Výsledky vyhledávání - "L. V. Anderson"

Risk of Pneumothorax Not Increased by Obstructive Lung Disease in Percutaneous Needle Biopsy

Autor: C. L. V. Anderson, J. C. A. Crespo, Thiam H. Lie

Publikováno v: Chest. 105:1705-1708

All computed tomography directed lung biopsies from 1987 to 1991 were retrospectively reviewed. Pneumothorax occurred in 33 of 93 (35 percent) patients; 16 of these patients or 17 percent overall required a chest tube. No correlation was found betwee

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::99bc651e375c4b09e4203c8d3dd652a4
https://doi.org/10.1378/chest.105.6.1705

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Partial alpha-sarcoglycan deficiency with retention of the dystrophin-glycoprotein complex in a LGMD2D family

Autor: M, Vainzof, E S, Moreira, M, Canovas, L V, Anderson, R C, Pavanello, M R, Passos-Bueno, M, Zatz

Publikováno v: Musclenerve. 23(6)

In patients with sarcoglycan (SG) deficiency, a primary defect in any one of the four SG proteins usually leads to reduced expression of the whole SG complex. We report a limb-girdle muscular dystrophy type 2D family (LGMD2D), with variable phenotype

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::099cf1bf33a3b5e8aab3768461a885ea
https://pubmed.ncbi.nlm.nih.gov/10842281

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Alternative dystrophin gene transcripts in golden retriever muscular dystrophy

Autor: S J, Schatzberg, L V, Anderson, S D, Wilton, J N, Kornegay, C J, Mann, G G, Solomon, N J, Sharp

Publikováno v: Musclenerve. 21(8)

Golden retriever muscular dystrophy (GRMD), the canine model of Duchenne muscular dystrophy (DMD), is caused by a splice site mutation in the dystrophin gene. This mutation predicts a premature termination codon in exon 8 and a peptide that is 5% the

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::a346abf5c39e2944472d5cf81242d063
https://pubmed.ncbi.nlm.nih.gov/9655116

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

Autor: C A, Sewry, J, Taylor, L V, Anderson, E, Ozawa, R, Pogue, F, Piccolo, K, Bushby, V, Dubowitz, F, Muntoni

Publikováno v: Neuromuscular disorders : NMD. 6(6)

We have identified 12 cases from a group of 45 patients with early onset limb-girdle muscular dystrophy (LGMD), who have a deficiency of the 50 kDa dystrophin-associated glycoprotein, alpha-sarcoglycan. An additional male sibling of one case was also

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::3afc779bae2c29d8ea5ded454ce91e23
https://pubmed.ncbi.nlm.nih.gov/9027857

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Characterization of dp6troglycan-laminin interaction in peripheral nerve

Autor: H, Yamada, A, Chiba, T, Endo, A, Kobata, L V, Anderson, H, Hori, H, Fukuta-Ohi, I, Kanazawa, K P, Campbell, T, Shimizu, K, Matsumura

Publikováno v: Journal of neurochemistry. 66(4)

Dystoroglycan is encoded by a single gene and cleaved into two proteins, alpha and beta-dystroglycan, by posttranslational processing. The 120kDa peripheral nerve isoform of alpha-dystroglycan binds laminin-2 comprised of the alpha 2, beta 1, and gam

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::b3951e9a03d9def9c10226f62fbefd83
https://pubmed.ncbi.nlm.nih.gov/8627307

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