The hypothalamus and neuropsychiatric disorders: psychiatry meets microscopy
暂无分享,去创建一个
[1] K. Schiltz,et al. Glucose homeostasis in major depression and schizophrenia: a comparison among drug-naïve first-episode patients , 2019, European Archives of Psychiatry and Clinical Neuroscience.
[2] B. Bogerts,et al. Postmortem studies indicate altered cell chemical composition of the suprachiasmatic nucleus in mood disorders , 2018, European Archives of Psychiatry and Clinical Neuroscience.
[3] E. Seifritz,et al. Anterior cingulate volume predicts response to psychotherapy and functional connectivity with the inferior parietal cortex in major depressive disorder , 2018, European Neuropsychopharmacology.
[4] Jinhui Wang,et al. Altered Volume and Functional Connectivity of the Habenula in Schizophrenia , 2017, Front. Hum. Neurosci..
[5] A. Cleare,et al. Hypothalamic-pituitary-adrenal (HPA) axis functioning as predictor of antidepressant response–Meta-analysis , 2017, Neuroscience & Biobehavioral Reviews.
[6] C. McClung,et al. Circadian Rhythm Disturbances in Mood Disorders: Insights into the Role of the Suprachiasmatic Nucleus , 2017, Neural plasticity.
[7] S. Nakagawa,et al. Neural basis of major depressive disorder: Beyond monoamine hypothesis , 2017, Psychiatry and clinical neurosciences.
[8] R. de Oliveira-Souza,et al. The hypothalamus at the crossroads of psychopathology and neurosurgery. , 2017, Neurosurgical focus.
[9] Ji-Hong Liu,et al. An astroglial basis of major depressive disorder? An overview , 2017, Glia.
[10] B. Bogerts,et al. Insulin-regulated aminopeptidase immunoreactivity is abundantly present in human hypothalamus and posterior pituitary gland, with reduced expression in paraventricular and suprachiasmatic neurons in chronic schizophrenia , 2017, European Archives of Psychiatry and Clinical Neuroscience.
[11] D. Swaab,et al. Increased glutamic acid decarboxylase expression in the hypothalamic suprachiasmatic nucleus in depression , 2017, Brain Structure and Function.
[12] J. Ribeiro,et al. Depression and psychodynamic psychotherapy , 2017, Revista brasileira de psiquiatria.
[13] S. Bouret. Development of Hypothalamic Circuits That Control Food Intake and Energy Balance , 2017 .
[14] Yuanyuan Xie,et al. Development of the hypothalamus: conservation, modification and innovation , 2017, Development.
[15] D. Swaab,et al. Sexually Dimorphic Changes of Hypocretin (Orexin) in Depression , 2017, EBioMedicine.
[16] J. Remes,et al. Long‐term antipsychotic use and brain changes in schizophrenia – a systematic review and meta‐analysis , 2017, Human psychopharmacology.
[17] Z. Jankowski,et al. Microglia in the dorsal raphe nucleus plays a potential role in both suicide facilitation and prevention in affective disorders , 2017, European Archives of Psychiatry and Clinical Neuroscience.
[18] R. Cui,et al. The Role of Neural Plasticity in Depression: From Hippocampus to Prefrontal Cortex , 2017, Neural plasticity.
[19] P. Falkai,et al. News from the graveyard: Neuropathological research on schizophrenia is alive and productive , 2016, Schizophrenia Research.
[20] J. Savitz,et al. Neuropathology of mood disorders: do we see the stigmata of inflammation? , 2016, Translational psychiatry.
[21] C. Sommer,et al. Reduced oxytocin receptor gene expression and binding sites in different brain regions in schizophrenia: A post-mortem study , 2016, Schizophrenia Research.
[22] Y. Kakinuma,et al. Loss of dopaminergic neurons occurs in the ventral tegmental area and hypothalamus of rats following chronic stress: Possible pathogenetic loci for depression involved in Parkinson's disease , 2016, Neuroscience Research.
[23] M. Berger,et al. Cortisol awakening response in patients with psychosis: Systematic review and meta-analysis , 2016, Neuroscience & Biobehavioral Reviews.
[24] T. Schneider-Axmann,et al. Decreased Oligodendrocyte and Neuron Number in Anterior Hippocampal Areas and the Entire Hippocampus in Schizophrenia: A Stereological Postmortem Study. , 2016, Schizophrenia bulletin.
