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1
Investigation of serum IL-12, IL-16, and IL-17A as diagnostic biomarkers in children with cow’s milk protein allergy
Investigation of serum IL-12, IL-16, and IL-17A as diagnostic biomarkers in children with cow’s milk protein allergy
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Investigation of serum IL-12, IL-16, and IL-17A as diagnostic biomarkers in children with cow’s milk protein allergy

Allergologia et immunopathologia, 2022-01, Vol.50 (5), p.162-168 [Peer Reviewed Journal]

2022. This work is published under https://creativecommons.org/licenses/by-nc-nd/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;ISSN: 0301-0546 ;EISSN: 1578-1267 ;DOI: 10.15586/aei.v50i5.592

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2
Factores asociados a casos probables de hipotiroidismo congénito en neonatos nacidos en Bucaramanga, Colombia
Factores asociados a casos probables de hipotiroidismo congénito en neonatos nacidos en Bucaramanga, Colombia
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Factores asociados a casos probables de hipotiroidismo congénito en neonatos nacidos en Bucaramanga, Colombia

C.E.S. medicina, 2023-04, Vol.37 (1), p.12-28 [Peer Reviewed Journal]

Copyright Universidad CES Jan-Apr 2023 ;ISSN: 0120-8705 ;EISSN: 2215-9177 ;DOI: 10.21615/cesmedicina.7020

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3
Clinical and immunological assessment of APDS2 with features of the SHORT syndrome related to a novel mutation in PIK3R1 with reduced penetrance
Clinical and immunological assessment of APDS2 with features of the SHORT syndrome related to a novel mutation in PIK3R1 with reduced penetrance
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Clinical and immunological assessment of APDS2 with features of the SHORT syndrome related to a novel mutation in PIK3R1 with reduced penetrance

Allergologia et immunopathologia, 2022-01, Vol.50 (4), p.1-9 [Peer Reviewed Journal]

2022. This work is published under https://creativecommons.org/licenses/by-nc-nd/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;ISSN: 0301-0546 ;EISSN: 1578-1267 ;DOI: 10.15586/aei.v50i4.510

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4
Diagnosis of primary immunodeficiency diseases in pediatric patients hospitalized for recurrent, severe, or unusual infections
Diagnosis of primary immunodeficiency diseases in pediatric patients hospitalized for recurrent, severe, or unusual infections
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Diagnosis of primary immunodeficiency diseases in pediatric patients hospitalized for recurrent, severe, or unusual infections

Allergologia et immunopathologia, 2022-01, Vol.50 (4), p.50-56 [Peer Reviewed Journal]

2022. This work is published under https://creativecommons.org/licenses/by-nc-nd/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;ISSN: 0301-0546 ;EISSN: 1578-1267 ;DOI: 10.15586/aei.v50i4.605

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5
Demographic and clinical characterization of pediatric group patients with inborn errors of the immune system in a Colombian tertiary hospital
Demographic and clinical characterization of pediatric group patients with inborn errors of the immune system in a Colombian tertiary hospital
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Demographic and clinical characterization of pediatric group patients with inborn errors of the immune system in a Colombian tertiary hospital

Allergologia et immunopathologia, 2022-01, Vol.50 (4), p.17-22 [Peer Reviewed Journal]

2022. This work is published under https://creativecommons.org/licenses/by-nc-nd/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;ISSN: 0301-0546 ;EISSN: 1578-1267 ;DOI: 10.15586/aei.v50i4.55

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6
The Buddhasothorn Asthma Severity Score (BASS): A practical screening tool for predicting severe asthma exacerbations for pediatric patients
The Buddhasothorn Asthma Severity Score (BASS): A practical screening tool for predicting severe asthma exacerbations for pediatric patients
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The Buddhasothorn Asthma Severity Score (BASS): A practical screening tool for predicting severe asthma exacerbations for pediatric patients

Allergologia et immunopathologia, 2023-01, Vol.51 (2), p.1-10 [Peer Reviewed Journal]

2023. This work is published under https://creativecommons.org/licenses/by-nc-nd/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;ISSN: 0301-0546 ;EISSN: 1578-1267 ;DOI: 10.15586/AEI.V51I2.690 ;PMID: 36916082

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7
Middle-Range Theory of Ineffective Breathing Pattern in children with Congenital Heart Disease
Middle-Range Theory of Ineffective Breathing Pattern in children with Congenital Heart Disease
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Middle-Range Theory of Ineffective Breathing Pattern in children with Congenital Heart Disease

