Nodular Lesions of Choroid Plexus in Hurler Disease

REFERENCES

• Dorfman A, Matalon R. The mucopolysaccharidoses (A Review). Proc Nat Acad Sci USA 73:630–637, 1976.
   PubMed Web of Science ®Google Scholar
• Matalon R, Dorfman A. Hurler's syndrome. An alpha-L-iduronidase deficiency. Biochem Biophys Res Chem 47:959–964, 1972.
   PubMed Web of Science ®Google Scholar
• Brante G. Gargoylism: A mucopolysaccharidosis. Scand J Clin Lab Invest 4:43–46, 1952.
   PubMed Web of Science ®Google Scholar
• Dorfman A, Lorincz AE. Occurrence of acid mucopolysaccharides in the Hurler syndrome. Proc Nat Acad Sci USA 43:443–446, 1957.
   PubMed Web of Science ®Google Scholar
• Haust MD, Orizago M, Bryans AM, Frank HF. The fine structure of liver in children with Hurler's syndrome. Exp Molec Path 10:141–161, 1969.
   PubMedGoogle Scholar
• Gordon BA, Haust MD. Hepatic acid mucopolysaccharides in the mucopolysaccharidoses type I, II and III. Clin Biochem 4:147–155, 1971.
   PubMed Web of Science ®Google Scholar
• Dekaban AS, Constanopoulos G. Mucopolysacchardosis types I, II, IIIA and V. Pathological and biochemical abnormalities in the neural and mesenchymal element of the brain. Acta Neuropath 39:1–7, 1977.
   PubMedGoogle Scholar
• Kint J.A, Decremont G, Carton D, Orye E, Hooft C. Mucopolysaccharidoses: secondarily induced abnormal distribution of lysosomal isoenzymes. Science 181:352–354, 1973.
   PubMedGoogle Scholar
• Suzuki K. Ganglioside pattern in normal and pathological brains. In: Aronson SM, Volk BW, eds., Inborn Disorders of Sphingolipids Metabolism. Oxford, UK: Pergamon Press, 215, 1967.
   Google Scholar
• Borri P, Hooghwinkel GJM, Edgar GP. Brain gangliosides in three forms of amaurotic idiocy and gargoylism. J Neurochem 18:1249–1256, 1966.
   Google Scholar
• Ballabio A, Gieselmann V. Lysosomal disorders: From storage to cellular damage. Biochim Biophys Acta 1793:684–696, 2009.
   Google Scholar
• Tuthill CR. Juvenile amaurotic idiocy. Arch Neurol Psych 32:198–209, 1937.
   Google Scholar
• Ashby WR, Steward EM, Watkin JH. Chondroosteodystrophy of the Hurler type. A pathological study. Brain 60:149–162, 1937.
   Google Scholar
• Henderson JL. Gargoylism. A review of principles features with report of five cases. Arch Dis Childhood 15:201–222, 1940.
   PubMedGoogle Scholar
• Strauss L. The pathology of gargoylism. Report of case and review of the literature. Am J Path 24:855–861, 1948.
   PubMedGoogle Scholar
• Lindsay S, Reilly WA, Gorham JT, Shaken R. Gargoylism. II Study of pathological lesions and clinical review of twelve cases. Am J Dis Childhood 76:239–306, 1948.
   PubMedGoogle Scholar
• Green MA. Gargoylism (Lipochondrodystrophy). J Neuropathol Exper Neurol 7:399–417, 1948.
   PubMedGoogle Scholar
• Magee RK. Leptomeningeal changes associated with lipochondrodystrophy/gargoylism. Report of case. Arch Neurol Psychiat 63:282–297, 1950.
   PubMedGoogle Scholar
• Henderson JK, MacGregor AR, Thannhauser SJ. Holden R. The pathology and biochemistry of gargoylism. Arch Dis Childhood 27:230–252, 1952.
   PubMedGoogle Scholar
• Naidoo D. Gargoylism/Hurler's disease. A neuropathological report. J Mental Sci 99:74–83, 1953.
   PubMedGoogle Scholar
• Norman RM, Urich H, France NE. Perivascular cavitation in the basal ganglia in gargoylism. J Mental Sci 105:1070–1077, 1959.
   PubMedGoogle Scholar
• Bishton R.L., Norman R.M., Tingey A. The pathology and chemistry of a case of gargoylism. J Clin Pathol 9:305–314, 1956.
