Detalhe da pesquisa
1.
Assessing the impact of long-term inhaled corticosteroid therapy on patients with COVID-19 and coexisting chronic lung disease: A multicenter retrospective cohort study.
Can J Respir Ther
; 60: 86-94, 2024.
Artigo
em Inglês
| MEDLINE | ID: mdl-38855380
2.
Nosocomial COVID-19: A Nationwide Spanish Study.
Gerontology
; 69(6): 671-683, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-36682355
3.
Malnutrition and sarcopenia worsen short- and long-term outcomes in internal medicine inpatients.
Postgrad Med J
; 99(1168): 56-62, 2023 Mar 31.
Artigo
em Inglês
| MEDLINE | ID: mdl-36828395
4.
WHO Ordinal Scale and Inflammation Risk Categories in COVID-19. Comparative Study of the Severity Scales.
J Gen Intern Med
; 37(8): 1980-1987, 2022 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-35396659
5.
Differences in clinical features and mortality in very old unvaccinated patients (≥ 80 years) hospitalized with COVID-19 during the first and successive waves from the multicenter SEMI-COVID-19 Registry (Spain).
BMC Geriatr
; 22(1): 546, 2022 06 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-35773622
6.
Generation of the First Human In Vitro Model for McArdle Disease Based on iPSC Technology.
Int J Mol Sci
; 23(22)2022 Nov 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-36430443
7.
Inadequate use of antibiotics in the covid-19 era: effectiveness of antibiotic therapy.
BMC Infect Dis
; 21(1): 1144, 2021 Nov 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-34749645
8.
CONCOMITANT MUTATIONS IN INHERITED RETINAL DYSTROPHIES: Why the Reproductive and Therapeutic Counseling Should Be Addressed Cautiously.
Retina
; 41(9): 1966-1975, 2021 Sep 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33411470
9.
Usher Syndrome: Genetics of a Human Ciliopathy.
Int J Mol Sci
; 22(13)2021 Jun 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-34201633
10.
Exome sequencing identifies PEX6 mutations in three cases diagnosed with Retinitis Pigmentosa and hearing impairment.
Mol Vis
; 26: 216-225, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-32214787
11.
Pathogenicity of novel atypical variants leading to choroideremia as determined by functional analyses.
Hum Mutat
; 40(1): 31-35, 2019 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-30341801
12.
Mutations in PLS1, encoding fimbrin, cause autosomal dominant nonsyndromic hearing loss.
Hum Mutat
; 40(12): 2286-2295, 2019 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-31397523
13.
The importance of biochemical and genetic findings in the diagnosis of atypical Norrie disease.
Clin Chem Lab Med
; 56(2): 229-235, 2018 01 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-28742514
14.
Novel deletions involving the USH2A gene in patients with Usher syndrome and retinitis pigmentosa.
Mol Vis
; 20: 1398-410, 2014.
Artigo
em Inglês
| MEDLINE | ID: mdl-25352746
15.
Deciphering complexity: TULP1 variants linked to an atypical retinal dystrophy phenotype.
Front Genet
; 15: 1352063, 2024.
Artigo
em Inglês
| MEDLINE | ID: mdl-38450199
16.
Prognostic Value of D-dimer to Lymphocyte Ratio (DLR) in Hospitalized Coronavirus Disease 2019 (COVID-19) Patients: A Validation Study in a National Cohort.
Viruses
; 16(3)2024 02 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-38543700
17.
The contribution of GPR98 and DFNB31 genes to a Spanish Usher syndrome type 2 cohort.
Mol Vis
; 19: 367-73, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-23441107
18.
PCR-Based Strategy for Introducing CRISPR/Cas9 Machinery into Hematopoietic Cell Lines.
Cancers (Basel)
; 15(17)2023 Aug 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-37686539
19.
TBC1D32 variants disrupt retinal ciliogenesis and cause retinitis pigmentosa.
JCI Insight
; 8(21)2023 Nov 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-37768732
20.
Mortality reduction in older COVID-19-patients hospitalized in Spain during the second pandemic wave from the SEMI-COVID-19 Registry.
Sci Rep
; 13(1): 17731, 2023 10 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-37853011