kumar, R; Pal, L; Krishnani, N; Husain, N; Gupta, RK
      Brain-within-brain appearance of a heterotopic neuronal mass on magnetic resonance imaging - Case illustration

      JOURNAL OF NEUROSURGERY
    32. Santi, MR; Golden, JA
      Periventricular heterotopia may result from radial glial fiber disruption

      JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY
    33. Gerhards, F; Buttner, R; Janicke, S
      Aberrant salivary gland tissue as a differential diagnosis of branchiogenic cysts: case report

      HNO
    34. Tassi, L; Pasquier, B; Minotti, L; Garbelli, R; Kahane, P; Benabid, AL; Battaglia, G; Munari, C; Spreafico, R
      Cortical dysplasia: Electroclinical, imaging, and neuropathologic study of13 patients

      EPILEPSIA
    35. Bernasconi, A; Martinez, V; Rosa-Neto, P; D'Agostino, D; Bernasconi, N; Berkovic, S; MacKay, M; Harvey, AS; Palmini, A; da Costa, JC; Paglioli, E; Kim, HI; Connolly, M; Olivier, A; Dubeau, F; Andermann, E; Guerrini, R; Whisler, W; de Toledo-Morrell, L; Morrell, F; Andermann, F
      Surgical resection for intractable epilepsy in "double cortex" syndrome yields inadequate results

      EPILEPSIA
    36. Houissa-Vuong, S; Martin, B; Lascar, G; Vuong, PN
      Multiple jejunal strictures caused by gastric heterotopia

      ANNALES DE CHIRURGIE
    37. Taylor, JP; Sater, R; French, J; Baltuch, G; Crino, PB
      Transcription of intermediate filament genes is enhanced in focal corticaldysplasia

      ACTA NEUROPATHOLOGICA
    38. Komatsu, S; Sakata-Haga, H; Sawada, K; Hisano, S; Fukui, Y
      Prenatal exposure to ethanol induces leptomeningeal heterotopia in the cerebral cortex of the rat fetus

      ACTA NEUROPATHOLOGICA
    39. Sakamoto, M; Ono, J; Okada, S; Nakamura, Y; Kurahashi, H
      Genetic alteration of the DCX gene in Japanese patients with subcortical laminar heterotopia or isolated lissencephaly sequence

      JOURNAL OF HUMAN GENETICS
    40. Oliveira, JRM
      News about disturbances of neuronal migration bring views to bipolar disorder

      MOLECULAR PSYCHIATRY
    41. Leventer, RJ; Pilz, DT; Matsumoto, N; Ledbetter, DH; Dobyns, WB
      Lissencephaly and subcortical band heterotopia: molecular basis and diagnosis

      MOLECULAR MEDICINE TODAY
    42. Yao, JL; Zhou, H; Roche, K; Bangaru, BS; Ginsburg, H; Greco, MA
      Adenomyoma arising in a Meckel diverticulum: Case report and review of theliterature

      PEDIATRIC AND DEVELOPMENTAL PATHOLOGY
    43. Lambert, MP; Heller, DS; Bethel, C
      Extensive gastric heterotopia of the small intestine resulting in massive gastrointestinal bleeding, rowel perforation, and death: Report of a case and review of the literature

      PEDIATRIC AND DEVELOPMENTAL PATHOLOGY
    44. Schwartzkroin, PA; Walsh, CA
      Cortical malformations and epilepsy

      MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS
    45. Caviness, VS; Takahashi, T; Nowakowski, RS
      Neocortical malformation as consequence of nonadaptive regulation of neuronogenetic sequence

      MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS
    46. Burgess, HA; Reiner, O
      Doublecortin-like kinase is associated with microtubules in neuronal growth cones

      MOLECULAR AND CELLULAR NEUROSCIENCE
    47. Tanaka, T; Gleeson, JG
      Genetics of brain development and malformation syndromes

