Congenital hyperinsulinism: clinical and molecular characterisation of compound heterozygous ABCC8 mutation responsive to Diazoxide therapy.

Arya, Ved Bhushan; Aziz, Qadeer; Nessa, Azizun; Tinker, Andrew; Hussain, Khalid

Arya, Ved Bhushan; Aziz, Qadeer; Nessa, Azizun; Tinker, Andrew; Hussain, Khalid.

Afiliação

Arya VB; London centre for Paediatric Endocrinology, Great Ormond Street Hospital for Children NHS Foundation Trust, London WC1N 3JH and The Institute of Child Health, University College London, London, WC1N 1EH UK.
Aziz Q; The Heart Centre, William Harvey Research Institute, Barts and the London School of Medicine and Dentistry, Charterhouse Square, London, UK.
Nessa A; The Institute of Child Health, University College London, London, WC1N 1EH UK.
Tinker A; The Heart Centre, William Harvey Research Institute, Barts and the London School of Medicine and Dentistry, Charterhouse Square, London, UK.
Hussain K; London centre for Paediatric Endocrinology, Great Ormond Street Hospital for Children NHS Foundation Trust, London WC1N 3JH and The Institute of Child Health, University College London, London, WC1N 1EH UK.

Int J Pediatr Endocrinol ; 2014(1): 24, 2014.

Article em En | MEDLINE | ID: mdl-25584046

Palavras-chave

ABCC8; Congenital hyperinsulinism; Diazoxide; Hypoglycaemia

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Int J Pediatr Endocrinol Ano de publicação: 2014 Tipo de documento: Article País de publicação: Reino Unido

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