Anderson LV - Search Results

1

Evaluation of the dystrophin-glycoprotein complex, alpha-actinin, dysferlin and calpain 3 in an autosomal recessive muscular dystrophy in Labrador retrievers.

Olby NJ, Sharp NJ, Anderson LV, Kunkel LM, Bönnemann CG. Olby NJ, et al. Among authors: anderson lv. Neuromuscul Disord. 2001 Jan;11(1):41-9. doi: 10.1016/s0960-8966(00)00166-8. Neuromuscul Disord. 2001. PMID: 11166165

2

Alternative dystrophin gene transcripts in golden retriever muscular dystrophy.

Schatzberg SJ, Anderson LV, Wilton SD, Kornegay JN, Mann CJ, Solomon GG, Sharp NJ. Schatzberg SJ, et al. Among authors: anderson lv. Muscle Nerve. 1998 Aug;21(8):991-8. doi: 10.1002/(sici)1097-4598(199808)21:8<991::aid-mus2>3.0.co;2-0. Muscle Nerve. 1998. PMID: 9655116

3

Molecular analysis of a spontaneous dystrophin 'knockout' dog.

Schatzberg SJ, Olby NJ, Breen M, Anderson LV, Langford CF, Dickens HF, Wilton SD, Zeiss CJ, Binns MM, Kornegay JN, Morris GE, Sharp NJ. Schatzberg SJ, et al. Among authors: anderson lv. Neuromuscul Disord. 1999 Jul;9(5):289-95. doi: 10.1016/s0960-8966(99)00011-5. Neuromuscul Disord. 1999. PMID: 10407848

4

Sarcoglycanopathies in Dutch patients with autosomal recessive limb girdle muscular dystrophy.

Ginjaar HB, van der Kooi AJ, Ceelie H, Kneppers AL, van Meegen M, Barth PG, Busch HF, Wokke JH, Anderson LV, Bönnemann CG, Jeanpierre M, Bolhuis PA, Moorman AF, de Visser M, Bakker E, Ommen GJ. Ginjaar HB, et al. Among authors: anderson lv. J Neurol. 2000 Jul;247(7):524-9. doi: 10.1007/s004150070151. J Neurol. 2000. PMID: 10993494

5

The sarcoglycan complex in the six autosomal recessive limb-girdle muscular dystrophies.

Vainzof M, Passos-Bueno MR, Canovas M, Moreira ES, Pavanello RC, Marie SK, Anderson LV, Bonnemann CG, McNally EM, Nigro V, Kunkel LM, Zatz M. Vainzof M, et al. Among authors: anderson lv. Hum Mol Genet. 1996 Dec;5(12):1963-9. doi: 10.1093/hmg/5.12.1963. Hum Mol Genet. 1996. PMID: 8968750

6

Abnormalities in alpha-, beta- and gamma-sarcoglycan in patients with limb-girdle muscular dystrophy.

Sewry CA, Taylor J, Anderson LV, Ozawa E, Pogue R, Piccolo F, Bushby K, Dubowitz V, Muntoni F. Sewry CA, et al. Among authors: anderson lv. Neuromuscul Disord. 1996 Dec;6(6):467-74. doi: 10.1016/s0960-8966(96)00389-6. Neuromuscul Disord. 1996. PMID: 9027857 Clinical Trial.

7

Strategy for mutation analysis in the autosomal recessive limb-girdle muscular dystrophies.

Pogue R, Anderson LV, Pyle A, Sewry C, Pollitt C, Johnson MA, Davison K, Moss JA, Mercuri E, Muntoni F, Bushby KM. Pogue R, et al. Among authors: anderson lv. Neuromuscul Disord. 2001 Jan;11(1):80-7. doi: 10.1016/s0960-8966(00)00154-1. Neuromuscul Disord. 2001. PMID: 11166169

8

Secondary reduction in calpain 3 expression in patients with limb girdle muscular dystrophy type 2B and Miyoshi myopathy (primary dysferlinopathies).

Anderson LV, Harrison RM, Pogue R, Vafiadaki E, Pollitt C, Davison K, Moss JA, Keers S, Pyle A, Shaw PJ, Mahjneh I, Argov Z, Greenberg CR, Wrogemann K, Bertorini T, Goebel HH, Beckmann JS, Bashir R, Bushby KM. Anderson LV, et al. Neuromuscul Disord. 2000 Dec;10(8):553-9. doi: 10.1016/s0960-8966(00)00143-7. Neuromuscul Disord. 2000. PMID: 11053681

9

Optimized protein diagnosis in the autosomal recessive limb-girdle muscular dystrophies.

Anderson LV. Anderson LV. Neuromuscul Disord. 1996 Dec;6(6):443-6. doi: 10.1016/s0960-8966(96)00385-9. Neuromuscul Disord. 1996. PMID: 9027853

10

Dysferlinopathy (LGMD2B): a 23-year follow-up study of 10 patients homozygous for the same frameshifting dysferlin mutations.

Mahjneh I, Marconi G, Bushby K, Anderson LV, Tolvanen-Mahjneh H, Somer H. Mahjneh I, et al. Among authors: anderson lv. Neuromuscul Disord. 2001 Jan;11(1):20-6. doi: 10.1016/s0960-8966(00)00157-7. Neuromuscul Disord. 2001. PMID: 11166162

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