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- Banna M., Hollenberg R. Compressive meningeal hypertrophy in mucopolysaccharidosis. AJNR Am J Neuroradiol. 1987 Mar-Apr;8(2):385–386. [PMC free article] [PubMed] [Google Scholar]
- Belani K. G., Krivit W., Carpenter B. L., Braunlin E., Buckley J. J., Liao J. C., Floyd T., Leonard A. S., Summers C. G., Levine S. Children with mucopolysaccharidosis: perioperative care, morbidity, mortality, and new findings. J Pediatr Surg. 1993 Mar;28(3):403–410. doi: 10.1016/0022-3468(93)90240-l. [DOI] [PubMed] [Google Scholar]
- Bunge S., Steglich C., Zuther C., Beck M., Morris C. P., Schwinger E., Schinzel A., Hopwood J. J., Gal A. Iduronate-2-sulfatase gene mutations in 16 patients with mucopolysaccharidosis type II (Hunter syndrome). Hum Mol Genet. 1993 Nov;2(11):1871–1875. doi: 10.1093/hmg/2.11.1871. [DOI] [PubMed] [Google Scholar]
- Cleary M. A., Wraith J. E. Management of mucopolysaccharidosis type III. Arch Dis Child. 1993 Sep;69(3):403–406. doi: 10.1136/adc.69.3.403. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Diaz J. H., Belani K. G. Perioperative management of children with mucopolysaccharidoses. Anesth Analg. 1993 Dec;77(6):1261–1270. doi: 10.1213/00000539-199312000-00028. [DOI] [PubMed] [Google Scholar]
- Donaldson M. D., Pennock C. A., Berry P. J., Duncan A. W., Cawdery J. E., Leonard J. V. Hurler syndrome with cardiomyopathy in infancy. J Pediatr. 1989 Mar;114(3):430–432. doi: 10.1016/s0022-3476(89)80565-7. [DOI] [PubMed] [Google Scholar]
- Fong L. V., Menahem S., Wraith J. E., Chow C. W. Endocardial fibroelastosis in mucopolysaccharidosis type VI. Clin Cardiol. 1987 Jun;10(6):362–364. doi: 10.1002/clc.4960100612. [DOI] [PubMed] [Google Scholar]
- Hayflick S., Rowe S., Kavanaugh-McHugh A., Olson J. L., Valle D. Acute infantile cardiomyopathy as a presenting feature of mucopolysaccharidosis VI. J Pediatr. 1992 Feb;120(2 Pt 1):269–272. doi: 10.1016/s0022-3476(05)80441-x. [DOI] [PubMed] [Google Scholar]
- Hopwood J. J., Morris C. P. The mucopolysaccharidoses. Diagnosis, molecular genetics and treatment. Mol Biol Med. 1990 Oct;7(5):381–404. [PubMed] [Google Scholar]
- SCHEIE H. G., HAMBRICK G. W., Jr, BARNESS L. A. A newly recognized forme fruste of Hurler's disease (gargoylism). Am J Ophthalmol. 1962 May;53:753–769. [PubMed] [Google Scholar]
- Scott H. S., Nelson P. V., Cooper A., Wraith J. E., Hopwood J. J., Morris C. P. Mucopolysaccharidosis type I (Hurler syndrome): linkage disequilibrium indicates the presence of a major allele. Hum Genet. 1992 Mar;88(6):701–702. doi: 10.1007/BF02265303. [DOI] [PubMed] [Google Scholar]
- Sjøgren P., Pedersen T., Steinmetz H. Mucopolysaccharidoses and anaesthetic risks. Acta Anaesthesiol Scand. 1987 Apr;31(3):214–218. doi: 10.1111/j.1399-6576.1987.tb02553.x. [DOI] [PubMed] [Google Scholar]
- Wraith J. E., Alani S. M. Carpal tunnel syndrome in the mucopolysaccharidoses and related disorders. Arch Dis Child. 1990 Sep;65(9):962–963. doi: 10.1136/adc.65.9.962. [DOI] [PMC free article] [PubMed] [Google Scholar]