Biblioteca Humberto Rosselli Quijano
Dialogues in Clinical Neuroscience . Año 2007 Vol. 9 - No. 2Mención de fecha: Junio Fecha de aparición: 12/09/2022 |
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Año 2007 Vol. 9 - No. 2 - Junio - Dialogues in Clinical Neuroscience [texto impreso] / Les Laboratoires Servier ((1999-); Francia), Autor . - 2022 . - pp. 105-226 : Cuadros, gráficas ; 27 cm. ISSN : 1294-8322 Idioma : Inglés (eng) Idioma original : Inglés (eng) |
Ejemplares (1)
Código de barras | Signatura | Tipo de medio | Ubicación | Sección | Estado |
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101700 | Dialogues in Clínical Neuroscience | Publicaciones seriadas | Biblioteca Instituto Colombiano del Sistema Nervioso | Hemeroteca | Disponible |
Artículos
Añadir el resultado a su cestaPsychiatric manifestations of neurologic disease: where are we headed? / Constantine G. Lyketsos en Dialogues in Clinical Neuroscience, Año 2007 Vol. 9 - No. 2 (Junio)
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Título : Psychiatric manifestations of neurologic disease: where are we headed? Tipo de documento: texto impreso Autores: Constantine G. Lyketsos, Autor ; Nicholas Kozauer, Autor ; Peter V. Rabin, Autor Fecha de publicación: 2022 Artículo en la página: pp. 111–124 Idioma : Inglés (eng) Idioma original : Inglés (eng) Palabras clave: Enfermedad cerebral, Depresión, Psicosis, Lesión cerebral traumática, Enfermedad de Alzheimer, Enfermedad de Parkinson, Accidente cerebrovascular Resumen: Neuropsychiatry represents a field of medicine situated at the crossroads of neurology and psychiatry, and deals with the interface of behavioral phenomena driven by brain dysfunction. Psychiatric symptoms are highly prevalent in these conditions, are a major source of disability and diminished quality of life, and potentially represent the target of treatment interventions that stand to significantly decrease the suffering they generate. Link: ./index.php?lvl=notice_display&id=28665
in Dialogues in Clinical Neuroscience > Año 2007 Vol. 9 - No. 2 (Junio) . - pp. 111–124[artículo] Psychiatric manifestations of neurologic disease: where are we headed? [texto impreso] / Constantine G. Lyketsos, Autor ; Nicholas Kozauer, Autor ; Peter V. Rabin, Autor . - 2022 . - pp. 111–124.
Idioma : Inglés (eng) Idioma original : Inglés (eng)
in Dialogues in Clinical Neuroscience > Año 2007 Vol. 9 - No. 2 (Junio) . - pp. 111–124
Palabras clave: Enfermedad cerebral, Depresión, Psicosis, Lesión cerebral traumática, Enfermedad de Alzheimer, Enfermedad de Parkinson, Accidente cerebrovascular Resumen: Neuropsychiatry represents a field of medicine situated at the crossroads of neurology and psychiatry, and deals with the interface of behavioral phenomena driven by brain dysfunction. Psychiatric symptoms are highly prevalent in these conditions, are a major source of disability and diminished quality of life, and potentially represent the target of treatment interventions that stand to significantly decrease the suffering they generate. Link: ./index.php?lvl=notice_display&id=28665 Neuropsychiatric manifestations of depression in multiple sclerosis / Michele L. Pucak en Dialogues in Clinical Neuroscience, Año 2007 Vol. 9 - No. 2 (Junio)
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Título : Neuropsychiatric manifestations of depression in multiple sclerosis : neuroinflammatory, neuroendocrine, and neurotrophic mechanisms in the pathogenesis of immune mediated depression Tipo de documento: texto impreso Autores: Michele L. Pucak, Autor ; Katherine A. L. Carroll, Autor ; Douglas A. Kerr, Autor Fecha de publicación: 2022 Artículo en la página: pp. 125–139 Idioma : Inglés (eng) Idioma original : Inglés (eng) Palabras clave: Citocina, Eje hipotálamo-pituitario-suprarrenal, Interferón, Tratamiento, Neuroimagen, Inflamación Resumen: Evidence suggests that depression in multiple sclerosis (MS) is largely biologically mediated by some of the same processes involved in the immunopathogenesis of this neurologic disease. In particular, the increase in proinflammatory cytokines, activation of the hypothalamic-pituitary-adrenal (HPA) axis, and reduction in neurotrophic factors that occur in MS may each account for the increased rate of depression seen in MS. Link: ./index.php?lvl=notice_display&id=28666
in Dialogues in Clinical Neuroscience > Año 2007 Vol. 9 - No. 2 (Junio) . - pp. 125–139[artículo] Neuropsychiatric manifestations of depression in multiple sclerosis : neuroinflammatory, neuroendocrine, and neurotrophic mechanisms in the pathogenesis of immune mediated depression [texto impreso] / Michele L. Pucak, Autor ; Katherine A. L. Carroll, Autor ; Douglas A. Kerr, Autor . - 2022 . - pp. 125–139.
