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Gastroenterology
|
September 1, 1989
Gallstone recurrence after successful oral bile acid treatment. A 12-year follow-up study and evaluation of long-term postdissolution treatment
N Villanova, F Bazzoli, F Taroni, et al.
Neurology
|
April 13, 2000
Cranial nerve involvement in CMT disease type 1 due to early growth response 2 gene mutation
D Pareyson, F Taroni, S Botti, et al.
Neurology
|
April 1, 1996
Phenotypic heterogeneity in hereditary neuropathy with liability to pressure palsies associated with chromosome 17p11.2-12 deletion
D Pareyson, V Scaioli, F Taroni, et al.
International Journal of Legal Medicine
|
September 1, 2005
Forensic identification of urine samples: a comparison between nuclear and mitochondrial DNA markers
V Castella, N Dimo-Simonin, C Brandt-Casadevall, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
January 15, 1991
cDNA cloning, sequence analysis, and chromosomal localization of the gene for human carnitine palmitoyltransferase
G Finocchiaro, F Taroni, M Rocchi, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
December 1, 1991
cDNA cloning, sequence analysis, and chromosomal localization of human carnitine palmitoyltransferase
G Finocchiaro, F Taroni, M Rocchi, et al.
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics
|
November 20, 2013
[Effect of prematurity on fat mass distribution and blood pressure at prepubertal age: a follow-up study]
P Piemontese, N Liotto, F Garbarino, et al.
Muscle & Nerve
|
December 8, 1998
Detection of hereditary neuropathy with liability to pressure palsies among patients with acute painless mononeuropathy or plexopathy
D Pareyson, A Solari, F Taroni, et al.
Journal of Health Services Research & Policy
|
September 4, 1997
Variation in hospital use and avoidable patient morbidity
F Taroni, F Repetto, D Z Louis, et al.
Neurology
|
May 29, 2003
Does CMT1A homozygosity cause more severe disease with root hypertrophy and higher CSF proteins?
D Pareyson, D Testa, M Morbin, et al.
Page
of 18
Search research articles
Search
Showing results (121-130 of 172) with videos related to
Sort By:
Page
of 18
Gastroenterology
|
September 1, 1989
Gallstone recurrence after successful oral bile acid treatment. A 12-year follow-up study and evaluation of long-term postdissolution treatment
N Villanova, F Bazzoli, F Taroni, et al.
Neurology
|
April 13, 2000
Cranial nerve involvement in CMT disease type 1 due to early growth response 2 gene mutation
D Pareyson, F Taroni, S Botti, et al.
Neurology
|
April 1, 1996
Phenotypic heterogeneity in hereditary neuropathy with liability to pressure palsies associated with chromosome 17p11.2-12 deletion
D Pareyson, V Scaioli, F Taroni, et al.
International Journal of Legal Medicine
|
September 1, 2005
Forensic identification of urine samples: a comparison between nuclear and mitochondrial DNA markers
V Castella, N Dimo-Simonin, C Brandt-Casadevall, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
January 15, 1991
cDNA cloning, sequence analysis, and chromosomal localization of the gene for human carnitine palmitoyltransferase
G Finocchiaro, F Taroni, M Rocchi, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
December 1, 1991
cDNA cloning, sequence analysis, and chromosomal localization of human carnitine palmitoyltransferase
G Finocchiaro, F Taroni, M Rocchi, et al.
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics
|
November 20, 2013
[Effect of prematurity on fat mass distribution and blood pressure at prepubertal age: a follow-up study]
P Piemontese, N Liotto, F Garbarino, et al.
Muscle & Nerve
|
December 8, 1998
Detection of hereditary neuropathy with liability to pressure palsies among patients with acute painless mononeuropathy or plexopathy
D Pareyson, A Solari, F Taroni, et al.
Journal of Health Services Research & Policy
|
September 4, 1997
Variation in hospital use and avoidable patient morbidity
F Taroni, F Repetto, D Z Louis, et al.
Neurology
|
May 29, 2003
Does CMT1A homozygosity cause more severe disease with root hypertrophy and higher CSF proteins?
D Pareyson, D Testa, M Morbin, et al.
Page
of 18