Anderson LV - Search Results

1

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

2

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

3

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

4

Immunomarkers for molecular mass.

Anderson LV. Anderson LV. Neuromuscul Disord. 1999 Oct;9(6-7):421-2. doi: 10.1016/s0960-8966(99)00043-7. Neuromuscul Disord. 1999. PMID: 10545048

5

Research database for dystrophin gene and protein expression. 35th ENMC Workshop, 6-8 October 1995, Naarden, The Netherlands.

Anderson LV. Anderson LV. Neuromuscul Disord. 1996 May;6(3):219. doi: 10.1016/0960-8966(96)00001-6. Neuromuscul Disord. 1996. PMID: 10712014 No abstract available.

6

Dysferlin expression after normal myoblast transplantation in SCID and in SJL mice.

Leriche-Guérin K, Anderson LV, Wrogemann K, Roy B, Goulet M, Tremblay JP. Leriche-Guérin K, et al. Among authors: anderson lv. Neuromuscul Disord. 2002 Feb;12(2):167-73. doi: 10.1016/s0960-8966(01)00254-1. Neuromuscul Disord. 2002. PMID: 11738359

7

Late onset in dysferlinopathy widens the clinical spectrum.

Klinge L, Dean AF, Kress W, Dixon P, Charlton R, Müller JS, Anderson LV, Straub V, Barresi R, Lochmüller H, Bushby K. Klinge L, et al. Among authors: anderson lv. Neuromuscul Disord. 2008 Apr;18(4):288-90. doi: 10.1016/j.nmd.2008.01.004. Neuromuscul Disord. 2008. PMID: 18396043

8

The differential gene expression profiles of proximal and distal muscle groups are altered in pre-pathological dysferlin-deficient mice.

von der Hagen M, Laval SH, Cree LM, Haldane F, Pocock M, Wappler I, Peters H, Reitsamer HA, Hoger H, Wiedner M, Oberndorfer F, Anderson LV, Straub V, Bittner RE, Bushby KM. von der Hagen M, et al. Among authors: anderson lv. Neuromuscul Disord. 2005 Dec;15(12):863-77. doi: 10.1016/j.nmd.2005.09.002. Epub 2005 Nov 8. Neuromuscul Disord. 2005. PMID: 16288871

9

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.

10

The phenotype of calpainopathy: diagnosis based on a multidisciplinary approach.

Pollitt C, Anderson LV, Pogue R, Davison K, Pyle A, Bushby KM. Pollitt C, et al. Among authors: anderson lv. Neuromuscul Disord. 2001 Apr;11(3):287-96. doi: 10.1016/s0960-8966(00)00197-8. Neuromuscul Disord. 2001. PMID: 11297944

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