Connective tissue and genetics in the pathogenesis of rectal prolapse: A scoping review. [PDF]
Davenport M +9 more
europepmc +1 more source
Case Report: Prenatal clues and postnatal evolution: a case of williams syndrome diagnosed following progressive cardiovascular phenotypes. [PDF]
Zeng Y +7 more
europepmc +1 more source
Case Report: Pediatric nephrology-expanding the genotypic spectrum of <i>COQ2</i>-related nephropathy with a novel splice site variant in CoQ10-responsive SRNS. [PDF]
Huang YR, Pal A, Tsai AC.
europepmc +1 more source
Metabolic-Immune Crosstalk in Pediatric Rheumatology: From Pathogenesis to Precision Therapy. [PDF]
Shashaani N +4 more
europepmc +1 more source
Congenital Diarrhoeas and Enteropathies. [PDF]
Köglmeier J, Lindley KJ.
europepmc +1 more source
A Case of Hyaline Fibromatosis Syndrome with a New Variant of Genetic Mutation in ANTXR2 Gene. [PDF]
Park CS +10 more
europepmc +1 more source
Very Rare Case of Hyaline Fibromatosis Syndrome Successfully Treated with Surgical Excision and Review of Literature. [PDF]
Jung YU, Kim BJ, Kim EH.
europepmc +1 more source
Adult-Onset Nephrotic Syndrome in the Older Adults: A Case Series. [PDF]
Choudhary N +4 more
europepmc +1 more source
Primary hyperoxaluria type I diagnosed after a kidney transplant presenting with subcutaneous calcification: a case report of sodium thiosulfate treatment. [PDF]
Wu M +6 more
europepmc +1 more source

