Andrea Martin-Nalda
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Explore the profile of Andrea Martin-Nalda including associated specialties, affiliations and a list of published articles.
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62
Citations
2227
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Recent Articles
1.
Tejedor Vaquero S, Neuman H, Comerma L, Marcos-Fa X, Corral-Vazquez C, Uzzan M, et al.
J Exp Med
. 2024 Nov;
221(12).
PMID: 39560666
The human gut includes plasma cells (PCs) expressing immunoglobulin A1 (IgA1) or IgA2, two structurally distinct IgA subclasses with elusive regulation, function, and reactivity. We show here that intestinal IgA1+...
2.
Saettini F, Guerra F, Mauri M, Salter C, Adam M, Adams D, et al.
J Clin Immunol
. 2024 Sep;
45(1):15.
PMID: 39312004
Purpose: PI4KA-related disorder is a highly clinically variable condition characterized by neurological (limb spasticity, developmental delay, intellectual disability, seizures, ataxia, nystagmus) and gastrointestinal (inflammatory bowel disease and multiple intestinal atresia)...
3.
Romero-Tamarit A, Valles X, Munar-Garcia M, Espinosa-Pereiro J, Saborit N, Tortola M, et al.
Infection
. 2024 Feb;
52(2):611-623.
PMID: 38349459
Purpose: This study investigates the potential of inflammatory parameters (IP), symptoms, and patient-related outcome measurements as biomarkers of severity and their ability to predict tuberculosis (TB) evolution. Methods: People with...
4.
Matuozzo D, Talouarn E, Marchal A, Zhang P, Manry J, Seeleuthner Y, et al.
Genome Med
. 2024 Jan;
16(1):6.
PMID: 38184654
No abstract available.
5.
Batlle-Maso L, Riviere J, Franco-Jarava C, Martin-Nalda A, Garcia-Prat M, Parra-Martinez A, et al.
J Clin Immunol
. 2023 Aug;
43(8):1953-1963.
PMID: 37597073
Chronic granulomatous disease (CGD) is a prototypical inborn error of immunity affecting phagocytes, in which these cells are unable to produce reactive oxygen species. CGD is caused by defects in...
6.
Matuozzo D, Talouarn E, Marchal A, Zhang P, Manry J, Seeleuthner Y, et al.
Genome Med
. 2023 Apr;
15(1):22.
PMID: 37020259
Background: We previously reported that impaired type I IFN activity, due to inborn errors of TLR3- and TLR7-dependent type I interferon (IFN) immunity or to autoantibodies against type I IFN,...
7.
Batlle-Maso L, Garcia-Prat M, Parra-Martinez A, Franco-Jarava C, Aguilo-Cucurull A, Velasco P, et al.
Front Immunol
. 2022 Dec;
13:1014984.
PMID: 36466883
Autoimmune lymphoproliferative syndrome (ALPS) is a rare primary immune disorder characterized by impaired apoptotic homeostasis. The clinical characteristics include lymphoproliferation, autoimmunity (mainly cytopenia), and an increased risk of lymphoma. A...
8.
Matuozzo D, Talouarn E, Marchal A, Manry J, Seeleuthner Y, Zhang Y, et al.
medRxiv
. 2022 Nov;
PMID: 36324795
Background: We previously reported inborn errors of TLR3- and TLR7-dependent type I interferon (IFN) immunity in 1-5% of unvaccinated patients with life-threatening COVID-19, and auto-antibodies against type I IFN in...
9.
Del Rosal T, Quintana-Ortega C, Deya-Martinez A, Soler-Palacin P, Goycochea-Valdivia W, Salmon N, et al.
Eur J Pediatr
. 2022 Sep;
181(11):3889-3898.
PMID: 36102997
Conclusion: Prevention and prompt control of cytomegalovirus infection, together with early HSCT/gene therapy, are crucial for improving the prognosis in children with IEI. What Is Known: • Cytomegalovirus is the...
10.
Gonzalez-Granado L, Martin-Nalda A, Alsina L, Neth O, Santamaria M, Soler-Palacin P
An Pediatr (Engl Ed)
. 2022 May;
96(6):492-500.
PMID: 35637145
Introduction: The aim of the study was to assess the incidence of hospital admission due to severe acute respiratory infection by respiratory syncytial virus (RSV-ARI) in children with primary immunodeficiencies...