Results 211 to 220 of about 68,329 (260)

Phenotype-Driven Next-Generation Sequencing and Structure-Based In Silico Analysis Reveal Disease-Specific Diagnostic Yield and Genotype-Phenotype Correlations in Inherited Kidney Diseases. [PDF]

Life (Basel)
Baris S, Terali K, Bozlak S, Yilmaz N, Yilmaz HI, Yavas C, Eroz R, Hazaloglu M, Ozen K, Gezdirici A, Dogan M, Kilic H, Demir S, Baris I.   +13 more
europepmc   +1 more source

Primary Retroperitoneal Mucinous Cystic Neoplasm Involving Adrenal Gland

The Kaohsiung Journal of Medical Sciences, Volume 42, Issue 8, August 2026.
Di‐Ping Yu, Xiao‐Long Liu, Xin‐Yu Li   +2 more
wiley   +1 more source

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Cystic kidney diseases in children

Archives De Pediatrie, 2023
Cystic kidney disease comprises a broad group of heterogeneous diseases, which differ greatly in age at onset, disease manifestation, systemic involvement, disease progression, and long-term prognosis. As our understanding of these diseases continues to evolve and new treatment strategies continue to emerge, correctly differentiating and diagnosing ...
Mekahli D, Luc Breysem
exaly   +3 more sources

Cystic kidney diseases

Current Opinion in Nephrology and Hypertension, 1997
The goal of understanding the primary defects that lead to renal cystic diseases has proved to be an elusive one, despite 3 decades of physiologic and genetic investigation. Within the past 2 years the genes responsible for type 1 and type 2 autosomal dominant polycystic kidney disease have been identified.
M D, Griffin, V E, Torres, R, Kumar
openaire   +4 more sources

Acquired cystic kidney disease

European Radiology, 2000
Acquired cystic kidney disease (ACKD), also known as acquired renal cystic disease (ARCD,) occurs in patients who are on dialysis for end-stage renal disease. It is generally accepted that ACKD develops as a consequence of sustained uremia and can first manifest even before dialysis is initiated while the patient is still in chronic renal failure.
J, Tantravahi, T I, Steinman
openaire   +4 more sources

Cystic Disease of the Kidney

Annual Review of Pathology: Mechanisms of Disease, 2007
This review focuses on the mechanisms that underlie the development of human renal cystic diseases. A pathological, clinical, and pathophysiological overview is given. Initial analysis of the cell biology of inappropriate hyperproliferation accompanied by fluid secretion of cyst-lining epithelia has been followed by the elucidation of fundamental ...
Patricia D, Wilson, Beatrice, Goilav
openaire   +2 more sources

Localized Cystic Disease of the Kidney

American Journal of Roentgenology, 2001
Localized cystic disease of the kidney is a benign nonsurgical condition. Its imaging and clinical features are characterized and differentiated from autosomal dominant polycystic kidney disease, multilocular cystic nephroma, and cystic neoplasm.Localized cystic disease was diagnosed in 18 patients on the basis of a review of imaging studies, clinical ...
C M, Slywotzky, M A, Bosniak
openaire   +2 more sources

ACQUIRED CYSTIC KIDNEY DISEASE

Radiologic Clinics of North America, 1995
ACKD is characterized by the development of many fluid-filled renal cysts and sometimes neoplasms in the kidneys of individuals with chronic renal failure but without a history of hereditary cystic disease. The condition is seen mainly in dialysis patients, but often begins in patients with ESRD before dialysis is started.
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CYSTIC DISEASE OF THE LIVER AND KIDNEY

Pediatrics, 1959
The subject of cystic disease of the liver and kidneys has been reviewed. A family has been studied in which at least four and probably six of seven children of normal parents have been affected by the disease, as shown by clinical study and biopsy, liver function and biopsy, and by pyelograms made after intravenous injection of radio ...
openaire   +2 more sources