Detalles de la búsqueda
1.
Trends and projections of inflammatory bowel disease at the global, regional and national levels, 1990-2050: a bayesian age-period-cohort modeling study.
BMC Public Health
; 23(1): 2507, 2023 12 14.
Artículo
en Inglés
| MEDLINE | ID: mdl-38097968
2.
Gestational weight gain and risk of autism spectrum disorders in offspring: a systematic review and meta-analysis.
J Obstet Gynaecol
; 40(7): 953-960, 2020 Oct.
Artículo
en Inglés
| MEDLINE | ID: mdl-31790315
3.
Therapeutic efficacy of nutritional support by percutaneous endoscopic gastrostomy in critically ill patients: A self-control clinical trial.
Pak J Med Sci
; 33(1): 75-80, 2017.
Artículo
en Inglés
| MEDLINE | ID: mdl-28367176
4.
Exome sequencing revealed novel germline mutations in Chinese Peutz-Jeghers syndrome patients.
Dig Dis Sci
; 59(1): 64-71, 2014 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-24154639
5.
RDH12-associated retinal degeneration caused by a homozygous pathogenic variant of 146C>T and literature review.
Int J Ophthalmol
; 17(2): 311-316, 2024.
Artículo
en Inglés
| MEDLINE | ID: mdl-38371258
6.
Ruxolitinib induces apoptosis and pyroptosis of anaplastic thyroid cancer via the transcriptional inhibition of DRP1-mediated mitochondrial fission.
Cell Death Dis
; 15(2): 125, 2024 02 09.
Artículo
en Inglés
| MEDLINE | ID: mdl-38336839
7.
Aplasia ras homolog member I is downregulated in gastric cancer and silencing its expression promotes cell growth in vitro.
J Gastroenterol Hepatol
; 27(8): 1395-404, 2012 Aug.
Artículo
en Inglés
| MEDLINE | ID: mdl-22497484
8.
[Hematologic Phenotype and Genotype Analysis of Patients with Hemoglobin Variants].
Zhongguo Shi Yan Xue Ye Xue Za Zhi
; 29(4): 1280-1288, 2021 Aug.
Artículo
en Zh
| MEDLINE | ID: mdl-34362517
9.
Rosiglitazone alleviates lipopolysaccharide-induced inflammation in RAW264.7 cells via inhibition of NF-κB and in a PPARγ-dependent manner.
Exp Ther Med
; 22(1): 743, 2021 Jul.
Artículo
en Inglés
| MEDLINE | ID: mdl-34055059
10.
[A preliminary study on intravitreal injection of bevacizumab for treatment of neovascular age-related macular degeneration].
Zhonghua Yan Ke Za Zhi
; 43(10): 890-6, 2007 Oct.
Artículo
en Zh
| MEDLINE | ID: mdl-18201525
11.
Factor X Shanghai and disruption of translocation to the endoplasmic reticulum.
Haematologica
; 90(12): 1659-64, 2005 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-16330440
12.
Characterization of molecular defect of 13387-9delG mutated antithrombin in inherited type I antithrombin deficiency.
Blood Coagul Fibrinolysis
; 16(2): 149-55, 2005 Mar.
Artículo
en Inglés
| MEDLINE | ID: mdl-15741804
13.
Biochemical activity and gene analysis of inherited protein C and antithrombin deficiency in two Chinese pedigrees.
Chin Med J (Engl)
; 117(6): 813-7, 2004 Jun.
Artículo
en Inglés
| MEDLINE | ID: mdl-15198878
14.
[Inherited coagulation factor VII deficiency caused by double heterozygotic mutations Arg304Gln and Arg304Trp].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 20(4): 279-83, 2003 Aug.
Artículo
en Zh
| MEDLINE | ID: mdl-12903033
15.
[Comparison and analysis of the clinical features of different types of gastrointestinal cancers].
Zhonghua Nei Ke Za Zhi
; 43(12): 900-2, 2004 Dec.
Artículo
en Zh
| MEDLINE | ID: mdl-15730733
16.
[Molecular genetic analysis for a pedigree with severe hereditary coagulation factor VII deficiency].
Zhonghua Nei Ke Za Zhi
; 42(10): 692-6, 2003 Oct.
Artículo
en Zh
| MEDLINE | ID: mdl-14633462
17.
[Two novel factor V gene mutations associated with congenital coagulation factor V deficiency, study of one pedigree].
Zhonghua Yi Xue Za Zhi
; 83(4): 312-5, 2003 Feb 25.
Artículo
en Zh
| MEDLINE | ID: mdl-12812650
18.
[Genetic analysis of a Chinese family with inherited afibrinogenemia].
Zhonghua Yi Xue Za Zhi
; 83(23): 2054-7, 2003 Dec 10.
Artículo
en Zh
| MEDLINE | ID: mdl-14703415
19.
[Type I hereditary protein C deficiency due to C5498T mutation in protein C gene].
Zhonghua Yi Xue Za Zhi
; 83(19): 1694-7, 2003 Oct 10.
Artículo
en Zh
| MEDLINE | ID: mdl-14642106
20.
[Molecular mechanisms of two novel mutations of factor XIII gene resulting in hereditary coagulation deficiency].
Zhonghua Yi Xue Za Zhi
; 83(24): 2158-61, 2003 Dec 25.
Artículo
en Zh
| MEDLINE | ID: mdl-14720426