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1.
[A clinical application study of digital manufacturing simple intraoral Gothic arch-tracing device in determining the centric relation of complete dentures].
Beijing Da Xue Xue Bao Yi Xue Ban
; 55(1): 101-107, 2023 Feb 18.
Artículo
en Zh
| MEDLINE | ID: mdl-36718696
2.
A Comparative Study on Efficacy and Safety of Propofol versus Dexmedetomidine in Sleep Apnea Patients undergoing Drug-Induced Sleep Endoscopy: A CONSORT-Prospective, Randomized, Controlled Clinical Trial.
Biomed Res Int
; 2018: 8696510, 2018.
Artículo
en Inglés
| MEDLINE | ID: mdl-30515416
3.
Microstructure and nanoindentation analyses of low-temperature aging on the zirconia-porcelain interface.
J Mech Behav Biomed Mater
; 66: 119-126, 2017 02.
Artículo
en Inglés
| MEDLINE | ID: mdl-27866055
4.
Stretchable and compressible strain sensors based on carbon nanotube meshes.
Nanoscale
; 8(46): 19352-19358, 2016 Nov 24.
Artículo
en Inglés
| MEDLINE | ID: mdl-27845462
5.
The natural history and genotype-phenotype nonconcordance of HLA identical siblings with the same mutations of the 21-hydroxylase gene.
J Pediatr Endocrinol Metab
; 18(2): 143-53, 2005 Feb.
Artículo
en Inglés
| MEDLINE | ID: mdl-15751603
6.
Rapid deoxyribonucleic acid analysis by allele-specific polymerase chain reaction for detection of mutations in the steroid 21-hydroxylase gene.
J Clin Endocrinol Metab
; 80(5): 1635-40, 1995 May.
Artículo
en Inglés
| MEDLINE | ID: mdl-7745011
7.
Prenatal treatment and diagnosis of congenital adrenal hyperplasia owing to steroid 21-hydroxylase deficiency.
J Clin Endocrinol Metab
; 80(7): 2014-20, 1995 Jul.
Artículo
en Inglés
| MEDLINE | ID: mdl-7608248
8.
Congenital adrenal hyperplasia (21-hydroxylase deficiency) without demonstrable genetic mutations.
J Clin Endocrinol Metab
; 84(1): 378-81, 1999 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-9920112
9.
Prenatal diagnosis for congenital adrenal hyperplasia in 532 pregnancies.
J Clin Endocrinol Metab
; 86(12): 5651-7, 2001 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-11739415
10.
Several homozygous mutations in the gene for 11 beta-hydroxysteroid dehydrogenase type 2 in patients with apparent mineralocorticoid excess.
J Clin Endocrinol Metab
; 80(11): 3145-50, 1995 Nov.
Artículo
en Inglés
| MEDLINE | ID: mdl-7593417
11.
A mutation in the HSD11B2 gene in a family with apparent mineralocorticoid excess.
J Clin Endocrinol Metab
; 80(7): 2263-6, 1995 Jul.
Artículo
en Inglés
| MEDLINE | ID: mdl-7608290
12.
A novel semiquantitative polymerase chain reaction/enzyme digestion-based method for detection of large scale deletions/conversions of the CYP21 gene and mutation screening in Turkish families with 21-hydroxylase deficiency.
J Clin Endocrinol Metab
; 88(12): 5893-7, 2003 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-14671187
13.
Examination of genotype and phenotype relationships in 14 patients with apparent mineralocorticoid excess.
J Clin Endocrinol Metab
; 83(7): 2244-54, 1998 Jul.
Artículo
en Inglés
| MEDLINE | ID: mdl-9661590
14.
Angle-dependent light emission from aligned multiwalled carbon nanotubes under CO(2) laser irradiation.
Nanotechnology
; 18(7): 075710, 2007 Feb 21.
Artículo
en Inglés
| MEDLINE | ID: mdl-21730518
15.
Optimization of an isocratic reversed phase liquid chromatographic system for the separation of fourteen steroids using factorial design and computer simulation.
Biomed Chromatogr
; 4(1): 34-8, 1990 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-2310840
16.
[Preventive effect of changzhankang in experimental intestinal adhesions in rats].
Zhong Xi Yi Jie He Za Zhi
; 11(8): 484-5, 454, 1991 Aug.
Artículo
en Zh
| MEDLINE | ID: mdl-1954667
17.
Simultaneous measurement of eight corticosteroids by liquid chromatography, and application of the procedure to diagnosis of congenital adrenal hyperplasia.
Clin Chem
; 33(8): 1354-9, 1987 Aug.
Artículo
en Inglés
| MEDLINE | ID: mdl-3496990
18.
Isocratic reversed phase high performance liquid chromatography determination of twelve natural corticosteroids in serum with on-line ultraviolet and fluorescence detection.
Biomed Chromatogr
; 4(4): 161-4, 1990 Jul.
Artículo
en Inglés
| MEDLINE | ID: mdl-2207378
19.
Serum steroid hormonal profiles by reversed-phase liquid chromatography in patients with 17-hydroxylase deficiency and in an affected family.
Clin Chem
; 38(1): 76-82, 1992 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-1310267
20.
A genetic defect resulting in mild low-renin hypertension.
Proc Natl Acad Sci U S A
; 95(17): 10200-5, 1998 Aug 18.
Artículo
en Inglés
| MEDLINE | ID: mdl-9707624
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