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Literature DB >> 25182308

ISPAD Clinical Practice Consensus Guidelines 2014. Management of cystic fibrosis-related diabetes in children and adolescents.

Antoinette Moran¹, Kubendran Pillay, Dorothy J Becker, Carlo L Acerini.

Abstract

Entities: Disease Species

Keywords: consensus; cystic-fibrosis; diabetes; guidelines

Mesh：

Year: 2014 PMID： 25182308 DOI： 10.1111/pedi.12178

Source DB: PubMed Journal: Pediatr Diabetes ISSN： 1399-543X Impact factor: 4.866

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Cited

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18 in total

Review 1. Methods for Measuring Risk for Type 2 Diabetes in Youth: the Oral Glucose Tolerance Test (OGTT).

Authors: Melinda E Chen; Rebecca S Aguirre; Tamara S Hannon
Journal: Curr Diab Rep Date: 2018-06-16 Impact factor: 4.810

Review 2. Endocrine Disorders in Cystic Fibrosis.

Authors: Scott M Blackman; Vin Tangpricha
Journal: Pediatr Clin North Am Date: 2016-08 Impact factor: 3.278

3. Continuous glucose monitoring abnormalities in cystic fibrosis youth correlate with pulmonary function decline.

Authors: Christine L Chan; Timothy Vigers; Laura Pyle; Philip S Zeitler; Scott D Sagel; Kristen J Nadeau
Journal: J Cyst Fibros Date: 2018-03-23 Impact factor: 5.482

4. Brazilian guidelines for the diagnosis and treatment of cystic fibrosis.

Authors: Rodrigo Abensur Athanazio; Luiz Vicente Ribeiro Ferreira da Silva Filho; Alberto Andrade Vergara; Antônio Fernando Ribeiro; Carlos Antônio Riedi; Elenara da Fonseca Andrade Procianoy; Fabíola Villac Adde; Francisco José Caldeira Reis; José Dirceu Ribeiro; Lídia Alice Torres; Marcelo Bicalho de Fuccio; Matias Epifanio; Mônica de Cássia Firmida; Neiva Damaceno; Norberto Ludwig-Neto; Paulo José Cauduro Maróstica; Samia Zahi Rached; Suzana Fonseca de Oliveira Melo
Journal: J Bras Pneumol Date: 2017 May-Jun Impact factor: 2.624

ISPAD Clinical Practice Consensus Guidelines 2014. Management of cystic fibrosis-related diabetes in children and adolescents.

Review 1. Methods for Measuring Risk for Type 2 Diabetes in Youth: the Oral Glucose Tolerance Test (OGTT).

Review 2. Endocrine Disorders in Cystic Fibrosis.

3. Continuous glucose monitoring abnormalities in cystic fibrosis youth correlate with pulmonary function decline.

4. Brazilian guidelines for the diagnosis and treatment of cystic fibrosis.

5. Determinants of Serum Glycerophospholipid Fatty Acids in Cystic Fibrosis.

Review 6. Dietary interventions for managing glucose abnormalities in cystic fibrosis: a systematic review protocol.

7. Clinical course and significance of nontuberculous mycobacteria and its subtypes in cystic fibrosis.

8. Cystic Fibrosis Mortality in Childhood. Data from European Cystic Fibrosis Society Patient Registry.

9. Diabetes outbreak during COVID19 lock-down in a prediabetic patient with cystic fibrosis long treated with glargine.

10. Pediatric Case Series of Cystic Fibrosis, Diabetes, and Islet Cell Autoimmunity.