Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Stefania Battistella"'
Autor:
Mandy Clayton, Glenda Fredman, Eleanor Martin, Eleanor Anderson, Stefania Battistella, Sarah Johnson, Alison Milton, Penny Rapaport
Publikováno v:
FPOP Bulletin: Psychology of Older People. 1:20-26
‘If it doesn’t start personal, it does not start. But if it ends personal then it ends.’(Pancho Arguelles, 2007)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4a981a21cf017c5c4bfbe8d87e759c53
https://doi.org/10.53841/bpsfpop.2012.1.121.20
https://doi.org/10.53841/bpsfpop.2012.1.121.20
Autor:
Stefania Battistella, H. Valerie Curran, Paul K. Davis, Celia J. A. Morgan, Natasha Constantinou, Dominic O’Ryan
Publikováno v:
Human Psychopharmacology: Clinical and Experimental. 27:499-506
Objective Despite a growing interest in memory functions of chronic drug users, investigation of semantic and episodic memory in opiate users is limited, and findings of studies have been inconsistent. The present study aimed to assess semantic memor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e63e9be2abe3be108895ed8b676682df
https://doi.org/10.1002/hup.2255
https://doi.org/10.1002/hup.2255
Autor:
Nadia Soriani, Maurizio Ferrari, S. Bernal, M. Baiget, Laura Cremonesi, Stefania Battistella, Stefania Stenirri
Publikováno v:
European Journal of Ophthalmology. 17:749-754
PURPOSE. Among the 500 ABCA4 mutations identified so far in the retina-specific ABC transporter (ABCA4) gene, only 20 have been described in patients with autosomal recessive retinitis pigmentosa (arRP). In this study the gene was screened for mutati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c2303c064d0e09af99b7e09b38930647
https://doi.org/10.1177/112067210701700510
https://doi.org/10.1177/112067210701700510
Autor:
Stefania, Battistella, Natasha, Constantinou, Celia J A, Morgan, Paul, Davis, Dominic, O'Ryan, H Valerie, Curran
Publikováno v:
Human psychopharmacology. 27(5)
Despite a growing interest in memory functions of chronic drug users, investigation of semantic and episodic memory in opiate users is limited, and findings of studies have been inconsistent. The present study aimed to assess semantic memory and epis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::947ad5141d0a9ace68d27c533a410a1c
https://pubmed.ncbi.nlm.nih.gov/22996617
https://pubmed.ncbi.nlm.nih.gov/22996617
Autor:
Laura Cremonesi, Maurizio Ferrari, Saul Surrey, Stefania Battistella, Kathleen Delgrosso, Marcella Chiari, Paolo Fortina, Francesco Damin
Publikováno v:
Clinical chemistry (Baltim. Md.) 54 (2008): 1657–1663.
info:cnr-pdr/source/autori:Battistella S.; Damin F.; Chiari M.; Delgrosso K.; Surrey S.; Fortina P.; Ferrari M.;Cremonesi L ./titolo:Genotyping beta-globin gene mutations on copolymer-coated glass slides with the ligation detection reaction/doi:/rivista:Clinical chemistry (Baltim. Md.)/anno:2008/pagina_da:1657/pagina_a:1663/intervallo_pagine:1657–1663/volume:54
info:cnr-pdr/source/autori:Battistella S.; Damin F.; Chiari M.; Delgrosso K.; Surrey S.; Fortina P.; Ferrari M.;Cremonesi L ./titolo:Genotyping beta-globin gene mutations on copolymer-coated glass slides with the ligation detection reaction/doi:/rivista:Clinical chemistry (Baltim. Md.)/anno:2008/pagina_da:1657/pagina_a:1663/intervallo_pagine:1657–1663/volume:54
Background: Methods are needed to analyze small amounts of samples for variation in disease-causing genes. One means is to couple the sensitivity and multiplexing capability of the ligation detection reaction (LDR) with the use of simple glass slides
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a1ebdf3b53adf80d07d3e9abf116a28d
http://www.cnr.it/prodotto/i/17560
http://www.cnr.it/prodotto/i/17560
Autor:
Maria Pia Manitto, Stefania Stenirri, Rosario Brancato, Laura Cremonesi, Maurizio Ferrari, Isabella Fermo, Elisabetta Martina, Stefania Battistella
Publikováno v:
Clinical Chemistry and Laboratory Medicine (CCLM). 44
Background: Mutations in the retina-specific ABC transporter (ABCA4) gene are associated with different types of macular degeneration, including Stargardt disease, cone-rod dystrophy, Fundus flavimaculatus, Retinitis pigmentosa and probably age-relat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::68bc94fccf17a8cff80e0cd9cefe6449
https://doi.org/10.1515/cclm.2006.116
https://doi.org/10.1515/cclm.2006.116
Autor:
Maurizio Ferrari, Rosario Brancato, Elisabetta Martina, Laura Cremonesi, Stefania Stenirri, Silvia Galbiati, Maria Pia Manitto, Isabella Fermo, Rita Paroni, Rando Allikmets, Nadia Soriani, Stefania Battistella
Background: Mutations in the retina-specific ABC transporter (ABCA4) gene have been associated with several forms of macular degenerations. Because the high complexity of the molecular genotype makes scanning of the ABCA4 gene cumbersome, we describe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::062ec9a29cc006963573837d6ae16eac