Zobrazeno 1 - 10
of 43
pro vyhledávání: '"V. Frontini"'
Autor:
Ana V. Frontini, Carlos D. De La Vega Elena, María V. Nicolorich, Ariel Naves, Pablo Schwarzbaum, Graciela D. Venera
Publikováno v:
Medicina (Buenos Aires), Vol 71, Iss 2, Pp 139-145 (2011)
The utilization of adenosine 5´-triphosphate (ATP ) infusions to inhibit the growth of some human and animals tumors was based on the anticancer activity observed in in vitro and in vivo experiments, but contradictory results make the use of ATP in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doajarticles::7bda35a1d5f835a15b036fa06bd8703a
http://www.scielo.org.ar/scielo.php?script=sci_arttext&pid=S0025-76802011000200005
http://www.scielo.org.ar/scielo.php?script=sci_arttext&pid=S0025-76802011000200005
Publikováno v:
Electronic Journal of Biomedicine, Vol 2008, Iss 1, Pp 36-42 (2008)
Este trabajo analiza, mediante densidad óptica (DO), residuos glucídicos en glomérulos y túbulos contorneados proximales, superficiales y yuxtamedulares, de dos líneas de ratas diabéticas: eSS y eSMT al año de edad. 10 ratas macho eSS, 12, eSM
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doajarticles::b68eff4baf573249fbf6c252b34858f2
http://biomed.uninet.edu/2008/n1/frontini.html
http://biomed.uninet.edu/2008/n1/frontini.html
Publikováno v:
Annales de Dermatologie et de Vénéréologie. 131:805-809
Resume Introduction La maladie de Darier ou dyskeratose folliculaire est une maladie autosomique dominante qui est frequemment le resultat d’une mutation spontanee. Elle peut etre generalisee ou localisee. La mutation, situee en 12q23-q24,1 code po
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dca4733fed2c1088006cdc39b116a6e3
https://doi.org/10.1016/s0151-9638(04)93765-9
https://doi.org/10.1016/s0151-9638(04)93765-9
Publikováno v:
Human Reproduction. 15:2375-2378
The aim of this controlled clinical study, performed in a specialized institutional unit for thalassaemic men, was to consider the possibility of restoring erection in beta-thalassaemic patients with erectile dysfunction by administering E(1) prostag
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a36c03da5e82fd1bc470fc526118d7fe
https://doi.org/10.1093/humrep/15.11.2375
https://doi.org/10.1093/humrep/15.11.2375
Publikováno v:
Clinical & Laboratory Haematology. 18:13-17
As thalassaemia patients live longer, compliance with chelation therapy becomes more and more of a problem. Teenagers rebel against the continual need for treatment, and young adults with jobs, active social lives and families, find it hard to find t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::88d22a5d02e4afafb913fb86edb01865
https://doi.org/10.1111/j.1365-2257.1996.tb00730.x
https://doi.org/10.1111/j.1365-2257.1996.tb00730.x
Autor:
Rubina Marzagalli, V Frontini, Anna Elisa Marchese, Giovanna Valenti, Martina Barchitta, Antonella Agodi
Publikováno v:
European journal of clinical nutrition. 65(12)
Folate has been recognized to ensure reproductive health and there is a growing body of epidemiological evidence suggesting that the methylenetetrahydrofolate reductase (MTHFR) 677T allele and reduced dietary folate may increase the risk of cervical
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::328ab83792397e69b026e452eb0f5ce7
https://pubmed.ncbi.nlm.nih.gov/21731042
https://pubmed.ncbi.nlm.nih.gov/21731042
Publikováno v:
Annales de dermatologie et de venereologie. 131(8-9)
Darier's disease or keratosis follicularis is an autosomal dominant acantholytic disorder that frequently arises as a result of spontaneous mutation. It is either a generalized or localized condition due to a mutation in the SERCA2 12q23-q24,1 result
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e46d6c994304472b9c33b5447b03349d
https://pubmed.ncbi.nlm.nih.gov/15505549
https://pubmed.ncbi.nlm.nih.gov/15505549
Publikováno v:
Pediatric dermatology. 20(6)
The coexistence of linear porokeratosis (LP) and disseminated superficial actinic porokeratosis (DSAP) in a 3-year-old girl with a family history of DSAP is presented. Happle proposed loss of heterozygosity (LOH) to explain the origin of this unusual
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::24a9bccfaf0e67c2842d58f877a424de
https://pubmed.ncbi.nlm.nih.gov/14651573
https://pubmed.ncbi.nlm.nih.gov/14651573
Publikováno v:
European journal of dermatology : EJD. 11(5)
We describe a girl with motor and mental retardation, macrocephaly, a "coarse" face, choanal atresia, postnatal feeding difficulty, redundant skin with deep palmar and plantar creases, and histopathological evidence of altered elastic fibers, who die
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::07e7c5fe1d46952ada8e80eb095539a7
https://pubmed.ncbi.nlm.nih.gov/11525956
https://pubmed.ncbi.nlm.nih.gov/11525956
Autor:
M. Lombardo, A. Ragusa, V. Frontini, S. Amata, Dominique Labie, Ronald L. Nagel, Turi Lombardo, R. Krishnamoorthy
Publikováno v:
American Journal of Hematology. 40:313-315
African admixture in Sicily has been long suspected because of the presence of the sickle gene. Nevertheless, the degree of African admixture cannot be derived from the study of HbS frequency, since this gene was most likely expanded by the selective
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ab6f002b7df37de3ceefe3667198450a
https://doi.org/10.1002/ajh.2830400413
https://doi.org/10.1002/ajh.2830400413