2784 Steroid Responsive Gastric Dysmotility - Seronegative Autoimmune Autonomic Neuropathy

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Experimental autoimmune autonomic neuropathy.

Antibodies specific for the neuronal ganglionic nicotinic acetylcholine receptor (nAChR) are found in high titer in serum of patients with subacute autonomic failure. This clinical disorder is known as autoimmune autonomic neuropathy (AAN). Rabbits immunized with a neuronal nAChR alpha3 subunit fusion protein produce ganglionic nAChR antibodies and develop autonomic failure (experimental AAN, o...

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translational physiology Experimental Autoimmune Autonomic Neuropathy

Vernino, Steven, Phillip A. Low, and Vanda A. Lennon. Experimental autoimmune autonomic neuropathy. J Neurophysiol 90: 2053–2059, 2003. First published May 28, 2003; 10.1152/jn.00408.2003. Antibodies specific for the neuronal ganglionic nicotinic acetylcholine receptor (nAChR) are found in high titer in serum of patients with subacute autonomic failure. This clinical disorder is known as autoim...

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Autoimmune autonomic ganglionopathy: a possible postganglionic neuropathy.

OBJECTIVE To evaluate postganglionic autonomic and somatic nerve fiber involvement in a patient with chronic autoimmune autonomic ganglionopathy. DESIGN Case report. SETTING Department of Neurological Sciences, University Federico II of Naples. PATIENT A patient with a 16-year history of severe autonomic failure and a high nicotinic acetylcholine receptor antibody titer underwent an exten...

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[Autoimmune autonomic ganglionopathy and acute autonomic and sensory neuropathy].

Autonomic neuropathies may occur primarily or secondarily to various underlying diseases. Primary autonomic neuropathies are divided into pure autonomic neuropathy, autonomic neuropathy with sensory impairment, and autonomic neuropathy with sensory and motor impairment based on the concomitance or absence of sensory or motor dysfunctions. Autoimmune autonomic ganglionopathy refers to a pure aut...

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Steroid-responsive encephalopathy associated with autoimmune thyroiditis.

BACKGROUND Steroid-responsive encephalopathy associated with autoimmune thyroiditis (SREAT), often termed Hashimoto encephalopathy, is a poorly understood and often misdiagnosed entity. OBJECTIVE To characterize the clinical, laboratory, and radiologic findings in patients with SREAT to potentially improve recognition of this treatable entity. DESIGN Retrospective analysis of clinical featu...

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ژورنال

عنوان ژورنال: American Journal of Gastroenterology

سال: 2019

ISSN: 0002-9270,1572-0241

DOI: 10.14309/01.ajg.0000600668.87883.c0