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Accessory spleen
Known as:
Spleniculus
, Supernumerary spleens
, Supernumerary spleen
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An accessory spleen is a round, iso-echogenic, homogenic and smooth structure and is seen as a normal variant mostly on the medial contour of the…
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National Institutes of Health
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Related topics
Related topics
10 relations
Acrocephalopolysyndactyly type 2
HYDROLETHALUS SYNDROME 1
Meckel syndrome type 1
Oculodigitoesophagoduodenal syndrome
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Broader (2)
Corticomedullary organ
accessory organ
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Review
2005
Review
2005
Heterotaxy Syndrome – Asplenia and Polysplenia as Indicators of Visceral Malposition and Complex Congenital Heart Disease
U. Bartram
,
J. Wirbelauer
,
C. Speer
Neonatology
2005
Corpus ID: 35753302
Heterotaxy results from failure of the developing embryo to establish normal left-right asymmetry. Typical manifestations include…
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Highly Cited
2003
Highly Cited
2003
Five- and 10-year survival rates after surgery for biliary atresia: a report from the Japanese Biliary Atresia Registry.
M. Nio
,
R. Ohi
,
T. Miyano
,
M. Saeki
,
K. Shiraki
,
Koichi Tanaka
Journal of Pediatric Surgery
2003
Corpus ID: 8474134
Review
2003
Review
2003
Congenital extrahepatic portosystemic shunts
C. Murray
,
S. Yoo
,
P. Babyn
Pediatric Radiology
2003
Corpus ID: 10615675
BackgroundA congenital extrahepatic portosystemic shunt (CEPS) is uncommon. A type 1 CEPS exists where there is absence of…
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Highly Cited
2002
Highly Cited
2002
Abdominal manifestations of situs anomalies in adults.
A. Fulcher
,
M. Turner
Radiographics
2002
Corpus ID: 575623
A study was made of 19 adults with situs anomalies (situs inversus [n = 10], situs ambiguous with polysplenia [n = 8], situs…
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Highly Cited
2000
Highly Cited
2000
Heterotaxy: Associated conditions and hospital-based prevalence in newborns
A. Lin
,
B. Ticho
,
K. Houde
,
M. Westgate
,
L. Holmes
Genetics in Medicine
2000
Corpus ID: 22452305
Purpose: To provide insight into the possible etiology and prevalence of heterotaxy, we studied conditions associated with…
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Review
1999
Review
1999
Situs revisited: imaging of the heterotaxy syndrome.
K. Applegate
,
M. Goske
,
G. Pierce
,
D. Murphy
Radiographics
1999
Corpus ID: 25885482
Situs anomalies present a diagnostic challenge to radiologists because of the overlapping spectrum of findings commonly seen in…
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Highly Cited
1995
Highly Cited
1995
Primary midline developmental field. I. Clinical and epidemiological characteristics.
M. Martínez‐Frías
American journal of medical genetics
1995
Corpus ID: 42375121
Opitz [BD:OAS XXIX(1):3-37, 1993] has postulated that during early blastogenesis the entire embryo represents a single…
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Review
1983
Review
1983
Polysplenia: A review of 146 cases
W. Peoples
,
J. Moller
,
J. Edwards
Pediatric Cardiology
1983
Corpus ID: 9856718
SummaryThe types of cardiac and visceral anomalies of 146 autopsied cases of polysplenia are described. One hundred and five of…
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Highly Cited
1982
Highly Cited
1982
ASPLENIA AND POLYSPLENIA SYNDROME
Y. Shinohara
,
S. Komiya
,
+10 authors
Akira Ichikawa
Acta pathologica japonica
1982
Corpus ID: 27316455
This report described the morphological characteristics of seven cases of asplenia syndrome and three of polysplenia syndrome…
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Highly Cited
1980
Highly Cited
1980
Morphological considerations pertaining to recognition of atrial isomerism. Consequences for sequential chamber localisation.
F. Macartney
,
J. R. Zuberbuhler
,
R. Anderson
British heart journal
1980
Corpus ID: 22371394
The atrial morphology and venous connections were assessed "blind" in 51 necropsy specimens from patients with visceral…
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