Results 131 to 140 of about 84,845 (281)

Polycystic liver disease: An uncommon genetic condition

open access: yesClinical Case Reports
Key Clinical Message Timely recognition, accurate diagnosis, and proper management are vital for preventing complications and improving outcomes in polycystic liver disease. Abstract Polycystic liver disease is an uncommon genetic condition characterized
Faten Limaiem, Mohamed Hajri
doaj   +1 more source

Hexafluoropropylene oxide-dimer acid (HFPO-DA or GenX) alters maternal and fetal glucose and lipid metabolism and produces neonatal mortality, low birthweight, and hepatomegaly in the Sprague-Dawley rat.

open access: yesEnvironment International, 2020
Justin M. Conley   +8 more
semanticscholar   +1 more source

tRF‐30‐FP18LPMBQ4NK in Systemic Juvenile Idiopathic Arthritis: A Promising Diagnostic and Disease Activity Biomarker

open access: yesAnnals of the New York Academy of Sciences, EarlyView.
ABSTRACT Diagnosing systemic juvenile idiopathic arthritis (sJIA) poses significant challenges. Accumulating evidence has indicated that tRNA‐derived fragments (tRFs) play integral roles in the pathogenesis of numerous diseases. Plasma samples were collected from individuals diagnosed with sJIA and healthy controls (HCs) from two medical centers and ...
Jiqian Huang   +6 more
wiley   +1 more source

A novel homozygous mutation in the glycerol-3-phosphate dehydrogenase 1 gene in a Chinese patient with transient infantile hypertriglyceridemia: a case report

open access: yesBMC Gastroenterology, 2018
Background Transient infantile hypertriglyceridemia (HTGTI) is an autosomal recessive disorder caused by mutations in the glycerol-3-phosphate dehydrogenase 1 (GPD1) gene. Case presentation We report a case of HTGTI in a Chinese female infant.
Jia-Qi Li   +7 more
doaj   +1 more source

Omalizumab for Pediatric Cutaneous Mastocytosis: Case Report and Review

open access: yesPediatric Dermatology, EarlyView.
ABSTRACT We report an 11‐month‐old boy with diffuse cutaneous mastocytosis whose severe pruritus and steroid dependence resolved following off‐label treatment with omalizumab. A literature review identified five additional pediatric cases in which omalizumab led to complete symptom resolution in an average of 2 months and permitted discontinuation of ...
Janis Chang   +3 more
wiley   +1 more source

Hereditary fibrosing poikiloderma with tendon contractures, myopathy, and pulmonary fibrosis: Hepatic disease in a child with a novel pathogenic variant of FAM111B

open access: yesJAAD Case Reports, 2020
Yelena Dokic, BSA   +6 more
doaj   +1 more source

HHV‐8/KSHV in Solid Organ Transplantation: Current Gaps of Knowledge and Future Directions

open access: yesTransplant Infectious Disease, EarlyView.
Risk mitigation strategies, including donors/recipients screening, DNAemia monitoring in recipients at risk, CNI‐to‐mTOR inhibitors switch, antivirals, and rituximab for KICS, may mitigate the impact of HHV‐8/KSHV infection in SOT. This review provides an update on KICS, identifies research gaps, and summarizes advances in screening and management ...
Alessandra Mularoni   +9 more
wiley   +1 more source

A Multi‐Institutional Retrospective Study of 21 Dogs Having Undergone Hypofractionated Radiotherapy for Adrenal Tumours (2017–2024)

open access: yesVeterinary and Comparative Oncology, EarlyView.
ABSTRACT Radiation therapy (RT) has emerged as a promising non‐surgical approach for treating canine adrenal tumours. This multi‐institutional, retrospective study describes clinical outcomes for 21 dogs having been prescribed a course of hypofractionated image‐guided intensity‐modulated RT (IMRT) entailing delivery of 25–35 Gy total in 5 fractions ...
Yen‐Hao Erik Lai   +4 more
wiley   +1 more source

Embolization by Gelatin Sponge for Tract Closure After Inappropriate Procedure of Percutaneous Endoscopic Gastrostomy: Safe Management of Hepatic Injury After Transhepatic Placement

open access: yesDEN Open, Volume 6, Issue 1, April 2026.
ABSTRACT Placement of percutaneous endoscopic gastrostomy (PEG) is generally safe and well‐tolerated. Transhepatic insertion of PEG tubes is an extremely rare but serious complication. Optimal management strategies for safe removal of PEG tubes remain unclear.
Hiroshi Yukimoto   +9 more
wiley   +1 more source

A Rare Case of Glycogenic Hepatopathy in a Child with Type 1 Diabetes: Reversible with Glycemic Control

open access: yesJournal of Diabetology
Glycogenic hepatopathy (GH) is an uncommon complication associated with poorly controlled diabetes mellitus (DM), more often with type 1 DM as compared to type 2 DM and is characterized by an enlarged liver and temporary increases in serum ...
Prabhat K. Agrawal   +3 more
doaj   +1 more source

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