      CURRENT OPINION IN PEDIATRICS
    48. Chiurazzi, P; Oostra, BA
      Genetics of mental retardation

      CURRENT OPINION IN PEDIATRICS
    49. Sapir, T; Horesh, D; Caspi, M; Atlas, R; Burgess, HA; Wolf, SG; Francis, F; Chelly, J; Elbaum, M; Pietrokovski, S; Reiner, O
      Doublecortin mutations cluster in evolutionarily conserved functional domains

      HUMAN MOLECULAR GENETICS
    50. Worthington, S; Turner, A; Elber, J; Andrews, PI
      22q11 deletion and polymicrogyria - cause or coincidence?

      CLINICAL DYSMORPHOLOGY
    51. Walsh, CA; Goffinet, AM
      Potential mechanisms of mutations that affect neuronal migration in man and mouse

      CURRENT OPINION IN GENETICS & DEVELOPMENT
    52. Erberich, H; Handt, S; Mittermayer, C; Tietze, L
      Simultaneous appearance of an adenomyoma and pancreatic heterotopia of thestomach

      VIRCHOWS ARCHIV-AN INTERNATIONAL JOURNAL OF PATHOLOGY
    53. Lammens, M
      Neuronal migration disorders in man

      EUROPEAN JOURNAL OF MORPHOLOGY
    54. McNamee, S
      Foucault's heterotopia and children's everyday lives

      CHILDHOOD-A GLOBAL JOURNAL OF CHILD RESEARCH
    55. Feng, YY; Olson, EC; Stukenberg, PT; Flanagan, LA; Kirschner, MW; Walsh, CA
      LIS1 regulates CNS lamination by interacting with mNudE, a central component of the centrosome

      NEURON
    56. Ozanne, DM; Brady, ME; Cook, S; Gaughan, L; Neal, DE; Robson, CN
      Androgen receptor nuclear translocation is facilitated by the f-actin cross-linking protein filamin

      MOLECULAR ENDOCRINOLOGY
    57. Guerreiro, MM; Andermann, E; Guerrini, R; Dobyns, WB; Kuzniecky, R; Silver, K; Van Bogaert, P; Gillain, C; David, P; Ambrosetto, G; Rosati, A; Bartolomei, F; Parmeggiani, A; Paetau, R; Salonen, O; Ignatius, J; Borgatti, R; Zucca, C; Bastos, AC; Palmini, A; Fernandes, W; Montenegro, MA; Cendes, F; Andermann, F
      Familiar perisylvian polymicrogyria: A new familial syndrome of cortical maldevelopment

      ANNALS OF NEUROLOGY
    58. Gleeson, JG; Luo, RF; Grant, PE; Guerrini, R; Huttenlocher, PR; Berg, MJ; Ricci, S; Cusmai, R; Wheless, JW; Berkovic, S; Scheffer, I; Dobyns, WB; Walsh, CA
      Genetic and neuroradiological heterogeneity of double cortex syndrome

      ANNALS OF NEUROLOGY
    59. Spreer, J; Dietz, M; Raab, P; Arnold, S; Klisch, J; Lanfermann, H
      Functional MRI of language-related activation in left frontal schizencephaly

      JOURNAL OF COMPUTER ASSISTED TOMOGRAPHY
    60. Lagae, L
      Cortical malformations: a frequent cause of epilepsy in children

      EUROPEAN JOURNAL OF PEDIATRICS
    61. Handra-Luca, A; Chabanne, A; Giglio, L; Flejou, JF
      An acid rectal polyp

      ANNALES DE PATHOLOGIE
    62. Colombat, M; Robbe, M; Chatelain, D; Thelu, F; Cordonnier, C; Leclercq, F; Ghighi, C; Sevestre, H; Gontier, MF
      A cutaneous neck flow

      ANNALES DE PATHOLOGIE
    63. Barkovich, AJ
      Morphologic characteristics of subcortical heterotopia: MR imaging study