   PubMedGoogle Scholar
• Schnabel R. Histochemische und biochemische Untersuchungen beim gargoylismus/ Pfaundler-Hurler Syndrome. Virchovs Arch Path Anat 334:379–398, 1961.
   PubMedGoogle Scholar
• Dekaban A, Rennert O. Histological, histochemical and chemical studies in Hurler's disease. J Neuropathol Exp Neurol 26:127, 1967.
   PubMedGoogle Scholar
• Aleu FP, Terry RD, Zellweger H. Electron microscopy of two cerebral biopsies in gargoylism. J Neuropath, Exper Neurol 24:304–317, 1965.
   PubMedGoogle Scholar
• Dekaban AS, Patton VM. Hurler's and Sanfilippo's variants of mucopolysaccharidosis. Cerebral pathology and lipid chemistry. Arch Pathol Lab Med 91:434–443, 1971.
   Google Scholar
• Gabrielli O, Polonara G, Regnicolo L, Petroni V, Scarabino T, Coppa GV, Salvolini U. Correlation between cerebral MRI abnormalities and mental retardation I patients with mucopolysaccharidoses. Am J Med Genet 125A:224–231, 2004.
   PubMedGoogle Scholar
• Vedolin L, Schwartz IVD, Komlos M, Schuch A, Azevedeo AC, Vieira T, Maeda FK, Marquez da Silva AM, Giuglani R. Brain MRI in mucopolysaccharidosis. Neurology 69:917–924, 2007.
   PubMed Web of Science ®Google Scholar
• Lee C, Dineen TE, Brack M, Kirsch JE, Runge VM, . The mucopolysaccharidoses: characterization by cranial MR imaging. Am J Neuroradiol 14:1285–1292, 1993.
   PubMed Web of Science ®Google Scholar
• Haust MD, Bryans AM, Frank HP. Children with Hurler's Syndrome institutionalized in Ontario's provincial facilities. Recent Adv Psych Press 5:93–101, 1963.
   Google Scholar
• Goldfischer S, Coltoff-Schiller B, Biempica L, Volinsky H. Lysosomes and the sclerotic arterial lesion in Hurler's disease. Human Pathol 6:633–637, 1975.
   PubMedGoogle Scholar
• Weller RO. Microscopic morphology and histology of human meninges. Morphologie 89:22–34, 2005.
   PubMedGoogle Scholar
• Shuangshoti S, Netsky MG. Histogenesis of choroid plexus in man. Am J Anat 118:283–316, 1970.
   PubMedGoogle Scholar
• Dorfman A, Matalon R. The Hurler and Hunter Syndromes. Am J Med 47:691–707, 1969.
   PubMed Web of Science ®Google Scholar
• Berra B, Riboni L, De Gasperi R, Gaini SM, Ragnotti G. Modification of gangliosides patterns in human meningiomas. J Neurochem 40:777–782, 1983.
   PubMed Web of Science ®Google Scholar
• Rhodin JAG. Ultrastructure of mammalian venous capillaries, venules and small collecting veins. J Ultrastruct Res 25:452–500, 1968.
   PubMedGoogle Scholar
• Sims ED. Diversity within pericytes. Clin. Exper Pharmacol Physiol 27:842–846, 2000.
   PubMed Web of Science ®Google Scholar
• Diaz-Flores L, Gutierrez R, Madrid JF, Varela H, Valladares F, Acosta E, Martin-Vassalo P, Diaz-Flores L, Jr. Pericytes. morphofunction, interactions and pathology in quiescent and activated mesenchymal niche. Review. Histol Histopathol 24:909–969, 2009.
   PubMed Web of Science ®Google Scholar
• Nicosia RF, Villaschi S. Rat aortic smooth muscle cells become pericytes during angiogenesis in vitro. Lab Invest 73:658–666, 1995.
   PubMed Web of Science ®Google Scholar
• Dunn J, Kernohan JW. Histologic changes within the choroid plexus of the lateral ventricle: their relation to age. Staff Meetings of the Mayo Clinic 30:607–615, 1955.
   PubMedGoogle Scholar
• Shuangshoti S, Netsky MG. Human choroid plexus: Morphologic and histochemical alterations with age. Am J Anat 128:73–96, 1970.
   PubMedGoogle Scholar