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339 results
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Heterozygous C2-deficiency and myasthenia gravis.
Riggs JE, Griggs RC, Rosenfeld SI, May AG, Penn AS. Riggs JE, et al. Among authors: griggs rc. Neurology. 1980 Aug;30(8):871-3. doi: 10.1212/wnl.30.8.871. Neurology. 1980. PMID: 7191069
Sjögren's syndrome and polymyositis or dermatomyositis.
Ringel SP, Forstot JZ, Tan EM, Wehling C, Griggs RC, Butcher D. Ringel SP, et al. Among authors: griggs rc. Arch Neurol. 1982 Mar;39(3):157-63. doi: 10.1001/archneur.1982.00510150027007. Arch Neurol. 1982. PMID: 7039564
Hereditary carnitine deficiency of muscle.
VanDyke DH, Griggs RC, Markesbery W, Dimauro S. VanDyke DH, et al. Among authors: griggs rc. Neurology. 1975 Feb;25(2):154-9. doi: 10.1212/wnl.25.2.154. Neurology. 1975. PMID: 123043
Recovery from the 'locked-in' syndrome.
McCusker EA, Rudick RA, Honch GW, Griggs RC. McCusker EA, et al. Among authors: griggs rc. Arch Neurol. 1982 Mar;39(3):145-7. doi: 10.1001/archneur.1982.00510150015004. Arch Neurol. 1982. PMID: 7065931
339 results