Porta G - Search Results

1

Autoimmune Hepatitis in Brazilian Children: IgE and Genetic Polymorphisms in Associated Genes.

de Oliveira LC, Goldberg AC, Marin ML, Schneidwind KR, Frade AF, Kalil J, Miura IK, Pugliese RP, Danesi VL, Porta G. de Oliveira LC, et al. Among authors: porta g. J Immunol Res. 2015;2015:679813. doi: 10.1155/2015/679813. Epub 2015 Nov 26. J Immunol Res. 2015. PMID: 26693492 Free PMC article.

2

Posttransplant lymphoproliferative disease of the liver successfully treated by retransplantation.

Chachap P, Carone Filho E, Porta G, Miura I, Zerbini MC, Gayotto LC, Maksoud JG. Chachap P, et al. Among authors: porta g. Transplantation. 1991 Oct;52(4):736-7. doi: 10.1097/00007890-199110000-00031. Transplantation. 1991. PMID: 1926356 No abstract available.

3

The endoscopic and surgical management of portal hypertension in children: analysis of 123 cases.

Maksoud JG, Gonçalves ME, Porta G, Miura I, Velhote MC. Maksoud JG, et al. Among authors: porta g. J Pediatr Surg. 1991 Feb;26(2):178-81. doi: 10.1016/0022-3468(91)90904-8. J Pediatr Surg. 1991. PMID: 2023079

4

Chronic active hepatitis associated with anti-liver-kidney microsome antibody type 1.

Porta G, Bonfa E, Miura IK, Pugliese RS, Cossermelli W, Oliveira RM. Porta G, et al. Arq Gastroenterol. 1988 Apr-Jun;25(2):86-8. Arq Gastroenterol. 1988. PMID: 3255276

5

Management of biliary atresia in the liver transplantation era: a 15-year, single-center experience.

Maksoud JG, Fauza DO, Silva MM, Porta G, Miura I, Zerbini CN. Maksoud JG, et al. Among authors: porta g. J Pediatr Surg. 1998 Jan;33(1):115-8. doi: 10.1016/s0022-3468(98)90375-x. J Pediatr Surg. 1998. PMID: 9473114

6

Different HLA profiles confer susceptibility to autoimmune hepatitis type 1 and 2.

Bittencourt PL, Goldberg AC, Cançado EL, Porta G, Laudanna AA, Kalil J. Bittencourt PL, et al. Among authors: porta g. Am J Gastroenterol. 1998 Aug;93(8):1394-5. doi: 10.1111/j.1572-0241.1998.1394a.x. Am J Gastroenterol. 1998. PMID: 9707090 No abstract available.

7

[3-Hydroxy-3-methyl-glutaryl-CoA-lyase deficiency as coma etiology in the neonatal period: case report].

Casella EB, Martins FR, Miura IK, Vieira MA, Porta G. Casella EB, et al. Among authors: porta g. Arq Neuropsiquiatr. 1998 Sep;56(3A):472-5. doi: 10.1590/s0004-282x1998000300019. Arq Neuropsiquiatr. 1998. PMID: 9754431 Portuguese.

8

Genetic heterogeneity in susceptibility to autoimmune hepatitis types 1 and 2.

Bittencourt PL, Goldberg AC, Cançado EL, Porta G, Carrilho FJ, Farias AQ, Palacios SA, Chiarella JM, Abrantes-Lemos CP, Baggio VL, Laudanna AA, Kalil J. Bittencourt PL, et al. Among authors: porta g. Am J Gastroenterol. 1999 Jul;94(7):1906-13. doi: 10.1111/j.1572-0241.1999.01229.x. Am J Gastroenterol. 1999. PMID: 10406258

9

Analysis of HLA haplotypes in autoimmune hepatitis type 1: identifying the major susceptibility locus.

Goldberg AC, Bittencourt PL, Mougin B, Cançado EL, Porta G, Carrilho F, Kalil J. Goldberg AC, et al. Among authors: porta g. Hum Immunol. 2001 Feb;62(2):165-9. doi: 10.1016/s0198-8859(00)00234-2. Hum Immunol. 2001. PMID: 11182227

10

Autoimmune hepatitis in Brazilian patients is not linked to tumor necrosis factor alpha polymorphisms at position -308.

Bittencourt PL, Palácios SA, Cançado EL, Porta G, Drigo S, Carrilho FJ, Laudanna AA, Kalil J, Goldberg AC. Bittencourt PL, et al. Among authors: porta g. J Hepatol. 2001 Jul;35(1):24-8. doi: 10.1016/s0168-8278(01)00072-1. J Hepatol. 2001. PMID: 11495038

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