Detalhe da pesquisa
1.
Role of anti-tissue transglutaminase IgA+IgG antibodies in detection of potential celiac disease in patients with type 1 diabetes.
Indian J Med Res
; 149(1): 18-25, 2019 Jan.
Artigo
Inglês
| MEDLINE | ID: mdl-31115370
2.
Lactase genetic polymorphisms and coeliac disease in children: a cohort study.
Ann Hum Biol
; 42(1): 101-4, 2015 Jan.
Artigo
Inglês
| MEDLINE | ID: mdl-25495501
3.
Frequency distribution of Q188R, N314D, Duarte 1, and Duarte 2 GALT variant alleles in an Indian galactosemia population.
Biochem Genet
; 50(11-12): 871-80, 2012 Dec.
Artigo
Inglês
| MEDLINE | ID: mdl-22798028
4.
Role of abdominal sonography in the preoperative diagnosis of extrahepatic biliary atresia in infants younger than 90 days.
AJR Am J Roentgenol
; 196(4): W438-45, 2011 Apr.
Artigo
Inglês
| MEDLINE | ID: mdl-21427309
5.
Natural history and predictive risk factors of prolonged unconjugated jaundice in the newborn.
Pediatr Int
; 52(5): 769-72, 2010 Oct.
Artigo
Inglês
| MEDLINE | ID: mdl-20497361
6.
Brush border enzyme activities in relation to histological lesion in pediatric celiac disease.
J Gastroenterol Hepatol
; 23(8 Pt 2): e348-52, 2008 Aug.
Artigo
Inglês
| MEDLINE | ID: mdl-18070009
7.
Lymphocytic gastritis and celiac disease in indian children: evidence of a positive relation.
J Pediatr Gastroenterol Nutr
; 47(5): 568-72, 2008 Nov.
Artigo
Inglês
| MEDLINE | ID: mdl-18979579
8.
Implication of the cystic fibrosis transmembrane conductance regulator gene in infertile family members of Indian CF patients.
Biochem Genet
; 46(11-12): 847-56, 2008 Dec.
Artigo
Inglês
| MEDLINE | ID: mdl-18810634
9.
Liver acoustic radiation force impulse (ARFI) in childhood obesity: comparison and correlation with biochemical markers.
J Ultrasound
; 20(1): 33-42, 2017 Mar.
Artigo
Inglês
| MEDLINE | ID: mdl-28298942
10.
Celiac Disease in a Boy with Duchenne Muscular Dystrophy: A Double Jeopardy!
Ann Indian Acad Neurol
; 23(5): 731-732, 2020.
Artigo
Inglês
| MEDLINE | ID: mdl-33623290
11.
Congenital Extrahepatic Portosystemic Shunts: Spectrum of Findings on Ultrasound, Computed Tomography, and Magnetic Resonance Imaging.
Radiol Res Pract
; 2015: 181958, 2015.
Artigo
Inglês
| MEDLINE | ID: mdl-26858845
12.
Ursodeoxycholic acid-augmented hepatobiliary scintigraphy in the evaluation of neonatal jaundice.
J Nucl Med
; 45(9): 1488-92, 2004 Sep.
Artigo
Inglês
| MEDLINE | ID: mdl-15347715
13.
HLA DRB1 Alleles Discriminate the Manifestation of Autoimmune Hepatitis as Type 1 or Type 2 in North Indian Population.
J Clin Exp Hepatol
; 4(1): 14-8, 2014 Mar.
Artigo
Inglês
| MEDLINE | ID: mdl-25755530
14.
Correlation of G/A -22018 single-nucleotide polymorphism with lactase activity and its usefulness in improving the diagnosis of adult-type hypolactasia among North Indian children.
Genes Nutr
; 8(1): 145-51, 2013 Jan.
Artigo
Inglês
| MEDLINE | ID: mdl-22763774
15.
Intravenous contrast enhanced computed tomography colonoscopy in children with suspected colonic polyps.
Eur J Radiol
; 82(6): 905-12, 2013 Jun.
Artigo
Inglês
| MEDLINE | ID: mdl-23332642
16.
Biochemical and molecular characterization of GALT gene from Indian galactosemia patients: identification of 10 novel mutations and their structural and functional implications.
Clin Chim Acta
; 414: 191-6, 2012 Dec 24.
Artigo
Inglês
| MEDLINE | ID: mdl-23022339
17.
Comparison of hospital versus rural eye cAMP based pediatric cataract surgery.
Middle East Afr J Ophthalmol
; 19(1): 141-6, 2012 Jan.
Artigo
Inglês
| MEDLINE | ID: mdl-22346130
18.
A prospective study comparing histology and enteric enzyme function of patients with extrahepatic portal vein obstruction before and after shunt surgery.
Eur J Gastroenterol Hepatol
; 24(10): 1219-26, 2012 Oct.
Artigo
Inglês
| MEDLINE | ID: mdl-22850192
19.
Clinical presentation of celiac disease among pediatric compared to adolescent and adult patients.
Indian J Gastroenterol
; 31(3): 116-20, 2012 Jun.
Artigo
Inglês
| MEDLINE | ID: mdl-22717947
20.
A case of classical galactosemia: identification and characterization of 3 distinct mutations in galactose-1-phosphate uridyl transferase (GALT) gene in a single family.
Indian J Pediatr
; 78(7): 874-6, 2011 Jul.
Artigo
Inglês
| MEDLINE | ID: mdl-21188552