Detalhe da pesquisa
1.
Genetics of inborn errors of immunity: Diagnostic strategies and new approaches to CNV detection.
Eur J Clin Invest
; 54(6): e14191, 2024 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-38440843
2.
Unexpected synergistic HIV neutralization by a triple microbicide produced in rice endosperm.
Proc Natl Acad Sci U S A
; 115(33): E7854-E7862, 2018 08 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-30061386
3.
New human combined immunodeficiency caused by interferon regulatory factor 4 (IRF4) deficiency inherited by uniparental isodisomy.
J Allergy Clin Immunol
; 141(5): 1924-1927.e18, 2018 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-29408330
4.
Description of Two New Cases of AQP1 Related Pulmonary Arterial Hypertension and Review of the Literature.
Genes (Basel)
; 13(5)2022 05 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-35627312
5.
[Prevalence and geographic distribution of the Wolf-Hirschhorn syndrome in Spain.] / Prevalencia y distribución geográfica del síndrome de Wolf-Hirschhorn en España.
Rev Esp Salud Publica
; 962022 Jun 08.
Artigo
em Espanhol
| MEDLINE | ID: mdl-35703131
6.
Prospective individual patient data meta-analysis of two randomized trials on convalescent plasma for COVID-19 outpatients.
Nat Commun
; 13(1): 2583, 2022 05 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-35546145
7.
Correlation between blood telomere length and CD4+ CD8+ T-cell subsets changes 96 weeks after initiation of antiretroviral therapy in HIV-1-positive individuals.
PLoS One
; 15(4): e0230772, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-32267847
8.
[Osteoporosis-pseudoglioma Syndrome: a pediatric case of primary osteoporosis]. / Síndrome de osteoporosis-pseudoglioma: a propósito de un caso pediátrico de osteoporosis primaria.
Arch Argent Pediatr
; 118(3): e300-e304, 2020 06.
Artigo
em Espanhol
| MEDLINE | ID: mdl-32470270
9.
[Wolf-Hirschhorn syndrome. Description of five cases characterized by means of single nucleotide polymorphism microarrays]. / Síndrome de Wolf-Hirschhorn. Descripción de cinco casos caracterizados por microarrays de polimorfismos de nucleótido único.
Arch Argent Pediatr
; 117(4): e406-e412, 2019 08 01.
Artigo
em Espanhol
| MEDLINE | ID: mdl-31339285
10.
A homozygous mutation in the highly conserved Tyr60 of the mature IGF1 peptide broadens the spectrum of IGF1 deficiency.
Eur J Endocrinol
; 181(5): K43-K53, 2019 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-31539878
11.
Author Correction: Prospective individual patient data meta-analysis of two randomized trials on convalescent plasma for COVID-19 outpatients.
Nat Commun
; 15(1): 4352, 2024 May 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-38778041
12.
Coupling solar photo-Fenton and biotreatment at industrial scale: main results of a demonstration plant.
J Hazard Mater
; 146(3): 440-6, 2007 Jul 31.
Artigo
em Inglês
| MEDLINE | ID: mdl-17532127
13.
Spontaneous remission in a child with an NPHS1-based congenital nephrotic syndrome.
Clin Kidney J
; 15(10): 1969-1970, 2022 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-36158155
14.
Síndrome de osteoporosis-pseudoglioma: a propósito de un caso pediátrico de osteoporosis primaria / Osteoporosis-pseudoglioma Syndrome: a pediatric case of primary osteoporosis
Arch. argent. pediatr
; 118(3): e300-e304, jun. 2020. ilus, tab
Artigo
em Espanhol
| BINACIS, LILACS | ID: biblio-1116991
15.
Síndrome de Wolf-Hirschhorn: Descripción de cinco casos caracterizados por microarrays de polimorfismos de nucleótido único / Wolf-Hirschhorn syndrome: Description of five cases characterized by means of single nucleotide polymorphism microarrays
Arch. argent. pediatr
; 117(4): 406-412, ago. 2019. ilus, tab
Artigo
em Espanhol
| LILACS, BINACIS | ID: biblio-1054946