Autosomal dominant hypoparathyroidism: a proband with concurrent nephrogenic diabetes insipidus.-Reference-Cited by-同舟云学术

Autosomal dominant hypoparathyroidism: a proband with concurrent nephrogenic diabetes insipidus.

Published:1981-12-01 Issue:6 Volume:18 Page:431-435
ISSN:1468-6244
Container-title:Journal of Medical Genetics
language:en
Short-container-title:Journal of Medical Genetics

Author:

Hunter A G,Heick H,Poznanski W J,McLaine P N

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Reference24 articles.

1. Five cases (three in siblings) of idiopathic hypoparathyroidism associated with moniliasis;Sutphin, A.; Albright, F.; McCune, D.J.;J Clin Endocrinol,1943

2. The spectrum of hypoparathyroid states: a classification based on physiological principles;Ml, Nusynowitz; B, Frame; FO, Kolb;Medicine,1976

3. Hypoparathyrodie familial. Etudes clinique, biologique et therapeutique;Chaptal, J.; Jean, R.; Bonnet, R.; Guillaumot, R.; Morel, G.;Arch FrPediatr

4. Familial hypoparathyroidism. JA;Goldman, R.; Reynolds, J.L.; Cummings, H.R.; Bassett, S.H.,1952

5. True idiopathic hypoparathyroidism as a sex-linked recessive trait;Peden, V.H.;Amn J Humn Genet,1960

Cited by 13 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. Autosomal Dominant Hypocalcemia Type 1: A Systematic Review;Journal of Bone and Mineral Research;2022-08-22

2. Gα11 mutation in mice causes hypocalcemia rectifiable by calcilytic therapy;JCI Insight;2017-02-09

3. Autosomal Dominant Hypoparathyroidism Caused by Germline Mutation inGNA11: Phenotypic and Molecular Characterization;The Journal of Clinical Endocrinology & Metabolism;2014-09-01

4. A Familial Syndrome of Hypocalcemia with Hypercalciuria Due to Mutations in the Calcium-Sensing Receptor;New England Journal of Medicine;1996-10-10

5. Autosomal dominant hypocalcaemia caused by a Ca2+-sensing receptor gene mutation;Nature Genetics;1994-11