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22. Pseudo-Hurler polydystrophy (mucolipidosis 3). A clinical, biochemical and ultrastructural study. Stein H; Berman ER; Livni N; Merin S; Sheskin J; Cohen T Isr J Med Sci; 1974 May; 10(5):463-75. PubMed ID: 4213328 [No Abstract] [Full Text] [Related]
23. A mucopolysaccharide storage disease with involvement of the renal glomerular epithelium. Scott CR; Lagunoff D; Pritzl P Am J Med; 1973 Apr; 54(4):549-56. PubMed ID: 4348719 [No Abstract] [Full Text] [Related]
24. The genetic mucopolysaccharidoses and mucolipidoses: review and comment. Legum CP; Schorr S; Berman ER Adv Pediatr; 1976; 22():305-47. PubMed ID: 131478 [No Abstract] [Full Text] [Related]
25. [Mucopolysaccharidoses in children. Experience of a general pediatric service. 11 cases]. Chaabouni M; Ben Slimen M; Boudawara M; Ben Amar H; Mahfoudh A; Ayadi F; Ben Halima N; Hachicha M; Karaay A; Triki A Tunis Med; 2001 Apr; 79(4):222-30. PubMed ID: 11515481 [TBL] [Abstract][Full Text] [Related]
26. The abnormalities of lysosomal enzymes in mucopolysacc- haridoses. Van Hoof F; Hers HG Eur J Biochem; 1968 Dec; 7(1):34-44. PubMed ID: 4236776 [No Abstract] [Full Text] [Related]
27. Macular cherry-red spot, corneal clouding, and beta-galactosidase deficiency. Clinical, biochemical, and electron microscopic study of a new autosomal recessive storage disease. Goldberg MF; Cotlier E; Fichenscher LG; Kenyon K; Enat R; Borowsky SA Arch Intern Med; 1971 Sep; 128(3):387-98. PubMed ID: 4999185 [No Abstract] [Full Text] [Related]
28. Case report. Case 2 (mucolipidosis III). Feingold M; Bull MJ; Darling DB Birth Defects Orig Artic Ser; 1974; 10(8):99-104. PubMed ID: 4218496 [No Abstract] [Full Text] [Related]
29. [Clinical, genetic and biochemical study of a case of gargoylism]. Lefebvre G; Duquennoy-Wanheuverswyn C Pediatrie; 1965; 20(5):604-9. PubMed ID: 4954479 [No Abstract] [Full Text] [Related]
30. Sanfilippo type C disease: clinical findings in four patients with a new variant of mucopolysaccharidosis III. Bartsocas C; Gröbe H; van de Kamp JJ; von Figura K; Kresse H; Klein U; Giesberts MA Eur J Pediatr; 1979 Apr; 130(4):251-8. PubMed ID: 108106 [TBL] [Abstract][Full Text] [Related]
31. Fucolipids and blood group glycolipids in normal and tumor tissue. Hakomori S Prog Biochem Pharmacol; 1975; 10():167-96. PubMed ID: 1093206 [No Abstract] [Full Text] [Related]
32. Letter: Chondroitinsulphaturia with alpha-L-iduronidase deficiency. Babarik A; Benson PF; Dean MF; Muir H Lancet; 1974 Aug; 2(7878):464-5. PubMed ID: 4136880 [No Abstract] [Full Text] [Related]
33. Letter: Phenotypic variation in alpha-L-iduronidase deficiency. Leisti J; Rimoin DL; Kaback MM; Hollister DW; DEn Tandt W; Neufeld E; Matalon R; Philippart M Lancet; 1975 Jun; 1(7920):1344. PubMed ID: 49545 [No Abstract] [Full Text] [Related]
35. Fucosidosis in Calabria: founder effect or high gene frequency. Romeo G; Borrone C; Gatti R; Durand P Lancet; 1977 Feb; 1(8007):368-9. PubMed ID: 64894 [No Abstract] [Full Text] [Related]
36. Mannosidosis: a clinical and histopathologic study. Kjellman B; Gamstorp I; Brun A; Ockerman PA; Palmgren B J Pediatr; 1969 Sep; 75(3):366-73. PubMed ID: 4979627 [No Abstract] [Full Text] [Related]
37. Acid hydrolases in the serum and liver in mucopolysaccharidoses types I and 3. Gordon BA; Feleki V Clin Biochem; 1970 Sep; 3(3):193-202. PubMed ID: 4258597 [No Abstract] [Full Text] [Related]
38. Mucopolysaccharidoses and mucolipidoses. Van Hoof F J Clin Pathol Suppl (R Coll Pathol); 1974; 8():64-93. PubMed ID: 4220223 [No Abstract] [Full Text] [Related]
39. [Mucosulfatidosis. Study of 3 familial cases]. Couchot J; Pluot M; Schmauch MA; Pennaforte F; Fandre M Arch Fr Pediatr; 1974 Oct; 31(8):775-95. PubMed ID: 4218948 [No Abstract] [Full Text] [Related]
40. Biochemical and molecular analysis in mucopolysaccharidoses: what a paediatrician must know. Filocamo M; Tomanin R; Bertola F; Morrone A Ital J Pediatr; 2018 Nov; 44(Suppl 2):129. PubMed ID: 30442161 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]