Menkes' disease: Clinical, therapeutic and biochemical studies
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://www.springerlink.com/index/pdf/10.1007/BF01810339
Reference11 articles.
1. Baerlocher, K., Nussbaumer, A., Werder, E. A. and Spycher, M. Menkes' kinky hair disease: confirmation of copper deficiency. Abstr.Pediatr. Res. 8 (1974) 135
2. Byers, P. H., Siegel, R. C., Holbrook, K. A., Narayanan, A. S., Bornstein, P. and Hall, J. G. X-linked cutis laxa. Defective cross-link formation in collagen due to decreased lysyl oxidase activity.N. Engl. J. Med. 303 (1980) 61–65
3. Danks, D. M., Campbell, P. E., Walker-Smith, J., Stevens, B. J., Gillespie, J. M., Blomfield, J. and Turner, B. Menkes' kinky-hair syndrome.Lancet 1 (1972) 1100–1102
4. Grover, W. D., Johnson, W. C. and Henkin, R. I. Clinical and biochemical aspects of trichopoliodystrophy.Ann. Neurol. 5 (1979) 65–71
5. Horn, N. Menkes X-linked disease: heterozygous phenotype in uncloned fibroblast cultures.J. Med. Genet. 17 (1980) 257–261
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1. Chelating principles in Menkes and Wilson diseases;Journal of Inorganic Biochemistry;2019-01
2. A 37-year-old Menkes disease patient-Residual ATP7A activity and early copper administration as key factors in beneficial treatment;Clinical Genetics;2017-10-09
3. Impaired osteogenesis in Menkes disease-derived induced pluripotent stem cells;Stem Cell Research & Therapy;2015-09-07
4. Life-span and Menkes kinky hair syndrome: report of a 13-year course of this disease;Clinical Genetics;2008-06-28
5. Treatment of Wilson and Menkes Diseases;Chemical Reviews;1999-08-20
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