Revista latino-americana de enfermagem, 2022-01, Vol.30, p.e3783-e3783 [Peer Reviewed Journal]

2022. This work is published under https://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;This work is licensed under a Creative Commons Attribution 4.0 International License. ;ISSN: 1518-8345 ;ISSN: 0104-1169 ;EISSN: 1518-8345 ;DOI: 10.1590/1518-8345.5826.3783 ;PMID: 36629731

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8
Pulmonary manifestations in a cohort of patients with inborn errors of immunity: an 8-year follow-up study
Pulmonary manifestations in a cohort of patients with inborn errors of immunity: an 8-year follow-up study
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Pulmonary manifestations in a cohort of patients with inborn errors of immunity: an 8-year follow-up study

Allergologia et immunopathologia, 2022, Vol.50 (1), p.80-84 [Peer Reviewed Journal]

2022. This work is published under https://creativecommons.org/licenses/by-nc-nd/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;ISSN: 0301-0546 ;EISSN: 1578-1267 ;DOI: 10.15586/aei.v50i1.388 ;PMID: 34935317

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9
MAORI (NEW ZEALAND) NPHS1 FOUNDER VARIANT IN A CHILEAN PATIENT WITH LESS SEVERE CONGENITAL NEPHROTIC SYNDROME PHENOTYPE
MAORI (NEW ZEALAND) NPHS1 FOUNDER VARIANT IN A CHILEAN PATIENT WITH LESS SEVERE CONGENITAL NEPHROTIC SYNDROME PHENOTYPE
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MAORI (NEW ZEALAND) NPHS1 FOUNDER VARIANT IN A CHILEAN PATIENT WITH LESS SEVERE CONGENITAL NEPHROTIC SYNDROME PHENOTYPE

BAG. Journal of basic and applied genetics, 2021-10, Vol.32, p.160 [Peer Reviewed Journal]

Copyright Sociedad Argentina de Genetica Oct 2021 ;ISSN: 1666-0390 ;EISSN: 1852-6233

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10
Síndrome de Herlyn-Werner-Wunderlich. Reporte de caso
Síndrome de Herlyn-Werner-Wunderlich. Reporte de caso
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Síndrome de Herlyn-Werner-Wunderlich. Reporte de caso

Revista de la Facultad de Medicina, Universidad Nacional de Colombia, 2022-10, Vol.69 (4), p.e83840 [Peer Reviewed Journal]

2021. This work is published under http://creativecommons.org/licenses/by/3.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;2022. This work is published under http://creativecommons.org/licenses/by/3.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;ISSN: 0120-0011 ;EISSN: 2357-3848 ;DOI: 10.15446/revfacmed.v69n4.83840

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11
Primary immunodeficiency and chronic mucocutaneous candidiasis: pathophysiological, diagnostic, and therapeutic approaches
Primary immunodeficiency and chronic mucocutaneous candidiasis: pathophysiological, diagnostic, and therapeutic approaches
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Primary immunodeficiency and chronic mucocutaneous candidiasis: pathophysiological, diagnostic, and therapeutic approaches

Allergologia et immunopathologia, 2021-01, Vol.49 (1), p.118-127 [Peer Reviewed Journal]

2021. This work is published under https://creativecommons.org/licenses/by-nc-nd/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;ISSN: 0301-0546 ;EISSN: 1578-1267 ;DOI: 10.15586/aei.v49i1.20 ;PMID: 33528939

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12
Enfermedades Huérfanas Orphaned Diseases
Enfermedades Huérfanas Orphaned Diseases
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Enfermedades Huérfanas Orphaned Diseases

Archivos venezolanos de farmacología y terapéutica, 2020-01, Vol.39 (5), p.627-634

Copyright Sociedad Latinoamericana de Hipertension 2020 ;ISSN: 0798-0264 ;EISSN: 2610-7988 ;DOI: 10.5281/zenodo.4263347

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13
Teoría de Mediano Alcance del Patrón de Respiración Ineficiente en niños con cardiopatías congénitas
Teoría de Mediano Alcance del Patrón de Respiración Ineficiente en niños con cardiopatías congénitas
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Teoría de Mediano Alcance del Patrón de Respiración Ineficiente en niños con cardiopatías congénitas

Revista latino-americana de enfermagem, 2022, Vol.30 [Peer Reviewed Journal]

2022. This work is published under https://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;ISSN: 1518-8345 ;ISSN: 0104-1169 ;EISSN: 1518-8345 ;DOI: 10.1590/1518-8345.5826.3782

