Search Results - "Tahmoush, A"

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  1. 1

    Long-term outcome following sympathectomy for complex regional pain syndrome type 1 (RSD) by Schwartzman, R.J, Liu, J.E, Smullens, S.N, Hyslop, T, Tahmoush, A.J

    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. 2

    Cramp-fasciculation syndrome : a treatable hyperexcitable peripheral nerve disorder by TAHMOUSH, A. J, ALONSO, R. J, TAHMOUSH, G. P, HEIMAN-PATTERSON, T. D

    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. 3

    Reflex sympathetic dystrophy revisited: MR imaging findings before and after infusion of contrast material by Schweitzer, M E, Mandel, S, Schwartzman, R J, Knobler, R L, Tahmoush, A J

    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. 4

    Sensing atmospheric structure using small-scale space geodetic networks by Elósegui, P., Davis, J. L., Gradinarsky, L. P., Elgered, G., Johansson, J. M., Tahmoush, D. A., Rius, A.

    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. 5

    Aphagia due to pharyngeal constrictor paresis from acute lateral medullary infarction by Vigderman, Anne M, Chavin, Jeffrey M, Kososky, Charles, Tahmoush, Albert J

    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. 6

    Biochemical and genetic studies in a family with mitochondrial myopathy by Heiman-Patterson, Terry D., Argov, Zohar, Chavin, Jeffrey M., Kalman, Bernadette, Alder, Hansjuerg, DiMauro, Salvatore, Bank, William, Tahmoush, Albert J.

    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. 7

    Shoulder-arm pain from cervical bands and scalene muscle anomalies by Liu, Jeffrey E., Tahmoush, Albert J., Roos, David B., Schwartzman, Robert J.

    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. 8

    Treatable lumbosacral polyradiculitis masquerading as diabetic amyotrophy by O'Neill, Bryan J, Flanders, Adam E, Escandon, Sandra L, Tahmoush, Albert J

    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. 9

    Antibodies to GM1 and GD1b in patients with motor neuron disease without plasma cell dyscrasia by Shy, M E, Evans, V A, Lublin, F D, Knobler, R L, Heiman-Patterson, T, Tahmoush, A J, Parry, G, Schick, P, DeRyk, T G

    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. 10

    Muscle involvement in polyarteritis nodosa: report of a patient presenting clinically as polymyositis and review of the literature by Fort, J G, Griffin, R, Tahmoush, A, Abruzzo, J L

    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. 11

    Quantitative Sensory Studies in Complex Regional Pain Syndrome Type 1/RSD by Tahmoush, Albert J, Schwartzman, R J, Hopp, J L, Grothusen, J R

    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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  12. 12

    Reflex sympathetic dystrophy: occurrence of chronic edema and nonimmune bullous skin lesions by Webster, G F, Iozzo, R V, Schwartzman, R J, Tahmoush, A J, Knobler, R L, Jacoby, R A

    “…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. 13

    No relationship between fiber type and halothane contracture test results in malignant hyperthermia by HEIMAN-PATTERSON, T, FLETCHER, J. E, ROSENBERG, H, TAHMOUSH, A. J

    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. 14

    Halothane-caffeine contracture testing in neuromuscular diseases by Heiman-Patterson, T D, Rosenberg, H, Fletcher, J E, Tahmoush, A J

    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. 15

    Anti-GM1/GD1b M-proteins damage human spinal cord neurons co-cultured with muscle by Heiman-Patterson, T, Krupa, T, Thompson, P, Nobile-Orazio, E, Tahmoush, A J, Shy, M E

    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. 16

    Muscle sodium channel inactivation defect in paramyotonia congenita with the thr1313met mutation by Tahmoush, A J, Schaller, K L, Zhang, P, Hyslop, T, Heiman-Patterson, T, Caldwell, J H

    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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  17. 17

    Malignant hyperthermia in myotonia congenita by HEIMAN-PATTERSON, T, MARTINO, C, ROSENBERG, H, FLETCHER, J, TAHMOUSH, A

    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. 18

    Peripheral neuropathy associated with eosinophilia-myalgia syndrome by Heiman-Patterson, T D, Bird, S J, Parry, G J, Varga, J, Shy, M E, Culligan, N W, Edelsohn, L, Tatarian, G T, Heyes, M P, Garcia, C A

    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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  20. 20

    Causalgia: redefinition as a clinical pain syndrome by Tahmoush, Albert J

    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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