Idioma : Inglés (eng) Idioma original : Inglés (eng)
in Dialogues in Clinical Neuroscience > Año 2007 Vol. 9 - No. 2 (Junio) . - pp. 125–139
Palabras clave: Citocina, Eje hipotálamo-pituitario-suprarrenal, Interferón, Tratamiento, Neuroimagen, Inflamación Resumen: Evidence suggests that depression in multiple sclerosis (MS) is largely biologically mediated by some of the same processes involved in the immunopathogenesis of this neurologic disease. In particular, the increase in proinflammatory cytokines, activation of the hypothalamic-pituitary-adrenal (HPA) axis, and reduction in neurotrophic factors that occur in MS may each account for the increased rate of depression seen in MS. Link: ./index.php?lvl=notice_display&id=28666 Frontal subcortical circuitry and behavior / Raphael M. Bonelli en Dialogues in Clinical Neuroscience, Año 2007 Vol. 9 - No. 2 (Junio)
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Título : Frontal subcortical circuitry and behavior Tipo de documento: texto impreso Autores: Raphael M. Bonelli, Autor ; Jeffrey L. Cummings, Autor Fecha de publicación: 2022 Artículo en la página: pp. 141–151. Idioma : Inglés (eng) Idioma original : Inglés (eng) Palabras clave: Circuito frontal-subcortical, Corteza prefrontal dorsolateral, Cingulado anterior, Corteza orbitofrontal, Síndrome disejecutivo Resumen: The neuropsychiatric manifestations of neurodegenerative diseases are closely linked to neurocircuitry defects. Frontal-subcortical circuits, in particular, are effector mechanisms that allow the organism to act on its environment In this paper, we present the three main frontal-subcortical circuits: the dorsolateral prefrontal circuit allows the organization of information to facilitate a response; the anterior cingulate circuit is required for motivated behavior; Link: ./index.php?lvl=notice_display&id=28667
in Dialogues in Clinical Neuroscience > Año 2007 Vol. 9 - No. 2 (Junio) . - pp. 141–151.[artículo] Frontal subcortical circuitry and behavior [texto impreso] / Raphael M. Bonelli, Autor ; Jeffrey L. Cummings, Autor . - 2022 . - pp. 141–151.
Idioma : Inglés (eng) Idioma original : Inglés (eng)
in Dialogues in Clinical Neuroscience > Año 2007 Vol. 9 - No. 2 (Junio) . - pp. 141–151.
Palabras clave: Circuito frontal-subcortical, Corteza prefrontal dorsolateral, Cingulado anterior, Corteza orbitofrontal, Síndrome disejecutivo Resumen: The neuropsychiatric manifestations of neurodegenerative diseases are closely linked to neurocircuitry defects. Frontal-subcortical circuits, in particular, are effector mechanisms that allow the organism to act on its environment In this paper, we present the three main frontal-subcortical circuits: the dorsolateral prefrontal circuit allows the organization of information to facilitate a response; the anterior cingulate circuit is required for motivated behavior; Link: ./index.php?lvl=notice_display&id=28667 Frontotemporal dementia to Alzheimer's disease / Maria Caterina Silveri en Dialogues in Clinical Neuroscience, Año 2007 Vol. 9 - No. 2 (Junio)
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Título : Frontotemporal dementia to Alzheimer's disease Tipo de documento: texto impreso Autores: Maria Caterina Silveri, Autor Fecha de publicación: 2022 Artículo en la página: pp. 153–160 Idioma : Inglés (eng) Idioma original : Inglés (eng) Palabras clave: Demencia frontotemporal, Enfermedad de Alzheimer, Trastorno del comportamiento, Teoría de la mente, Cognición social Resumen: Behavioral manifestations may dominate the clinical picture of the frontal variant of frontotemporal dementia (fv-FTD) for a long time before the appearance of true cognitive deficits. On the other hand, a deficit in the episodic memory domain represents the main manifestation of Alzheimer's disease (AD), Many behavioral disorders have been described in the clinical course of both FTD and AD;... Link: ./index.php?lvl=notice_display&id=28668
in Dialogues in Clinical Neuroscience > Año 2007 Vol. 9 - No. 2 (Junio) . - pp. 153–160[artículo] Frontotemporal dementia to Alzheimer's disease [texto impreso] / Maria Caterina Silveri, Autor . - 2022 . - pp. 153–160.
