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La ricerca find articoli where soggetti phrase all words 'syndrome X' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 1300 riferimenti
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    1. Laederach-Hofmann, K; Truniger, C; Mussgay, L; Jurgensen, R
      Sensory and affective components in the use of pain words in patients suffering from angina pectoris due to coronary artery disease or syndrome-x

      ZEITSCHRIFT FUR KLINISCHE PSYCHOLOGIE UND PSYCHOTHERAPIE
    2. Sun, SS; Huang, JL; Tsai, SC; Ho, YJ; Kao, CH
      The higher likelihood of developing cardiomegaly during follow-up in patients with syndrome X and abnormal thallium-201 myocardial perfusion SPECT

      INTERNATIONAL JOURNAL OF CARDIOVASCULAR IMAGING
    3. Kenneson, A; Warren, ST
      The female and the fragile X reviewed

      SEMINARS IN REPRODUCTIVE MEDICINE
    4. Duplantier, JE; Seyama, K; Day, NK; Hitchcock, R; Nelson, RP; Ochs, HD; Haraguchi, S; Klemperer, MR; Good, RA
      Immunologic reconstitution following bone marrow transplantation for X-linked hyper IgM syndrome

      CLINICAL IMMUNOLOGY
    5. Lewis, J; Eiben, LJ; Nelson, DL; Cohen, JI; Nichols, KE; Ochs, HD; Notarangelo, LD; Duckett, CS
      Distinct interactions of the X-linked lymphoproliferative syndrome gene product SAP with cytoplasmic domains of members of the CD2 receptor family

      CLINICAL IMMUNOLOGY
    6. Kallinen, J; Marin, K; Heinonen, S; Mannermaa, A; Palotie, A; Ryynanen, M
      Wide scope prenatal diagnosis at Kuopio University Hospital 1997-1998: integration of gene tests and fetal karyotyping

      BRITISH JOURNAL OF OBSTETRICS AND GYNAECOLOGY
    7. Simonsson, T
      G-quadruplex DNA structures - Variations on a theme

      BIOLOGICAL CHEMISTRY
    8. Timmermann, S; Lehrmann, H; Polesskaya, A; Harel-Bellan, A
      Histone acetylation and disease

      CELLULAR AND MOLECULAR LIFE SCIENCES
    9. Musumeci, SA; Ferri, R; Scuderi, C; Bosco, P; Elia, M
      Seizures and epileptiform EEG abnormalities in FRAXE syndrome

      CLINICAL NEUROPHYSIOLOGY
    10. Evenhuis, H; Henderson, CM; Beange, H; Lennox, N; Chicoine, B
      Healthy ageing - Adults with intellectual disabilities: Physical health issues

      JOURNAL OF APPLIED RESEARCH IN INTELLECTUAL DISABILITIES
    11. Akiyama, T; Gohda, J; Shibata, S; Nomura, Y; Azuma, S; Ohmori, Y; Sugano, S; Arai, H; Yamamoto, T; Inoue, J
      Mammalian homologue of E-coli ras-like GTPase (ERA) is a possible apoptosis regulator with RNA binding activity

      GENES TO CELLS
    12. Scheen, AJ
      The insulin sensitivity concept

      DIABETES & METABOLISM
    13. Crawford, DC; Acuna, JM; Sherman, SL
      FMR1 and the fragile X syndrome: Human genome epidemiology review

      GENETICS IN MEDICINE
    14. Worbs, M; Bourenkov, GP; Bartunik, HD; Huber, R; Wahl, MC
      An extended RNA binding surface through arrayed S1 and KH domains in transcription factor NusA

      MOLECULAR CELL
    15. Hagerman, RJ; Hagerman, PJ
      Fragile X syndrome: A model of gene-brain-behavior relationships

      MOLECULAR GENETICS AND METABOLISM
    16. Castellvi-Bel, S; Mila, M
      Genes responsible for nonspecific mental retardation

      MOLECULAR GENETICS AND METABOLISM
    17. Hegde, MR; Fawkner, M; Chong, B; McGaughran, J; Gilbert, D; Love, DR
      Compound heterozygosity at the FMR1 gene

