Detalhe da pesquisa
1.
Citizens from 13 countries share similar preferences for COVID-19 vaccine allocation priorities.
Proc Natl Acad Sci U S A
; 118(38)2021 09 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-34526400
2.
Detecting Förster resonance energy transfer in living cells by conventional and spectral flow cytometry.
Cytometry A
; 101(10): 818-834, 2022 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-34128311
3.
A systematic review of common genetic variation and biological pathways in autism spectrum disorder.
BMC Neurosci
; 22(1): 60, 2021 10 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-34627165
4.
Endothelial CD99 supports arrest of mouse neutrophils in venules and binds to neutrophil PILRs.
Blood
; 129(13): 1811-1822, 2017 Mar 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-28223280
5.
Atypical Activin A and IL-10 Production Impairs Human CD16+ Monocyte Differentiation into Anti-Inflammatory Macrophages.
J Immunol
; 196(3): 1327-37, 2016 Feb 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-26729812
6.
Inhibition of PIM Kinases in DLBCL Targets MYC Transcriptional Program and Augments the Efficacy of Anti-CD20 Antibodies.
Cancer Res
; 81(23): 6029-6043, 2021 12 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34625423
7.
Molecular characterization of 22 novel UDP-N-acetylglucosamine-1-phosphate transferase alpha- and beta-subunit (GNPTAB) gene mutations causing mucolipidosis types IIalpha/beta and IIIalpha/beta in 46 patients.
Hum Mutat
; 30(11): E956-73, 2009 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-19634183
8.
Blood flow guides sequential support of neutrophil arrest and diapedesis by PILR-ß1 and PILR-α.
Elife
; 82019 08 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-31385804
9.
Cotargeting of BCL2 with Venetoclax and MCL1 with S63845 Is Synthetically Lethal In Vivo in Relapsed Mantle Cell Lymphoma.
Clin Cancer Res
; 25(14): 4455-4465, 2019 07 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-31004002
10.
Pompe disease (glycogen storage disease type II) in Argentineans: clinical manifestations and identification of 9 novel mutations.
Neuromuscul Disord
; 17(1): 16-22, 2007 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-17056254
11.
HS1 deficiency impairs neutrophil recruitment in vivo and activation of the small GTPases Rac1 and Rap1.
J Leukoc Biol
; 101(5): 1133-1142, 2017 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-28122813
12.
Tay-Sachs and Sandhoff diseases: enzymatic diagnosis in dried blood spots on filter paper: retrospective diagnoses in newborn-screening cards.
Clin Chim Acta
; 318(1-2): 133-7, 2002 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-11880123
13.
Glycogen storage disease type II: enzymatic screening in dried blood spots on filter paper.
Clin Chim Acta
; 347(1-2): 97-102, 2004 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-15313146
14.
Gaucher and Niemann-Pick diseases--enzymatic diagnosis in dried blood spots on filter paper: retrospective diagnoses in newborn-screening cards.
Clin Chim Acta
; 317(1-2): 191-7, 2002 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-11814475
15.
[Mucopolysaccharidosis type VI: clinical aspects, diagnosis and treatment with enzyme replacement therapy]. / Mucopolisacaridosis VI: aspectos clínicos, iagnósticos y del tratamiento con terapia de eemplazo enzimático.
Arch Argent Pediatr
; 112(3): 258-62, 2014 Jun.
Artigo
em Espanhol
| MEDLINE | ID: mdl-24862809
16.
Molecular analysis of HEXA gene in Argentinean patients affected with Tay-Sachs disease: possible common origin of the prevalent c.459+5A>G mutation.
Gene
; 499(2): 262-5, 2012 May 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-22441121
17.
Retrospective diagnosis of glycogen storage disease type II by use of a newborn-screening card.
Clin Chim Acta
; 359(1-2): 205-6, 2005 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-15963968
18.
Mucopolisacaridosis VI: aspectos clínicos, iagnósticos y del tratamiento con terapia de eemplazo enzimático / Mucopolysaccharidosis type VI: clinical aspects, diagnosis and treatment with enzyme replacement therapy
Arch. argent. pediatr
; 112(3): 258-262, jun. 2014. ilus
Artigo
em Espanhol
| LILACS, BINACIS | ID: biblio-1159607
19.
Vertebrobasilar Dolichoectasia in Fabry Disease: The Earliest Marker of Neurovascular Involvement?
J. inborn errors metab. screen
; 2: e130003, 2014. tab, graf
Artigo
em Inglês
|
LILACS-Express
| ID: biblio-1090856
20.
Rapid diagnostic testing procedures for lysosomal storage disorders: alpha-glucosidase and beta-galactosidase assays on dried blood spots.
Clin Chim Acta
; 402(1-2): 38-41, 2009 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-19111682