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14
Anxiety of mothers of newborns with congenital malformations in the pre- and postnatal periods
Anxiety of mothers of newborns with congenital malformations in the pre- and postnatal periods
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Anxiety of mothers of newborns with congenital malformations in the pre- and postnatal periods

Revista latino-americana de enfermagem, 2018-11, Vol.26, p.e3080-e3080 [Peer Reviewed Journal]

2018. This work is published under https://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;2018 Revista Latino-Americana de Enfermagem 2018 SciELO ;This work is licensed under a Creative Commons Attribution 4.0 International License. ;ISSN: 1518-8345 ;ISSN: 0104-1169 ;EISSN: 1518-8345 ;DOI: 10.1590/1518-8345.2482.3080 ;PMID: 30462791

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15
22q11.2 deletion syndrome: 20 years of experience from two pediatric immunology units and review of clues for diagnosis and disease management
22q11.2 deletion syndrome: 20 years of experience from two pediatric immunology units and review of clues for diagnosis and disease management
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22q11.2 deletion syndrome: 20 years of experience from two pediatric immunology units and review of clues for diagnosis and disease management

Allergologia et immunopathologia, 2021-01, Vol.49 (1), p.95-100 [Peer Reviewed Journal]

2021. This work is published under https://creativecommons.org/licenses/by-nc-nd/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;ISSN: 0301-0546 ;EISSN: 1578-1267 ;DOI: 10.15586/aei.v49i1.24 ;PMID: 33528935

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16
Capacidad de respuesta y desafíos del sistema de salud cubano frente a las enfermedades transmisibles
Capacidad de respuesta y desafíos del sistema de salud cubano frente a las enfermedades transmisibles
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Capacidad de respuesta y desafíos del sistema de salud cubano frente a las enfermedades transmisibles

Revista panamericana de salud pública, 2018, Vol.42, p.1-9 [Peer Reviewed Journal]

Copyright Pan American Health Organization (Organizacion Panamericana de la Salud) 2018 ;ISSN: 1020-4989 ;EISSN: 1680-5348 ;DOI: 10.26633/RPSP.2018.30

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17
Modelo teórico de cuidado de niños con síndrome capilar congénito por el virus del Zika en el contexto familiar
Modelo teórico de cuidado de niños con síndrome capilar congénito por el virus del Zika en el contexto familiar
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Modelo teórico de cuidado de niños con síndrome capilar congénito por el virus del Zika en el contexto familiar

Revista latino-americana de enfermagem, 2021-01, Vol.29 [Peer Reviewed Journal]

2021. This work is published under https://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;ISSN: 0104-1169 ;EISSN: 1518-8345 ;DOI: 10.1590/1518-8345.4057.3458

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18
Síndrome deleción de 22q11.2: a propósito de dos casos
Síndrome deleción de 22q11.2: a propósito de dos casos
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Síndrome deleción de 22q11.2: a propósito de dos casos

Duazary, 2023-09, Vol.20 (3), p.224-230 [Peer Reviewed Journal]

2023. This work is published under https://creativecommons.org/licenses/by-nc-sa/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;ISSN: 1794-5992 ;EISSN: 2389-783X ;DOI: 10.21676/2389783X.5365

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19
Reporte de una nueva mutación en Colombia: un paciente con síndrome de Kabuki
Reporte de una nueva mutación en Colombia: un paciente con síndrome de Kabuki
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Reporte de una nueva mutación en Colombia: un paciente con síndrome de Kabuki

Iatreia (Medellín, Colombia), 2020-01, Vol.33 (1), p.78-83 [Peer Reviewed Journal]

COPYRIGHT 2020 Universidad de Antioquia, Facultad de Medicina ;COPYRIGHT 2020 Universidad de Antioquia, Facultad de Medicina ;2020. This work is licensed under https://creativecommons.org/licenses/by-nc-sa/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. ;ISSN: 0121-0793 ;EISSN: 2011-7965 ;DOI: 10.17533/udea.iatreia.38

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20
Analysis of the effect of interventional therapy for congenital heart disease complicated with pulmonary artery hypertension
Analysis of the effect of interventional therapy for congenital heart disease complicated with pulmonary artery hypertension
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Analysis of the effect of interventional therapy for congenital heart disease complicated with pulmonary artery hypertension

Revista argentina de clínica psicológica, 2020-01, Vol.29 (3), p.498

Copyright FUNDACIÓN AIGLÉ 2020 ;ISSN: 0327-6716 ;EISSN: 1851-7951 ;DOI: 10.24205/03276716.2020.748

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