      GENETIC TESTING
    18. Merz, CNB; Johnson, BJ; Kelsey, SF; Reis, SE; Lewis, JF; Reichek, N; Rogers, WJ; Pepine, CF; Shaw, LJ
      Diagnostic, prognostic, and cost assessment of coronary artery disease in women

      AMERICAN JOURNAL OF MANAGED CARE
    19. Abbeduto, L; Evans, J; Dolan, T
      Theoretical perspectives on language and communication problems in mental retardation and developmental disabilities

      MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS
    20. Adamson, DL; Webb, CM; Collins, P
      Esterified estrogens combined with methyltestosterone improve emotional well-being in postmenopausal women with chest pain and normal coronary angiograms

      MENOPAUSE-THE JOURNAL OF THE NORTH AMERICAN MENOPAUSE SOCIETY
    21. Mallolas, J; Duran, M; Sanchez, A; Jimenez, D; Castellvi-Bel, S; Rife, M; Mila, M
      Implications of the FMR1 gene in menopause: study of 147 Spanish women

      MENOPAUSE-THE JOURNAL OF THE NORTH AMERICAN MENOPAUSE SOCIETY
    22. Jacobson, JW
      Environmental postmodernism and rehabilitation of the borderline of mentalretardation

      BEHAVIORAL INTERVENTIONS
    23. Santos, CB; Lima, MAC; Pimentel, MMG
      A new PCR assay useful for screening of FRAXE/FMR2 mental impairment amongmales

      HUMAN MUTATION
    24. Sabaratnam, M; Vroegop, PG; Gangadharan, SK
      Epilepsy and EEG findings in 18 males with fragile X syndrome

      SEIZURE-EUROPEAN JOURNAL OF EPILEPSY
    25. Plomin, R
      Genetic factors contributing to learning and language delays and disabilities

      CHILD AND ADOLESCENT PSYCHIATRIC CLINICS OF NORTH AMERICA
    26. Tzeng, CC; Lin, SJ; Chen, YJ; Kuo, PL; Jong, YJ; Tsai, LP; Chen, RM
      An effective strategy of using molecular testing to screen mentally retarded individuals for fragile X syndrome

      DIAGNOSTIC MOLECULAR PATHOLOGY
    27. Sun, SS; Shiau, YC; Tsai, SC; Ho, YJ; Wang, JJ; Kao, CH
      Cerebral perfusion in patients with syndrome X: A single photon emission computed tomography study

      JOURNAL OF NEUROIMAGING
    28. Larsen, LA; Vuust, J; Nystad, M; Evseeva, I; Van Ghelue, M; Tranebjaerg, L
      Analysis of FMR1 (CGG)(n) alleles and DXS548-FRAXAC1 haplotypes in three European circumpolar populations: traces of genetic relationship with Asia

      EUROPEAN JOURNAL OF HUMAN GENETICS
    29. Kooy, RF; Verhoye, M; Lemmon, V; Van Der Linden, A
      Brain studies of mouse models for neurogenetic disorders using in vivo magnetic resonance imaging (MRI)

      EUROPEAN JOURNAL OF HUMAN GENETICS
    30. Kwon, SH; Lee, KS; Hyun, MC; Song, KE; Kim, JK
      Molecular screening for Fragile X syndrome in mentally handicapped children in Korea

      JOURNAL OF KOREAN MEDICAL SCIENCE
    31. Fulmer-Smentek, SB; Francke, U
      Association of acetylated histones with paternally expressed genes in the Prader-Willi deletion region

      HUMAN MOLECULAR GENETICS
    32. Richards, RI
      Dynamic mutations: a decade of unstable expanded repeats in human genetic disease

      HUMAN MOLECULAR GENETICS
    33. Bontekoe, CJM; Bakker, CE; Nieuwenhuizen, IM; van der Linde, H; Lans, H; de Lange, D; Hirst, MC; Oostra, BA
      Instability of a (CGG)(98) repeat in the Fmr1 promoter

      HUMAN MOLECULAR GENETICS
    34. Kenneson, A; Zhang, FP; Hagedorn, CH; Warren, ST
      Reduced FMRP and increased FMR1 transcription is proportionally associatedwith CGG repeat number in intermediate-length and premutation carriers