[25] P Hagmann,et al. Impaired fornix–hippocampus integrity is linked to peripheral glutathione peroxidase in early psychosis , 2016, Translational Psychiatry.
[26] P. Xie,et al. Hypothalamic Proteomic Analysis Reveals Dysregulation of Glutamate Balance and Energy Metabolism in a Mouse Model of Chronic Mild Stress-Induced Depression , 2016, Neurochemical Research.
[27] N. Parizad,et al. The Relationship Between Depression and Metabolic Syndrome: Systematic Review and Meta-Analysis Study , 2016, Iranian Red Crescent medical journal.
[28] J. Lieberman,et al. Association of orexin receptor polymorphisms with antipsychotic-induced weight gain , 2016, The world journal of biological psychiatry : the official journal of the World Federation of Societies of Biological Psychiatry.
[29] S. Ogawa,et al. Reproductive Neuroendocrine Pathways of Social Behavior , 2016, Front. Endocrinol..
[30] A. Jaggi,et al. An Integrative Review on Role and Mechanisms of Ghrelin in Stress, Anxiety and Depression. , 2016, Current drug targets.
[31] T. Horvath,et al. Metabolism and Mental Illness. , 2016, Trends in molecular medicine.
[32] S. Heringa,et al. Sex hormones and oxytocin augmentation strategies in schizophrenia: A quantitative review , 2015, Schizophrenia Research.
[33] C. H. Summers,et al. Evidence for the role of corticotropin-releasing factor in major depressive disorder , 2015, Neuroscience & Biobehavioral Reviews.
[34] H. Zhao,et al. Early life adversity induced third ventricular enlargement in young adult male patients suffered from major depressive disorder: a study of brain morphology. , 2015, Folia morphologica.
[35] J. Irazusta,et al. Plasma peptidases as prognostic biomarkers in patients with first-episode psychosis , 2015, Psychiatry Research.
[36] P. Andrews,et al. Is serotonin an upper or a downer? The evolution of the serotonergic system and its role in depression and the antidepressant response , 2015, Neuroscience & Biobehavioral Reviews.
[37] B. Bogerts,et al. Glial cells as key players in schizophrenia pathology: recent insights and concepts of therapy , 2015, Schizophrenia Research.
[38] C. Hölscher,et al. Increased number of orexin/hypocretin neurons with high and prolonged external stress-induced depression , 2014, Behavioural Brain Research.
[39] D. Atkinson,et al. Schizophrenia: overview and treatment options. , 2014, P & T : a peer-reviewed journal for formulary management.
[40] A. Bao,et al. Nitric oxide synthase and nitric oxide alterations in chronically stressed rats: A model for nitric oxide in major depressive disorder , 2014, Psychoneuroendocrinology.
[41] E. Drews,et al. Enkephalin knockout male mice are resistant to chronic mild stress , 2014, Genes, brain, and behavior.
[42] R. Rajkumar. Prolactin and Psychopathology in Schizophrenia: A Literature Review and Reappraisal , 2014, Schizophrenia research and treatment.
[43] B. Bogerts,et al. Volumetric analysis of the hypothalamus, amygdala and hippocampus in non-suicidal and suicidal mood disorder patients--a post-mortem study. , 2013, CNS & neurological disorders drug targets.
[44] G. Rajkowska,et al. Astrocyte pathology in major depressive disorder: insights from human postmortem brain tissue. , 2013, Current drug targets.
[45] R. Kahn,et al. Brain volumes in schizophrenia: a meta-analysis in over 18 000 subjects. , 2013, Schizophrenia bulletin.
[46] P. Guest,et al. Metabolic, hormonal and stress-related molecular changes in post-mortem pituitary glands from schizophrenia subjects , 2013, The world journal of biological psychiatry : the official journal of the World Federation of Societies of Biological Psychiatry.
[47] J. Wiltfang,et al. Structural brain alterations associated with schizophrenia preceded by conduct disorder: a common and distinct subtype of schizophrenia? , 2013, Schizophrenia bulletin.
[48] B. Bogerts,et al. Some notes on insulin-regulated aminopeptidase in depression. , 2013, The international journal of neuropsychopharmacology.
[49] B. Bogerts,et al. Increased nuclear Olig1-expression in the pregenual anterior cingulate white matter of patients with major depression: a regenerative attempt to compensate oligodendrocyte loss? , 2013, Journal of psychiatric research.
