Results 151 to 160 of about 2,012 (189)
Foregut Duplication Cysts in a Patient With Congenital Diaphragmatic Hernia: A Case Report. [PDF]
CureusSadecka AI, Slowik-Moczydlowska Z.
europepmc +1 more source
Pheochromocytoma in a patient with heterotaxy syndrome: a case report. [PDF]
BMC Endocr DisordRad FF +3 more
europepmc +1 more source
Some of the next articles are maybe not open access.
Related searches:
Related searches:
Journal of Computer Assisted Tomography, 1981
A case of polysplenia associated with total abdominal situs inversus, central localization of the liver, and incomplete development of the inferior vena cava is reported. Various components of the syndrome were easily demonstrated by CT.
P, De Maeyer, G, Wilms, A L, Baert
openaire +2 more sources
A case of polysplenia associated with total abdominal situs inversus, central localization of the liver, and incomplete development of the inferior vena cava is reported. Various components of the syndrome were easily demonstrated by CT.
P, De Maeyer, G, Wilms, A L, Baert
openaire +2 more sources
The British Journal of Radiology, 1975
Polysplenia is a rare syndrome of visceral anomalies. The diagnosis in vivo may be difficult. Recently Vaughan, Hawkins and Elliott (1971) stressed the importance of visceral arteriography for a correct diagnosis. A patient with this condition was seen by us and the angiographic findings are reported hereby.
A L, Baert, J, Myle
openaire +2 more sources
Polysplenia is a rare syndrome of visceral anomalies. The diagnosis in vivo may be difficult. Recently Vaughan, Hawkins and Elliott (1971) stressed the importance of visceral arteriography for a correct diagnosis. A patient with this condition was seen by us and the angiographic findings are reported hereby.
A L, Baert, J, Myle
openaire +2 more sources
American Journal of Medical Genetics, 1985
AbstractThe pathogenesis of asplenia and polysplenia in humans is unknown. The conditions have been regarded as duplication of sidedness or abnormalities of embryonic curvature. The resemblance of the abnormalities in an autosomal recessive mutation (iv) in mice to those in humans with asplenia or polysplenia suggest the possibility of a genetic basis ...
Suzanne M. De La Monte +3 more
openaire +2 more sources
AbstractThe pathogenesis of asplenia and polysplenia in humans is unknown. The conditions have been regarded as duplication of sidedness or abnormalities of embryonic curvature. The resemblance of the abnormalities in an autosomal recessive mutation (iv) in mice to those in humans with asplenia or polysplenia suggest the possibility of a genetic basis ...
Suzanne M. De La Monte +3 more
openaire +2 more sources
ASPLENIA AND POLYSPLENIA SYNDROME
Acta Pathologica Japonica, 1982This report described the morphological characteristics of seven cases of asplenia syndrome and three of polysplenia syndrome. Each syndrome has been characterized by a tendency for symmetric development of normally asymmetric organs, with varying degrees of cardiovascular anomalies.
Y, Shinohara +12 more
openaire +2 more sources
Diagnosis of Polysplenia Syndrome
Radiology, 1971Three cases of polysplenia were diagnosed by visceral arteriography. Each patient had a common celiacomesenteric artery. The origin of supply to the dislocated splenic lobules was variable. Such lobules were readily demonstrated at various sites along the greater curvature of the stomach.
T J, Vaughan, I F, Hawkins, L P, Elliott
openaire +2 more sources