Showing results (11-20 of 117) with videos related to
Sort By:
Pageof 12
Birth Defects Original Article Series|January 1, 1980
The uptake of enzymes into lysosomes: an overviewE F NeufeldClinical Genetics|February 1, 1984
Mucopolysaccharidosis III B: hybridization studies on fibroblasts from a mild case and fibroblasts from severe patientsA Ballabio, R Pallini, P Di NataleHuman Genetics|October 1, 1993
Heterogeneity of DNA and RNA in Hunter patientsT Annella, A Daniele, P Di NataleBollettino Della Societa Italiana Di Biologia Sperimentale|September 15, 1978
[Preparation of iduronate sulfatase from the human placenta]P Di Natale, P Murino, A PerfumoMolecular and Cellular Biochemistry|March 5, 1990
Synthesis of rhodanese in Hep 3B cellsR Pallini, C Cannella, P Di NataleAmerican Journal of Human Genetics|March 7, 1998
NAGLU mutations underlying Sanfilippo syndrome type BA Schmidtchen, D Greenberg, H G Zhao, et al.Biochemical and Biophysical Research Communications|April 15, 1983
Synthesis and maturation of cross-reactive glycoprotein in fibroblasts deficient in arylsulfatase A activityG Bach, E F NeufeldHuman Mutation|April 17, 1999
Two novel mutations of the arylsulfatase B gene in two Italian patients with severe form of mucopolysaccharidosis. Mutations in brief no. 127. OnlineG R Villani, N Balzano, P Di NataleAmerican Journal of Human Genetics|January 1, 1979
Detection of hunter heterozygotes by enzymatic analysis of hair rootsN Nwokoro, E F NeufeldScience (New York, N.Y.)|July 3, 1970
Scheie and Hurler syndromes: apparent identity of the biochemical defectU Wiesmann, E F NeufeldPageof 12