Results 71 to 80 of about 1,134,664 (163)

The L‐type calcium channel CaV1.3: A potential target for cancer therapy

open access: yesJournal of Cellular and Molecular Medicine, Volume 28, Issue 19, October 2024.
Abstract Cancer remains a prominent cause to life expectancy, and targeted cancer therapy stands as a pivotal approach in contemporary therapy. Calcium (Ca2+) signalling plays a multifaceted role in cancer progression, such as proliferation, invasion and distant metastasis.
Xuerun Liu   +4 more
wiley   +1 more source

Mitral Regurgitation: A Rare Cause of Ortner’s Syndrome [PDF]

open access: yesJournal of Clinical and Diagnostic Research, 2012
Ortner’s syndrome (Cadriovocal syndrome) is characterized by left recurrent laryngeal nerve palsy due to cardiovascular diseases. Very rarely, it can be caused by mitral regurgitation.
Sibes Kumar Das   +3 more
doaj  

A morphological and molecular approach to investigating infectious disease in early medieval Iberia: The necropolis of La Olmeda (Palencia, Spain)

open access: yesAmerican Journal of Biological Anthropology, Volume 185, Issue 1, September 2024.
Abstract Objective Here we investigate infectious diseases that potentially contribute to osteological lesions in individuals from the early medieval necropolis of La Olmeda (6th‐11th c. CE) in North Iberia. Materials and methods We studied a minimum number of 268 individuals (33 adult females; 38 adult males, 77 unknown/indeterminate sex; and 120 non ...
L. Coppola Bove   +4 more
wiley   +1 more source

Losing the Voice to the Lungs: Ortner’s Syndrome in Pulmonary Vascular Disease

open access: yes
Ortner’s syndrome, also known as cardiovocal syndrome, is a rare clinical condition marked by left recurrent laryngeal nerve palsy. It is most commonly caused by mechanical compression or traction of the nerve between the aortic arch and the pulmonary ...
Ramakant Dixit, Haseef Ahammed
core   +1 more source

Prevalence of Metabolic Syndrome in Psychiatric Inpatients: A Naturalistic Study [PDF]

open access: yes, 2010
The aim of this naturalistic survey was to measure the prevalence of metabolic syndrome by collating data on routine physical investigation in an acute psychiatric inpatient population.
Batugedara, Anuja   +4 more
core   +2 more sources

SARS‐CoV‐2 Vaccination is Not Associated With Involuntary Childlessness in Female Healthcare Workers: A Multicenter Cohort Study

open access: yesInfluenza and Other Respiratory Viruses, Volume 18, Issue 6, June 2024.
ABSTRACT Background There is debate about the causes of the recent birth rate decline in high‐income countries worldwide. During the pandemic, concern about the effects on reproductive health has caused vaccine hesitancy. We investigated the association of SARS‐CoV‐2 vaccination and infection with involuntary childlessness. Methods Females in fertility
Tamara Dörr   +19 more
wiley   +1 more source

Ortner’s Syndrome: A Rare Presentation of Thoracic Aortic Aneurysm

open access: yes
Thoracic aortic aneurysms (TAAs) are often silent and asymptomatic, but may present with nonspecific symptoms or life-threatening complications. We report a rare case of a 73-year-old male with acute decompensated heart failure and 3-month history of ...
Normalinda Yaacob   +4 more
core   +1 more source

Scimitar syndrome in infancy [PDF]

open access: yes, 2008
Scimitar syndrome, if presenting in infancy, is associated with signs of heart failure and pulmonary hypertension. The typical pathological features are sequestration of a segment of the lung, usually the right lower lobe, with arterial supply ...
Sreeram, Narayanswami   +3 more
core  

Ortner's Syndrome in an Infant With Congenital Heart Disease. [PDF]

open access: yesJ Med Cases, 2022
Murillo-Deluquez M   +4 more
europepmc   +1 more source

Clinical manifestations of Deletion 22q11.2 syndrome (DiGeorge/Velo-CardioFacial syndrome) [PDF]

open access: yes, 2005
Deletion 22q11.2 syndrome (Del22) (DiGeorge/Velo-Cardio-Facial syndrome) is characterized by congenital heart defect (CHD), palatal anomalies, facial dysmorphisms, neonatal hypocalcemia, immune deficit, speech and learning disabilities. CHD is present
Marino, Bonnie   +3 more
core  

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