[50] M. Olive,et al. Neuropeptide systems and schizophrenia. , 2013, CNS & neurological disorders drug targets.
[51] D. Swaab,et al. Reduced GAD(65/67) immunoreactivity in the hypothalamic paraventricular nucleus in depression: a postmortem study. , 2013, Journal of affective disorders.
[52] F. Scheer,et al. Alterations of melatonin receptors MT1 and MT2 in the hypothalamic suprachiasmatic nucleus during depression. , 2013, Journal of affective disorders.
[53] Y. Michotte,et al. Antidepressant-like effects of oxytocin in mice are dependent on the presence of insulin-regulated aminopeptidase. , 2013, The international journal of neuropsychopharmacology.
[54] V. Mondelli,et al. A systematic review of the activity of the hypothalamic–pituitary–adrenal axis in first episode psychosis , 2013, Psychoneuroendocrinology.
[55] D. Swaab,et al. Unaltered histaminergic system in depression: a postmortem study. , 2013, Journal of affective disorders.
[56] Y. Goumon,et al. Endogenous morphine and its metabolites in mammals: History, synthesis, localization and perspectives , 2013, Neuroscience.
[57] R. Toni,et al. Functional Anatomy of the Hypothalamus and Pituitary , 2013 .
[58] A. Beltramello,et al. Enlarged hypothalamic volumes in schizophrenia , 2012, Psychiatry Research: Neuroimaging.
[59] S. Stahl,et al. Glutamate Neurocircuitry: Theoretical Underpinnings in Schizophrenia , 2012, Front. Pharmacol..
[60] B. Bogerts,et al. Reduced density of hypothalamic VGF-immunoreactive neurons in schizophrenia: a potential link to impaired growth factor signaling and energy homeostasis , 2012, European Archives of Psychiatry and Clinical Neuroscience.
[61] R. Murray,et al. Hypothalamic–pituitary–adrenal axis and clinical symptoms in first-episode psychosis , 2012, Psychoneuroendocrinology.
[62] Vaughan J. Carr,et al. Systematic meta-review and quality assessment of the structural brain alterations in schizophrenia , 2012, Neuroscience & Biobehavioral Reviews.
[63] M. Azevedo,et al. Revisiting Thyroid Hormones in Schizophrenia , 2012, Journal of thyroid research.
[64] R. Kahn,et al. Hypothalamus and pituitary volume in schizophrenia: a structural MRI study. , 2012, The international journal of neuropsychopharmacology.
[65] B. Bogerts,et al. A postmortem assessment of mammillary body volume, neuronal number and densities, and fornix volume in subjects with mood disorders , 2012, European Archives of Psychiatry and Clinical Neuroscience.
[66] R. Turner,et al. Structural studies of the hypothalamus and its nuclei in mood disorders , 2012, Psychiatry Research: Neuroimaging.
[67] M. Banasr,et al. Cell atrophy and loss in depression: reversal by antidepressant treatment. , 2011, Current opinion in cell biology.
[68] P. Falkai,et al. Schizophrenia as a disorder of disconnectivity , 2011, European Archives of Psychiatry and Clinical Neuroscience.
[69] Michael D. Spain,et al. Altered levels of circulating insulin and other neuroendocrine hormones associated with the onset of schizophrenia , 2011, Psychoneuroendocrinology.
[70] V. Steen,et al. Olanzapine-Induced Hyperphagia and Weight Gain Associate with Orexigenic Hypothalamic Neuropeptide Signaling without Concomitant AMPK Phosphorylation , 2011, PloS one.
[71] A. Bao,et al. Corticotropin-Releasing Hormone, Glutamate, and γ-Aminobutyric Acid in Depression , 2011, The Neuroscientist : a review journal bringing neurobiology, neurology and psychiatry.
[72] T. Dinan,et al. A systematic review of hypothalamic–pituitary–adrenal axis function in schizophrenia: implications for mortality , 2010, Journal of psychopharmacology.
[73] B. Bogerts,et al. The Hypothalamus in Schizophrenia Research: No Longer a Wallflower Existence~!2009-12-09~!2010-02-07~!2010-08-09~! , 2010 .
[74] Edward T Bullmore,et al. Morphometric brain abnormalities in schizophrenia in a population-based sample: relationship to duration of illness. , 2010, Schizophrenia bulletin.
[75] C. Hendrie,et al. Depression as an evolutionary adaptation: anatomical organisation around the third ventricle. , 2010, Medical hypotheses.
