Detalhe da pesquisa
1.
Clinical, immunological, and genetic description of a Mexican cohort of patients with DOCK8 deficiency.
Pediatr Allergy Immunol
; 35(2): e14073, 2024 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-38351896
2.
Efficacy and Safety of Interferon-Gamma in Chronic Granulomatous Disease: a Systematic Review and Meta-analysis.
J Clin Immunol
; 43(3): 578-584, 2023 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-36385358
3.
Mendelian Susceptibility to Mycobacterial Disease: Retrospective Clinical and Genetic Study in Mexico.
J Clin Immunol
; 43(1): 123-135, 2023 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36044171
4.
Clinical manifestations and expression of CD18 to guide the diagnosis of leukocyte adhesion deficiency type 1: Mexico experience.
Allergol Immunopathol (Madr)
; 51(6): 89-96, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37937501
5.
[Guidelines on atopic dermatitis for Mexico (GUIDAMEX): using the ADAPTE methodology]. / Guía de dermatitis atópica para México (GUIDAMEX): lineamientos usando metodología ADAPTE.
Gac Med Mex
; 158(Suplement 2): 1-116, 2023 Jan 20.
Artigo
em Espanhol
| MEDLINE | ID: mdl-36763412
6.
Severe congenital neutropenia due to G6PC3 deficiency: Case series of five patients and literature review.
Scand J Immunol
; 95(4): e13136, 2022 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-34964150
7.
Coronavirus disease 2019 in patients with inborn errors of immunity: An international study.
J Allergy Clin Immunol
; 147(2): 520-531, 2021 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-32980424
8.
COVID-19 in the Context of Inborn Errors of Immunity: a Case Series of 31 Patients from Mexico.
J Clin Immunol
; 41(7): 1463-1478, 2021 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-34114122
9.
Clinical Manifestations, Mutational Analysis, and Immunological Phenotype in Patients with RAG1/2 Mutations: First Cases Series from Mexico and Description of Two Novel Mutations.
J Clin Immunol
; 41(6): 1291-1302, 2021 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-33954879
10.
Diagnostic and therapeutic caveats in Griscelli syndrome.
Scand J Immunol
; 93(6): e13034, 2021 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-33660295
11.
Latin American consensus on the supportive management of patients with severe combined immunodeficiency.
J Allergy Clin Immunol
; 144(4): 897-905, 2019 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-31419546
12.
Hematopoietic stem cell transplantation in 29 patients hemizygous for hypomorphic IKBKG/NEMO mutations.
Blood
; 130(12): 1456-1467, 2017 09 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-28679735
13.
A Variety of Alu-Mediated Copy Number Variations Can Underlie IL-12Rß1 Deficiency.
J Clin Immunol
; 38(5): 617-627, 2018 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-29995221
14.
Pulmonary nodules and nodular scleritis in a teenager with superficial granulomatous pyoderma gangrenosum.
Pediatr Dermatol
; 35(1): e35-e38, 2018 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-29243307
15.
Clinical Features, Non-Infectious Manifestations and Survival Analysis of 161 Children with Primary Immunodeficiency in Mexico: A Single Center Experience Over two Decades.
J Clin Immunol
; 36(1): 56-65, 2016 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-26707787
16.
Primary Immunodeficiency Diseases in Aguascalientes, Mexico: Results from an Educational Program.
J Clin Immunol
; 36(3): 173-8, 2016 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-26898367
17.
Correction to: Clinical Manifestations, Mutational Analysis, and Immunological Phenotype in Patients with RAG1/2 Mutations: First Cases Series from Mexico and Description of Two Novel Mutations.
J Clin Immunol
; 41(7): 1708, 2021 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-34136975
18.
A male infant with COVID-19 in the context of ARPC1B deficiency.
Pediatr Allergy Immunol
; 32(1): 199-201, 2021 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-32683750
19.
Corrigendum to "Sphingolipids as Mediators in the Crosstalk between Microbiota and Intestinal Cells: Implications for Inflammatory Bowel Disease".
Mediators Inflamm
; 2016: 7267956, 2016.
Artigo
em Inglês
| MEDLINE | ID: mdl-27965522
20.
Disseminated Infectious Disease Caused by Histoplasma capsulatum in an Adult Patient as First Manifestation of Inherited IL-12Rß1 Deficiency.
J Clin Immunol
; 40(7): 1051-1054, 2020 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-32710397