      HUMAN MOLECULAR GENETICS
    35. Perez-Canadillas, JM; Varani, G
      Recent advances in RNA-protein recognition

      CURRENT OPINION IN STRUCTURAL BIOLOGY
    36. Grosso, S; Balestri, P; Anichini, C; Bartalini, G; Pucci, L; Morgese, G; Berardi, R
      Pubertal disorders in inv dup(15) syndrome

      GYNECOLOGICAL ENDOCRINOLOGY
    37. Lebovitz, HE
      Insulin resistance: definition and consequences

      EXPERIMENTAL AND CLINICAL ENDOCRINOLOGY & DIABETES
    38. Rickert, CH; Grabellus, F; Varchmin-Schultheiss, K; Stoss, H; Paulus, W
      Sudden unexpected death in young adults with chronic hydrocephalus

      INTERNATIONAL JOURNAL OF LEGAL MEDICINE
    39. Ho, YL; Wu, CC; Yen, RF; Hung, SR; Chen, MF; Huang, PJ
      Comparison of ischemic patterns in myocardial bridge and syndrome X: Evaluation by dobutamine stress echocardiography and stress thallium-201 SPECT

      JOURNAL OF THE FORMOSAN MEDICAL ASSOCIATION
    40. Botker, HE
      Vascular and metabolic abnormalities in patients with angina pectoris and normal coronary angiograms

      DANISH MEDICAL BULLETIN
    41. Cornish, KM; Munir, F; Cross, G
      Differential impact of the FMR-1 full mutation on memory and attention functioning: A neuropsychological perspective

      JOURNAL OF COGNITIVE NEUROSCIENCE
    42. Ethell, IM; Irie, F; Kalo, MS; Couchman, JR; Pasquale, EB; Yamaguchi, Y
      EphB/syndecan-2 signaling in dendritic spine morphogenesis

      NEURON
    43. Bailey, DB; Roberts, JE; Mirrett, P; Hatton, DD
      Identifying infants and toddlers with fragile X syndrome: Issues and recommendations

      INFANTS AND YOUNG CHILDREN
    44. Hodapp, RM; Dykens, EM
      Strengthening behavioral research on genetic mental retardation syndromes

      AMERICAN JOURNAL ON MENTAL RETARDATION
    45. Bakris, GL
      Angiotensin-converting enzyme inhibition to enhance vascular health-clinical and research models

      AMERICAN JOURNAL OF HYPERTENSION
    46. Chen, W; Srinivasan, SR; Berenson, GS
      Plasma renin activity and insulin resistance in African American and whitechildren: The Bogalusa Heart Study

      AMERICAN JOURNAL OF HYPERTENSION
    47. Miatello, R; Risler, N; Castro, C; Gonzalez, S; Ruttler, M; Cruzado, M
      Aortic smooth muscle cell proliferation and endothelial nitric oxide synthase activity in fructose-fed rats

      AMERICAN JOURNAL OF HYPERTENSION
    48. Bustamante-Calvillo, ME; Velazquez, FR; Cabrera-Munoz, L; Torres, J; Gomez-Delgado, A; Moreno, JAE; Munoz-Hernandez, O
      Molecular detection of respiratory syncytial virus in postmortem lung tissue samples from Mexican children deceased with pneumonia

      PEDIATRIC INFECTIOUS DISEASE JOURNAL
    49. Lee, MH; Schedl, T
      Identification of in vivo mRNA targets of GLD-1, a maxi-KH motif containing protein required for C-elegans germ cell development

      GENES & DEVELOPMENT
    50. Moldavsky, M; Lev, D; Lerman-Sagie, T
      Behavioral phenotypes of genetic syndromes: A reference guide for psychiatrists

      JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY
    51. Ferri, R; Elia, M; Musumeci, SA; Cosentino, FII; Roccasalva, G; Spada, RS; Toscano, G
      Somatosensory evoked potentials in patients affected by unilateral cerebrovascular lesions with onset during the perinatal period or adulthood

