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Annali Italiani Di Chirurgia
|
January 1, 1991
[The role of endoscopy in the hemorrhagic complications of gastroduodenal ulcer]
A Scamporrino, U De Petris, G Novelli, et al.
American Journal of Human Genetics
|
January 1, 1995
Is congenital bilateral absence of vas deferens a primary form of cystic fibrosis? Analyses of the CFTR gene in 67 patients
B Mercier, C Verlingue, W Lissens, et al.
Cellular and Molecular Life Sciences : CMLS
|
November 2, 2005
Rescue of heterochromatin organization in Hutchinson-Gilford progeria by drug treatment
M Columbaro, C Capanni, E Mattioli, et al.
Biochemistry and Molecular Biology International
|
April 17, 1999
Cellular uptake and delivery monitoring of liposome/DNA complexes during in vitro transfection of CFTR gene
A L Serafino, G Novelli, S Di Sario, et al.
La Clinica Terapeutica
|
December 31, 1985
[Comparative evaluation in the treatment of arterial hypertension between prolonged-action clonidine and atenolol]
M La Vecchia, G Vergara, G Iannuzzi, et al.
Clinical and Experimental Immunology
|
June 26, 2016
Polymorphisms in STAT-4, IL-10, PSORS1C1, PTPN2 and MIR146A genes are associated differently with prognostic factors in Italian patients affected by rheumatoid arthritis
C Ciccacci, P Conigliaro, C Perricone, et al.
American Journal of Medical Genetics
|
April 1, 1990
Autosomal dominant polycystic kidney disease: a linkage evaluation of heterogeneity in Italy. Italian Collaborative Group on Polycystic Kidney Disease
P Mandich, G Restagno, G Novelli, et al.
American Journal of Medical Genetics
|
February 13, 2001
Exclusion of the elastin gene in the pathogenesis of Costello syndrome
C Tandoi, A Botta, G Fini, et al.
Mutation Research
|
September 1, 1989
Identification of 4 ataxia telangiectasia cell lines hypersensitive to gamma-irradiation but not to hydrogen peroxide
O Cantoni, P Sestili, M Fiorilli, et al.
Neurogenetics
|
May 17, 2001
Dopamine D4 receptor (DRD4) polymorphism and adaptability trait during infancy: a longitudinal study in 1- to 5-month-old neonates
A De Luca, M Rizzardi, I Torrente, et al.
Page
of 33
Search research articles
Search
Showing results (181-190 of 330) with videos related to
Sort By:
Page
of 33
Annali Italiani Di Chirurgia
|
January 1, 1991
[The role of endoscopy in the hemorrhagic complications of gastroduodenal ulcer]
A Scamporrino, U De Petris, G Novelli, et al.
American Journal of Human Genetics
|
January 1, 1995
Is congenital bilateral absence of vas deferens a primary form of cystic fibrosis? Analyses of the CFTR gene in 67 patients
B Mercier, C Verlingue, W Lissens, et al.
Cellular and Molecular Life Sciences : CMLS
|
November 2, 2005
Rescue of heterochromatin organization in Hutchinson-Gilford progeria by drug treatment
M Columbaro, C Capanni, E Mattioli, et al.
Biochemistry and Molecular Biology International
|
April 17, 1999
Cellular uptake and delivery monitoring of liposome/DNA complexes during in vitro transfection of CFTR gene
A L Serafino, G Novelli, S Di Sario, et al.
La Clinica Terapeutica
|
December 31, 1985
[Comparative evaluation in the treatment of arterial hypertension between prolonged-action clonidine and atenolol]
M La Vecchia, G Vergara, G Iannuzzi, et al.
Clinical and Experimental Immunology
|
June 26, 2016
Polymorphisms in STAT-4, IL-10, PSORS1C1, PTPN2 and MIR146A genes are associated differently with prognostic factors in Italian patients affected by rheumatoid arthritis
C Ciccacci, P Conigliaro, C Perricone, et al.
American Journal of Medical Genetics
|
April 1, 1990
Autosomal dominant polycystic kidney disease: a linkage evaluation of heterogeneity in Italy. Italian Collaborative Group on Polycystic Kidney Disease
P Mandich, G Restagno, G Novelli, et al.
American Journal of Medical Genetics
|
February 13, 2001
Exclusion of the elastin gene in the pathogenesis of Costello syndrome
C Tandoi, A Botta, G Fini, et al.
Mutation Research
|
September 1, 1989
Identification of 4 ataxia telangiectasia cell lines hypersensitive to gamma-irradiation but not to hydrogen peroxide
O Cantoni, P Sestili, M Fiorilli, et al.
Neurogenetics
|
May 17, 2001
Dopamine D4 receptor (DRD4) polymorphism and adaptability trait during infancy: a longitudinal study in 1- to 5-month-old neonates
A De Luca, M Rizzardi, I Torrente, et al.
Page
of 33