Literature DB >> 10352113

Pseudohypohyperparathyroidism-pseudohypoparathyroidism type Ib.

Z Farfel.   

Abstract

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Year:  1999        PMID： 10352113     DOI： 10.1359/jbmr.1999.14.6.1016

Source DB:  PubMed          Journal:  J Bone Miner Res        ISSN： 0884-0431            Impact factor:   6.741


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  6 in total

Review 1.  Genetics of endocrine and metabolic disorders: parathyroid.

Authors:  R V Thakker
Journal:  Rev Endocr Metab Disord       Date:  2004-03       Impact factor: 6.514

2.  Paternal uniparental isodisomy of chromosome 20q--and the resulting changes in GNAS1 methylation--as a plausible cause of pseudohypoparathyroidism.

Authors:  M Bastepe; A H Lane; H Jüppner
Journal:  Am J Hum Genet       Date:  2001-04-09       Impact factor: 11.025

3.  Cinacalcet as adjunctive therapy in pseudohypoparathyroidism type 1b.

Authors:  Tarak Srivastava; Jeffrey Krudys; Neil J Mardis; Judith Sebestyen-VanSickle; Uri S Alon
Journal:  Pediatr Nephrol       Date:  2015-12-01       Impact factor: 3.714

4.  Paternal uniparental isodisomy of the entire chromosome 20 as a molecular cause of pseudohypoparathyroidism type Ib (PHP-Ib).

Authors:  Murat Bastepe; Ozge Altug-Teber; Chhavi Agarwal; Sharon E Oberfield; Michael Bonin; Harald Jüppner
Journal:  Bone       Date:  2010-10-19       Impact factor: 4.398

Review 5.  Use of calcimimetics in children with normal kidney function.

Authors:  Judith Sebestyen VanSickle; Tarak Srivastava; Uri S Alon
Journal:  Pediatr Nephrol       Date:  2018-03-19       Impact factor: 3.714

6.  Loss of XLαs (extra-large αs) imprinting results in early postnatal hypoglycemia and lethality in a mouse model of pseudohypoparathyroidism Ib.

Authors:  Eduardo Fernández-Rebollo; Akira Maeda; Monica Reyes; Serap Turan; Leopold F Fröhlich; Antonius Plagge; Gavin Kelsey; Harald Jüppner; Murat Bastepe
Journal:  Proc Natl Acad Sci U S A       Date:  2012-04-10       Impact factor: 11.205
  6 in total

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