[76] A. Sawa,et al. Review of pathological hallmarks of schizophrenia: comparison of genetic models with patients and nongenetic models. , 2010, Schizophrenia bulletin.
[77] B. Bogerts,et al. Schizophrenia, sleep disturbances and the suprachiasmatic nucleus: reduced nitric oxide synthase may matter. , 2010, Medical hypotheses.
[78] G. Yadid,et al. The β-Endorphin Role in Stress-Related Psychiatric Disorders , 2009 .
[79] R. Lanius,et al. The role of β-endorphin in the pathophysiology of major depression , 2009, Neuropeptides.
[80] J. Bundzikova,et al. Different antipsychotics elicit different effects on magnocellular oxytocinergic and vasopressinergic neurons as revealed by Fos immunohistochemistry , 2009, Journal of neuroscience research.
[81] B. Bogerts,et al. Reduced neuronal expression of insulin-degrading enzyme in the dorsolateral prefrontal cortex of patients with haloperidol-treated, chronic schizophrenia. , 2009, Journal of psychiatric research.
[82] Jordan Grafman,et al. The functional neuroanatomy of depression: Distinct roles for ventromedial and dorsolateral prefrontal cortex , 2009, Behavioural Brain Research.
[83] B. Bogerts,et al. Evidence for structural abnormalities of the human habenular complex in affective disorders but not in schizophrenia , 2009, Psychological Medicine.
[84] B. Bogerts,et al. Cathepsin K generates enkephalin from β-endorphin: A new mechanism with possible relevance for schizophrenia , 2009, Neurochemistry International.
[85] Z. Chemali. Long-Term Antipsychotic Use in Alzheimer Disease , 2009 .
[86] T. Schneider-Axmann,et al. Stereologic investigation of the posterior part of the hippocampus in schizophrenia , 2009, Acta Neuropathologica.
[87] C. Schwarzer,et al. Prodynorphin-Derived Peptides Are Critical Modulators of Anxiety and Regulate Neurochemistry and Corticosterone , 2009, Neuropsychopharmacology.
[88] B. Bogerts,et al. The volumes of the fornix in schizophrenia and affective disorders: A post-mortem study , 2008, Psychiatry Research: Neuroimaging.
[89] E. Bullmore,et al. The anatomy of first-episode and chronic schizophrenia: an anatomical likelihood estimation meta-analysis. , 2008, The American journal of psychiatry.
[90] D F Swaab,et al. Gene expression analysis in the human hypothalamus in depression by laser microdissection and real-time PCR: the presence of multiple receptor imbalances , 2008, Molecular Psychiatry.
[91] E. Frank,et al. The vasopressin system--from antidiuresis to psychopathology. , 2008, European journal of pharmacology.
[92] B. Bogerts,et al. Beacon-like/ubiquitin-5-like immunoreactivity is highly expressed in human hypothalamus and increased in haloperidol-treated schizophrenics and a rat model of schizophrenia , 2008, Psychoneuroendocrinology.
[93] Hilleke E. Hulshoff Pol,et al. Hypothalamus volume in twin pairs discordant for schizophrenia , 2008, European Neuropsychopharmacology.
[94] D. Marazziti,et al. The role of oxytocin in neuropsychiatric disorders. , 2008, Current medicinal chemistry.
[95] M. Engelmann,et al. Neuronal nitric oxide synthase gene inactivation reduces the expression of vasopressin in the hypothalamic paraventricular nucleus and of catecholamine biosynthetic enzymes in the adrenal gland of the mouse , 2008, Stress.
[96] S. Keller,et al. Vasopressin is a physiological substrate for the insulin-regulated aminopeptidase IRAP. , 2007, American journal of physiology. Endocrinology and metabolism.
[97] A. Giusti-Paiva,et al. Central nitric oxide blocks vasopressin, oxytocin and atrial natriuretic peptide release and antidiuretic and natriuretic responses induced by central angiotensin II in conscious rats , 2007, Experimental physiology.
[98] N. Uranova,et al. The role of oligodendrocyte pathology in schizophrenia. , 2007, The international journal of neuropsychopharmacology.
[99] N. Makris,et al. Hypothalamic Abnormalities in Schizophrenia: Sex Effects and Genetic Vulnerability , 2007, Biological Psychiatry.