Idioma : Inglés (eng) Idioma original : Inglés (eng)
in Dialogues in Clinical Neuroscience > Año 2007 Vol. 9 - No. 2 (Junio) . - pp. 153–160
Palabras clave: Demencia frontotemporal, Enfermedad de Alzheimer, Trastorno del comportamiento, Teoría de la mente, Cognición social Resumen: Behavioral manifestations may dominate the clinical picture of the frontal variant of frontotemporal dementia (fv-FTD) for a long time before the appearance of true cognitive deficits. On the other hand, a deficit in the episodic memory domain represents the main manifestation of Alzheimer's disease (AD), Many behavioral disorders have been described in the clinical course of both FTD and AD;... Link: ./index.php?lvl=notice_display&id=28668 Tourette's syndrome / Norbert Müller en Dialogues in Clinical Neuroscience, Año 2007 Vol. 9 - No. 2 (Junio)
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Título : Tourette's syndrome : clinical features, pathophysiology, and therapeutic approaches. Tipo de documento: texto impreso Autores: Norbert Müller, Autor Fecha de publicación: 2022 Artículo en la página: pp. 161–171 Idioma : Inglés (eng) Idioma original : Inglés (eng) Palabras clave: Síndrome de Tourette, Diagnóstico, Fisiopatología, Genética, Inflamación, Infección, Terapia Resumen: Tourette's syndrome (TS) is a disorder characterized by simple and complex motor tics, vocal tics, and frequently obsessive-compulsive symptoms, its onset occurs before the age of 21. Typically, TS shows a waxing and waning course, but a chronification of the tics, even during later life, is often observed, TS mainly occurs in boys, and shows genetic heritability with differing penetrance. Link: ./index.php?lvl=notice_display&id=28669
in Dialogues in Clinical Neuroscience > Año 2007 Vol. 9 - No. 2 (Junio) . - pp. 161–171[artículo] Tourette's syndrome : clinical features, pathophysiology, and therapeutic approaches. [texto impreso] / Norbert Müller, Autor . - 2022 . - pp. 161–171.
Idioma : Inglés (eng) Idioma original : Inglés (eng)
in Dialogues in Clinical Neuroscience > Año 2007 Vol. 9 - No. 2 (Junio) . - pp. 161–171
Palabras clave: Síndrome de Tourette, Diagnóstico, Fisiopatología, Genética, Inflamación, Infección, Terapia Resumen: Tourette's syndrome (TS) is a disorder characterized by simple and complex motor tics, vocal tics, and frequently obsessive-compulsive symptoms, its onset occurs before the age of 21. Typically, TS shows a waxing and waning course, but a chronification of the tics, even during later life, is often observed, TS mainly occurs in boys, and shows genetic heritability with differing penetrance. Link: ./index.php?lvl=notice_display&id=28669 Visual hallucinatory syndromes / Dominic H. Ffytche en Dialogues in Clinical Neuroscience, Año 2007 Vol. 9 - No. 2 (Junio)
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Título : Visual hallucinatory syndromes : past, present, and future Tipo de documento: texto impreso Autores: Dominic H. Ffytche, Autor Fecha de publicación: 2022 Artículo en la página: pp. 173–189 Idioma : Inglés (eng) Idioma original : Inglés (eng) Palabras clave: Síndrome de Charles Bonnet, Alucinación visual, Alucinación liliputiense, Zoopsia, Automatismo mental, Neurofenomenología, Deaferentación, Serotonina, Acetilcolina Resumen: In 1936, two clinical rewiews, one by de Morsier, the other by L'Hermitte and de Ajuriaguerra, formulated an approach to visual hallucinations that continues to this day. Breaking with previous traditions, the papers championed visual hallucinations as worthy of study in their own right, de-emphasizing the clinical significance of their visual contents and distancing them from visual illusions. Link: ./index.php?lvl=notice_display&id=28670
in Dialogues in Clinical Neuroscience > Año 2007 Vol. 9 - No. 2 (Junio) . - pp. 173–189[artículo] Visual hallucinatory syndromes : past, present, and future [texto impreso] / Dominic H. Ffytche, Autor . - 2022 . - pp. 173–189.