      JOURNAL OF CHILD NEUROLOGY
    52. Kovtun, IV; Goellner, G; McMurray, CT
      Structural features of trinucleotide repeats associated with DNA expansion

      BIOCHEMISTRY AND CELL BIOLOGY-BIOCHIMIE ET BIOLOGIE CELLULAIRE
    53. Huckell, VF
      Angiogenesis (clinical trials) - Case 1

      CANADIAN JOURNAL OF CARDIOLOGY
    54. Sharma, D; Gupta, M; Thelma, BK
      Expansion mutation frequency and CGG/GCC repeat polymorphism in FMR1 and FMR2 genes in an Indian population

      GENETIC EPIDEMIOLOGY
    55. Brockhurst, V; Barnard, R; Wolter, L; Giffard, P; Timms, P
      Development of ligase-assisted spacer addition for the measurement of microsatellites

      BIOTECHNIQUES
    56. Bassett, AS; Chow, EWC; O'Neill, S; Brzustowicz, LM
      Genetic insights into the neurodevelopmental hypothesis of schizophrenia

      SCHIZOPHRENIA BULLETIN
    57. Saenger, P; DiMartino-Nardi, J
      Premature adrenarche

      JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION
    58. Lane, RH; Kelley, DE; Gruetzmacher, EM; Devaskar, SU
      Uteroplacental insufficiency alters hepatic fatty acid-metabolizing enzymes in juvenile and adult rats

      AMERICAN JOURNAL OF PHYSIOLOGY-REGULATORY INTEGRATIVE AND COMPARATIVE PHYSIOLOGY
    59. Masino, L; Pastore, A
      A structural approach to trinucleotide expansion diseases

      BRAIN RESEARCH BULLETIN
    60. Kral, JG; Buckley, MC; Kissileff, HR; Schaffner, F
      Metabolic correlates of eating behavior in severe obesity

      INTERNATIONAL JOURNAL OF OBESITY
    61. Mori, S; Murano, S; Yokote, K; Takemoto, M; Asaumi, S; Take, A; Saito, Y
      Enhanced intra-abdominal visceral fat accumulation in patients with Werner's syndrome

      INTERNATIONAL JOURNAL OF OBESITY
    62. Nguyen, MC; Stewart, RB; Banerji, MA; Gordon, DH; Kral, JG
      Relationships between tamoxifen use, liver fat and body fat distribution in women with breast cancer

      INTERNATIONAL JOURNAL OF OBESITY
    63. Chen, L; Toth, M
      Fragile X mice develop sensory hyperreactivity to auditory stimuli

      NEUROSCIENCE
    64. Grishin, NV
      KH domain: one motif, two folds

      NUCLEIC ACIDS RESEARCH
    65. Rojsitthisak, P; Romero, RM; Haworth, IS
      Extrahelical cytosine bases in DNA duplexes containing d[GCC](n)center dotd[GCC](n) repeats: detection by a mechlorethamine crosslinking reaction

      NUCLEIC ACIDS RESEARCH
    66. Thurston, RC; Keefe, FJ; Bradley, L; Krishnan, KRR; Caldwell, DS
      Chest pain in the absence of coronary artery disease: A biopsychosocial perspective

      PAIN
    67. Sermon, K; Seneca, S; De Rycke, M; Goossens, V; Van de Velde, H; De Vos, A; Platteau, P; Lissens, W; Van Steirteghem, A; Liebaers, I
      PGD in the lab for triplet repeat diseases - myotonic dystrophy, Huntington's disease and Fragile-X syndrome

      MOLECULAR AND CELLULAR ENDOCRINOLOGY
    68. Lombardi, G; Zarrilli, S; Colao, A; Paesano, L; Di Somma, C; Rossi, F; De Rosa, M
      Estrogens and health in males

      MOLECULAR AND CELLULAR ENDOCRINOLOGY
    69. Smith, M; Escamilla, JR; Filipek, P; Bocian, ME; Modahl, C; Flodman, P; Spence, MA
      Molecular genetic delineation of 2q37.3 deletion in autism and osteodystrophy: report of a case and of new markers for deletion screening by PCR

