Detalles de la búsqueda
1.
Mutations of the Transcriptional Corepressor ZMYM2 Cause Syndromic Urinary Tract Malformations.
Am J Hum Genet
; 107(4): 727-742, 2020 10 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-32891193
2.
Clinical characteristics and early recognition of thrombotic microangiopathy in children with systemic lupus erythematosus / 中国小儿急救医学
Chinese Pediatric Emergency Medicine
; (12): 868-873, 2021.
Artículo
en Zh
| WPRIM | ID: wpr-908385
3.
Childhood primary Sjogren syndrome with central nervous system symptoms as the first manifestation: a case report and literature review / 临床儿科杂志
Journal of Clinical Pediatrics
; (12): 775-777, 2017.
Artículo
en Zh
| WPRIM | ID: wpr-661176
4.
Childhood primary Sjogren syndrome with central nervous system symptoms as the first manifestation: a case report and literature review / 临床儿科杂志
Journal of Clinical Pediatrics
; (12): 775-777, 2017.
Artículo
en Zh
| WPRIM | ID: wpr-658281
5.
The role of urinary kidney injury molecule-1 in pediatric Henoch-Sch?nlein purpura / 临床儿科杂志
Journal of Clinical Pediatrics
; (12): 918-920, 2014.
Artículo
en Zh
| WPRIM | ID: wpr-459311
6.
Clinical observation of multi-target therapy in children with lupus nephritis / 中华风湿病学杂志
Chinese Journal of Rheumatology
; (12): 607-611, 2014.
Artículo
en Zh
| WPRIM | ID: wpr-453852
7.
Application of immune cell functional assay in monitoring immune status in renal transplant recipients / 中华肾脏病杂志
Chinese Journal of Nephrology
; (12): 345-350, 2014.
Artículo
en Zh
| WPRIM | ID: wpr-447088
Resultados
1 -
7
de 7
1
Próxima >
>>