Detalhe da pesquisa
1.
Comprehensive genetic analysis confers high diagnostic yield in 16 Japanese patients with corpus callosum anomalies.
J Hum Genet
; 66(11): 1061-1068, 2021 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-33958710
2.
LMX1B mutation with residual transcriptional activity as a cause of isolated glomerulopathy.
Nephrol Dial Transplant
; 29(1): 81-8, 2014 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-24042019
3.
Clinical and genetic characterization of nephropathy in patients with nail-patella syndrome.
Eur J Hum Genet
; 28(10): 1414-1421, 2020 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-32457516
4.
Improvement of nephrotic syndrome by intensive lipid-lowering therapy in a patient with lipoprotein glomerulopathy.
Clin Exp Nephrol
; 13(6): 659-62, 2009 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-19603250
5.
Careful Clinical Surveillance Is Important for the Identification of Parechovirus Type A3-Associated Myalgia/Myositis: a Sporadic Case Found in a Season with a Low Level of Its Activity in Yamagata, Japan in 2017.
Jpn J Infect Dis
; 72(1): 71-72, 2019 Jan 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-30504645