Results 231 to 240 of about 423,580 (268)
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Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy.
Science, 1988Leber's hereditary optic neuropathy is a maternally inherited disease resulting in optic nerve degeneration and cardiac dysrhythmia. A mitochondrial DNA replacement mutation was identified that correlated with this disease in multiple families.
D. Wallace+7 more
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Medical Clinics of North America, 1998
Better clinical characteristics and a standardized approach to the definition of neuropathy has enabled us to define more precisely the natural history of diabetic neuropathy. Detailed studies on the pathology and pathogenesis have allowed dissection of important pathogenetic pathways.
A J, Boulton, R A, Malik
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Better clinical characteristics and a standardized approach to the definition of neuropathy has enabled us to define more precisely the natural history of diabetic neuropathy. Detailed studies on the pathology and pathogenesis have allowed dissection of important pathogenetic pathways.
A J, Boulton, R A, Malik
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Muscle & Nerve, 1995
AbstractA 29‐year‐old Haitian man had a sore throat with a marked tonsillar exudate followed by the onset of increasingly blurred vision with swallowing difficulties and, then, a diffuse acute demyelinating neuropathy. Cerebrospinal fluid showed moderate pleiocytosis and elevated protein content.
Jean-Denis Degos+4 more
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AbstractA 29‐year‐old Haitian man had a sore throat with a marked tonsillar exudate followed by the onset of increasingly blurred vision with swallowing difficulties and, then, a diffuse acute demyelinating neuropathy. Cerebrospinal fluid showed moderate pleiocytosis and elevated protein content.
Jean-Denis Degos+4 more
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Current Opinion in Neurology, 1994
A limited autonomic neuropathy may underlie some unusual clinical syndromes, including the postural tachycardia syndrome, pseudo-obstruction syndrome, heat intolerance, and perhaps chronic fatigue syndrome. Antibodies to autonomic structures are common in diabetes, but their specificity is unknown. The presence of autonomic failure worsens prognosis in
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A limited autonomic neuropathy may underlie some unusual clinical syndromes, including the postural tachycardia syndrome, pseudo-obstruction syndrome, heat intolerance, and perhaps chronic fatigue syndrome. Antibodies to autonomic structures are common in diabetes, but their specificity is unknown. The presence of autonomic failure worsens prognosis in
openaire +4 more sources
Paraneoplastic vasculitic neuropathy: A treatable neuropathy
Muscle & Nerve, 1991AbstractParaneoplastic vasculitic neuropathy has been recently described. We report the first case of this disorder which responded both clinically and electrophysiologically to cyclophosphamide treatment. A 54hyphen;year‐old women with a history of metastatic endometrial carcinoma in remission had asymmetrical polyneuropathy, electrophysiological ...
Shin J. Oh+2 more
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Neurologic Clinics, 2007
ABSTRACT OBJECTIVE This article reviews the etiologies, presentations, and management of neuropathies related to nutritional deficiencies. LATEST DEVELOPMENTS Peripheral neuropathy can be the predominant or only manifestation of certain nutrient deficiencies.
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ABSTRACT OBJECTIVE This article reviews the etiologies, presentations, and management of neuropathies related to nutritional deficiencies. LATEST DEVELOPMENTS Peripheral neuropathy can be the predominant or only manifestation of certain nutrient deficiencies.
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Oral Diseases, 2007
Trigeminal neuropathies (TNs) are well recognized disorders characterized and manifesting as skin and mucosal numbness in the region innervated by the trigeminal nerve. Facial numbness indicates trigeminal sensory alteration affecting the trigeminal system. TNs always pose differential location difficulties as multiple diseases are capable of producing
E Martí+3 more
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Trigeminal neuropathies (TNs) are well recognized disorders characterized and manifesting as skin and mucosal numbness in the region innervated by the trigeminal nerve. Facial numbness indicates trigeminal sensory alteration affecting the trigeminal system. TNs always pose differential location difficulties as multiple diseases are capable of producing
E Martí+3 more
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BMJ, 2017
A 26 year old woman was referred to dermatology with a one year history of a rash on her lower legs, abdomen, and arms, and a six month history of paraesthesia in her right hand and left foot. She had no history of fatigue, weight loss, fever, or arthralgia. There was palpable retiform erythema and broken livedo on her abdomen, arms, and legs (fig 1).
Fangyi Xie, Daniel Creamer
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A 26 year old woman was referred to dermatology with a one year history of a rash on her lower legs, abdomen, and arms, and a six month history of paraesthesia in her right hand and left foot. She had no history of fatigue, weight loss, fever, or arthralgia. There was palpable retiform erythema and broken livedo on her abdomen, arms, and legs (fig 1).
Fangyi Xie, Daniel Creamer
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Paraproteinemia and neuropathy
Neurological Sciences, 2021Paraproteinemia is associated with different peripheral neuropathies. The major causes of neuropathy correlated with paraproteinemia are the deposition of immunoglobulin in the myelin, represented by anti-myelin-associated glycoprotein (MAG) neuropathy; deposition of immunoglobulin or its fragment in the interstitium, represented by immunoglobulin ...
Haruki Koike, Masahisa Katsuno
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2016
Peripheral neuropathies are diseases of the peripheral nervous system that can be divided into mononeuropathies, multifocal neuropathies, and polyneuropathies. Symptoms usually include numbness and paresthesia. These symptoms are often accompanied by weakness and can be painful. Polyneuropathies can be divided into axonal and demyelinating forms, which
Rens Hanewinckel+2 more
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Peripheral neuropathies are diseases of the peripheral nervous system that can be divided into mononeuropathies, multifocal neuropathies, and polyneuropathies. Symptoms usually include numbness and paresthesia. These symptoms are often accompanied by weakness and can be painful. Polyneuropathies can be divided into axonal and demyelinating forms, which
Rens Hanewinckel+2 more
openaire +4 more sources