Search Results - "Tahmoush, A"
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Long-term outcome following sympathectomy for complex regional pain syndrome type 1 (RSD)
Published in Journal of the neurological sciences (10-09-1997)“…We performed a retrospective study of 29 patients with CRPS1 (RSD) who were initially examined between 1983 and 1993, and had either transthoracic (lower third…”
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2
Cramp-fasciculation syndrome : a treatable hyperexcitable peripheral nerve disorder
Published in Neurology (01-07-1991)“…We report nine patients with muscle aching, cramps, stiffness, exercise intolerance, and peripheral nerve hyperexcitability. Neurologic examination showed calf…”
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3
Reflex sympathetic dystrophy revisited: MR imaging findings before and after infusion of contrast material
Published in Radiology (01-04-1995)“…To determine the appearance of reflex sympathetic dystrophy (RSD) at magnetic resonance (MR) imaging. Fifty-one patients with suspected RSD were prospectively…”
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4
Sensing atmospheric structure using small-scale space geodetic networks
Published in Geophysical research letters (15-08-1999)“…We describe two ways in which horizontal atmospheric structure affects GPS observations. For a single site, such structure results in azimuthal variations in…”
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5
Aphagia due to pharyngeal constrictor paresis from acute lateral medullary infarction
Published in Journal of the neurological sciences (05-03-1998)“…Although swallowing difficulties (dysphagia) frequently occur in acute brainstem infarction, physiological studies of dysphagia (videofluoroscopy, manometry)…”
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6
Biochemical and genetic studies in a family with mitochondrial myopathy
Published in Muscle & nerve (01-10-1997)“…We present a family with severe exercise intolerance, progressive proximal weakness, and lactic acidemia. Fifteen of 24 family members in five generations were…”
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7
Shoulder-arm pain from cervical bands and scalene muscle anomalies
Published in Journal of the neurological sciences (01-02-1995)“…Fourteen patients were identified with (1) pain and sensory changes in a brachial plexus distribution, (2) aggravation of pain with use of the affected…”
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8
Treatable lumbosacral polyradiculitis masquerading as diabetic amyotrophy
Published in Journal of the neurological sciences (22-10-1997)“…Patients with diabetic amyotrophy may have an inflammatory vasculopathy and may obtain reversal of neurological deficits with immunosuppression. We present a…”
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9
Antibodies to GM1 and GD1b in patients with motor neuron disease without plasma cell dyscrasia
Published in Annals of neurology (01-05-1989)“…Fifty-nine percent of 49 patients with motor neuron disease and 25% of 91 control subjects had IgM antibodies to ganglioside GM1 but usually not to GD1b at…”
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10
Muscle involvement in polyarteritis nodosa: report of a patient presenting clinically as polymyositis and review of the literature
Published in Journal of rheumatology (01-05-1994)“…Muscle symptoms, especially myalgias, appear to be common in patients with polyarteritis nodosa (PAN). We describe a patient who presented with a generalized…”
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11
Quantitative Sensory Studies in Complex Regional Pain Syndrome Type 1/RSD
Published in The Clinical journal of pain (01-12-2000)“…OBJECTIVE:Patients with complex regional pain syndrome type 1 (CRPSD1) may have thermal allodynia after application of a non-noxious thermal stimulus to the…”
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Reflex sympathetic dystrophy: occurrence of chronic edema and nonimmune bullous skin lesions
Published in Journal of the American Academy of Dermatology (01-01-1993)“…Reflex sympathetic dystrophy (RSD) is a poorly understood syndrome of post-traumatic pain, autonomic dysfunction, and progressive tissue atrophy. Classical…”
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13
No relationship between fiber type and halothane contracture test results in malignant hyperthermia
Published in Anesthesiology (Philadelphia) (01-07-1987)“…Previous studies in cat, rat, and swine have implicated fiber type as influencing the halothane and caffeine contracture test used to diagnose malignant…”
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14
Halothane-caffeine contracture testing in neuromuscular diseases
Published in Muscle & nerve (01-05-1988)“…The association of malignant hyperthermia (MH) with neuromuscular disorders has been recognized since 1970. These disorders include central core disease,…”
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15
Anti-GM1/GD1b M-proteins damage human spinal cord neurons co-cultured with muscle
Published in Journal of the neurological sciences (01-12-1993)“…IgM M-proteins in some motor neuron disease (MND) patients bind immunologically to shared determinants on gangliosides GM1 and GD1b. Since patients with these…”
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16
Muscle sodium channel inactivation defect in paramyotonia congenita with the thr1313met mutation
Published in Neuromuscular disorders : NMD (01-09-1994)“…Mutations of the skeletal muscle sodium (Na) channel have been reported in families with paramyotonia congenita (PC), an autosomal dominant disorder with cold…”
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Malignant hyperthermia in myotonia congenita
Published in Neurology (01-05-1988)“…We report a family in which two sisters with myotonia congenita (MyC) were referred for malignant hyperthermia (MH) evaluation after each developed muscle…”
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18
Peripheral neuropathy associated with eosinophilia-myalgia syndrome
Published in Annals of neurology (01-10-1990)“…In 1989, the Centers for Disease Control recognized the existence of an epidemic illness characterized by myalgia and eosinophilia in individuals taking…”
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Myopathy, antineutrophil cytoplasmic antibodies, and glomerulonephritis
Published in Muscle & nerve (01-04-1995)Get more information
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Causalgia: redefinition as a clinical pain syndrome
Published in Pain (Amsterdam) (01-04-1981)“…In this report, the following criteria were used for the diagnosis of causalgia: (a) the presence of continuous, burning pain distal to a site of injury; (b)…”
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