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Oligomeganephronia
Congenital renal hypoplasia characterized by small kidneys; reduced nephron number; tubular and glomerular hypertrophy.(NICHD)
National Institutes of Health
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Related topics
Related topics
5 relations
Broader (1)
Congenital hypoplasia of kidney
Kidney
Kidney Diseases
Renal cysts and diabetes syndrome
Urinary system
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Review
2011
Review
2011
Renal coloboma syndrome
L. Schimmenti
European Journal of Human Genetics
2011
Corpus ID: 35641595
Renal coloboma syndrome (RCS), also called papillorenal syndrome, is an autosomal dominant condition characterized by optic nerve…
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2011
2011
Three cases of late-onset oligomeganephronia
K. Kawanishi
,
T. Takei
,
+7 authors
K. Nitta
NDT plus
2011
Corpus ID: 13539224
Oligomeganephronia is classified as a subgroup of renal hypoplasia, characterized by histopathologic abnormalities which progress…
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2011
2011
Oligomeganephronia in an adult without end stage renal failure
Y. Fuke
,
S. Hemmi
,
M. Kajiwara
,
M. Yabuki
,
T. Fujita
,
M. Soma
Clinical and Experimental Nephrology
2011
Corpus ID: 483924
A 23 year-old male was investigated for hypertension, moderate renal insufficiency, persistent proteinuria and bilateral small…
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Review
2004
Review
2004
Renal outcome of children exposed to cyclosporine in utero.
P. Cochat
,
S. Decramer
,
E. Robert-Gnansia
,
L. Dubourg
,
P. Audra
Transplantation proceedings
2004
Corpus ID: 24372806
The number of pregnancies in immunosuppressed women has increased during the recent years and this has become a major part of the…
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Highly Cited
2003
Highly Cited
2003
Distinct molecular and morphogenetic properties of mutations in the human HNF1beta gene that lead to defective kidney development.
S. Bohn
,
H. Thomas
,
+4 authors
G. Ryffel
Journal of the American Society of Nephrology…
2003
Corpus ID: 24400787
The homeobox transcription factor hepatocyte nuclear factor 1beta (HNF1beta) is a tissue-specific regulator that plays an…
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Highly Cited
2001
Highly Cited
2001
PAX2 mutations in oligomeganephronia.
R. Salomon
,
A. Tellier
,
+7 authors
M. Broyer
Kidney international
2001
Corpus ID: 31051106
BACKGROUND Oligomeganephronia (OMN) is a rare congenital and usually sporadic anomaly. It is characterized by bilateral renal…
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1993
1993
Oligomeganephronia associated with 4p deletion type chromosomal anomaly.
S. Park
,
J. G. Chi
Pediatric pathology
1993
Corpus ID: 20518081
Oligomeganephronia is a rare congenital renal hypoplasia that is characterized histologically by a reduction in the number of…
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1977
1977
Bilateral renal hypoplasia with oligomeganephronia.
R. Adelman
,
S. Shapiro
Urology
1977
Corpus ID: 28791378
Abstract A patient with clinical, laboratory, and biopsy findings of bilateral renal hypoplasia with oligomeganephronia is…
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1973
1973
Bilateral renal hypoplasia with oligomeganephronia: quantitative and electron microsopic study.
T. Morita
,
J. Wenzl
,
J. McCoy
,
J. Porch
,
P. Kimmelstiel
American journal of clinical pathology
1973
Corpus ID: 19170289
The case of a 12-year-old boy with oligomeganephronic renal hypoplasia is reported. On light microscopy the histologic findings…
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1970
1970
Bilateral renal hypoplasia with oligomeganephronia. Oligomeganephronic renal hypoplasia.
J. Carter
,
D. Lirenman
American journal of diseases of children
1970
Corpus ID: 38606640
The syndrome of congenital bilateral renal hypoplasia with hypertrophy of nephrons has been well documented in the French…
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