Results 171 to 180 of about 2,246,280 (273)

Perinatal and Infant Outcomes of Prenatal Diagnosis of Heterotaxy Syndrome (Asplenia and Polysplenia)

open access: green, 2014
Maria C. Escobar‐Diaz   +9 more
openalex   +2 more sources

Incidental abdominal heterotaxy syndrome [PDF]

open access: yesANZ Journal of Surgery, 2019
Janaka Lovell   +2 more
openaire   +3 more sources

A novel biallelic loss-of-function variant in DAND5 causes heterotaxy syndrome. [PDF]

open access: yesCold Spring Harb Mol Case Stud, 2022
Ganapathi M   +9 more
europepmc   +1 more source

Analysis of associated malformations by computed tomography in adults with polysplenia syndrome: A pilot study.

open access: yesPLoS ONE
ObjectiveTo analytically depict the associated malformations of polysplenia syndrome (PS) in adults via computed tomography (CT).Materials and methodsThe incidence of malformations associated with PS in twelve adult patients was retrospectively analyzed ...
Xinru Gu   +8 more
doaj   +1 more source

Computed tomography of congenital heart disease in patients with heterotaxy syndrome [PDF]

open access: diamond, 2018
Nadiia Rokytska   +5 more
openalex   +1 more source

Congenital heart disease and inverse situs as a prenatal expression of Ivemark Syndrome

open access: yesUniversidad Médica Pinareña, 2019
Introduction: Ivemark Syndrome is a rare congenital condition that affects multiple organs of the body; it is classified as a disorder of heterotaxiaor laterally disorder.
Melissa Toledo Licourt   +2 more
doaj  

Heterotaxy Syndrome with Polysplenism and Left Atrial Isomerism. [PDF]

open access: yesJ Gen Intern Med, 2021
See J, Daingerfield EC, Santos MA.
europepmc   +1 more source

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