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Enhanced intestinal 2-deoxy-2-[18F]fluoro-D-glucose uptake under metformin is not fully suppressed by loperamide

, Fiz F, Democrito A, Amaro A, Morbelli S, Piana M, Maggi D, Cilli M, Pfeffer U, Sambuceti G. Metformin temporal and localized effects on gut glucose metabolism assessed using 18F-FDG PET in mice. J Nucl Med 54, 259-266, 2013. McCreight LJ, Bailey CJ, Pearson ER. Metformin and the gastrointestinal tract. Diabetologia 59, 426-435, 2016. Oh JR, Song HC, Chong A, Ha JM, Jeong SY, Min JJ, Bom HS. Impact of medication discontinuation on increased intestinal FDG accumulation in diabetic patients treated with metformin. Am J Roentgenol 195

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Genetic and environmental factors in the etiology of schizophrenia - towards mainstreaming

analysis of differentially methylated genes in schizophrenia, implicating GABA receptor B1 [GABBR1] and protein kinase B [AKT1], 2015. 12. Ripke S., Sanders A.R., Kendler K.S. Genome-wide association study identifies five new schizophrenia loci, 2011. 13. Kirov G., Pocklington A.J., Holmans P., Ivanov D., Ikeda M. De novo CNV analysis implicates specific abnormalities of postsynaptic signalling complexes in the pathogenesis of schizophrenia, 2012. 14. Gulsuner S., Walsh T., Watts A.C., Lee M.K., Thornton A.M. Spatial and Temporal Mapping of De Novo

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Hyper-coherence and increased energy of gamma oscillations in patient with first onset schizophrenia and cerebral white matter damage

disorder and schizophrenia. Journal of Psychiatric Research, 2013: 47(12), 1893-1901. 17. Stoica P., Moses R. Spectral Analysis of Signals. Upper Saddle River, NJ: Prentice Hall, 2005 18. Mallat S. G., Zhang Z. Matching Pursuit with time-frequency dictionaries. IEEE Transactions On Signal Processing,1993; 41(12), 3397-3415. 19. Franaszczuk P. J, Bergey G. K., Durka P. J., Eisenberg H. M. Time-frequency analysis using the matching pursuit algorithm to seizures originating from mesial temporal lobe. Electroencephalography and Clinical Neurophysiology

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Implantation and pregnancy outcome of Sprague-Dawley rats exposed to pirimiphos-methyl

polymorphisms, haplotypes, and enzyme activity in Latino mothers and newborns. Environ Health Perspect 114, 985–999, 2006. Iranloye B, Oyeusi K. Alada A. Effect of aqueous extract of Phyllanthus amarus leaf on implantation and pregnancy in rats. Niger J Physiol Sci 25, 63–66, 2010. Iranloye BO, Oyesola TO. The organophosphate - pirimiphos-methyl alters estrous cycle and hormone concentrations in female Sprague-Dawley rats. World Journal of Pharmaceutical and Life Sciences 4, 207–211, 2018. Koch D, Lu C, Fisker-Andersen J, Jolley L, Fenske R. Temporal

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Modern faces of hysteria, or some of the dissociative disorders

and brain PET findings in 3 cases of dissociative amnesia: disproportionate retrograde deficit and posterior middle temporal gyrus hypometabolism. Neurophysiol Clin., 2014; 44(4): 355-362. 14. Jha M. i Sharma V. Dissociative Fugue Disorder: Identification and Psychological Intervention. Psychol Stud, 2015; 60 (1): 17-24. 15. Igwe M.N. Dissociative fugue symptoms in a 28-year-old male Nigerian medical student: a case report. J Med Case Rep., 2013; 7: 143. 16. Tomalski R. Aleksytymia i dysocjacja. Psychoterapia, 2008, 2(145): 35-43. 17

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The prepulse inhibition deficit appearance is largely independent on the circadian cycle, body weight, and the gender of vasopressin deficient Brattleboro rat

, Jonsson S. Reduced concentrations of galanin, arginine vasopressin, neuropeptide Y and peptide YY in the temporal cortex but not in the hypothalamus of brains from schizophrenics. Acta Psychiatr Scand 83, 273–277, 1991. Geyer MA, Krebs-Thomson K, Braff DL, Swerdlow NR. Pharmacological studies of prepulse inhibition models of sensorimotor gating deficits in schizophrenia: a decade in review. Psychopharmacology (Berl) 156, 117–154, 2001. Goldman MB, Robertson GL, Luchins DJ, Hedeker D, Pandey GN. Psychotic exacerbations and enhanced vasopressin secretion in

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Clinical Manifestations of Self-disorders in Schizophrenia Spectrum Conditions

: 79–83. 55. Nordgaard J., Revsbech R., Henriksen M.G. Self-disorders, neurocognition, and rationality in schizophrenia: A preliminary study. Psychopathology, 2015; 48: 310–316. 56. Nordgaard J., Handest P., Vollmer-Larsen A., Sæbye D., Thejlade Pedersen J., Parnas J. Temporal persistence of anomalous self-experience: A 5 years follow-up. Schizophr Res, 2017; 179: 36-40. 57. Maj M. The critique of DSM-IV operational criteria for schizophrenia. Brit J Psychiatry, 1998; 172: 458–460.

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Towards integrating phenomenology and neurocognition: Possible neurocognitive correlates of basic self-disturbance in schizophrenia

;30:14-21. 68 Blakemore S-J, Smith J, Steel R, Johnstone EC, Frith CD: The perception of self-produced sensory stimuli in patients with auditory hallucinations and passivity experiences: Evidence for a breakdown in self-monitoring. Psychological Medicine 2000;30:1131-1139. 69 Ford JM, Mathalon DH, Whitfield S, Faustman WO, Roth WT: Reduced communication between frontal and temporal lobes during talking in schizophrenia. Biological psychiatry 2002;51:485-492. 70 Ford JM, Gray M, Faustman WO, Heinks TH, Mathalon DH: Reduced gamma-band coherence to distorted feedback

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Obstetric complications in women with schizophrenia

. Schizophr Res. 2001; 47: 167–175. 26. Castle DJ, Mc Garth J, Kulakarni J. Women and schizophrenia: an epidemiological perspective. New York; wyd. Cambridge University Press: 2000. 27. Takahashi S, Matsuura M, Tanabe E, Yara K, Nonaka K, Fukura Y et al. Age at onset of schizophrenia: Gender differences and influence of temporal socioeconomic change. Psychiatry Clin Neurosci 2001; 52:153-6. 28. Jaracz K, Górna K, Kiejda J, Rybakowski J, Prospektywna ocena wczesnego przebiegu schizofrenii u kobiet i mężczyzn po pierwszej hospitalizacji psychiatrycznej

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Uncommon psychopathological syndromes in psychiatry

, 20:283–284. 83. Kearns A., Cotard’s syndrome in a mentally handicapped man. Br. J. Psychiatry, 1987, 150:112–114. 84. Campbell S., Volow M.R., Cavenar J.O., Cotard’s syndrome and the psychiatric manifestations of typhoid fever, Am J Psychiatry, 1981, 138:1377–1378. 85. Drake M.E.J., Cotard’s syndrome and temporal lobe epilepsy, Psychiatry J. Univ Ott, 1988, 13:36–39. 86. Hu W.T., Diesing T.S., Meissner I., Cotard’s syndrome in a patient with superior sagittal sinus thrombosis [abstract], Biol Psychiatry, 2006, 56:263S. 87. Bathia M

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