X-linked hypophosphataemic rickets in children: clinical phenotype, therapeutic strategies, and molecular background-Reference-Cited by-同舟云学术

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X-linked hypophosphataemic rickets in children: clinical phenotype, therapeutic strategies, and molecular background

Published:2021-04-30 Issue:2 Volume:72 Page:108-119
ISSN:2299-8306
Container-title:Endokrynologia Polska
language:
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Author:

Obara-Moszynska Monika,Rojek Aleksandra,Kolesinska Zofia,Jurkiewicz Dorota,Chrzanowska Krystyna H.,Niedziela Marek

Publisher

VM Media SP. zo.o VM Group SK

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism

Cited by 4 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Clinical efficacy and safety of use of alfacalcidol and calcitriol in daily endocrinological practice;Endokrynologia Polska;2023-02-27

2. Whole exome sequencing identifies two novel variants in PHEX and DMP1 in Malaysian children with hypophosphatemic rickets;Italian Journal of Pediatrics;2022-12-08

3. PHEXL222P Mutation Increases Phex Expression in a New ENU Mouse Model for XLH Disease;Genes;2022-07-28

4. Genetic basis of hereditary hypophosphataemic rickets and phenotype presentation in children and adults;Endokrynologia Polska;2021-08-11

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