Literature DB >> 21457340

A proposal of warning signs for primary immunodeficiencies in the first year of life.

Magda Carneiro-Sampaio, Cristina Miuki Abe Jacob, Cléa Rodrigues Leone.   

Abstract

Entities:  

Mesh：

Year:  2011        PMID： 21457340     DOI： 10.1111/j.1399-3038.2010.01084.x

Source DB:  PubMed          Journal:  Pediatr Allergy Immunol        ISSN： 0905-6157            Impact factor:   6.377


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  11 in total

1.  The Duesseldorf warning signs for primary immunodeficiency: is it time to change the rules?

Authors:  Petra Lankisch; Julia Schiffner; Sujal Ghosh; Florian Babor; Arndt Borkhardt; Hans-Jürgen Laws
Journal:  J Clin Immunol       Date:  2015-03-08       Impact factor: 8.317

2.  Inborn Errors of Immunity in Patients with Adverse Events Following BCG Vaccination in Brazil.

Authors:  Paula T Lyra; Edvaldo Souza; Ana Carla A Moura; Marina C Matta; Leuridan C Torres; Antonio Victor Campos Coelho; Maria Ângela W Rocha; Luiz Arraes; João Bosco Oliveira
Journal:  J Clin Immunol       Date:  2022-07-30       Impact factor: 8.542

Review 3.  Inborn Errors of Immunity With Fetal or Perinatal Clinical Manifestations.

Authors:  Magda Carneiro-Sampaio; Adriana Almeida de Jesus; Silvia Yumi Bando; Carlos Alberto Moreira-Filho
Journal:  Front Pediatr       Date:  2022-05-06       Impact factor: 3.569

4.  Primary immunodeficiency diseases in different age groups: a report on 1,008 cases from a single Brazilian reference center.

Authors:  Magda Carneiro-Sampaio; Dewton Moraes-Vasconcelos; Cristina M Kokron; Cristina M A Jacob; Myrthes Toledo-Barros; Mayra B Dorna; Letícia A Watanabe; Ana Karolina B B Marinho; Ana Paula Moschione Castro; Antonio C Pastorino; Clóvis Artur A Silva; Maurício D Ferreira; Luiz V Rizzo; Jorge E Kalil; Alberto J S Duarte
Journal:  J Clin Immunol       Date:  2013-01-29       Impact factor: 8.317

Review 5.  A family history of serious complications due to BCG vaccination is a tool for the early diagnosis of severe primary immunodeficiency.

Authors:  Pérsio Roxo-Junior; Jorgete Silva; Mauro Andrea; Larissa Oliveira; Fernando Ramalho; Thiago Bezerra; Altacílio A Nunes
Journal:  Ital J Pediatr       Date:  2013-09-10       Impact factor: 2.638

6.  Congenital Heart Disease as a Warning Sign for the Diagnosis of the 22q11.2 Deletion.

Authors:  Marcília S Grassi; Cristina M A Jacob; Leslie D Kulikowski; Antonio C Pastorino; Roberta L Dutra; Nana Miura; Marcelo B Jatene; Stephanie P Pegler; Chong A Kim; Magda Carneiro-Sampaio
Journal:  Arq Bras Cardiol       Date:  2014-10-10       Impact factor: 2.000

7.  Exome sequencing identifies a novel TTC37 mutation in the first reported case of Trichohepatoenteric syndrome (THE-S) in South Africa.

Authors:  Craig Kinnear; Brigitte Glanzmann; Eric Banda; Nikola Schlechter; Glenda Durrheim; Annika Neethling; Etienne Nel; Mardelle Schoeman; Glynis Johnson; Paul D van Helden; Eileen G Hoal; Monika Esser; Michael Urban; Marlo Möller
Journal:  BMC Med Genet       Date:  2017-03-14       Impact factor: 2.103

8.  Microbial Disease Spectrum Linked to a Novel IL-12Rβ1 N-Terminal Signal Peptide Stop-Gain Homozygous Mutation with Paradoxical Receptor Cell-Surface Expression.

Authors:  Thais Louvain de Souza; Regina C de Souza Campos Fernandes; Juliana Azevedo da Silva; Vladimir Gomes Alves Júnior; Adelia Gomes Coelho; Afonso C Souza Faria; Nabia M Moreira Salomão Simão; João T Souto Filho; Caroline Deswarte; Stéphanie Boisson-Dupuis; Dara Torgerson; Jean-Laurent Casanova; Jacinta Bustamante; Enrique Medina-Acosta
Journal:  Front Microbiol       Date:  2017-04-13       Impact factor: 5.640

Review 9.  Attending to warning signs of primary immunodeficiency diseases across the range of clinical practice.

Authors:  Beatriz Tavares Costa-Carvalho; Anete Sevciovic Grumach; José Luis Franco; Francisco Javier Espinosa-Rosales; Lily E Leiva; Alejandra King; Oscar Porras; Liliana Bezrodnik; Mathias Oleastro; Ricardo U Sorensen; Antonio Condino-Neto
Journal:  J Clin Immunol       Date:  2013-11-16       Impact factor: 8.317

10.  Identifying Mutations of the Tetratricopeptide Repeat Domain 37 (TTC37) Gene in Infants With Intractable Diarrhea and a Comparison of Asian and Non-Asian Phenotype and Genotype: A Global Case-report Study of a Well-Defined Syndrome With Immunodeficiency.

Authors:  Wen-I Lee; Jing-Long Huang; Chien-Chang Chen; Ju-Li Lin; Ren-Chin Wu; Tang-Her Jaing; Liang-Shiou Ou
Journal:  Medicine (Baltimore)       Date:  2016-03       Impact factor: 1.889
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