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S Marinoni

Showing results (11-20 of 24) with videos related to

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Minerva Pediatrica|September 15, 1984
[Group B streptococcus infections in newborn infants]U de Vonderweid, S Marinoni, F Colonna, et al.
Mutation Research|March 1, 1992
DNA repair investigations in nine Italian patients affected by trichothiodystrophyM Stefanini, S Giliani, T Nardo, et al.
American Journal of Human Genetics|October 3, 1998
Analysis of mutations in the XPD gene in Italian patients with trichothiodystrophy: site of mutation correlates with repair deficiency, but gene dosage appears to determine clinical severityE Botta, T Nardo, B C Broughton, et al.
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics|September 1, 1988
[Changes in the immunologic profile of newly-diagnosed diabetic patients during the first year of the disease]M G Pizzul, C Betterle, C De Campo, et al.
Helvetica Paediatrica Acta|February 1, 1989
High frequency of empty sella syndrome in children with growth hormone deficiencyM Pocecco, C de Campo, S Marinoni, et al.
Journal of Pineal Research|February 19, 1998
Melatonin regulates the respiratory burst of human neutrophils and their depolarizationC Pieri, R Recchioni, F Moroni, et al.
Mutation Research|July 1, 1988
Chromosome and blood marker studies in families of patients affected by xeroderma pigmentosum and trichothiodystrophyF Nuzzo, M Stefanini, M Rocchi, et al.
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics|July 1, 1991
[Comparison of high-dose immunoglobulin and cyclosporine in newly diagnosed diabetic children]C Romanello, F Grossi, L Radillo, et al.
Journal of Medical Genetics|January 1, 1990
Search for consanguinity within and among families of patients with trichothiodystrophy associated with xeroderma pigmentosumF Nuzzo, G Zei, M Stefanini, et al.
Human Genetics|October 1, 1986
Xeroderma pigmentosum (complementation group D) mutation is present in patients affected by trichothiodystrophy with photosensitivityM Stefanini, P Lagomarsini, C F Arlett, et al.
Pageof 3

Showing results (11-20 of 24) with videos related to

Sort By:
Pageof 3
Minerva Pediatrica|September 15, 1984
[Group B streptococcus infections in newborn infants]U de Vonderweid, S Marinoni, F Colonna, et al.
Mutation Research|March 1, 1992
DNA repair investigations in nine Italian patients affected by trichothiodystrophyM Stefanini, S Giliani, T Nardo, et al.
American Journal of Human Genetics|October 3, 1998
Analysis of mutations in the XPD gene in Italian patients with trichothiodystrophy: site of mutation correlates with repair deficiency, but gene dosage appears to determine clinical severityE Botta, T Nardo, B C Broughton, et al.
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics|September 1, 1988
[Changes in the immunologic profile of newly-diagnosed diabetic patients during the first year of the disease]M G Pizzul, C Betterle, C De Campo, et al.
Helvetica Paediatrica Acta|February 1, 1989
High frequency of empty sella syndrome in children with growth hormone deficiencyM Pocecco, C de Campo, S Marinoni, et al.
Journal of Pineal Research|February 19, 1998
Melatonin regulates the respiratory burst of human neutrophils and their depolarizationC Pieri, R Recchioni, F Moroni, et al.
Mutation Research|July 1, 1988
Chromosome and blood marker studies in families of patients affected by xeroderma pigmentosum and trichothiodystrophyF Nuzzo, M Stefanini, M Rocchi, et al.
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics|July 1, 1991
[Comparison of high-dose immunoglobulin and cyclosporine in newly diagnosed diabetic children]C Romanello, F Grossi, L Radillo, et al.
Journal of Medical Genetics|January 1, 1990
Search for consanguinity within and among families of patients with trichothiodystrophy associated with xeroderma pigmentosumF Nuzzo, G Zei, M Stefanini, et al.
Human Genetics|October 1, 1986
Xeroderma pigmentosum (complementation group D) mutation is present in patients affected by trichothiodystrophy with photosensitivityM Stefanini, P Lagomarsini, C F Arlett, et al.
Pageof 3