[100] B. Bogerts,et al. Cathepsin K and schizophrenia , 2007, Synapse.
[101] D. Swaab,et al. Hypothalamic oxytocin mRNA expression and melancholic depression , 2007, Molecular Psychiatry.
[102] B. Bogerts,et al. Strongly Reduced Number of Parvalbumin‐Immunoreactive Projection Neurons in the Mammillary Bodies in Schizophrenia , 2007, Annals of the New York Academy of Sciences.
[103] D. Swaab,et al. Increased Arginine Vasopressin mRNA Expression in the Human Hypothalamus in Depression: A Preliminary Report , 2006, Biological Psychiatry.
[104] M. Keshavan,et al. Pituitary Volume in Treatment-Naïve Pediatric Major Depressive Disorder , 2006, Biological Psychiatry.
[105] K. Elliott,et al. Association of Genetic Variation Within UBL5 with Phenotypes of Metabolic Syndrome , 2006, Human Biology: The Official Publication of the American Association of Anthropological Genetics.
[106] Carl-Fredrik Westin,et al. Fornix Integrity and Hippocampal Volume in Male Schizophrenic Patients , 2006, Biological Psychiatry.
[107] K. Lesch,et al. Neural stem cell proliferation is decreased in schizophrenia, but not in depression , 2006, Molecular Psychiatry.
[108] D. Swaab,et al. Absence of a Difference in the Neurosecretory Activity of Supraoptic Nucleus Vasopressin Neurons of Neuroleptic-Treated Schizophrenic Patients , 2006, Neuroendocrinology.
[109] L. Caregaro,et al. Disorders of eating behavior: Correlation between hypothalamo-pituitary–thyroid function and psychopathological aspects , 2006, Psychoneuroendocrinology.
[110] Bernhard Bogerts,et al. The many faces of nitric oxide in schizophrenia. A review , 2005, Schizophrenia Research.
[111] B. Bogerts,et al. Hypothalamic nitric oxide synthase in affective disorder: focus on the suprachiasmatic nucleus. , 2005, Cellular and molecular biology.
[112] B. Bogerts,et al. Volume deficits of subcortical nuclei in mood disorders , 2005, European Archives of Psychiatry and Clinical Neuroscience.
[113] P. Kelly,et al. Selective Neuron Loss in the Paraventricular Nucleus of Hypothalamus in Patients Suffering from Major Depression and Bipolar Disorder , 2005, Journal of neuropathology and experimental neurology.
[114] G. Mastorakos,et al. The Hypothalamic-Pituitary-Adrenal Axis in the Neuroendocrine Regulation of Food Intake and Obesity: The Role of Corticotropin Releasing Hormone , 2004, Nutritional neuroscience.
[115] B. Bogerts,et al. Further Immunohistochemical Evidence for Impaired NO Signaling in the Hypothalamus of Depressed Patients , 2002, Annals of the New York Academy of Sciences.
[116] E. Young,et al. The hypothalamic-pituitary-gonadal axis in mood disorders. , 2002, Endocrinology and metabolism clinics of North America.
[117] D. Swaab,et al. Alterations in arginine vasopressin neurons in the suprachiasmatic nucleus in depression. , 2001, Archives of general psychiatry.
[118] L. Selemon,et al. Reductions in neuronal and glial density characterize the dorsolateral prefrontal cortex in bipolar disorder , 2001, Biological Psychiatry.
[119] Ron Kikinis,et al. A quantitative MR measure of the fornix in schizophrenia , 2001, Schizophrenia Research.
[120] Paul J. Harrison. Postmortem studies in schizophrenia , 2000, Dialogues in clinical neuroscience.
[121] B. Bogerts,et al. Low and infrequent expression of nitric oxide synthase/NADPH-diaphorase in neurons of the human supraoptic nucleus: a histochemical study , 2000, Journal of Chemical Neuroanatomy.
[122] T. Sharma,et al. Third ventricle enlargement and developmental delay in first-episode psychosis: preliminary findings. , 2000, The British journal of psychiatry : the journal of mental science.
[123] Janine McMillan,et al. Beacon: A novel gene involved in the regulation of energy balance , 2000, Regulatory Peptides.
[124] D. Swaab,et al. Brain alterations in depression , 2000, Acta Neuropsychiatrica.
[125] A. Altamura,et al. HPA axis and cytokines dysregulation in schizophrenia: potential implications for the antipsychotic treatment , 1999, European Neuropsychopharmacology.
