Results 231 to 240 of about 2,817,125 (290)
A pilot study of magnetic resonance fingerprinting and radiomics analysis in autosomal dominant polycystic kidney disease. [PDF]
Kidney IntKremer LE +10 more
europepmc +1 more source
Urology, 1976 Renal cystic disorders have long represented an area of diagnostic confusion. We have attempted to correlate renal microdissection findings with clinically established renal cystic disorders by examining each disorder in sequential fashion. The clinical presentation of a child with a multicystic kidney is followed by a review of the cystic diseases ...
E M, Mullin, D F, Paulson
core +4 more sources
Some of the next articles are maybe not open access.
Related searches:
Related searches:
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 ...
Peter C Harris +2 more
exaly +3 more sources
European Radiology, 1997
Renal cystic disease comprises a mixed group of heritable, developmental, and acquired disorders. Because of their diverse etiology, histology, and clinical presentation, no single scheme of classification has gained acceptance. Conditions include autosomal dominant polycystic kidney disease, acquired renal cystic disease, medullary sponge kidney ...
H S, Thomsen +6 more
openaire +2 more sources
Renal cystic disease comprises a mixed group of heritable, developmental, and acquired disorders. Because of their diverse etiology, histology, and clinical presentation, no single scheme of classification has gained acceptance. Conditions include autosomal dominant polycystic kidney disease, acquired renal cystic disease, medullary sponge kidney ...
H S, Thomsen +6 more
openaire +2 more sources
Magnetic Resonance Imaging Clinics of North America, 2004
Renal cysts are relatively common radiographic and clinical abnormalities. Cystic renal disease is a heterogeneous entity comprised of heritable, developmental, and acquired disorders. During the last decade, considerable progress has been made in reaching a consensus for standard terminologies and classifications of cystic renal disease among ...
Fadi M, EL-Merhi, Kyongtae T, Bae
openaire +2 more sources
Renal cysts are relatively common radiographic and clinical abnormalities. Cystic renal disease is a heterogeneous entity comprised of heritable, developmental, and acquired disorders. During the last decade, considerable progress has been made in reaching a consensus for standard terminologies and classifications of cystic renal disease among ...
Fadi M, EL-Merhi, Kyongtae T, Bae
openaire +2 more sources
Advances in Anatomic Pathology, 2006
This review aims to assist in the categorization of inherited, developmental, and acquired cystic disease of the kidney as well as to provide a pertinent, up-to-date bibliography. The conditions included are autosomal-dominant polycystic kidney disease, autosomal-recessive polycystic kidney disease, unilateral renal cystic disease (localized cystic ...
Michele, Bisceglia +4 more
openaire +2 more sources
This review aims to assist in the categorization of inherited, developmental, and acquired cystic disease of the kidney as well as to provide a pertinent, up-to-date bibliography. The conditions included are autosomal-dominant polycystic kidney disease, autosomal-recessive polycystic kidney disease, unilateral renal cystic disease (localized cystic ...
Michele, Bisceglia +4 more
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
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
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