Results 111 to 120 of about 1,479 (176)

Endocrine Alterations in Patients With Pachydermoperiostosis. [PDF]

J Clin Endocrinol Metab
Stelmachowska-Banaś M, Barry S, Angurala I, Rice T, Magid K, Carreira A, Rai A, Evans A, Bollington M, Kaur V, Singhmar S, Silaghi CA, Mandisodza K, McGregor A, Sahoo J, Gupta R, Behera KK, Roy A, Carr IM, Loughrey PB, Dutta P, Korbonits M.   +21 more
europepmc   +1 more source

A rare clinical image of pachydermoperiostosis (Touraine-Solente-Gole syndrome). [PDF]

Pan Afr Med J
Joshi T, Patharkar J.
europepmc   +1 more source

GLIS3, a novel regulator of eicosanoid gene expression and metabolism in normal kidney and polycystic kidney disease. [PDF]

Biochem Pharmacol
Srivastava C, Kang HS, Edin ML, Mukherjee T, Lih FB, Grimm SA, Collier JB, Zeldin DC, Jetten AM.   +8 more
europepmc   +1 more source

An environmentally relevant phthalate mixture impairs ovulatory prostaglandin and progesterone receptor pathways in human granulosa cells in vitro. [PDF]

Environ Int
Land KL, Xu H, Akin JW, Hannon PR.
europepmc   +1 more source

Cryptogenic multifocal ulcerative stenosing enteritis (CMUSE): a rare case and a review of the literature. [PDF]

J Surg Case Rep
Hudson L, Grayson N, Toomey D.
europepmc   +1 more source

Cryptogenic Multifocal Ulcerating Stenosing Enteritis (CMUSE) in a Patient with Down Syndrome: A Case Report. [PDF]

Reports (MDPI)
Patel AB, Zula D, Varshney K, Thompson D, Bolshinsky V.   +4 more
europepmc   +1 more source

PGR-mediated transcriptome identifies SOX9 as a critical regulator of progesterone production in human ovulatory follicles. [PDF]

iScience
Jeon H, Choi Y, Brännström M, Akin JW, Curry TE, Jo M.   +5 more
europepmc   +1 more source

Genotype-Phenotype Correlation Insights in a Rare Case Presenting with Multiple Osteodysplastic Syndromes. [PDF]

Genes (Basel)
Yapijakis C, Gintoni I, Chamakioti M, Koniari E, Papanikolaou E, Kassi E, Vlachakis D, Chrousos GP.   +7 more
europepmc   +1 more source

Reactive Therapeutic Drug Monitoring Guides Optimal Management of Adalimumab Failure in Pediatric Crohn's Disease: A Real-World Single-Center Experience. [PDF]

Pediatr Gastroenterol Hepatol Nutr
Jeong IS, Kim TG, Yi DY, Kim KM.
europepmc   +1 more source

A novel compound mutation of SLCO2A1 in a Chinese patient with primary hypertrophic osteoarthropathy

Indian Journal of Dermatology, Venereology and Leprology, 2023
openaire   +2 more sources