      AMERICAN JOURNAL OF NEURORADIOLOGY
    64. Mitchell, LA; Simon, EM; Filly, RA; Barkovich, AJ
      Antenatal diagnosis of subependymal heterotopia

      AMERICAN JOURNAL OF NEURORADIOLOGY
    65. Aigner, L; Fluegel, D; Dietrich, J; Ploetz, S; Winkler, J
      Isolated lissencephaly sequence and double-cortex syndrome in a German family with a novel doublecortin mutation

      NEUROPEDIATRICS
    66. Agaimy, A; Mandl, L
      Papillary fibroelastoma of the aortic valve coexisting with a cystic tumorof the atrioventricular nodal region: a case report

      PATHOLOGE
    67. Gleeson, JG; Walsh, CA
      Neuronal migration disorders: from genetic diseases to developmental mechanisms

      TRENDS IN NEUROSCIENCES
    68. Leventer, RJ; Mills, PL; Dobyns, WB
      X-linked malformations of cortical development

      AMERICAN JOURNAL OF MEDICAL GENETICS
    69. Carney, JA
      Salivary heterotopia, cysts, and the parathyroid gland - Branchial pouch derivatives and remnants

      AMERICAN JOURNAL OF SURGICAL PATHOLOGY
    70. Schroth, M; Wolf, S; Bentzien, SC; Wagner, M; Rupprecht, T
      Relapsing nasal glioma in a three-week-old infant

      MEDICAL AND PEDIATRIC ONCOLOGY
    71. Landrieu, P
      Progress in pediatric neurology.

      REVUE NEUROLOGIQUE
    72. Barkovich, AJ; Kuzniecky, RI
      Gray matter heterotopia

      NEUROLOGY
    73. Pinard, JM; Feydy, A; Carlier, R; Perez, N; Pierot, L; Burnod, Y
      Functional MRI in double cortex: Functionality of heterotopia

      NEUROLOGY
    74. Guerrini, R; Barkovich, AJ; Sztriha, L; Dobyns, WB
      Bilateral frontal polymicrogyria - A newly recognized brain malformation syndrome

      NEUROLOGY
    75. Hagemann, G; Redecker, C; Witte, OW
      Cortical dysgenesis: present classification, MRI diagnostics, and clinicaloverview

      NERVENARZT
    76. Redecker, C; Hagemann, G; Gressens, P; Evrard, P; Witte, OW
      Cortical dysgenesis: recent aspects regarding pathogenesis and pathophysiology

      NERVENARZT
    77. Gyure, KA; Thompson, LDR; Morrison, AL
      A clinicopathological study of 15 patients with neuroglial heterotopias and encephaloceles of the middle ear and mastoid region

      LARYNGOSCOPE
    78. Shin, CE; Kim, SS; Chwals, WJ
      Salivary gland choristoma of the anterior chest wall

      JOURNAL OF PEDIATRIC SURGERY
    79. Yoshiura, K; Noda, Y; Kinoshita, A; Niikawa, N
      Colocalization of doublecortin with the microtubules: An ex vivo colocalization study of mutant doublecortin

      JOURNAL OF NEUROBIOLOGY
    80. Taylor, KR; Holzer, AK; Bazan, JF; Walsh, CA; Gleeson, JG
      Patient mutations in doublecortin define a repeated tubulin-binding domain

      JOURNAL OF BIOLOGICAL CHEMISTRY
    81. Chen, ZF; Schottler, F; Bertram, E; Gall, CM; Anzivino, MJ; Lee, KS
      Distribution and initiation of seizure activity in a rat brain with subcortical band heterotopia

      EPILEPSIA
    82. Sisodiya, SM; Free, SL; Duncan, JS; Stevens, JM
      Bilateral periventricular and subcortical heterotopia in a man with refractory epilepsy

      EPILEPSIA
    83. Rosen, GD; Galaburda, AM
      Single cause, polymorphic neuronal migration disorders: an animal model

      DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY
    84. Uher, BF; Golden, JA
      Neuronal migration defects of the cerebral cortex: a destination debacle

      CLINICAL GENETICS
    85. Qin, J; Mizuguchi, M; Itoh, M; Takashima, S
      Immunohistochemical expression of doublecortin in the human cerebrum: comparison of normal development and neuronal migration disorders

      BRAIN RESEARCH
    86. Sisodiya, SM
      Surgery for malformations of cortical development causing epilepsy

      BRAIN
    87. Gleeson, JG; Minnerath, S; Kuzniecky, RI; Dobyns, WB; Young, ID; Ross, ME; Walsh, CA
      Somatic and germline mosaic mutations in the doublecortin gene are associated with variable phenotypes

      AMERICAN JOURNAL OF HUMAN GENETICS
    88. Ono-Yagi, K; Ohno, M; Iwami, M; Takano, T; Yamano, T; Shimada, M
      Heterotopia in microcephaly induced by cytosine arabinoside: hippocampus in the neocortex

      ACTA NEUROPATHOLOGICA
    89. Brodtkorb, E; Myhr, G; Gimse, R
      Is monochorionic twinning a risk factor for focal cortical dysgenesis?

      ACTA NEUROLOGICA SCANDINAVICA
    90. Suzuki, K; Uchida, T; Nakayama, H; Ugajin, W; Inaniwa, Y; Sugitani, M; Mori, Y
      Heterotopic pancreatic tissue associated with intra- and extrahepatic choledochal cysts

      PATHOLOGY INTERNATIONAL
    91. Nakanishi, Y; Ochiai, A; Shimoda, T; Yamaguchi, H; Tachimori, Y; Kato, H; Watanabe, H; Hirohashi, S
      Heterotopic sebaceous glands in the esophagus: Histopathological and immunohistochemical study of a resected esophagus

      PATHOLOGY INTERNATIONAL
    92. Suarez-Mier, MP; Sanchez-de-Leon, S; Cohle, SD
      An unusual site for the AV node tumor: Report of two cases

      CARDIOVASCULAR PATHOLOGY
    93. Horesh, D; Sapir, T; Francis, F; Wolf, SG; Caspi, M; Elbaum, M; Chelly, J; Reiner, O
      Doublecortin, a stabilizer of microtubules

      HUMAN MOLECULAR GENETICS
    94. Pilz, DT; Kuc, J; Matsumoto, N; Bodurtha, J; Bernadi, B; Tassinari, CA; Dobyns, WB; Ledbetter, DH
      Subcortical band heterotopia in rare affected males can be caused by missense mutations in DCX (XLIS) or LIS1

      HUMAN MOLECULAR GENETICS
    95. Chelly, J
      Breakthroughs in molecular and cellular mechanisms underlying X-linked mental retardation

      HUMAN MOLECULAR GENETICS
    96. Slaney, SF; Chong, WK; Winter, RM
      A new syndrome of short stature, distinctive facial features and periventricular grey matter heterotopia

      CLINICAL DYSMORPHOLOGY
    97. Allen, KM; Walsh, CA
      Genes that regulate neuronal migration in the cerebral cortex

      EPILEPSY RESEARCH
    98. Jacobs, KM; Kharazia, VN; Prince, DA
      Mechanisms underlying epileptogenesis in cortical malformations

      EPILEPSY RESEARCH
    99. Francis, F; Koulakoff, A; Boucher, D; Chafey, P; Schaar, B; Vinet, MC; Friocourt, G; McDonnell, N; Reiner, O; Kahn, A; McConnell, SK; Berwald-Netter, Y; Denoulet, P; Chelly, J
      Doublecortin is a developmentally regulated, microtubule-associated protein expressed in migrating and differentiating neurons

      NEURON
    100. Reiner, O
      The unfolding story of two lissencephaly genes and brain development

      MOLECULAR NEUROBIOLOGY


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Documento generato il 01/06/20 alle ore 10:20:46