Detalhe da pesquisa
1.
Maternal socio-demographic and psychological predictors for risk of developmental delays among young children in Mongolia.
BMC Pediatr
; 18(1): 68, 2018 02 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-29458342
2.
An hour-specific transcutaneous bilirubin nomogram for Mongolian neonates.
Eur J Pediatr
; 174(10): 1299-304, 2015 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-25869495
3.
Validation of a transcutaneous bilirubin meter in Mongolian neonates: comparison with total serum bilirubin.
BMC Pediatr
; 13: 151, 2013 Sep 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-24074043
4.
Novel COL2A1 variants in Japanese patients with spondyloepiphyseal dysplasia congenita.
Hum Genome Var
; 9(1): 16, 2022 May 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-35581182
5.
Deletion of ERF and CIC causes abnormal skull morphology and global developmental delay.
Cold Spring Harb Mol Case Stud
; 7(3)2021 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-34117072
6.
Cutaneous immunization rapidly activates liver invariant Valpha14 NKT cells stimulating B-1 B cells to initiate T cell recruitment for elicitation of contact sensitivity.
J Exp Med
; 198(12): 1785-96, 2003 Dec 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-14676294
7.
B cell-dependent T cell responses: IgM antibodies are required to elicit contact sensitivity.
J Exp Med
; 196(10): 1277-90, 2002 Nov 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-12438420
8.
Discordant phenotype caused by CASK mutation in siblings with NF1.
Hum Genome Var
; 6: 20, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-31044082
9.
Novel SYNGAP1 variant in a patient with intellectual disability and distinctive dysmorphisms.
Congenit Anom (Kyoto)
; 58(6): 188-190, 2018 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-29381230
10.
Refining the clinical phenotype of Okur-Chung neurodevelopmental syndrome.
Hum Genome Var
; 5: 18011, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-29619237
11.
Novel COL4A1 mutation in a fetus with early prenatal onset of schizencephaly.
Hum Genome Var
; 5: 4, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-29760938
12.
Republication: Two Premature Neonates of Congenital Syphilis with Severe Clinical Manifestations.
Trop Med Health
; 43(3): 165-70, 2015 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-26543391
13.
A Japanese neonatal case of glucose-6-phosphate dehydrogenase deficiency presenting as severe jaundice and hemolytic anemia without apparent trigger.
Springerplus
; 2: 434, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-24052930
14.
B-1 B cells mediate required early T cell recruitment to elicit protein-induced delayed-type hypersensitivity.
J Immunol
; 171(11): 6225-35, 2003 Dec 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-14634139
15.
Early delayed-type hypersensitivity eosinophil infiltrates depend on T helper 2 cytokines and interferon-gamma via CXCR3 chemokines.
Immunology
; 111(3): 306-17, 2004 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-15009431