The peculiar role of vitamin D in the pathophysiology of cardiovascular and neurodegenerative diseases

M Janjusevic, G Gagno, AL Fluca, L Padoan… - Life sciences, 2022 - Elsevier
Vitamin D is a hormone with both genomic and non-genomic actions. It exerts its activity by
binding vitamin D receptor (VDR), which belongs to the superfamily of nuclear receptors and …

[HTML][HTML] Autoimmunity in primary immunodeficiency disorders: an updated review on pathogenic and clinical implications

G Costagliola, S Cappelli, R Consolini - Journal of Clinical Medicine, 2021 - mdpi.com
During the last years, studies investigating the intriguing association between
immunodeficiency and autoimmunity led to the discovery of new monogenic disorders, the …

[HTML][HTML] Could nutritional supplements act as therapeutic adjuvants in COVID-19?

G Costagliola, E Spada, P Comberiati… - Italian journal of …, 2021 - Springer
Background The role of the immune system and inflammatory response in the pathogenesis
of the severe manifestations of coronavirus disease 2019 (COVID-19) is well known …

[HTML][HTML] Nutraceuticals in viral infections: an overview of the immunomodulating properties

G Costagliola, G Nuzzi, E Spada, P Comberiati… - Nutrients, 2021 - mdpi.com
Nutraceuticals, including vitamin D, vitamin A, zinc, lactoferrin, polyphenols coenzyme Q,
magnesium, and selenium, are implicated in the modulation of the complex molecular …

[HTML][HTML] Dendritic cells in inborn errors of immunity

S Gupta, A Agrawal - Frontiers in Immunology, 2023 - frontiersin.org
Dendritic cells (DCs) are crucial cells for initiating and maintaining immune response. They
play critical role in homeostasis, inflammation, and autoimmunity. A number of molecules …

[HTML][HTML] Clinical, immunological, and genetic findings in a cohort of patients with the diGeorge phenotype without 22q11. 2 deletion

AMQ Alberio, A Legitimo, V Bertini… - Journal of Clinical …, 2022 - mdpi.com
Chromosome 22q11. 2 deletion syndrome (22q11. 2DS) is a primary immunodeficiency
characterized by a broad and heterogeneous clinical presentation associated with various …

[HTML][HTML] Distinct Immunophenotypic Features in Patients Affected by 22q11. 2 Deletion Syndrome with Immune Dysregulation and Infectious Phenotype

G Costagliola, A Legitimo, V Bertini… - Journal of Clinical …, 2023 - mdpi.com
The clinical expression of 22q11. 2 deletion syndrome (22q11. 2 DS) is extremely variable,
as patients can present with recurrent or severe infections, immune dysregulation, atopic …

Síndrome deleción de 22q11. 2: a propósito de dos casos

MC Gutiérrez-Vargas, H Ostos-Alfonso - Duazary, 2023 - revistas.unimagdalena.edu.co
El síndrome de deleción 22q11 es la microdeleción cromosómica más frecuente, con una
prevalencia de 1 en 3 a 6000 nacidos vivos. Se presentarán dos casos femeninos …

[HTML][HTML] Systemic Screening for 22q11. 2 Copy Number Variations in Hungarian Pediatric and Adult Patients With Congenital Heart Diseases Identified Rare …

GKE Zodanu, M Oszlánczi, K Havasi, A Kalapos… - Frontiers in …, 2021 - frontiersin.org
Congenital heart defects (CHD) are the most common developmental abnormalities,
affecting approximately 0.9% of livebirths. Genetic factors, including copy number variations …

Kromozom 22q11. 2 Delesyon Sendromu Tanılı Hastaların Klinik ve Laboratuvar Özellikleri.

F HAZAN, Ö NALBANTOĞLU… - … Klinikleri Journal of …, 2021 - search.ebscohost.com
Amaç: Bu çalışmada; kromozom 22q11. 2 Delesyon Sendromu (22q11. 2DS) tanısı konulan
hastaların, genetik polikliniğine başvuru nedenleri ile birlikte, klinik ve laboratuvar …