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1
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 [Tạp chí có phản biện]

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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2
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 [Tạp chí có phản biện]

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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3
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 [Tạp chí có phản biện]

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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4
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 [Tạp chí có phản biện]

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

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5
Dental Rehabilitation of a Rare Hallermann-Streiff Syndrome with Olygodontia: A Case Report
Dental Rehabilitation of a Rare Hallermann-Streiff Syndrome with Olygodontia: A Case Report
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Dental Rehabilitation of a Rare Hallermann-Streiff Syndrome with Olygodontia: A Case Report

Odovtos, 2020-01, Vol.22 (3), p.54 [Tạp chí có phản biện]

2020. This work is published under http://creativecommons.org/licenses/by-nc/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;ISSN: 1659-1046 ;EISSN: 2215-3411 ;DOI: 10.15517/ijds.2020.42072

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6
Improvement in Oral Health and Compliance in a Child with Congenital Hypothyroidism. Case Report
Improvement in Oral Health and Compliance in a Child with Congenital Hypothyroidism. Case Report
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Improvement in Oral Health and Compliance in a Child with Congenital Hypothyroidism. Case Report

Odovtos, 2019-01, Vol.21 (3), p.45 [Tạp chí có phản biện]

2019. This work is published under http://creativecommons.org/licenses/by-nc/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;ISSN: 1659-1046 ;EISSN: 2215-3411 ;DOI: 10.15517/ijds.2019.37850

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