Author:
van der Knaap Marjo S.,Valk Jacob
Publisher
Springer Berlin Heidelberg
Reference37 articles.
1. Beard ME, Sapirstein V, Kolodny EH, Holtzman E (1985) Peroxisomes in fibroblasts from skin of Refsums disease patients. J Histochem Cytochem 33: 480–484
2. Cammermeijer J (1956) Neuropathological changes in hereditary neuropathies: manifestation of the syndrome heredopathia atactica polyneuritiformis in the presence of interstitial hypertrophic polyneuropathy. J Neuropathol Exp Neurol 15: 340–367
3. Dick JPR, Meeran K, Gibberd FB, Clifford Rose F (1993) Hypokalaemia in acute Refsums disease. J R Soc Med 86: 17 1172
4. Dickson N, Mortimer JG, Faed JM, Pollard AC, Styles M, Peart DA (1989) A child with Refsums disease: successful treat-ment with diet and plasma exchange. Dev Med Child Neurol 31: 81–97
5. Djupesland G, Flottorp G, Refsum S (1983) Phytanic acid storage disease:hearing maintained after 15 years of dietary treatment. Neurology 33: 237–240