Literature DB >> 4835124

A defective thyroid peroxidase solubilized from a familial goiter with iodine organification defect.

J Pommier, J Tourniaire, D Dème, D Chalendar, H Bornet, J Nunez.   

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Year:  1974        PMID： 4835124     DOI： 10.1210/jcem-39-1-69

Source DB:  PubMed          Journal:  J Clin Endocrinol Metab        ISSN： 0021-972X            Impact factor:   5.958


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  5 in total

1.  Partial and total iodide organification defect in different sibships in a kindred.

Authors:  E Perez-Cuvit; J F Crigler; J B Stanbury
Journal:  Am J Hum Genet       Date:  1977-03       Impact factor: 11.025

2.  Deficient thyroid peroxidase causing organification defect and goitrous hypothyroidism.

Authors:  G A Medeiros-Neto; M Knobel; K Yamamoto; H Cavaliere; W Kallas
Journal:  J Endocrinol Invest       Date:  1979 Oct-Dec       Impact factor: 4.256

3.  Identification of a mutation in the coding sequence of the human thyroid peroxidase gene causing congenital goiter.

Authors:  M J Abramowicz; H M Targovnik; V Varela; P Cochaux; L Krawiec; M A Pisarev; F V Propato; G Juvenal; H A Chester; G Vassart
Journal:  J Clin Invest       Date:  1992-10       Impact factor: 14.808

4.  Autoantibodies to the thyroid microsomal/thyroid peroxidase antigen are polyclonal and directed to several distinct antigenic sites.

Authors:  N D Doble; J P Banga; R Pope; E Lalor; P Kilduff; A M McGregor
Journal:  Immunology       Date:  1988-05       Impact factor: 7.397

5.  Association of peroxidase enzyme defect and low thyroglobulin content in a case of endemic cretinism.

Authors:  N Ait Hammou; N Abdelmoumene; M Benmiloud
Journal:  J Endocrinol Invest       Date:  1985-06       Impact factor: 4.256
  5 in total

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