      CYTOGENETICS AND CELL GENETICS
    70. Gianarris, WJ; Golden, CJ; Greene, L
      The Conners' Parent Rating Scales: A critical review of the literature

      CLINICAL PSYCHOLOGY REVIEW
    71. Castren, M; Haapasalo, A; Oostra, BA; Castren, E
      Subcellular localization of fragile X mental retardation protein with the I304N mutation in the RNA-binding domain in cultured hippocampal neurons

      CELLULAR AND MOLECULAR NEUROBIOLOGY
    72. Imai, T; Tokunaga, A; Yoshida, T; Hashimoto, M; Mikoshiba, K; Weinmaster, G; Nakafuku, M; Okano, H
      The neural RNA-binding protein Musashi1 translationally regulates mammalian numb gene expression by interacting with its mRNA

      MOLECULAR AND CELLULAR BIOLOGY
    73. Nimchinsky, EA; Oberlander, AM; Svoboda, K
      Abnormal development of dendritic spines in FMR1 knock-out mice

      JOURNAL OF NEUROSCIENCE
    74. Picano, E; Palinkas, A; Amyot, R
      Diagnosis of myocardial ischemia in hypertensive patients

      JOURNAL OF HYPERTENSION
    75. Schaeffer, C; Bardoni, B; Mandel, JL; Ehresmann, B; Ehresmann, C; Moine, H
      The fragile X mental retardation protein binds specifically to its mRNA via a purine quartet motif

      EMBO JOURNAL
    76. Fichera, M; Silengo, M; Spalletta, A; Lo Giudice, M; Romano, C; Ragusa, A
      Prenatal diagnosis of ATR-X syndrome in a fetus with a new G > T splicing mutation in the XNP/ATR-X gene

      PRENATAL DIAGNOSIS
    77. Apessos, A; Abou-Sleiman, PM; Harper, JC; Delhanty, JDA
      Preimplantation genetic diagnosis of the fragile X syndrome by use of linked polymorphic markers

      PRENATAL DIAGNOSIS
    78. Kaski, JC; Garcia, LFV
      Therapeutic options for the management of patients with cardiac syndrome X

      EUROPEAN HEART JOURNAL
    79. Rosano, GMC; Fini, M; Mercuro, G
      Hormone replacement therapy in women with angina with normal coronary arteriograms. Pathogenetic or symptomatic therapy?

      EUROPEAN HEART JOURNAL
    80. Sitges, M; Heras, M; Roig, E; Durcan, M; Masotti, M; Zurbano, MJ; Roque, M; Sanz, G
      Acute and mid-term combined hormone replacement therapy improves endothelial function in post-menopausal women with angina and angiographically normal coronary arteries

      EUROPEAN HEART JOURNAL
    81. Lanza, GA; Andreotti, F; Sestito, A; Sciahbasi, A; Crea, F; Maseri, A
      Platelet aggregability in cardiac syndrome X

      EUROPEAN HEART JOURNAL
    82. Hughes, AD; Thom, S
      Wearing your heart in your sleeve?

      EUROPEAN HEART JOURNAL
    83. Antonios, TFT; Kaski, JC; Hasan, KM; Brown, SJ; Singer, DRJ
      Rarefaction of skin capillaries in patients with anginal chest pain and normal coronary arteriograms

      EUROPEAN HEART JOURNAL
    84. Roberts, CK; Vaziri, ND; Liang, KH; Barnard, RJ
      Reversibility of chronic experimental syndrome X by diet modification

      HYPERTENSION
    85. Gresl, TA; Colman, RJ; Roecker, EB; Havighurst, TC; Huang, Z; Allison, DB; Bergman, RN; Kemnitz, JW
      Dietary restriction and glucose regulation in aging rhesus monkeys: a follow-up report at 8.5 yr

      AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM
    86. Sung, WC; Lee, GB; Tzeng, CC; Chen, SH
      Plastic microchip electrophoresis for genetic screening: The analysis of polymerase chain reactions products of fragile X (CGG)n alleles

