Results 251 to 260 of about 101,655 (304)
Some of the next articles are maybe not open access.
Inherited renal cystic diseases
Abdominal Radiology, 2016A number of inherited renal diseases present with renal cysts and often lead to end-stage renal disease. With recent advances in genetics, increasing number of genes and mutations have been associated with cystic renal diseases. Although genetic testing can provide a definite diagnosis, it is often reserved for equivocal cases or for ongoing ...
Bohyun, Kim +5 more
openaire +2 more sources
Neonatal renal cystic diseases
The Journal of Maternal-Fetal & Neonatal Medicine, 2017Neonatal renal cystic diseases have a great impact on the morbidity and mortality of the affected neonates and infants. A good insight into the pathophysiology, diagnosis and treatment options of various neonatal renal cystic diseases aid in early diagnosis and intervention, thereby preventing complications.PubMed search was done for articles on ...
Anshika Khare +3 more
openaire +2 more sources
Current Opinion in Pediatrics, 1999
Renal cystic diseases constitute the most common genetic cause for end-stage renal disease in children and young adults. Recently, there has been rapid progress regarding the identification or chromosomal localization of some of the responsible disease genes.
openaire +2 more sources
Renal cystic diseases constitute the most common genetic cause for end-stage renal disease in children and young adults. Recently, there has been rapid progress regarding the identification or chromosomal localization of some of the responsible disease genes.
openaire +2 more sources
2020
Renal cystic diseases may be inherited or acquired. The most common renal cystic disease is multicystic dysplastic kidney, which is essentially a nonfunctioning kidney. Most renal cysts and cystic diseases do not require intervention, with the exception of multilocular cystic nephroma. Cases of multilocular cystic nephroma cannot be differentiated from
Alexandra Rehfuss +3 more
openaire +1 more source
Renal cystic diseases may be inherited or acquired. The most common renal cystic disease is multicystic dysplastic kidney, which is essentially a nonfunctioning kidney. Most renal cysts and cystic diseases do not require intervention, with the exception of multilocular cystic nephroma. Cases of multilocular cystic nephroma cannot be differentiated from
Alexandra Rehfuss +3 more
openaire +1 more source
Seminars in ultrasound, CT, and MR, 1991
Cystic lesions are one of the most common abnormalities of the kidneys and are the most common asymptomatic space-occupying lesions (Lang 1973, 1980, 1986). While the vast majority of renal cysts are of the uncomplicated simple cyst variety, renal cystic disease comprises a heterogeneous group of developmental, acquired, and hereditary entities.
C K, Hayden, L E, Swischuk
openaire +3 more sources
Cystic lesions are one of the most common abnormalities of the kidneys and are the most common asymptomatic space-occupying lesions (Lang 1973, 1980, 1986). While the vast majority of renal cysts are of the uncomplicated simple cyst variety, renal cystic disease comprises a heterogeneous group of developmental, acquired, and hereditary entities.
C K, Hayden, L E, Swischuk
openaire +3 more sources
1990
Acquired renal cystic disease (ARCD) is a recently described disorder. It was appreciated only after the survival of patients with endstage renal disease was prolonged by dialysis. ARCD is a bilateral multiple cystic disorder occurring in patients whose original renal illness was unrelated to cystic disease.
openaire +2 more sources
Acquired renal cystic disease (ARCD) is a recently described disorder. It was appreciated only after the survival of patients with endstage renal disease was prolonged by dialysis. ARCD is a bilateral multiple cystic disorder occurring in patients whose original renal illness was unrelated to cystic disease.
openaire +2 more sources
Cystic fibrosis and renal disease
Paediatric Respiratory Reviews, 2002Renal disease is relatively rare in cystic fibrosis even though the cystic fibrosis transmembrane regulator (CFTR) protein is expressed in abundance in the kidney. Aberrant CFTR expression probably explains the subtle abnormalities in renal concentrating and diluting ability described in cystic fibrosis and possibly the increased incidence of ...
S E, Stephens, S P A, Rigden
openaire +2 more sources
Cystic Disease of Renal Medulla
Annals of Internal Medicine, 1971Excerpt To the editor: We read with interest the paper by Dr. Gardner in the January ANNALS(73:47-54, 1971) suggesting that cystic disease of the renal medulla in adults be distinguished from famil...
W M, Bennett, N, Simon, K D, Gardner
openaire +2 more sources
2013
Renal cysts represent a wide spectrum of conditions ranging from simple cysts with little or no clinical significance to severe developmental renal abnormalities and progressive (polycystic) kidney disease or syndromes with multiple organ involvement.
Indra Gupta, Martin Bitzan
openaire +1 more source
Renal cysts represent a wide spectrum of conditions ranging from simple cysts with little or no clinical significance to severe developmental renal abnormalities and progressive (polycystic) kidney disease or syndromes with multiple organ involvement.
Indra Gupta, Martin Bitzan
openaire +1 more source
Unilateral Renal Cystic Disease
Journal of Computer Assisted Tomography, 1989Unilateral renal cystic disease (URCD) is characterized by replacement of most of one kidney by multiple cysts scattered diffusely throughout the parenchyma without the formation of a distinct, encapsulated renal mass. There are no cysts in the opposite kidney or liver. The condition is nonfamilial and does not cause renal functional impairment.
E, Levine, M, Huntrakoon
openaire +2 more sources