Results 131 to 140 of about 2,246,280 (273)

Heterotaxy syndrome with polysplenia: case report

Brazilian Journal of Health Review
Heterotaxy syndrome (HS) or situs ambiguus is a rare condition, more common in women, in which internal organs are abnormally arranged within the thoracic and abdominal cavities. The condition may manifest as asplenia or polysplenia, characterized by the
Stephania Neves Scapim, Sarah Verdan Moreira, Priscila Rizutti Ferreira, Vinícius Neves Marcos   +3 more
semanticscholar   +1 more source

Factors Affecting Immune Reconstitution Post‐Allogeneic HSCT in Children: The Case for an Individualized Approach to Vaccination

European Journal of Haematology, EarlyView.
ABSTRACT Allogeneic hematopoietic stem cell transplantation (HSCT) is increasingly used to treat malignant and non‐malignant diseases. Following allogeneic HSCT, patients are particularly vulnerable to vaccine‐preventable diseases (VPD) because conditioning depletes immune cells, including memory cells.
Hélène Buvelot, Frederic Baleydier, Laure Pittet, Geraldine Blanchard‐Rohner   +3 more
wiley   +1 more source

The Role of Cardiovascular Magnetic Resonance in Pediatric Congenital Heart Disease [PDF]

, 2011
Cardiovascular magnetic resonance (CMR) has expanded its role in the diagnosis and management of congenital heart disease (CHD) and acquired heart disease in pediatric patients.
Hughes, ML, Ntsinjana, HN, Taylor, AM
core   +2 more sources

Cyclin‐dependent kinase 13 is indispensable for normal mouse heart development

Journal of Anatomy, Volume 246, Issue 4, Page 616-630, April 2025.
Congenital heart disease (CHD) is the most common defect in live births. The role of cyclin‐dependent kinase (CDK13) in cardiogenesis and CHD was studied using a transgenic mouse model (Cdk13tm1b) carrying deletion of exons 3 and 4, causing loss of function.
Qazi Waheed‐Ullah, Anna Wilsdon, Aseel Abbad, Sophie Rochette, Frances Bu'Lock, Asma Ali Saed, Marc‐Phillip Hitz, J. David Brook, Siobhan Loughna   +8 more
wiley   +1 more source

Polysplenia syndrome in adulthood: A case report of incidental discovery

Radiology Case Reports
The Polysplenia Syndrome (PSS) is a form of heterotaxy, a rare congenital anomaly with an estimated incidence of 1 in 250,000 live births, first described by Helwig in 1929.
Jihane El Houssni, Sanae Jellal, Ismail Neftah, Fariss Dehayni, Siham El Haddad, Nazik Allali, Latifa Chat   +6 more
doaj   +1 more source

Desired and Feared Identities and Their Role in Occupational Identity Regulation

Journal of Management Studies, EarlyView.
Abstract This paper extends theory by showing how occupational identity regulation operates jointly through both desired and feared identities which, in combination, enforce normative control. Taking a narrative identity perspective and drawing on an ethnographic and interview‐based study of veterinarians, we make three principal contributions to our ...
Sarah Page‐Jones, Andrew D. Brown
wiley   +1 more source

Polüspleeniaga heterotaksia sündroom [PDF]

, 2015
Eesti Arst 2015; 94(11):675 ...
Tiivel, Marek
core   +2 more sources

Surgery for Functional Single Ventricle Associated with Heterotaxy Syndrome: Common Atrioventricular Valve Repair

, 2021
Takaya Hoashi, Hajime Ichikawa
openalex   +2 more sources

Use of hyperglycemic clamp to assess pancreatectomy and islet cell autotransplant in patient with heterotaxy syndrome and dorsal pancreas agenesis leading to chronic pancreatitis [PDF]

, 2020
Diedert Luc De Paep, Pieter Gillard, Zhidong Ling, H. Verbeke, Geert Maleux, Vincent Vandecaveye, Yves Debaveye, Bart Keymeulen, Van der Merwe, Daniël Pipeleers, Jacques Pirenne, Hannah van Malenstein, Daniel Jacobs‐Tulleneers‐Thevissen   +12 more
openalex   +1 more source

The Evolving Landscape of CHD Genetics: A Contemporary Guide to Genetic Testing and Management

Journal of Paediatrics and Child Health, EarlyView.
ABSTRACT Congenital heart disease (CHD) is the most common birth defect, affecting an estimated 9.4/1000 infants globally. The genetics of CHD is complex, with most cases thought to have multifactorial aetiology, implicating both genetic and environmental factors.
Bridget R. O'Malley, Gary F. Sholler, Janine Smith, Gillian M. Blue   +3 more
wiley   +1 more source