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PubMed This is a summary of 8 peer-reviewed journal articles Updated

Research & Literature

Explore the leading researchers and institutions driving advances in this area, and dive into the full body of literature that informs this resource.

Explore the Literature Visualize citation networks across 8 referenced papers

References

References (8)
  1. 1

    Growth in Infants and Children With Intestinal Failure-associated Liver Disease Treated With Intravenous Fish Oil.

    Raphael BP, Mitchell PD, Gura KM, et al.

    Journal of pediatric gastroenterology and nutrition 2020; (70(2)):261-268 doi:10.1097/MPG.0000000000002551.

    PMID: 31978030
  2. 2

    Efficacy and safety of parenteral vitamin D therapy in infants and children with vitamin D deficiency caused by intestinal malabsorption.

    Yu SB, Lee Y, Oh A, et al.

    Annals of pediatric endocrinology & metabolism 2020; (25(2)):112-117 doi:10.6065/apem.1938142.071.

    PMID: 32615691
  3. 3

    Novel Compound Heterozygous TMPRSS15 Gene Variants Cause Enterokinase Deficiency.

    Wang L, Zhang D, Fan C, et al.

    Frontiers in genetics 2020; (11()):538778 doi:10.3389/fgene.2020.538778.

    PMID: 33061943
  4. 4

    Enterokinase deficiency with novel TMPRSS15 gene mutation masquerading as acrodermatitis enteropathica.

    Chen Y, Li Z, Liu C, Wang S

    Pediatric dermatology 2023; (40(2)):389-391 doi:10.1111/pde.15197.

    PMID: 36410965
  5. 5

    Activation of Human Pancreatic Proteolytic Enzymes: The Role of Enteropeptidase and Trypsin.

    Freiburghaus AU, Roduner J, Hadorn HB

    JPGN reports 2021; (2(4)):e138 doi:10.1097/PG9.0000000000000138.

    PMID: 37206452
  6. 6

    Enterokinase deficiency associated with novel TMPRSS15 gene mutations: a case report.

    Li Y, Li R, Pan Y, et al.

    Frontiers in pediatrics 2025; (13()):1484208 doi:10.3389/fped.2025.1484208.

    PMID: 39944319
  7. 7

    Secondary Hyperparathyroidism in Primary Intestinal Lymphangiectasia: A Report of Four Cases.

    Zhang DX, Hao K, Zhang L, et al.

    Gastroenterology research 2025; (18(3)):152-158 doi:10.14740/gr2022.

    PMID: 40503188
  8. 8

    A Rare Case of Congenital Glucose Galactose Malabsorption Due to SLC5A1 Mutation.

    Muralidharan H, Sajith A, ElSayed N, et al.

    Cureus 2025; (17(12)):e98692 doi:10.7759/cureus.98692.

    PMID: 41510412