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Page 1
Cerebellar hypoplasia in respiratory chain dysfunction.
Lincke CR, van den Bogert C, Nijtmans LG, Wanders RJ, Tamminga P, Barth PG. Lincke CR, et al. Among authors: barth pg. Neuropediatrics. 1996 Aug;27(4):216-8. doi: 10.1055/s-2007-973792. Neuropediatrics. 1996. PMID: 8892374
Cultured human muscle cells and respiratory chain deficiencies.
Herzberg NH, Bolhuis PA, van den Bogert C, Barth PG. Herzberg NH, et al. Among authors: barth pg. Neuromuscul Disord. 1994 Jan;4(1):3-11. doi: 10.1016/0960-8966(94)90042-6. Neuromuscul Disord. 1994. PMID: 8173349 Review.
Defective remodeling of cardiolipin and phosphatidylglycerol in Barth syndrome.
Vreken P, Valianpour F, Nijtmans LG, Grivell LA, Plecko B, Wanders RJ, Barth PG. Vreken P, et al. Among authors: barth pg. Biochem Biophys Res Commun. 2000 Dec 20;279(2):378-82. doi: 10.1006/bbrc.2000.3952. Biochem Biophys Res Commun. 2000. PMID: 11118295
In this paper we present evidence that patients with the rare disorder X-linked cardioskeletal myopathy and neutropenia (Barth syndrome, MIM 302060) have a primary defect in CL and PG remodeling. We investigated phospholipid metabolism in cultured skin fibroblasts o …
In this paper we present evidence that patients with the rare disorder X-linked cardioskeletal myopathy and neutropenia (Barth syndro …
Peroxisomal disorders: a review.
Wanders RJ, Schutgens RB, Barth PG. Wanders RJ, et al. Among authors: barth pg. J Neuropathol Exp Neurol. 1995 Sep;54(5):726-39. doi: 10.1097/00005072-199509000-00016. J Neuropathol Exp Neurol. 1995. PMID: 7545216 Review.
251 results