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Connection

Sirish Palle to Humans

This is a "connection" page, showing publications Sirish Palle has written about Humans.
Connection Strength

0.389
  1. Advanced cystic fibrosis liver disease: Endovascular, endoscopic, radiologic, and surgical considerations. Pediatr Pulmonol. 2024 Sep; 59 Suppl 1:S115-S122.
    View in: PubMed
    Score: 0.053
  2. Gastric Duplication Cyst. J Pediatr Gastroenterol Nutr. 2022 Nov 01; 75(5):e106-e107.
    View in: PubMed
    Score: 0.045
  3. CholbamĀ® and Zellweger spectrum disorders: treatment implementation and management. Orphanet J Rare Dis. 2021 09 14; 16(1):388.
    View in: PubMed
    Score: 0.043
  4. Novel compound heterozygous variants in the NBAS gene in a child with osteogenesis imperfecta and recurrent acute liver failure. BMJ Case Rep. 2021 Feb 04; 14(2).
    View in: PubMed
    Score: 0.041
  5. Racial disparities in presentation and outcomes of paediatric autoimmune hepatitis. Liver Int. 2019 05; 39(5):976-984.
    View in: PubMed
    Score: 0.036
  6. Approach to a Child with Colitis. Indian J Pediatr. 2016 Nov; 83(12-13):1444-1451.
    View in: PubMed
    Score: 0.029
  7. Oxidized high-density lipoprotein and low-density lipoprotein in adolescents with obesity and metabolic dysfunction-associated steatotic liver disease. Pediatr Obes. 2025 Feb; 20(2):e13194.
    View in: PubMed
    Score: 0.013
  8. Serum adropin is unaltered in adolescents with histology-confirmed steatotic liver disease. J Pediatr Gastroenterol Nutr. 2025 Jan; 80(1):182-188.
    View in: PubMed
    Score: 0.013
  9. Concordance of MASLD and NAFLD nomenclature in youth participating in the TARGET-NASH real-world cohort. Hepatol Commun. 2024 Nov 01; 8(11).
    View in: PubMed
    Score: 0.013
  10. Postprandial triglycerides and fibroblast growth factor 19 as potential screening tools for paediatric non-alcoholic fatty liver disease. Pediatr Obes. 2023 04; 18(4):e13007.
    View in: PubMed
    Score: 0.012
  11. Diagnostic challenges and disease management in patients with a mild Zellweger spectrum disorder phenotype. Mol Genet Metab. 2021 11; 134(3):217-222.
    View in: PubMed
    Score: 0.011
  12. Whole-genome sequencing of African Americans implicates differential genetic architecture in inflammatory bowel disease. Am J Hum Genet. 2021 03 04; 108(3):431-445.
    View in: PubMed
    Score: 0.010
  13. A two decade long study of disease progression of de novo and recurrent autoimmune hepatitis in the pediatric population. Pediatr Transplant. 2021 Aug; 25(5):e13978.
    View in: PubMed
    Score: 0.010
  14. The Sclerosing Cholangitis Outcomes in Pediatrics (SCOPE) Index: A Prognostic Tool for Children. Hepatology. 2021 03; 73(3):1074-1087.
    View in: PubMed
    Score: 0.010
  15. Pediatric Non-Alcoholic Fatty Liver Disease: Nutritional Origins and Potential Molecular Mechanisms. Nutrients. 2020 Oct 16; 12(10).
    View in: PubMed
    Score: 0.010
  16. The expanding LARS2 phenotypic spectrum: HLASA, Perrault syndrome with leukodystrophy, and mitochondrial myopathy. Hum Mutat. 2020 08; 41(8):1425-1434.
    View in: PubMed
    Score: 0.010
  17. Assessing the Validity of Adult-derived Prognostic Models for Primary Sclerosing Cholangitis Outcomes in Children. J Pediatr Gastroenterol Nutr. 2020 01; 70(1):e12-e17.
    View in: PubMed
    Score: 0.010
  18. Epidemiology, Clinical Presentation, and Seasonal Variation in the Diagnosis of Children with Eosinophilic Esophagitis in Oklahoma. South Med J. 2020 01; 113(1):37-41.
    View in: PubMed
    Score: 0.010
  19. Ursodeoxycholic Acid Therapy in Pediatric Primary Sclerosing Cholangitis: Predictors of Gamma Glutamyltransferase Normalization and Favorable Clinical Course. J Pediatr. 2019 06; 209:92-96.e1.
    View in: PubMed
    Score: 0.009
Connection Strength

The connection strength for concepts is the sum of the scores for each matching publication.

Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.