Results 251 to 260 of about 65,744 (296)
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Degenerative cervical myelopathy — update and future directions
Nature Reviews Neurology, 2020J. Badhiwala+8 more
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Journal of Clinical Gastroenterology, 1991
Postshunt myelopathy is a rare, severely debilitating syndrome complicating portosystemic shunts that is characterized by spastic paraparesis. In this report we describe a 39-year-old woman with alcoholic liver disease and postshunt myelopathy resulting in an inability to walk.
V G, Bain, R J, Bailey, J H, Jhamandas
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Postshunt myelopathy is a rare, severely debilitating syndrome complicating portosystemic shunts that is characterized by spastic paraparesis. In this report we describe a 39-year-old woman with alcoholic liver disease and postshunt myelopathy resulting in an inability to walk.
V G, Bain, R J, Bailey, J H, Jhamandas
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Seminars in Neurology, 2010
Both general neurologists and neurologists with a broad spectrum of subspecialty interests are often asked to evaluate patients with disorders of the spinal cord. Over the past decade, there have been significant advances in our understanding of a wide spectrum of immune-mediated, infectious, metabolic, hereditary, paraneoplastic, and compressive ...
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Both general neurologists and neurologists with a broad spectrum of subspecialty interests are often asked to evaluate patients with disorders of the spinal cord. Over the past decade, there have been significant advances in our understanding of a wide spectrum of immune-mediated, infectious, metabolic, hereditary, paraneoplastic, and compressive ...
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Seminars in Neurology, 2012
Inherited myelopathies are a small, but important subset of diseases that cause dysfunction of the spinal cord. Manifestations can include various combinations of signs and symptoms, including disturbance of gait, spasticity, paraplegia, amyotrophy, sensory loss, and urinary sphincter dysfunction. These diseases can be divided into classes that include
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Inherited myelopathies are a small, but important subset of diseases that cause dysfunction of the spinal cord. Manifestations can include various combinations of signs and symptoms, including disturbance of gait, spasticity, paraplegia, amyotrophy, sensory loss, and urinary sphincter dysfunction. These diseases can be divided into classes that include
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CONTINUUM: Lifelong Learning in Neurology
ABSTRACT OBJECTIVE Vascular injuries of the spinal cord are less common than those involving the brain; however, they can be equally devastating. This article discusses the diagnosis and management of ischemic and hemorrhagic vascular disorders of the spinal cord. LATEST DEVELOPMENTS
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ABSTRACT OBJECTIVE Vascular injuries of the spinal cord are less common than those involving the brain; however, they can be equally devastating. This article discusses the diagnosis and management of ischemic and hemorrhagic vascular disorders of the spinal cord. LATEST DEVELOPMENTS
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CONTINUUM: Lifelong Learning in Neurology
ABSTRACT OBJECTIVE This article provides an overview of genetic myelopathies, a diverse group of inherited, degenerative conditions that may be broadly categorized as motor neuron disorders, disorders of spinocerebellar degeneration, leukodystrophies, and hereditary spastic paraplegia.
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ABSTRACT OBJECTIVE This article provides an overview of genetic myelopathies, a diverse group of inherited, degenerative conditions that may be broadly categorized as motor neuron disorders, disorders of spinocerebellar degeneration, leukodystrophies, and hereditary spastic paraplegia.
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CONTINUUM: Lifelong Learning in Neurology, 2015
Involvement of the spinal cord by cancer is seen in 5% to 10% of all patients with cancer. This article reviews disorders in which cancer results in spinal cord dysfunction.Involvement of the spinal cord in patients with cancer occurs by either direct or indirect mechanisms.
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Involvement of the spinal cord by cancer is seen in 5% to 10% of all patients with cancer. This article reviews disorders in which cancer results in spinal cord dysfunction.Involvement of the spinal cord in patients with cancer occurs by either direct or indirect mechanisms.
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HTLV-I ASSOCIATED MYELOPATHY, A NEW CLINICAL ENTITY
The Lancet, 1986M. Osame+7 more
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CONTINUUM: Lifelong Learning in Neurology
ABSTRACT Objective This article illustrates the clinical importance, diagnosis, and management of degenerative and nondegenerative structural myelopathies. It also aims to create a diagnostic approach for the evaluation of patients with suspected degenerative myelopathies.
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ABSTRACT Objective This article illustrates the clinical importance, diagnosis, and management of degenerative and nondegenerative structural myelopathies. It also aims to create a diagnostic approach for the evaluation of patients with suspected degenerative myelopathies.
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