Literature DB >> 21423243

Autoimmunity: acquired versus inherited pituitary deficiency - same difference?

Jacques Drouin, Shinobu Takayasu.   

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Year:  2011        PMID： 21423243     DOI： 10.1038/nrendo.2011.53

Source DB:  PubMed          Journal:  Nat Rev Endocrinol        ISSN： 1759-5029            Impact factor:   43.330


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  7 in total

1.  Congenital isolated adrenocorticotropin deficiency: an underestimated cause of neonatal death, explained by TPIT gene mutations.

Authors:  Sophie Vallette-Kasic; Thierry Brue; Anne-Marie Pulichino; Magali Gueydan; Anne Barlier; Michel David; Marc Nicolino; Georges Malpuech; Pierre Déchelotte; Cheri Deal; Guy Van Vliet; Monique De Vroede; Felix G Riepe; Carl-Joachim Partsch; Wolfgang G Sippell; Merih Berberoglu; Begüm Atasay; Francis de Zegher; Dominique Beckers; Jennifer Kyllo; Patricia Donohoue; Martin Fassnacht; Stefanie Hahner; Bruno Allolio; C Noordam; Leo Dunkel; Matti Hero; B Pigeon; Jacques Weill; Sevket Yigit; Raja Brauner; Juan Jorge Heinrich; Elizabeth Cummings; Christie Riddell; Alain Enjalbert; Jacques Drouin
Journal:  J Clin Endocrinol Metab       Date:  2004-12-21       Impact factor: 5.958

2.  Adult combined GH, prolactin, and TSH deficiency associated with circulating PIT-1 antibody in humans.

Authors:  Masaaki Yamamoto; Genzo Iguchi; Ryoko Takeno; Yasuhiko Okimura; Toshiaki Sano; Michiko Takahashi; Hitoshi Nishizawa; Anastasia Evi Handayaningshi; Hidenori Fukuoka; Maya Tobita; Takatoshi Saitoh; Katsuyoshi Tojo; Atsuko Mokubo; Akio Morinobu; Keiji Iida; Hidesuke Kaji; Susumu Seino; Kazuo Chihara; Yutaka Takahashi
Journal:  J Clin Invest       Date:  2010-12-01       Impact factor: 14.808

3.  PROP1 gene screening in patients with multiple pituitary hormone deficiency reveals two sites of hypermutability and a high incidence of corticotroph deficiency.

Authors:  S Vallette-Kasic; A Barlier; C Teinturier; A Diaz; M Manavela; F Berthezène; P Bouchard; J L Chaussain; R Brauner; I Pellegrini-Bouiller; P Jaquet; A Enjalbert; T Brue
Journal:  J Clin Endocrinol Metab       Date:  2001-09       Impact factor: 5.958

Review 4.  Autoimmune polyglandular syndromes.

Authors:  Aaron W Michels; Peter A Gottlieb
Journal:  Nat Rev Endocrinol       Date:  2010-03-23       Impact factor: 43.330

5.  Pituitary lineage determination by the Prophet of Pit-1 homeodomain factor defective in Ames dwarfism.

Authors:  M W Sornson; W Wu; J S Dasen; S E Flynn; D J Norman; S M O'Connell; I Gukovsky; C Carrière; A K Ryan; A P Miller; L Zuo; A S Gleiberman; B Andersen; W G Beamer; M G Rosenfeld
Journal:  Nature       Date:  1996-11-28       Impact factor: 49.962

6.  Human and mouse TPIT gene mutations cause early onset pituitary ACTH deficiency.

Authors:  Anne-Marie Pulichino; Sophie Vallette-Kasic; Catherine Couture; Yves Gauthier; Thierry Brue; Michel David; Georges Malpuech; Cheri Deal; Guy Van Vliet; Monique De Vroede; Felix G Riepe; Carl-Joachim Partsch; Wolfgang G Sippell; Merih Berberoglu; Begüm Atasay; Jacques Drouin
Journal:  Genes Dev       Date:  2003-03-15       Impact factor: 11.361

Review 7.  Genetic regulation of pituitary gland development in human and mouse.

Authors:  Daniel Kelberman; Karine Rizzoti; Robin Lovell-Badge; Iain C A F Robinson; Mehul T Dattani
Journal:  Endocr Rev       Date:  2009-10-16       Impact factor: 19.871
  7 in total
  1 in total

1.  A novel thymoma-associated autoimmune disease: Anti-PIT-1 antibody syndrome.

Authors:  Hironori Bando; Genzo Iguchi; Yasuhiko Okimura; Yukiko Odake; Kenichi Yoshida; Ryusaku Matsumoto; Kentaro Suda; Hitoshi Nishizawa; Hidenori Fukuoka; Atsuko Mokubo; Katsuyoshi Tojo; Yoshimasa Maniwa; Wataru Ogawa; Yutaka Takahashi
Journal:  Sci Rep       Date:  2017-02-20       Impact factor: 4.379
  1 in total

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