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F Taroni

Showing results (151-160 of 172) with videos related to

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Annals of the New York Academy of Sciences|December 10, 1999
Heterozygous null mutation in the P0 gene associated with mild Charcot-Marie-Tooth diseaseD Pareyson, D Menichella, S Botti, et al.
Neurology|July 23, 1998
Facial nerve is liable to pressure palsyT E Poloni, I M Merlo, E Alfonsi, et al.
Annals of the New York Academy of Sciences|November 1, 2017
Heterozygous Null Mutation in the P<sub>0</sub> Gene Associated with Mild Charcot-Marie-Tooth DiseaseD Pareyson, D Menichella, S Botti, et al.
Hepatology (Baltimore, Md.)|November 1, 1982
Ursodeoxycholic acid vs. chenodeoxycholic acid as cholesterol gallstone-dissolving agents: a comparative randomized studyE Roda, F Bazzoli, A M Labate, et al.
Neuroscience Letters|September 11, 2012
Novel and recurrent spastin mutations in a large series of SPG4 Italian familiesL Nanetti, S Baratta, M Panzeri, et al.
Human Mutation|May 26, 1998
Two CPT2 mutations in three Japanese patients with carnitine palmitoyltransferase II deficiency: functional analysis and association with polymorphic haplotypes and two clinical phenotypesK Wataya, J Akanuma, P Cavadini, et al.
Hepatology (Baltimore, Md.)|September 1, 1983
Diagnostic effectiveness of serum bile acids in liver diseases as evaluated by multivariate statistical methodsD Festi, A M Morselli Labate, A Roda, et al.
Neurology|November 17, 2010
Four novel cases of periaxin-related neuropathy and review of the literatureC Marchesi, M Milani, M Morbin, et al.
Health Policy (Amsterdam, Netherlands)|February 8, 1991
Hospital comparisons using a Euro Health Data Base for resource management and strategic planningF H France, A Alban, B Barber, et al.
Hepatology (Baltimore, Md.)|September 1, 1987
A population study on the prevalence of gallstone disease: the Sirmione StudyL Barbara, C Sama, A M Morselli Labate, et al.
Pageof 18

Showing results (151-160 of 172) with videos related to

Sort By:
Pageof 18
Annals of the New York Academy of Sciences|December 10, 1999
Heterozygous null mutation in the P0 gene associated with mild Charcot-Marie-Tooth diseaseD Pareyson, D Menichella, S Botti, et al.
Neurology|July 23, 1998
Facial nerve is liable to pressure palsyT E Poloni, I M Merlo, E Alfonsi, et al.
Annals of the New York Academy of Sciences|November 1, 2017
Heterozygous Null Mutation in the P<sub>0</sub> Gene Associated with Mild Charcot-Marie-Tooth DiseaseD Pareyson, D Menichella, S Botti, et al.
Hepatology (Baltimore, Md.)|November 1, 1982
Ursodeoxycholic acid vs. chenodeoxycholic acid as cholesterol gallstone-dissolving agents: a comparative randomized studyE Roda, F Bazzoli, A M Labate, et al.
Neuroscience Letters|September 11, 2012
Novel and recurrent spastin mutations in a large series of SPG4 Italian familiesL Nanetti, S Baratta, M Panzeri, et al.
Human Mutation|May 26, 1998
Two CPT2 mutations in three Japanese patients with carnitine palmitoyltransferase II deficiency: functional analysis and association with polymorphic haplotypes and two clinical phenotypesK Wataya, J Akanuma, P Cavadini, et al.
Hepatology (Baltimore, Md.)|September 1, 1983
Diagnostic effectiveness of serum bile acids in liver diseases as evaluated by multivariate statistical methodsD Festi, A M Morselli Labate, A Roda, et al.
Neurology|November 17, 2010
Four novel cases of periaxin-related neuropathy and review of the literatureC Marchesi, M Milani, M Morbin, et al.
Health Policy (Amsterdam, Netherlands)|February 8, 1991
Hospital comparisons using a Euro Health Data Base for resource management and strategic planningF H France, A Alban, B Barber, et al.
Hepatology (Baltimore, Md.)|September 1, 1987
A population study on the prevalence of gallstone disease: the Sirmione StudyL Barbara, C Sama, A M Morselli Labate, et al.
Pageof 18