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UNITED STATES of America, Plaintiff-Appellee,v.Eddie L. TRIMBLE, Defendant-Appellant.
No. 94-8164.
United States Court of Appeals,Sixth Circuit.
Sept. 29, 1995.

Before: SUHRHEINRICH, DAUGHTREY, and MOORE, Circuit Judges.

ORDER

1
The parties having agreed that this case may be submitted upon the briefs and the record, the judgment is affirmed for the reasons set forth in the memorandum opinion of the district court. United States v. Trimble, 815 F.Supp. 577 (W.D.Mich.1993). In addition, we note that the district court properly denied the defendant’s motion for sentencing credit for time served in the state penal system.

Progressive neuromuscular weakness in a patient with anti-GQ1b antibodies.
Although myasthenia gravis-related antibodies are most commonly directed to the acetylcholine receptor, antibodies to ganglioside GQ1b, which are present in a subset of patients with myasthenia gravis, are sometimes associated with extraocular, small fiber neuropathy. In this report, we document a patient with progressive weakness in axial, proximal, and distal muscles, as well as in the tongue, but who lacks an ocular component of the disease. This patient was previously tested for anti-myasthenia gravis-related antibodies, but only after having presented with arthralgia and weakness in the limbs. The IgG fraction of the patient’s serum contained anti-GQ1b antibodies, and the IgM fraction contained anti-AChR antibodies. Prolonged repetitive nerve stimulation studies and magnetic resonance imaging of the brain were diagnostic of a small fiber neuropathy. This is the first case of motor

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