R. Pallini

发表

Chemical modification of rhodanese with sulphite.

R. Berni, G. Musci, C. Cannella, 1991, Free radical research communications.

GM2 gangliosidosis with hexosaminidase A and B defect: Report of a family with motor neuron disease-like phenotype

A. Rossi, G. Guazzi, A. Federico, 1986, Journal of Inherited Metabolic Disease.

Synthesis of rhodanese in Hep 3B cells

P. Natale, C. Cannella, R. Pallini, 1990, Molecular and Cellular Biochemistry.

Biochemical diagnosis of mucopolysaccharidoses: Experience of 297 diagnoses in a 15-year period (1977–1991)

P. Natale, A. Daniele, T. Annella, 1993, Journal of Inherited Metabolic Disease.

Normal rhodanese activity in leukocytes from Leber patients

G. Guazzi, A. Federico, P. Martelli, 1987, Neurology.

Mucopolysaccharidosis III B: hybridization studies on fibroblasts from a mild case and fibroblasts from severe patients

A. Ballabio, P. Natale, R. Pallini, 1984, Clinical genetics.

Sanfilippo Type C Diagnosis: Assay of Acetyl-CoA: αGlucosaminide N-Acetyltransferase Using [14C]Glucosamine as Substrate and Leukocytes as Enzyme Source

P. Natale, I. G. Leder, R. Pallini, 1984, Pediatric Research.

Cloning and sequence analysis of the human liver rhodanese: comparison with the bovine and chicken enzymes.

G. Guazzi, M. Cacace, C. Cannella, 1991, Biochemical and biophysical research communications.

Electrocardiographic abnormalities in Leber's hereditary optic atrophy

G. Guazzi, A. Federico, M. Dotti, 1987, Journal of Inherited Metabolic Disease.