Results 221 to 230 of about 587,070 (347)

Mixed Erdheim-Chester disease with thoraco-abdominal involvement. [PDF]

Acta Radiol Open
Saliba T, Rotzinger D, Haefliger L, Fahrni G.   +3 more
europepmc   +1 more source

Apoptosis and loss of renal tissue in polycystic kidney diseases.

New England Journal of Medicine, 1995
David D. L. Woo
semanticscholar   +1 more source

Primary Hyperparathyroidism With Brown Tumor—A Case Mistaken as Non‐Ossifying Fibroma Resolved by Biochemical and Radiological Correlation

Clinical Case Reports, Volume 14, Issue 2, February 2026.
ABSTRACT Primary hyperparathyroidism (PHPT) is uncommon in the pediatric population and rarely presents with overt skeletal complications such as brown tumors. This case study describes a 16‐year‐old female who initially presented with abdominal pain and was subsequently found to have severe hypercalcemia (serum calcium 16.4 mg/dL) and markedly ...
Dosti Regmi, Uma Bhatta, Madhur Bhattarai, Saurav Jha, Akriti Baral   +4 more
wiley   +1 more source

Giant Pyonephrosis Diagnosed Using POCUS in a Resource-Limited Setting. [PDF]

POCUS J
Menager R, Louis RS, Gelin A, Jacques FD.   +3 more
europepmc   +1 more source

A genetic screen in zebrafish identifies cilia genes as a principal cause of cystic kidney

Development, 2004
Zhaoxia Sun, A. Amsterdam, G. Pazour, D. Cole, M. S. Miller, N. Hopkins   +5 more
semanticscholar   +1 more source

Dual Monogenic Cystic Disease Case Report: Autosomal Dominant Polycystic Kidney Disease and Autosomal Dominant Polycystic Liver Disease

Clinical Case Reports, Volume 14, Issue 2, February 2026.
ABSTRACT Autosomal dominant polycystic kidney disease (ADPKD) and autosomal dominant polycystic liver disease (ADPLD) are inherited cystic conditions with overlapping features but distinct genetic causes and clinical courses. Here, we report a case of a 50‐year‐old woman with a clinical diagnosis of ADPKD, hypertension, preserved kidney function ...
Anna Katya Brossart, Kathryn Curry, Sumit Punj, Tarek Darwish, Hossein Tabriziani   +4 more
wiley   +1 more source

Fumarate hydratase-deficient renal cell carcinoma arising in acquired cystic kidney disease in a hemodialysis patient: Diagnostic clues from percutaneous renal mass core needle biopsy: A case report. [PDF]

Oncol Lett
Oba Y, Kamido H, Kono K, Miki K, Ito S, Sekine A, Kurihara S, Yamanouchi M, Suwabe T, Takazawa Y, Ohashi K, Nagashima Y, Nakamura Y, Ubara Y, Sawa N.   +14 more
europepmc   +1 more source

Cystic kidney disease.

Indian pediatrics, 1996
S, Mishra, S, Kumari, S, Niranjan, C P, Sachdev, P, Bajaj   +4 more
openaire   +1 more source

Clinical and radiographic features of a family with hypochondroplasia owing to a novel Asn540Ser mutation in the fibroblast growth factor receptor 3 gene [PDF]

, 2000
Craen, Margarita, De Paepe, Anne, Leroy, Juliaan, Mortier, Geert, Nuytinck, Lieve, Renard, Jean-Pierre   +5 more
core   +3 more sources

Spontaneous Perirenal Hemorrhage Mimicking Renal Rupture in a Long‐Term Hemodialysis Patient: A Case Report

Clinical Case Reports, Volume 14, Issue 2, February 2026.
ABSTRACT Spontaneous perirenal hemorrhage (SPH) and spontaneous renal rupture (SRR) are rare emergencies that can be radiologically indistinguishable when hematomas are large, especially in hemodialysis patients. We report a 53‐year‐old man on long‐term hemodialysis who developed acute left flank pain 19 h after low‐molecular‐weight heparin.
Zhen Wang, Bo Yang, Yi Zhang, Xiaoqiang Li, Bin Wang, Jinghan Chen   +5 more
wiley   +1 more source