Detalles de la búsqueda
1.
[Analysis of clinical features, biochemical indices and genetic variants among children with Short/branched-chain acyl-CoA dehydrogenase deficiency detected by neonatal screening].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 40(2): 155-160, 2023 Feb 10.
Artículo
en Zh
| MEDLINE | ID: mdl-36709932
2.
Application of genetic screening processor in screening neonatal glucose-6-phosphate dehydrogenase deficiency.
Zhejiang Da Xue Xue Bao Yi Xue Ban
; 50(4): 487-493, 2021 Aug 25.
Artículo
en Inglés
| MEDLINE | ID: mdl-34704417
3.
Rapid detection of common variants and deletions of CYP21A2 using MALDI-TOF MS.
Eur J Med Genet
; 69: 104950, 2024 Jun.
Artículo
en Inglés
| MEDLINE | ID: mdl-38830573
4.
Newborn screening for 3-methylcrotonyl-CoA carboxylase deficiency in Zhejiang province, China.
Clin Chim Acta
; 542: 117266, 2023 Mar 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-36822454
5.
Recurrence of ameloblastoma in bone grafts of a fibula free flap: A case report and literature review.
J Stomatol Oral Maxillofac Surg
; 123(6): 663-665, 2022 11.
Artículo
en Inglés
| MEDLINE | ID: mdl-35697254
6.
Newborn Screening for Mitochondrial Carnitine-Acylcarnitine Cycle Disorders in Zhejiang Province, China.
Front Genet
; 13: 823687, 2022.
Artículo
en Inglés
| MEDLINE | ID: mdl-35360862
7.
Biochemical, molecular, and clinical features of patients with glutaric acidemia type 1 identified through large-scale newborn screening in Zhejiang Province, China.
Clin Chim Acta
; 530: 113-118, 2022 May 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-35367405
8.
Dynamic changes of metabolic characteristics in neonatal intrahepatic cholestasis caused by citrin deficiency.
Front Mol Biosci
; 9: 939837, 2022.
Artículo
en Inglés
| MEDLINE | ID: mdl-36090036
9.
Fabrication of NaYF4:Yb,Er Nanoprobes for Cell Imaging Directly by Using the Method of Hydrion Rivalry Aided by Ultrasonic.
Nanoscale Res Lett
; 11(1): 441, 2016 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-27696322
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