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Neurology|May 16, 2002
A one-year study on the pharmacodynamic profile of interferon-beta1a in MSF Bagnato, C Pozzilli, C Scagnolari, et al.
Acta Neurologica Scandinavica|April 1, 1992
HLA-linked spinocerebellar ataxia: a clinical and genetic study of large Italian kindredsM Spadaro, P Giunti, P Lulli, et al.
Human Molecular Genetics|September 1, 1993
The gene for spinal cerebellar ataxia 1 (SCA1) is flanked by two closely linked highly polymorphic microsatellite lociC Jodice, M Frontali, F Persichetti, et al.
Environmental Toxicology and Chemistry|August 13, 2024
Dissolved Barium Causes Toxicity to Groundwater CyclopoidaMerrin S Adams, Kitty S McKnight, David M Spadaro, et al.
American Journal of Human Genetics|June 1, 1994
Effect of trinucleotide repeat length and parental sex on phenotypic variation in spinocerebellar ataxia IC Jodice, P Malaspina, F Persichetti, et al.
Brain : a Journal of Neurology|December 1, 1992
Autosomal dominant pure cerebellar ataxia. Neurological and genetic studyM Frontali, M Spadaro, P Giunti, et al.
Rivista Di Neurologia|January 1, 1987
Non-clinical tests for the diagnosis of multiple sclerosisP M Rossini, M Caramia, F Lavaroni, et al.
Cancer Research|April 18, 2001
A light, nontoxic interleukin 12 protocol inhibits HER-2/neu mammary carcinogenesis in BALB/c transgenic mice with established hyperplasiaL Cifaldi, E Quaglino, E Di Carlo, et al.
American Journal of Human Genetics|July 1, 1991
The gene for autosomal dominant spinocerebellar ataxia (SCA1) maps telomeric to the HLA complex and is closely linked to the D6S89 locus in three large kindredsH Y Zoghbi, C Jodice, L A Sandkuijl, et al.
Human Molecular Genetics|September 25, 1997
Episodic ataxia type 2 (EA2) and spinocerebellar ataxia type 6 (SCA6) due to CAG repeat expansion in the CACNA1A gene on chromosome 19pC Jodice, E Mantuano, L Veneziano, et al.
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