Engel AG - Search Results

1

Myofibrillar myopathy. III. Abnormal expression of cyclin-dependent kinases and nuclear proteins.

Nakano S, Engel AG, Akiguchi I, Kimura J. Nakano S, et al. Among authors: engel ag. J Neuropathol Exp Neurol. 1997 Aug;56(8):850-6. doi: 10.1097/00005072-199708000-00002. J Neuropathol Exp Neurol. 1997. PMID: 9258254

2

Myasthenia gravis: quantitative immunocytochemical analysis of inflammatory cells and detection of complement membrane attack complex at the end-plate in 30 patients.

Nakano S, Engel AG. Nakano S, et al. Among authors: engel ag. Neurology. 1993 Jun;43(6):1167-72. doi: 10.1212/wnl.43.6.1167. Neurology. 1993. PMID: 8170563

3

Myofibrillar myopathy with abnormal foci of desmin positivity. I. Light and electron microscopy analysis of 10 cases.

Nakano S, Engel AG, Waclawik AJ, Emslie-Smith AM, Busis NA. Nakano S, et al. Among authors: engel ag. J Neuropathol Exp Neurol. 1996 May;55(5):549-62. doi: 10.1097/00005072-199605000-00008. J Neuropathol Exp Neurol. 1996. PMID: 8627346

4

The spectrum of mutations causing end-plate acetylcholinesterase deficiency.

Ohno K, Engel AG, Brengman JM, Shen XM, Heidenreich F, Vincent A, Milone M, Tan E, Demirci M, Walsh P, Nakano S, Akiguchi I. Ohno K, et al. Among authors: engel ag. Ann Neurol. 2000 Feb;47(2):162-70. Ann Neurol. 2000. PMID: 10665486

5

Congenital endplate acetylcholinesterase deficiency.

Hutchinson DO, Walls TJ, Nakano S, Camp S, Taylor P, Harper CM, Groover RV, Peterson HA, Jamieson DG, Engel AG. Hutchinson DO, et al. Among authors: engel ag. Brain. 1993 Jun;116 ( Pt 3):633-53. doi: 10.1093/brain/116.3.633. Brain. 1993. PMID: 8390325

6

Myasthenic syndromes attributed to mutations affecting the epsilon subunit of the acetylcholine receptor.

Engel AG, Hutchinson DO, Nakano S, Murphy L, Griggs RC, Gu Y, Hall ZW, Lindstrom J. Engel AG, et al. Ann N Y Acad Sci. 1993 Jun 21;681:496-508. doi: 10.1111/j.1749-6632.1993.tb22933.x. Ann N Y Acad Sci. 1993. PMID: 8357190 No abstract available.

7

The spectrum of congenital end-plate acetylcholinesterase deficiency.

Hutchinson DO, Engel AG, Walls TJ, Nakano S, Camp S, Taylor P, Harper CM, Brengman JM. Hutchinson DO, et al. Among authors: engel ag. Ann N Y Acad Sci. 1993 Jun 21;681:469-86. doi: 10.1111/j.1749-6632.1993.tb22931.x. Ann N Y Acad Sci. 1993. PMID: 8395162 No abstract available.

8

Congenital myasthenic syndrome caused by decreased agonist binding affinity due to a mutation in the acetylcholine receptor epsilon subunit.

Ohno K, Wang HL, Milone M, Bren N, Brengman JM, Nakano S, Quiram P, Pruitt JN, Sine SM, Engel AG. Ohno K, et al. Among authors: engel ag. Neuron. 1996 Jul;17(1):157-70. doi: 10.1016/s0896-6273(00)80289-5. Neuron. 1996. PMID: 8755487 Free article.

9

1,1'-Ethylidenebis[tryptophan] induces pathologic alterations in muscle similar to those observed in the eosinophilia-myalgia syndrome.

Emslie-Smith AM, Mayeno AN, Nakano S, Gleich GJ, Engel AG. Emslie-Smith AM, et al. Among authors: engel ag. Neurology. 1994 Dec;44(12):2390-2. doi: 10.1212/wnl.44.12.2390. Neurology. 1994. PMID: 7991132

10

New mutations in acetylcholine receptor subunit genes reveal heterogeneity in the slow-channel congenital myasthenic syndrome.

Engel AG, Ohno K, Milone M, Wang HL, Nakano S, Bouzat C, Pruitt JN 2nd, Hutchinson DO, Brengman JM, Bren N, Sieb JP, Sine SM. Engel AG, et al. Hum Mol Genet. 1996 Sep;5(9):1217-27. doi: 10.1093/hmg/5.9.1217. Hum Mol Genet. 1996. PMID: 8872460

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