[126] T. Crow,et al. Fiber content of the fornix in schizophrenia: lack of evidence for a primary limbic encephalopathy. , 1999, The American journal of psychiatry.
[127] P S Kalra,et al. Interacting appetite-regulating pathways in the hypothalamic regulation of body weight. , 1999, Endocrine reviews.
[128] P. Goldman-Rakic,et al. The reduced neuropil hypothesis: a circuit based model of schizophrenia , 1999, Biological Psychiatry.
[129] B. Bogerts,et al. Expression of Hypothalamic Peptides in Mice Lacking Neuronal Nitric Oxide Synthase: Reduced β-END Immunoreactivity in the Arcuate Nucleus , 1998, Neuroendocrinology.
[130] I. Everall,et al. Mamillary body abnormalities in schizophrenia , 1998, The Lancet.
[131] C. Nemeroff. Structural Brain Alterations in Polysubstance Abusers , 1998 .
[132] P. Goldman-Rakic,et al. Neuronal and glial somal size in the prefrontal cortex: a postmortem morphometric study of schizophrenia and Huntington disease. , 1998, Archives of general psychiatry.
[133] B. Bogerts,et al. Nitric oxide synthase-containing neurons in the human hypothalamus: reduced number of immunoreactive cells in the paraventricular nucleus of depressive patients and schizophrenics , 1998, Neuroscience.
[134] B. Bogerts,et al. Changes in CSF spaces differ in endogenous and neurotic depression. A planimetric CT scan study. , 1997, Journal of affective disorders.
[135] D. Swaab,et al. Increased number of vasopressin- and oxytocin-expressing neurons in the paraventricular nucleus of the hypothalamus in depression. , 1996, Archives of general psychiatry.
[136] D F Swaab,et al. Corticotropin-releasing hormone mRNA levels in the paraventricular nucleus of patients with Alzheimer's disease and depression. , 1995, The American journal of psychiatry.
[137] N. Butters,et al. Magnetic resonance imaging and mood disorders. Localization of white matter and other subcortical abnormalities. , 1995, Archives of general psychiatry.
[138] J. Palacios,et al. In situ hybridization for vasopressin mRNA in the human supraoptic and paraventricular nucleus; quantitative aspects of formalin-fixed paraffin-embedded tissue sections as compared to cryostat sections , 1995, Journal of Neuroscience Methods.
[139] K. A. Kadir,et al. High Prevalence of Thyroid Function Test Abnormalities in Chronic Schizophrenia , 1994, The Australian and New Zealand journal of psychiatry.
[140] D. Swaab,et al. Increased numbers of corticotropin-releasing hormone expressing neurons in the hypothalamic paraventricular nucleus of depressed patients. , 1994, Neuroendocrinology.
[141] P. Emson,et al. Up-regulation of nitric oxide synthase (NOS) gene expression together with NOS activity in the rat hypothalamo-hypophysial system after chronic salt loading: evidence of a neuromodulatory role of nitric oxide in arginine vasopressin and oxytocin secretion. , 1994, Endocrinology.
[142] M. Timsit-Berthier,et al. Apomorphine stimulation of vasopressin- and oxytocin-neurophysins. Evidence for increased oxytocinergic and decreased vasopressinergic function in schizophrenics , 1992, Psychoneuroendocrinology.
[143] N. Kowall,et al. NADPH diaphorase histochemistry of the human hypothalamus , 1991, Neuroscience.
[144] R. Ekman,et al. Reduced concentrations of galanin, arginine vasopressin, neuropeptide Y and peptide YY in the temporal cortex but not in the hypothalamus of brains from schizophrenics , 1991, Acta psychiatrica Scandinavica.
[145] Darrell M. Wilson,et al. Growth hormone response to growth hormone releasing hormone in depression and schizophrenia , 1990, Psychiatry Research.
[146] J. Kleinman,et al. Neurotransmitter amino acids in post-mortem brains of chronic schizophrenic patients , 1987, Psychiatry Research.
[147] H. Emrich,et al. Dopamine and the action of opiates: A reevaluation of the dopamine hypothesis of schizophrenia with special consideration of the role of endogenous opioids in the pathogenesis of schizophrenia , 1985, Biological Psychiatry.
[148] C. Golden,et al. Ventricular enlargement in major depression , 1983, Psychiatry Research.
