Literature DB >> 3373402

Increased serum level of 1,25-dihydroxyvitamin D3 after parathyroid hormone in the normocalcemic phase of idiopathic hypercalcemia.

E Pronicka1, H Kulczycka, R Lorenc, K Prószyńska, J Gradzka, E Rowińska.   

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Year:  1988        PMID： 3373402     DOI： 10.1016/s0022-3476(88)80221-x

Source DB:  PubMed          Journal:  J Pediatr        ISSN： 0022-3476            Impact factor:   4.406


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  3 in total

1.  Genetic defect in CYP24A1, the vitamin D 24-hydroxylase gene, in a patient with severe infantile hypercalcemia.

Authors:  Andrew Dauber; Thutrang T Nguyen; Etienne Sochett; David E C Cole; Ronald Horst; Steven A Abrams; Thomas O Carpenter; Joel N Hirschhorn
Journal:  J Clin Endocrinol Metab       Date:  2011-11-23       Impact factor: 5.958

2.  Biallelic mutations in CYP24A1 or SLC34A1 as a cause of infantile idiopathic hypercalcemia (IIH) with vitamin D hypersensitivity: molecular study of 11 historical IIH cases.

Authors:  Ewa Pronicka; Elżbieta Ciara; Paulina Halat; Agnieszka Janiec; Marek Wójcik; Elżbieta Rowińska; Dariusz Rokicki; Paweł Płudowski; Ewa Wojciechowska; Aldona Wierzbicka; Janusz B Książyk; Agnieszka Jacoszek; Martin Konrad; Karl P Schlingmann; Mieczysław Litwin
Journal:  J Appl Genet       Date:  2017-05-03       Impact factor: 3.240

3.  Long-term outcome of the survivors of infantile hypercalcaemia with CYP24A1 and SLC34A1 mutations.

Authors:  Agnieszka Janiec; Paulina Halat-Wolska; Łukasz Obrycki; Elżbieta Ciara; Marek Wójcik; Paweł Płudowski; Aldona Wierzbicka; Ewa Kowalska; Janusz B Książyk; Zbigniew Kułaga; Ewa Pronicka; Mieczysław Litwin
Journal:  Nephrol Dial Transplant       Date:  2021-07-23       Impact factor: 5.992
  3 in total

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