Results 211 to 220 of about 488,068 (360)

A Case of Gastric Cancer with Autosomal Dominant Polycystic Kidney Disease

open access: diamond, 2010
Hidetaka YAMANAKA   +7 more
openalex   +2 more sources

Exploring the Role of Kisspeptin in Polycystic Ovary Syndrome and Its Associated Pregnancy Complications

open access: yesObesity Reviews, Volume 27, Issue 1, Page 1-21, January 2026.
ABSTRACT Polycystic ovary syndrome (PCOS) is a common endocrine disorder with a complex pathogenesis that includes disordered follicle development, hypothalamic–pituitary–ovarian (HPO) axis dysfunction, hyperandrogenemia, and insulin resistance. The risk of complications during pregnancy, such as gestational diabetes mellitus (GDM) and preeclampsia (PE)
Shaohua Zhang   +5 more
wiley   +1 more source

Overweight and Obesity Are Predictors of Progression in Early Autosomal Dominant Polycystic Kidney Disease.

open access: yesJournal of the American Society of Nephrology, 2017
Kristen L. Nowak   +15 more
semanticscholar   +1 more source

Exploring the Role of Plant-Based Nutrition in Polycystic Kidney Disease. [PDF]

open access: yesNutrients
Sarmad A   +6 more
europepmc   +1 more source

Quantification of angiotensin II-regulated proteins in urine of patients with polycystic and other chronic kidney diseases by selected reaction monitoring [PDF]

open access: gold, 2016
Ana Konvalinka   +10 more
openalex   +1 more source

POLYCYSTIC KIDNEY DISEASE IN A PERSIAN CAT – A CASE REPORT

open access: bronze, 2023
Majida Farzana P.   +2 more
openalex   +1 more source

Pigmented Birthmarks and Spinal Neurofibromas in KRAS Mosaicism—Not to Be Confused With NF1

open access: yesPediatric Dermatology, Volume 43, Issue 1, Page 128-131, January/February 2026.
ABSTRACT We report a child presenting with pigmentary skin lesions and spinal neurofibromas who was diagnosed molecularly with KRAS mosaicism. We review the previous literature of two cases of congenital skin lesions and neurofibromas and spinal nerve root hypertrophy caused by KRAS variants and highlight this presentation as an important differential ...
Karina M. Forde   +3 more
wiley   +1 more source

Mutations in DZIP1L, which encodes a ciliary-transition-zone protein, cause autosomal recessive polycystic kidney disease

open access: yesNature Genetics, 2017
Hao Lu   +38 more
semanticscholar   +1 more source

A stepwise approach for effective management of chronic pain in autosomal-dominant polycystic kidney disease [PDF]

open access: bronze, 2014
Niek F. Casteleijn   +12 more
openalex   +1 more source

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