These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
140 related articles for article (PubMed ID: 2128891)
41. [Hereditary bone dystrophy. Pyknodysostosis]. Sada Moreno E; Martinez Lage JL; Vazquez Ajuria F; Jimenez Burkhardt A Rev Esp Estomatol; 1980; 28(6):331-6. PubMed ID: 6798645 [No Abstract] [Full Text] [Related]
42. [Impossibility of detecting heterozygote mucopolysaccharidosis by lymphocyte metachromasia in culture]. de Magalhaes J; Maroteaux P Ann Genet; 1974 Mar; 17(1):41-4. PubMed ID: 4135577 [No Abstract] [Full Text] [Related]
43. [Computer-assisted genetic files and diagnosis]. Schorderet D Schweiz Rundsch Med Prax; 1985 Apr; 74(14):347-50. PubMed ID: 3922033 [No Abstract] [Full Text] [Related]
46. [Sanfilippo's disease--accompanying findings in maxillofacial surgery as an aid to differential diagnosis of type III mucopolysaccharidosis]. Radtke J Dtsch Z Mund Kiefer Gesichtschir; 1988; 12(4):289-92. PubMed ID: 3149221 [No Abstract] [Full Text] [Related]
47. [Global functional management of mucopolysaccharidoses]. Boulay C; Lemoine M; Chabrol B Arch Pediatr; 2014 Jun; 21 Suppl 1():S46-9. PubMed ID: 25063385 [TBL] [Abstract][Full Text] [Related]
49. [Treatment of mucopolysaccharidoses with perfusions of human plasma. Changes in mucopolysaccharides of high and low molecular weight]. Lambotte C; Winand R; Chantraine JM; Biertho G; Leruth-Fafchamps Y Acta Paediatr Belg; 1971; 25(6):297-309. PubMed ID: 4258789 [No Abstract] [Full Text] [Related]
50. [Biochemical characteristics and diagnosis of lysosomal diseases related to hereditary glycosidase deficiency]. Vidershaĭn GIa Vestn Akad Med Nauk SSSR; 1982; (6):42-7. PubMed ID: 6810572 [No Abstract] [Full Text] [Related]
51. [Test for the characterization of hypermucopolysaccharidurias]. Rufini S; Ghebregzabher M; Lato M Minerva Pediatr; 1980 Dec; 32(24):1371-4. PubMed ID: 6454060 [No Abstract] [Full Text] [Related]
52. [Achievements of biochemical genetics in studying hereditary pathology of the connective tissue]. Krasnopol'skaia KD Vestn Akad Med Nauk SSSR; 1982; (6):70-6. PubMed ID: 6810573 [No Abstract] [Full Text] [Related]
53. Musculoskeletal manifestations of lysosomal storage disorders. Aldenhoven M; Sakkers RJ; Boelens J; de Koning TJ; Wulffraat NM Ann Rheum Dis; 2009 Nov; 68(11):1659-65. PubMed ID: 19822711 [TBL] [Abstract][Full Text] [Related]
54. Early diagnosis of mucopolysaccharidosis. Hugh-Jones K Lancet; 1983 Dec; 2(8362):1300. PubMed ID: 6139633 [No Abstract] [Full Text] [Related]
55. Comments on the plasma treatment of the mucopolysaccharidoses. Diferrante NM; Nicholds BL Birth Defects Orig Artic Ser; 1974; 10(12):234-8. PubMed ID: 4218768 [No Abstract] [Full Text] [Related]
56. Otorhinolaryngological manifestations of the mucopolysaccharidoses. Simmons MA; Bruce IA; Penney S; Wraith E; Rothera MP Int J Pediatr Otorhinolaryngol; 2005 May; 69(5):589-95. PubMed ID: 15850680 [TBL] [Abstract][Full Text] [Related]
57. [Pathological and histochemical findings in a case of gargoylism]. Perper I; Wolman M Dapim Refuiim; 1965 Oct; 24(5):477-82. PubMed ID: 4956029 [No Abstract] [Full Text] [Related]
58. Phenotypic and population features of MPS IH in Quibor, Venezuela. Arias S; Zimmer E; Pinto-Cisternas J; Quero J Prog Clin Biol Res; 1982; 104():487-98. PubMed ID: 6819578 [No Abstract] [Full Text] [Related]
60. The Hurler/Scheie phenotype in children from a consanguineous marriage: case report with electronmicroscopy of the conjunctiva and ERG. Jensen OA; Pedersen C; Vestermark S; Warburg M Metab Pediatr Ophthalmol; 1980; 4(3):133-4. PubMed ID: 6779061 [No Abstract] [Full Text] [Related] [Previous] [Next] [New Search]