Mutation in the novel nuclear-encoded mitochondrial protein CHCHD10 in a family with autosomal dominant mitochondrial myopathy von Ajroud-Driss, Senda, Fecto, Faisal, Ajroud, Kaouther, Lalani, Irfan, Calvo, Sarah E., Mootha, Vamsi K., Deng, Han-Xiang, Siddique, Nailah, Tahmoush, Albert J., Heiman-Patterson, Terry D., Siddique, Teepu

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

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

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Patch clamp studies of the Thr1313met mutant sodium channel causing paramyotonia congenita von Boulos, Paul T., Heiman-Patterson, Terry D., Alexander, Guillermo M., Tahmoush, Albert J.

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

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Causalgia: Redefinition as a clinical pain syndrome von Tahmoush, Albert J.

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

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

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Quantitative sensory studies in complex regional pain syndrome type 1/RSD. (MCP Hahnemann University, Philadelphia, PA) Clin J Pain. 2000;16:340-344 von Tahmoush, Albert J., Schwartzman, R. J., Hopp, J. L., Grothusen, J. R.

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Antibodies to GM1 and GD1b in patients with motor neuron disease without plasma cell dyscrasia von Shy, Michael E., Evans, Vance A., Lublin, Fred D., Knobler, Robert L., Heiman-Patterson, Terry, Tahmoush, Albert J., Parry, Gareth, Schick, Paul, Deryk, Theodora G.

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Anti-GM1/GD1b M-proteins damage human spinal cord neurons co-cultured with muscle von HEIMAN-PATTERSON, T, KRUPA, T, THOMPSON, P, NOBILE-ORAZIO, E, TAHMOUSH, A. J, SHY, M. E

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Muscle sodium channel inactivation defect in paramyotonia congenita with the thr1313met mutation von Tahmoush, Albert J., Schaller, Kristen L., Zhang, Ping, Hyslop, Terry, Heiman-Patterson, Terry, Caldwell, John H.

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Myopathy, antineutrophil cytoplasmic antibodies, and glomerulonephritis von Tahmoush, Albert J., Liu, Jeffrey E., Amir, Mary S., Heiman-Patterson, Terry

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Anti-GM 1/GD 1b M-proteins damage human spinal cord neurons co-cultured with muscle von Heiman-Patterson, Terry, Krupa, Thomas, Thompson, Preston, Nobile-Orazio, Eduardo, Tahmoush, Albert J., Shy, Michael E.

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In Vitro Studies of the Pulsatile Radiometric Signal von Tahmoush, Albert J., Francis, Mildred E.

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Malignant hyperthermia susceptibility in X-linked muscle dystrophies von Heiman-Patterson, Terry D., Natter, Howard M., Rosenberg, Henry R., Fletcher, Jeffrey E., Tahmoush, Albert J.

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Antibodies to GM 1 and GD 1b in patients with motor neuron disease without plasma cell dyscrasia von Shy, Michael E., Evans, Vance A., Lublin, Fred D., Knobler, Robert L., Heiman‐Patterson, Terry, Tahmoush, Albert J., Parry, Gareth, Schick, Paul, Deryk, Theodora G.

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King-Denborough syndrome: Contracture testing and literature review von Heiman-Patterson, Terry D., Rosenberg, Henry R., Binning, Chinder PS, Tahmoush, Albert J.

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The presence of antibodies reacting with GM1 in motor neuron disease patients without plasma cell dyscrasia von Shy, Michael E., Evans, Vance A., Lublin, Fred D., Knobler, Robert L., Heiman-Patternson, Terry, Tahmoush, Albert J., Parry, Gareth

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Characteristics of a Light Emitting Diode-Transistor Photoplethysmograph von Tahmoush, Albert J., Jkennings, J. Richard, Lee, Alison L., Camp, Stephen, Webhr, Frederick

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