Idioma : Inglés (eng) Idioma original : Inglés (eng)
in Dialogues in Clinical Neuroscience > Año 2007 Vol. 9 - No. 2 (Junio) . - pp. 173–189
Palabras clave: Síndrome de Charles Bonnet, Alucinación visual, Alucinación liliputiense, Zoopsia, Automatismo mental, Neurofenomenología, Deaferentación, Serotonina, Acetilcolina Resumen: In 1936, two clinical rewiews, one by de Morsier, the other by L'Hermitte and de Ajuriaguerra, formulated an approach to visual hallucinations that continues to this day. Breaking with previous traditions, the papers championed visual hallucinations as worthy of study in their own right, de-emphasizing the clinical significance of their visual contents and distancing them from visual illusions. Link: ./index.php?lvl=notice_display&id=28670 Neuropsychiatry of Huntington's disease / Adam Rosenblatt en Dialogues in Clinical Neuroscience, Año 2007 Vol. 9 - No. 2 (Junio)
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Título : Neuropsychiatry of Huntington's disease Tipo de documento: texto impreso Autores: Adam Rosenblatt, Autor Fecha de publicación: 2022 Artículo en la página: pp. 191–197 Idioma : Inglés (eng) Idioma original : Inglés (eng) Palabras clave: Enfermedad de Huntington, Neuropsiquiatría, Subcortical, Ejecutiva, Frontal, Neurodegenerativa, Corea, Demencia Resumen: Psychiatric manifestations are an integral part of Huntington's disease. They may be divided into those syndromes which resemble idiopathic disorders, but for which HD patients may be particularly at risk, those constellations which are peculiar to HD and related conditions, such as the executive dysfunction syndrome, and those symptoms that can truly be regarded as nonspecific, such as delirium. Link: ./index.php?lvl=notice_display&id=28671
in Dialogues in Clinical Neuroscience > Año 2007 Vol. 9 - No. 2 (Junio) . - pp. 191–197[artículo] Neuropsychiatry of Huntington's disease [texto impreso] / Adam Rosenblatt, Autor . - 2022 . - pp. 191–197.
Idioma : Inglés (eng) Idioma original : Inglés (eng)
in Dialogues in Clinical Neuroscience > Año 2007 Vol. 9 - No. 2 (Junio) . - pp. 191–197
Palabras clave: Enfermedad de Huntington, Neuropsiquiatría, Subcortical, Ejecutiva, Frontal, Neurodegenerativa, Corea, Demencia Resumen: Psychiatric manifestations are an integral part of Huntington's disease. They may be divided into those syndromes which resemble idiopathic disorders, but for which HD patients may be particularly at risk, those constellations which are peculiar to HD and related conditions, such as the executive dysfunction syndrome, and those symptoms that can truly be regarded as nonspecific, such as delirium. Link: ./index.php?lvl=notice_display&id=28671 Neuropsychiatric manifestations in CADASIL / Hugues Chabriat en Dialogues in Clinical Neuroscience, Año 2007 Vol. 9 - No. 2 (Junio)
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Título : Neuropsychiatric manifestations in CADASIL Tipo de documento: texto impreso Autores: Hugues Chabriat, Autor ; Marie Germaine Bousser, Autor Fecha de publicación: 2022 Artículo en la página: pp. 199–208 Idioma : Inglés (eng) Idioma original : Inglés (eng) Palabras clave: CADASIL, RM, Sustancia blanca, Infarto lacunar, Notch3, Trastorno del estado de ánimo, Vascular, Deterioro cognitivo, Demencia vascular isquémica subcortical Resumen: Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy(CADASIL) is an inherited small-artery disease of mid-adulthood caused by mutations of the NOTCH3 gene. The disease is responsible for widespread white-matter Iesions associated with lacunar infarctions in varinus subcortical areas. Link: ./index.php?lvl=notice_display&id=28672
in Dialogues in Clinical Neuroscience > Año 2007 Vol. 9 - No. 2 (Junio) . - pp. 199–208[artículo] Neuropsychiatric manifestations in CADASIL [texto impreso] / Hugues Chabriat, Autor ; Marie Germaine Bousser, Autor . - 2022 . - pp. 199–208.
Idioma : Inglés (eng) Idioma original : Inglés (eng)
in Dialogues in Clinical Neuroscience > Año 2007 Vol. 9 - No. 2 (Junio) . - pp. 199–208
Palabras clave: CADASIL, RM, Sustancia blanca, Infarto lacunar, Notch3, Trastorno del estado de ánimo, Vascular, Deterioro cognitivo, Demencia vascular isquémica subcortical Resumen: Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy(CADASIL) is an inherited small-artery disease of mid-adulthood caused by mutations of the NOTCH3 gene. The disease is responsible for widespread white-matter Iesions associated with lacunar infarctions in varinus subcortical areas. Link: ./index.php?lvl=notice_display&id=28672