[149] O. Hornykiewicz,et al. Norepinephrine in chronic paranoid schizophrenia: above-normal levels in limbic forebrain. , 1978, Science.
[150] M. Kedinger,et al. Survival of chick embryonic organs submitted to high hydrostatic pressures. , 1973, Biomedicine / [publiee pour l'A.A.I.C.I.G.].
[151] Kraines Sh. Manic depressive syndrome: a physiologic disease. II. , 1966 .
[152] S. H. Kraines. The physiologic basis of the manic-depressive illness: a theory. , 1957, The American journal of psychiatry.
[153] B. Hechst. Zur Histopathologie der Schizophrenie mit besonderer Berücksichtigung der Ausbreitung des Prozessses , 1931 .
[154] W. K. Simmons,et al. Depression and obesity: evidence of shared biological mechanisms , 2018, Molecular Psychiatry.
[155] A. Riecher-Rössler. Oestrogens, prolactin, hypothalamic-pituitary-gonadal axis, and schizophrenic psychoses. , 2017, The lancet. Psychiatry.
[156] A. Cleare,et al. HPA axis functioning predicts antidepressant response Hypothalamic-pituitary-adrenal ( HPA ) axis functioning as predictor of antidepressant response – meta-analysis , 2017 .
[157] M. Kanehisa,et al. The thyrotropin-releasing hormone test may predict recurrence of clinical depression within ten years after discharge. , 2013, Neuro endocrinology letters.
[158] P. Kreczmański. Neuropathology of schizophrenia : a new vistas , 2009 .
[159] B. Bogerts,et al. Immunological aspects in the neurobiology of suicide: elevated microglial density in schizophrenia and depression is associated with suicide. , 2008, Journal of psychiatric research.
[160] Anneke Alkemade,et al. Hypothalamic thyroid hormone feedback in health and disease. , 2006, Progress in brain research.
[161] B. Bogerts,et al. The diencephalon in schizophrenia: Evidence for reduced thickness of the periventricular grey matter , 2004, European archives of psychiatry and neurological sciences.
[162] THE CHANGES OF HYPOTHALAMIC NUCLEI IN SCHIZOPHRENIA , 2003 .
[163] J. Macher,et al. Disturbances in hypothalamo pituitary adrenal and thyroid axis identify different sleep EEG patterns in major depressed patients. , 2003, Journal of psychiatric research.
[164] B. Bogerts,et al. Fewer beta-endorphin expressing arcuate nucleus neurons and reduced beta-endorphinergic innervation of paraventricular neurons in schizophrenics and patients with depression. , 2002, Cellular and molecular biology.
[165] D. Lewis,et al. Decreased dendritic spine density on prefrontal cortical pyramidal neurons in schizophrenia. , 2000, Archives of general psychiatry.
[166] S. Heckers,et al. Neuropathology of schizophrenia: cortex, thalamus, basal ganglia, and neurotransmitter-specific projection systems. , 1997, Schizophrenia bulletin.
[167] J. K. Mai,et al. Morphometric evaluation of neurophysin-immunoreactivity in the human brain: pronounced inter-individual variability and evidence for altered staining patterns in schizophrenia. , 1993, Journal fur Hirnforschung.
[168] J. Burbach,et al. Increased concentration of alpha- and gamma-endorphin in post mortem hypothalamic tissue of schizophrenic patients. , 1988, Life sciences.
[169] J. Burbach,et al. Increased concentration of α- and γ-endorphin in post mortem hypothalamic tissue of schizophrenic patients , 1988 .
[170] P. Seeburg,et al. The mammalian GnRH gene and its pivotal role in reproduction. , 1987, Recent progress in hormone research.
[171] C. Nemeroff,et al. Somatostatin and Behavior: Preclinical and Clinical Studies , 1987 .
[172] J. Haracz. The dopamine hypothesis: an overview of studies with schizophrenic patients. , 1982, Schizophrenia bulletin.
[173] W. Vale,et al. Regulatory peptides of the hypothalamus. , 1977, Annual review of physiology.
[174] A. Lohman,et al. Structure and fiber connections of the hypothalamus in mammals. , 1974, Progress in brain research.
[175] E. Gerber. [Histopathology of neurosecretory nuclei in different types of schizophrenia]. , 1966, Vestnik Akademii meditsinskikh nauk SSSR.
[176] S. H. Kraines. Manic depressive syndrome: a physiologic disease. , 1966, Diseases of the nervous system.