Results 11 to 20 of about 15,117 (303)

Syndrome of right isomerism: Ivemark syndrome

open access: yesJournal of Mahatma Gandhi Institute of Medical Sciences, 2018
Heterotaxy Syndrome is a complex syndrome that occurs when the axes of the body fail to rotate correctly when developing in the uterus. This can result in many different organ systems being affected.
Dipti Jain, Bhushan Chavan, Anita Manoj
doaj   +2 more sources

Bodily isomerism is an independent risk factor for pulmonary hypertension in adults with congenital heart disease

open access: yesTherapeutic Advances in Respiratory Disease, 2016
Introduction: Bodily isomerism, or heterotaxy is a unique entity on which there is mirror imagery in various organ systems, leading to a deviation from the normal lateral arrangements of the viscera.
Rohit S. Loomba   +3 more
doaj   +2 more sources

Isomerism in the setting of the so-called “heterotaxy”: The usefulness of computed tomographic analysis

open access: yesAnnals of Pediatric Cardiology, 2017
The most complex combinations of congenital cardiac malformations are found in the setting of bodily isomerism. The question remains, however, as to whether evidence of cardiac isomerism is always to be found in the setting of bodily isomerism, also ...
Shumpei Mori   +4 more
doaj   +2 more sources

Ion Mobility–Mass Spectrometry Imaging: Advances in Biomedical Research [PDF]

open access: yesBioTech
Mass spectrometry imaging (MSI) visualizes the spatial distribution of biomolecules in tissues, whereas ion mobility–mass spectrometry (IM-MS) separates ions through the collision cross-section (CCS) with an inert gas, providing the structural ...
Mengya Liu   +10 more
doaj   +2 more sources

Ventricular Topology in Congenital Heart Defects Associated with Heterotaxy: Can We Find Patterns Reflecting the Syndrome-Specific Tendency for Visceral Symmetry? [PDF]

open access: yesJournal of Cardiovascular Development and Disease
Heterotaxy syndrome is characterized by a tendency for bilaterally symmetric arrangement (isomerism) of inner organs. It is frequently associated with complex congenital heart defects (CHDs).
Takhfif Othman   +4 more
doaj   +2 more sources

Left Isomerism With Normal Bronchopulmonary Anatomy: Broadening the Heterotaxy Spectrum [PDF]

open access: yesCase Reports in Radiology
Situs ambiguous is a rare congenital condition characterized by the abnormal arrangement of thoracoabdominal organs along the left–right axis. This condition often presents as either left or right isomerism, leading to complex anatomical variations and ...
Zach Sukin   +4 more
doaj   +2 more sources

Isomerism as a general scientific concept

open access: yesТонкие химические технологии, 2011
Consideration of objects of various fields of knowledge has shown that isomerism is a general scientific concept. Examples illustrating its manifestation in heterogeneous equilibria thermodynamics and chemical technology are given.
L. A. Serafimov   +2 more
doaj   +2 more sources

The Development and Validation of a Targeted LC-HRAM-MS/MS Methodology to Separate and Quantify p-Synephrine and m-Synephrine in Dietary Supplements and Herbal Preparations

open access: yesSeparations, 2023
Dietary supplements containing Citrus aurantium or p-synephrine remain very popular in Europe and the United States of America (USA). They are primarily sold as weight loss enhancers, although their efficacy and the safety are still under scrutiny.
Celine Vanhee   +6 more
doaj   +1 more source

Left isomerism with bilateral superior vena cava, interrupted inferior vena cava and tetralogy of Fallot

open access: yesAnnals of Pediatric Cardiology, 2020
The association of left isomerism with tetralogy of Fallot (TOF) is rare and reported as scattered case reports. Complex congenital cardiac and noncardiac malformations are known to be associated with left isomerism, but right-sided obstructive lesions ...
Nikhil Bansal   +5 more
doaj   +1 more source

Which side are they on? A review and case series of diagnosing primary ciliary dyskinesias in low- or middle-income countries.

open access: yesAfrican Journal of Thoracic and Critical Care Medicine, 2023
Primary ciliary dyskinesia (PCD) is a rare genetic condition with a variable clinical presentation, making its diagnosis a challenge. The authors describe two unrelated sibling pairs with PCD: adult siblings in the first  and perinatal/neonatal in the ...
S P Surdut   +3 more
doaj   +1 more source

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