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22. The diagnostic value of ultrastructural studies of skin-punch biopsies and buffy coat for the early diagnosis of some neurodegenerative diseases. Wisniewski KE Ann N Y Acad Sci; 1986; 477():285-311. PubMed ID: 3028228 [No Abstract] [Full Text] [Related]
23. Variation in protein structure and inborn errors in metabolism. Poole AE Dent Clin North Am; 1975 Jan; 19(1):47-62. PubMed ID: 803265 [No Abstract] [Full Text] [Related]
24. Ultrastructure of the human placenta in metabolic storage disease. Jones CJ; Lendon M; Chawner LE; Jauniaux E Placenta; 1990; 11(5):395-411. PubMed ID: 2127960 [TBL] [Abstract][Full Text] [Related]
27. [Experimental and prenatal diagnosis of lysosomal storage diseases]. Shi HP Zhonghua Yi Xue Za Zhi; 1988 Mar; 68(3):124-7, 10. PubMed ID: 3136887 [No Abstract] [Full Text] [Related]
29. Tay-Sachs disease as a model for screening inborn errors. Blitzer MG; McDowell GA Clin Lab Med; 1992 Sep; 12(3):463-80. PubMed ID: 1355703 [TBL] [Abstract][Full Text] [Related]
30. Acid maltase deficiency in adults: studies in four cases of a syndrome which may mimic muscular dystrophy or other myopathies. Engel AG Brain; 1970; 93(3):599-616. PubMed ID: 4918728 [No Abstract] [Full Text] [Related]
32. [Inborn errors of metabolism (author's transl)]. Bulovic D Srp Arh Celok Lek; 1973 Jun; 101(6):441-55. PubMed ID: 4206852 [No Abstract] [Full Text] [Related]
33. [Progress in the diagnosis of congenital metabolic central nervous system diseases. Review]. Nevsímalová S Cesk Neurol; 1973 Mar; 36(2):120-7. PubMed ID: 4266580 [No Abstract] [Full Text] [Related]
34. The liver in lipid storage disease: biochemical basis of pathogenesis and clinical features. Brady RO; James SP; Barranger JA Prog Liver Dis; 1982; 7():331-46. PubMed ID: 6810410 [No Abstract] [Full Text] [Related]
35. Prenatal diagnosis of GM2 gangliosidoses using a fluorogenic sulfated substrate. Inui K; Wenger DA; Furukawa M; Suehara N; Yutaka Y; Okada S; Tanizawa O; Yabuuchi H Clin Chim Acta; 1986 Jan; 154(2):145-50. PubMed ID: 3955840 [No Abstract] [Full Text] [Related]
36. Inborn errors of carbohydrate metabolism. Mayatepek E; Hoffmann B; Meissner T Best Pract Res Clin Gastroenterol; 2010 Oct; 24(5):607-18. PubMed ID: 20955963 [TBL] [Abstract][Full Text] [Related]
37. Identification of Sandhoff disease in a Thai family: clinical and biochemical characterization. Sakpichaisakul K; Taeranawich P; Nitiapinyasakul A; Sirisopikun T J Med Assoc Thai; 2010 Sep; 93(9):1088-92. PubMed ID: 20873083 [TBL] [Abstract][Full Text] [Related]
40. Changes of serum hexosaminidase for the presumptive diagnosis of type I Gaucher disease in Tay-Sachs carrier screening. Nakagawa S; Kumin S; Sachs G; Nitowsky HM Am J Med Genet; 1983 Mar; 14(3):525-32. PubMed ID: 6859103 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]