      ELECTROPHORESIS
    87. Dudek, D; Rzeszutko, L; Dimitrow, PP; Bartus, S; Sorysz, D; Chyrchel, M; Rakowski, T; Zdzienicka, A; Guevara, I; Dembinska-Kiec, A; Dubiel, JS
      Circulating N-terminal brain natriuretic peptide precursor and endothelin levels in patients with syndrome X and left bundle branch block with preserved systolic function

      INTERNATIONAL JOURNAL OF CARDIOLOGY
    88. Yaymaci, B; Dagdelen, S; Bozbuga, N; Demirkol, O; Say, B; Guzelmeric, F; Dindar, I
      The response of the myocardial metabolism to atrial pacing in patients with coronary slow flow

      INTERNATIONAL JOURNAL OF CARDIOLOGY
    89. Latif, OA; Nedeljkovic, SS; Stevenson, LW
      Spinal cord stimulation for chronic intractable angina pectoris: A unifiedtheory on its mechanism

      CLINICAL CARDIOLOGY
    90. Tousoulis, D; Davies, GJ; Asimakopoos, G; Homaei, H; Zouridakis, E; Ahmed, N; Kaski, JC
      Vascular cell adhesion molecule-1 and intercellular adhesion molecule-1 serum level in patients with chest pain and normal coronary arteries (syndrome X)

      CLINICAL CARDIOLOGY
    91. Coupland, NJ
      Social phobia: Etiology, neurobiology, and treatment

      JOURNAL OF CLINICAL PSYCHIATRY
    92. Sanderson, JE; Haines, CJ; Yeung, L; Yip, GWK; Tang, K; Yim, SF; Jorgensen, LN; Woo, J
      Anti-ischemic action of estrogen-progestogen continuous combined hormone replacement therapy in postmenopausal women with established angina pectoris: A randomized, placebo-controlled, double-blind, parallel-group trial

      JOURNAL OF CARDIOVASCULAR PHARMACOLOGY
    93. Limprasert, P; Saechan, V; Ruangdaraganon, N; Sura, T; Vasiknanote, P; Jaruratanasirikul, S; Brown, WT
      Haplotype analysis at the FRAXA locus in Thai subjects

      AMERICAN JOURNAL OF MEDICAL GENETICS
    94. Irwin, SA; Patel, B; Idupulapati, M; Harris, JB; Crisostomo, RA; Larsen, BP; Kooy, F; Willems, PJ; Cras, P; Kozlowski, PB; Swain, RA; Weiler, IJ; Greenough, WT
      Abnormal dendritic spine characteristics in the temporal and visual cortices of patients with fragile-X syndrome: A quantitative examination

      AMERICAN JOURNAL OF MEDICAL GENETICS
    95. McConkie-Rosell, A; Spiridigliozzi, GA; Sullivan, JA; Dawson, DV; Lachiewicz, AM
      Longitudinal study of the carrier testing process for fragile X syndrome: Perceptions and coping

      AMERICAN JOURNAL OF MEDICAL GENETICS
    96. Maat-Kievit, A; Helderman-van den Enden, P; Losekoot, M; de Knijff, P; Belfroid, R; Vegter-van der Vlis, M; Roos, R; Breuning, M
      Using a roster and haplotyping is useful in risk assessment for persons with intermediate and reduced penetrance alleles in Huntington disease

      AMERICAN JOURNAL OF MEDICAL GENETICS
    97. Johnston, C; Eliez, S; Dyer-Friedman, J; Hessl, D; Glaser, B; Blasey, C; Taylor, A; Reiss, A
      Neurobehavioral phenotype in carriers of the fragile X premutation

      AMERICAN JOURNAL OF MEDICAL GENETICS
    98. Mazzocco, MMM; Kelley, RI
      Preliminary evidence for a cognitive phenotype in Barth syndrome

      AMERICAN JOURNAL OF MEDICAL GENETICS
    99. Musunuru, K; Darnell, RB
      Paraneoplastic neurologic disease antigens: RNA-binding proteins and signaling proteins in neuronal degeneration

      ANNUAL REVIEW OF NEUROSCIENCE
    100. O'Rourke, RA
      Optimal medical management of patients with chronic ischemic heart disease

      CURRENT PROBLEMS IN CARDIOLOGY


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 05/06/20 alle ore 22:00:32