E-LIB Suche - Ergebnisse für: Bisceglia, L.

1

PB0222 A Novel c.952G>T Mutation in the FGG Gene Exon 8 Cau..:

Casoria, A. ; Miele, C. ; Capasso, F....
Research and Practice in Thrombosis and Haemostasis. 7 (2023) - p. 101269 , 2023

Link: https://doi.org/10.1016/..

2

Risk of Sars-CoV-2 infection and disease severity in people..:

Mazzilli, S ; Chieti, A ; Casigliani, V...
European Journal of Public Health. 31 (2021) Supplement_3 - p. , 2021

Link: https://doi.org/10.1093/..

3

A Swine In-vivo Liver Model for Morphometric Characterizati..:

Pregel, P. ; Bullone, M. ; Martano, M....
Journal of Comparative Pathology. 174 (2020) - p. 180 , 2020

Link: https://doi.org/10.1016/..

4

Association between particulate matter and cause-specific m..:

M, Renzi ; C, Gariazzo ; P, Michelozzi...
Environmental Epidemiology. 3 (2019) Supplement 1 - p. 329-330 , 2019

Link: https://doi.org/10.1097/..

5

The use of high resolution temperature exposure data to est..:

F, de'Donato ; M, Scortichini ; P, Michelozzi...
Environmental Epidemiology. 3 (2019) Supplement 1 - p. 94-94 , 2019

Link: https://doi.org/10.1097/..

6

Clinical, biochemical and molecular characterization of Cys..:

Barbosa, M ; Lopes, A ; Mota, C...
Clinical Genetics. 81 (2011) 1 - p. 47-55 , 2011

Link: https://doi.org/10.1111/..

7

The Missing ApoE Allele:

Seripa, D. ; Matera, M. G. ; Daniele, A....
Annals of Human Genetics. 71 (2007) 4 - p. 496-500 , 2007

Link: https://doi.org/10.1111/..

8

Posttransplant Recurrence of Proteinuria in a Case of Focal..:

Ghiggeri, G.M. ; Aucella, F. ; Caridi, G....
American Journal of Transplantation. 6 (2006) 9 - p. 2208-2211 , 2006

Link: https://doi.org/10.1111/..

9

C677T variant form at the MTHFR gene and CL/P: A risk facto..:

Martinelli, M. ; Scapoli, L. ; Pezzetti, F....
American Journal of Medical Genetics. 98 (2001) 4 - p. 357-360 , 2001

Link: https://doi.org/10.1002/..

10

Cellular Retinol Binding Protein 1 (RBP1): A frequent polym..:

Bisceglia, L ; d»Ambrosio, L ; Piemontese, M.R...
Molecular and Cellular Probes. 12 (1998) 4 - p. 255-258 , 1998

Link: https://doi.org/10.1006/..

11

Detection of dystrophin deletion carriers using FISH analys..:

Calvano, S. ; Memeo, E. ; Piemontese, M. R....
Clinical Genetics. 52 (1997) 1 - p. 17-22 , 1997

Link: https://doi.org/10.1111/..

12

The molecular basis of cystinuria: the role of the rBAT gen:

Palacín, M. ; Mora, C. ; Chillarón, J....
Amino Acids. 11 (1996) 2 - p. 225-246 , 1996

Link: https://doi.org/10.1007/..

13

Phenotype characterization and prevalence of rBAT M467T mut..:

de Sanctis, L. ; Bruno, M. ; Bonetti, G....
Journal of Inherited Metabolic Disease. 19 (1996) 2 - p. 243-245 , 1996

Link: https://doi.org/10.1007/..

14

Molecular screening of genetic defects with RNA–SSCP analys..:

Giannattasio, S. ; Bisceglia, L. ; Lattanzio, P....
Molecular and Cellular Probes. 9 (1995) 3 - p. 201-205 , 1995

Link: https://doi.org/10.1006/..

15

Genetic heterogeneity in cystinuria: the SLC3A1 gene is lin..:

Calonge, M J ; Volpini, V ; Bisceglia, L...
Proceedings of the National Academy of Sciences. 92 (1995) 21 - p. 9667-9671 , 1995

Link: https://doi.org/10.1073/..