Angela Rogers

Truro, ENG TR13LJ, United Kingdom

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 17 publications

Reply to Kambhampati B.

Reply to Kambhampati B.

Journal: Pediatric radiology

Published: July 23, 2025

Frequency and outcomes of gastrojejunostomy tube replacement in children - a single-centre experience.

Frequency and outcomes of gastrojejunostomy tube replacement in children - a single-centre experience.

Journal: Pediatric radiology

Published: April 28, 2025

GNA11 Variants Identified in Patients with Hypercalcemia or Hypocalcemia.

GNA11 Variants Identified in Patients with Hypercalcemia or Hypocalcemia.

Journal: Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research

Published: January 18, 2023

Multiple Endocrine Neoplasia Type 1 (MEN1) 5'UTR Deletion, in MEN1 Family, Decreases Menin Expression.

Multiple Endocrine Neoplasia Type 1 (MEN1) 5'UTR Deletion, in MEN1 Family, Decreases Menin Expression.

Journal: Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research

Published: March 04, 2020

Association of prolactin receptor (PRLR) variants with prolactinomas.

Association of prolactin receptor (PRLR) variants with prolactinomas.

Journal: Human molecular genetics

Published: August 07, 2018

N-ethyl-N-nitrosourea-Induced Adaptor Protein 2 Sigma Subunit 1 (Ap2s1) Mutations Establish Ap2s1 Loss-of-Function Mice.

N-ethyl-N-nitrosourea-Induced Adaptor Protein 2 Sigma Subunit 1 (Ap2s1) Mutations Establish Ap2s1 Loss-of-Function Mice.

Journal: JBMR plus

Published: February 27, 2018

AP2σ Mutations Impair Calcium-Sensing Receptor Trafficking and Signaling, and Show an Endosomal Pathway to Spatially Direct G-Protein Selectivity.

AP2σ Mutations Impair Calcium-Sensing Receptor Trafficking and Signaling, and Show an Endosomal Pathway to Spatially Direct G-Protein Selectivity.

Journal: Cell reports

Published: June 16, 2017

Gα11 mutation in mice causes hypocalcemia rectifiable by calcilytic therapy.

Gα11 mutation in mice causes hypocalcemia rectifiable by calcilytic therapy.

Journal: JCI insight

Published: February 15, 2017

Cinacalcet for Symptomatic Hypercalcemia Caused by AP2S1 Mutations.

Cinacalcet for Symptomatic Hypercalcemia Caused by AP2S1 Mutations.

Journal: The New England journal of medicine

Published: April 07, 2016

Adaptor protein-2 sigma subunit mutations causing familial hypocalciuric hypercalcaemia type 3 (FHH3) demonstrate genotype-phenotype correlations, codon bias and dominant-negative effects.

Adaptor protein-2 sigma subunit mutations causing familial hypocalciuric hypercalcaemia type 3 (FHH3) demonstrate genotype-phenotype correlations, codon bias and dominant-negative effects.

Journal: Human molecular genetics

Published: May 01, 2015

Diagnosis and management of prolactinomas and non-functioning pituitary adenomas.

Diagnosis and management of prolactinomas and non-functioning pituitary adenomas.

Journal: BMJ (Clinical research ed.)

Published: September 12, 2014

Mutational analysis of the adaptor protein 2 sigma subunit (AP2S1) gene: search for autosomal dominant hypocalcemia type 3 (ADH3).

Mutational analysis of the adaptor protein 2 sigma subunit (AP2S1) gene: search for autosomal dominant hypocalcemia type 3 (ADH3).

Journal: The Journal of clinical endocrinology and metabolism

Published: April 09, 2014

Showing 1-12 of 17

Last Updated: 09/26/2026