Results 291 to 300 of about 567,471 (395)

Bilateral nontraumatic subcapsular renal haematoma (Wunderlich syndrome) in a Thoroughbred broodmare

Equine Veterinary Education, EarlyView.
Summary This case report describes a Thoroughbred broodmare referred for colic and pyrexia. The mare had a history of repeated urinary tract infections, placentitis, abortion and endotoxaemia. A diagnosis of bilateral subcapsular renal haematoma was made by ultrasonography and standing laparoscopy and confirmed on post‐mortem.
M. Hannan, D. Verwilghen, F. Gibbons, C. Burden, R. Liechti, O. Forde, N. Meyer, V. Roati, B. Remaj, G. van Galen   +9 more
wiley   +1 more source

Lysophosphatidic Acid is a Modulator of Cyst Growth in Autosomal Dominant Polycystic Kidney Disease [PDF]

, 2011
Bonnie L. Blazer‐Yost, Brenda J. Blacklock, Stephanie Flaig, Robert L. Bacallao, Vincent H. Gattone   +4 more
openalex   +1 more source

Posttranslational modifications of phosphodiesterase type 4 enzymes represent novel points for therapeutic targeting

The FEBS Journal, EarlyView.
Enzymes from the phosphodiesterase type 4 family (PDE4) coordinate physiological events driven by the cyclic AMP s(cAMP) signaling pathway by tightly controlling cAMP dynamics in many cell types. Key to this strict regulation is the myriad of posttranslational modifications that alter PDE4 activity, cellular location, and binding partner selection ...
Madihah Hussain, Gonzalo S. Tejeda, George S. Baillie   +2 more
wiley   +1 more source

Congenital Cystic Disease of the Kidneys [PDF]

Proceedings of the Royal Society of Medicine, 1909
openaire   +3 more sources

Renal cell carcinoma with fibromyomatous stroma (RCC FMS) and with hemangioblastoma‐like areas is part of the RCC FMS spectrum in patients with tuberous sclerosis complex

Histopathology, EarlyView.
We report on three patients with Tuberous Sclerosis Complex (TSC) who had renal cell carcinomas with fibromyomatous stroma (RCC FMS), demonstrating a coexistent haemangioblastoma (HB)‐like morphology. Our findings support the conclusion that HB‐like features are part of the spectrum of RCC FMS with TSC/MTOR alterations.
Katherina Baranova, Jacob A Houpt, Deaglan Arnold, Andrew A House, Laura Lockau, Lindsay Ninivirta, Stephen Pautler, Haiying Chen, Madeleine Moussa, Rola Saleeb, Jose A Gomez, Asli Yilmaz, Farshid Siadat, Adrian Box, Douglas J Mahoney, Franz J Zemp, Manal Gabril, Kiril Trpkov   +17 more
wiley   +1 more source

Cystic kidney diseases: many ways to form a cyst [PDF]

, 2012
Hannah Loftus, Albert Ong
openalex   +1 more source

Initial assessment of the infant with neonatal cholestasis--Is this biliary atresia? [PDF]

, 2017
et al.,, Turmelle, Yumirle P
core   +2 more sources

Molecular Genetic Diagnosis of Omani Patients With Inherited Cystic Kidney Disease. [PDF]

Kidney Int Rep, 2019
Al Alawi I, Al Salmi I, Al Rahbi F, Al Riyami M, Al Kalbani N, Al Ghaithi B, Al Mawali A, Sayer JA.   +7 more
europepmc   +1 more source

Current Evidences and Future Perspectives in the Management of Metastatic Non‐Clear Cell Renal Cell Carcinoma

International Journal of Urology, EarlyView.
ABSTRACT Renal cell carcinoma is a heterogeneous disease with diverse phenotypes. Renal cell carcinoma classification is based on morphological and molecular characteristics and falls into 2 main categories: clear cell renal cell carcinoma and non‐clear cell renal cell carcinoma.
Shotaro Nakanishi, Junichi Inokuchi
wiley   +1 more source

G-protein signaling modulator 1 deficiency accelerates cystic disease in an orthologous mouse model of autosomal dominant polycystic kidney disease [PDF]

, 2012
Michelle Kwon, Tengis S. Pavlov, Kandai Nozu, Shauna A. Rasmussen, Daria V. Ilatovskaya, Alexandra Lerch‐Gaggl, Lauren M. North, Hyunho Kim, Feng Qian, William E. Sweeney, Ellis D. Avner, J Blumer, Alexander Staruschenko, Frank Park   +13 more
openalex   +1 more source