Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

G Misiano

Showing results (11-20 of 17) with videos related to

Pageof 2
Sort By:
You have reached the last page of results.This site can display upto 17 results.
Journal of Endocrinological Investigation|September 1, 1994
Immunological pattern in patients with 21-hydroxylase deficiencyF Parlato, G Pisano, M Brillante, et al.
Digestive and Liver Disease : Official Journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver|August 3, 2004
C4BQ0: a genetic marker of familial HCV-related liver cirrhosisL Pasta, G Pietrosi, C Marrone, et al.
Scandinavian Journal of Immunology|May 1, 1992
Complement deficiency and antibody profile in survivors of meningococcal meningitis due to common serogroups in ItalyR D'Amelio, A Agostoni, R Biselli, et al.
European Journal of Pharmacology|July 4, 1998
Tetracycline inhibits the nitric oxide synthase activity induced by endotoxin in cultured murine macrophagesP D'Agostino, F Arcoleo, C Barbera, et al.
Burns : Journal of the International Society for Burn Injuries|November 15, 2011
Analysis of IL-6, IL-10 and IL-17 genetic polymorphisms as risk factors for sepsis development in burned patientsA Accardo Palumbo, G I Forte, D Pileri, et al.
Clinical and Experimental Immunology|November 11, 1999
Properdin deficiency in a large Swiss family: identification of a stop codon in the properdin gene, and association of meningococcal disease with lack of the IgG2 allotype marker G2m(n)P J Späth, A G Sjöholm, G N Fredrikson, et al.
Thyroid : Official Journal of the American Thyroid Association|May 1, 2001
Differential regulation of Fas-mediated apoptosis in both thyrocyte and lymphocyte cellular compartments correlates with opposite phenotypic manifestations of autoimmune thyroid diseaseC Giordano, P Richiusa, M Bagnasco, et al.
Pageof 2

Showing results (11-20 of 17) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 17 results.
Journal of Endocrinological Investigation|September 1, 1994
Immunological pattern in patients with 21-hydroxylase deficiencyF Parlato, G Pisano, M Brillante, et al.
Digestive and Liver Disease : Official Journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver|August 3, 2004
C4BQ0: a genetic marker of familial HCV-related liver cirrhosisL Pasta, G Pietrosi, C Marrone, et al.
Scandinavian Journal of Immunology|May 1, 1992
Complement deficiency and antibody profile in survivors of meningococcal meningitis due to common serogroups in ItalyR D'Amelio, A Agostoni, R Biselli, et al.
European Journal of Pharmacology|July 4, 1998
Tetracycline inhibits the nitric oxide synthase activity induced by endotoxin in cultured murine macrophagesP D'Agostino, F Arcoleo, C Barbera, et al.
Burns : Journal of the International Society for Burn Injuries|November 15, 2011
Analysis of IL-6, IL-10 and IL-17 genetic polymorphisms as risk factors for sepsis development in burned patientsA Accardo Palumbo, G I Forte, D Pileri, et al.
Clinical and Experimental Immunology|November 11, 1999
Properdin deficiency in a large Swiss family: identification of a stop codon in the properdin gene, and association of meningococcal disease with lack of the IgG2 allotype marker G2m(n)P J Späth, A G Sjöholm, G N Fredrikson, et al.
Thyroid : Official Journal of the American Thyroid Association|May 1, 2001
Differential regulation of Fas-mediated apoptosis in both thyrocyte and lymphocyte cellular compartments correlates with opposite phenotypic manifestations of autoimmune thyroid diseaseC Giordano, P Richiusa, M Bagnasco, et al.
Pageof 2