Literature DB >> 22322538

Variable clinical presentations in a family with neurohypophysial diabetes insipidus.

E Passeri, A Tufano, S Perrotta, B Ambrosi, S Corbetta.   

Abstract

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Year:  2011        PMID： 22322538     DOI： 10.1007/BF03346735

Source DB:  PubMed          Journal:  J Endocrinol Invest        ISSN： 0391-4097            Impact factor:   4.256


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  4 in total

1.  A new type of familial central diabetes insipidus caused by a single base substitution in the neurophysin II coding region of the vasopressin gene.

Authors:  Y Ueta; S Taniguchi; A Yoshida; I Murakami; Y Mitani; I Hisatome; I Manabe; R Sato; M Tsuboi; A Ohtahara; E Nanba; C Shigemasa
Journal:  J Clin Endocrinol Metab       Date:  1996-05       Impact factor: 5.958

2.  Growth retardation in untreated autosomal dominant familial neurohypophyseal diabetes insipidus caused by one recurring and two novel mutations in the vasopressin-neurophysin II gene.

Authors:  Cécile Brachet; Julia Birk; Catherine Christophe; Sylvie Tenoutasse; Brigitte Velkeniers; Claudine Heinrichs; Jonas Rutishauser
Journal:  Eur J Endocrinol       Date:  2010-11-18       Impact factor: 6.664

3.  A novel mutation in the coding region for neurophysin-II is associated with autosomal dominant neurohypophyseal diabetes insipidus.

Authors:  F Rauch; C Lenzner; P Nürnberg; C Frömmel; U Vetter
Journal:  Clin Endocrinol (Oxf)       Date:  1996-01       Impact factor: 3.478

Review 4.  The diagnosis of children with central diabetes insipidus.

Authors:  Stefano Ghirardello; Maria-Luisa Garrè; Andrea Rossi; Mohamad Maghnie
Journal:  J Pediatr Endocrinol Metab       Date:  2007-03       Impact factor: 1.634
  4 in total

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