Detalhe da pesquisa
1.
A multi-population-based genomic analysis uncovers unique haplotype variants and crucial mutant genes in SARS-CoV-2.
J Genet Eng Biotechnol;
20(1): 149, 2022 Nov 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36318347
2.
Unfavorable neuroblastoma prognostic factor NLRR2 inhibits cell differentiation by transcriptional induction through JNK pathway.
Cancer Sci;
107(9): 1223-32, 2016 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-27357360
3.
Persistent mullerian duct syndrome: A 24-year experience.
J Pediatr Surg;
51(10): 1721-4, 2016 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-27329391
4.
Additive loss-of-function proteasome subunit mutations in CANDLE/PRAAS patients promote type I IFN production.
J Clin Invest;
126(2): 795, 2016 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-26829627
5.
Additive loss-of-function proteasome subunit mutations in CANDLE/PRAAS patients promote type I IFN production.
J Clin Invest;
125(11): 4196-211, 2015 Nov 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-26524591
6.
Protective effects of Moringa oleifera Lam. leaves against arsenic-induced toxicity in mice.
Asian Pac J Trop Biomed;
4(Suppl 1): S353-8, 2014 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-25183111
7.
Mortality in a case of crystal gel ball ingestion: an alert for parents.
APSP J Case Rep;
3(1): 6, 2012 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-22953300
8.
A case of fetus in fetu.
APSP J Case Rep;
3(2): 9, 2012 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-22953303
9.
Biliary atresia associated with polysplenia syndrome, situs inversus abdominus, and reverse rotation of intestine.
APSP J Case Rep;
3(2): 14, 2012 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-22953308
10.
Duodenal Duplication Cyst having Ectopic Gastric and Pancreatic Tissues.
APSP J Case Rep;
3(2): 15, 2012 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-22953309
11.
Gastric volvulus in children: our experience.
Indian J Gastroenterol;
31(5): 258-62, 2012 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-22983838
12.
A hypermorphic missense mutation in PLCG2, encoding phospholipase Cγ2, causes a dominantly inherited autoinflammatory disease with immunodeficiency.
Am J Hum Genet;
91(4): 713-20, 2012 Oct 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-23000145
13.
Pheochromocytoma: a rare cause of childhood hypertensive encephalopathy.
J Coll Physicians Surg Pak;
22(8): 536-8, 2012 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-22868025
14.
Laparoscopic management of 128 undescended testes: our experience.
Afr J Paediatr Surg;
9(2): 106-8, 2012.
Artigo
em Inglês
| MEDLINE | ID: mdl-22878756
15.
Reply: Congenital pouch colon with ileovesical and colovesical fistulae: A new variant.
J Indian Assoc Pediatr Surg;
17(2): 91, 2012 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-22529563
16.
Congenital right hemidiaphragmatic agenesis.
Lung India;
29(1): 53-5, 2012 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-22345915
17.
Elevated levels of plasma Big endothelin-1 and its relation to hypertension and skin lesions in individuals exposed to arsenic.
Toxicol Appl Pharmacol;
259(2): 187-94, 2012 Mar 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-22245594
18.
Mutations in proteasome subunit ß type 8 cause chronic atypical neutrophilic dermatosis with lipodystrophy and elevated temperature with evidence of genetic and phenotypic heterogeneity.
Arthritis Rheum;
64(3): 895-907, 2012 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-21953331
19.
Prognosis of surgical neonates.
J Neonatal Surg;
1(1): 1, 2012.
Artigo
em Inglês
| MEDLINE | ID: mdl-26023360
20.
Multiple associated anomalies in patients of duodenal atresia: a case series.
J Neonatal Surg;
1(2): 23, 2012.
Artigo
em Inglês
| MEDLINE | ID: mdl-26023382