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.
48. Clinical, biochemical and ultrastructural studies of an atypical form of mucopolysaccharidosis. Loeb H; Tondeur M; Toppet M; Cremer N Acta Paediatr Scand; 1969 May; 58(3):220-8. PubMed ID: 4239322 [No Abstract] [Full Text] [Related]
49. Leukocyte beta-galactosidase activity in the diagnosis of generalized GM 1 gangliosidosis. Singer HS; Nankervis GA; Schafer IA Pediatrics; 1972 Mar; 49(3):352-61. PubMed ID: 4258708 [No Abstract] [Full Text] [Related]
50. Atypical mucopolysaccharidosis and successful keratoplasty. Gollance RB; D'Amico RA Am J Ophthalmol; 1967 Oct; 64(4):707-16. PubMed ID: 4228834 [No Abstract] [Full Text] [Related]
51. [Generalized, Norman-Landing type, GM1 gangliosidosis: study of a case diagnosed during the life of the patient]. Seringe P; Plainfosse B; Lautmann F; Lorilloux J; Calamy G; Berry JP; Watchi JM Ann Pediatr (Paris); 1968 Mar; 15(3):165-84. PubMed ID: 5744290 [No Abstract] [Full Text] [Related]
52. Further studies of congenital hereditary endothelial dystrophy of the cornea. Kenyon KR; Maumenee AE Am J Ophthalmol; 1973 Oct; 76(4):419-39. PubMed ID: 4270338 [No Abstract] [Full Text] [Related]
53. GM1-gangliosidosis without chondrodystrophy or visceromegaly. B-galactosidase deficiency with gangliosidosis and the excessive excretion of a keratan sulfate. Wolfe LS; Callahan J; Fawcett JS; Andermann F; Scriver CR Neurology; 1970 Jan; 20(1):23-44. PubMed ID: 4243740 [No Abstract] [Full Text] [Related]
54. Enzymatic and biochemical diagnosis of inborn lysosomal diseases with neurological symptoms. Hultberg B; Ockerman PA; Sjöblad S Eur Neurol; 1972; 7(1):101-18. PubMed ID: 4259742 [No Abstract] [Full Text] [Related]
55. Corneal clouding with increased acid mucopolysaccharide accumulation in Bowman's membrane. Rodrigues MM; Calhoun J; Harley RD Am J Ophthalmol; 1975 Jun; 79(6):916-24. PubMed ID: 49147 [TBL] [Abstract][Full Text] [Related]
56. [Ocular histopathologic study of Marfan syndrome in a newborn infant]. Verstappen A; Haumont D; Depierreux M; Danis P J Fr Ophtalmol; 1982; 5(11):699-705. PubMed ID: 7153470 [No Abstract] [Full Text] [Related]
57. Ultrastructure of the skin in the genetic mucopolysaccharidoses. Belcher RW Arch Pathol; 1972 Dec; 94(6):511-8. PubMed ID: 4263882 [No Abstract] [Full Text] [Related]