Articles with "paucity" as a keyword



Photo from archive.org

Intersections of binary quadratic forms in primes and the paucity phenomenon

Sign Up to like & get
recommendations!
Published in 2021 at "Journal of Number Theory"

DOI: 10.1016/j.jnt.2021.06.035

Abstract: Abstract. The number of solutions to a+b = c+d ≤ x in integers is a well-known result, while if one restricts all the variables to primes Erdős [4] showed that only the diagonal solutions, namely,… read more here.

Keywords: binary quadratic; primes paucity; paucity; quadratic forms ... See more keywords
Photo from wikipedia

A Case of Dubin-Johnson Syndrome Presenting as Neonatal Cholestasis With Paucity of Interlobular Bile Ducts

Sign Up to like & get
recommendations!
Published in 2021 at "Pediatric and Developmental Pathology"

DOI: 10.1177/1093526620980577

Abstract: Dubin-Johnson syndrome (DJS) is a rare autosomal recessive disorder that typically manifests in young adulthood as jaundice with conjugated hyperbilirubinemia. We report a case presenting as neonatal cholestasis with the unexpected histologic finding of paucity… read more here.

Keywords: bile; dubin johnson; neonatal cholestasis; paucity ... See more keywords
Photo from wikipedia

Alagille syndrome and non-syndromic paucity of the intrahepatic bile ducts.

Sign Up to like & get
recommendations!
Published in 2021 at "Translational gastroenterology and hepatology"

DOI: 10.21037/tgh-2020-03

Abstract: The observation of bile duct paucity is an important diagnostic finding in children, occurring in roughly 11% of pediatric liver biopsies. Alagille syndrome (ALGS) is a well-defined syndromic form of intrahepatic bile duct paucity that… read more here.

Keywords: bile duct; paucity; alagille syndrome; intrahepatic bile ... See more keywords

Downregulation of Protease Cathepsin D and Upregulation of Pathologic α-Synuclein Mediate Paucity of DNAJC6-Induced Degeneration of Dopaminergic Neurons

Sign Up to like & get
recommendations!
Published in 2024 at "International Journal of Molecular Sciences"

DOI: 10.3390/ijms25126711

Abstract: A homozygous mutation of the DNAJC6 gene causes autosomal recessive familial type 19 of Parkinson’s disease (PARK19). To test the hypothesis that PARK19 DNAJC6 mutations induce the neurodegeneration of dopaminergic cells by reducing the protein… read more here.

Keywords: dopaminergic neurons; dnajc6; dnajc6 paucity; paucity ... See more keywords