Results 111 to 120 of about 24,959 (186)

Mitral regurgitation and decompensated heart failure in a young pregnant pony mare: An aetiological challenge

Equine Veterinary Education, Volume 38, Issue 10, Page e676-e685, October 2026.
Summary A 4‐year‐old, 6‐month pregnant, Welsh pony mare presented with severe acute clinical signs including depression, anorexia, pale mucous membranes, tachycardia with a grade 4/6 holosystolic murmur and moderate expiratory dyspnoea with diffuse wheezes. There was no evidence of placentitis or fetal distress.
M. F. David, L. Cannon, A. Tortereau, A. Thomas‐Cancian, I. Desjardins   +4 more
wiley   +1 more source

PEBP1 Regulates Ferroptosis in Acute Glaucoma: Targeted Therapy Using Engineered Exosomes

The FASEB Journal, Volume 40, Issue 17, 15 September 2026.
General schematic diagram of Spatial and Single‐Cell Transcriptomics Identifies PEBP1 as a Ferroptosis Mediator in Glaucoma: Targeted Intervention by Engineered Stem Cell Exosomes. ABSTRACT Glaucoma is the leading cause of irreversible blindness worldwide, primarily driven by the progressive loss of retinal ganglion cells (RGCs) under pathological high
Yijia Huang, Di Gong, Junhong Guo, Wei Huang, Tingyu Hu, Shengbin Tang, Li Li, Bingkai Feng, Kuanrong Dang, Simin Deng, Yong Liu, Chunyan Tan, Fei Yao, Jiantao Wang   +13 more
wiley   +1 more source

Prospective evaluation of kidney and liver disease in autosomal recessive polycystic kidney disease-congenital hepatic fibrosis. [PDF]

Mol Genet Metab, 2020
Abdul Majeed N, Font-Montgomery E, Lukose L, Bryant J, Veppumthara P, Choyke PL, Turkbey IB, Heller T, Gahl WA, Gunay-Aygun M.   +9 more
europepmc   +1 more source

Joubert Syndrome and Related Disorders: Congenital Hepatic Fibrosis, Autosomal Recessive Polycystic Kidney Disease, and Pigmentary Retinopathy

Case Reports in Clinical Practice, 2017
Joubert syndrome and related disorders (JSRDs) are a group of anomalies characterized by hypotonia, ataxia, developmental delay, intellectual disability, abnormal eye movements, and apnea and hyperpnea in infancy with multiorgan involvement in which the ...
Fatemeh Farahmand, Hojjatollah Jafari-Fesharaki, Rouhullah Edalatkhah, Mohammad Eshagh Rozeh   +3 more
doaj  

Congenital hepatic fibrosis and related ciliopathies across the life course: current management, disease burden, and unmet needs in the era of genomic diagnosis and translational therapeutics. [PDF]

Front Pediatr
Wang A, He J, Liu K, Fu J, Chen J.
europepmc   +1 more source

Congenital Hepatic Fibrosis and/or Autosomal Recessive Polycystic Kidney Disease: A Single-center Experience. [PDF]

Pediatr Gastroenterol Hepatol Nutr
Altay D, Yel S, Dursun İ, Arslan D.
europepmc   +1 more source

Terlipressin-Induced Hyponatremic Seizures in a Patient With Congenital Hepatic Fibrosis. [PDF]

HCA Healthc J Med
Gauci L, Gafa J, Cauchi S, Gerada J.
europepmc   +1 more source

An Unusual Case of Congenital Hepatic Fibrosis with Retinitis Pigmentosa. [PDF]

Cureus, 2019
Butt N, Akbar A, Fahad A.
europepmc   +1 more source

Congenital hepatic fibrosis and coexistent retinal macular degeneration: A case report. [PDF]

Medicine (Baltimore), 2019
Li D, Qin J, Sun S, Li X.
europepmc   +1 more source

[A case of congenital hepatic fibrosis accompanied with multiple system abnormalities]. [PDF]

Zhonghua Gan Zang Bing Za Zhi
Liu TF, Kong Y, Zhang LY, Wang L.
europepmc   +1 more source