Annette Gruters

Berlin, BE 13353, Germany

Last Updated: 09/26/2026

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Found 30 publications

Precision Medicine in patients with rare forms of genetic obesity: Necessity for coordinated and structured care.

Precision Medicine in patients with rare forms of genetic obesity: Necessity for coordinated and structured care.

Journal: The Journal of clinical endocrinology and metabolism

Published: May 01, 2026

IMPROVE 2022 International Meeting on Pathway-Related Obesity: Vision of Excellence.

IMPROVE 2022 International Meeting on Pathway-Related Obesity: Vision of Excellence.

Journal: Clinical obesity

Published: February 22, 2024

It is finally time to stop causing anxiety for mothers with autoimmune thyroiditis during the early postpartum period.

It is finally time to stop causing anxiety for mothers with autoimmune thyroiditis during the early postpartum period.

Journal: Acta paediatrica (Oslo, Norway : 1992)

Published: February 18, 2024

Transition for adolescents with a rare disease: results of a nationwide German project.

Transition for adolescents with a rare disease: results of a nationwide German project.

Journal: Orphanet journal of rare diseases

Published: September 22, 2022

The Interdisciplinary Diagnosis of Rare Diseases.

The Interdisciplinary Diagnosis of Rare Diseases.

Journal: Deutsches Arzteblatt international

Published: December 23, 2021

A New Multisystem Disorder Caused by the Gαs Mutation p.F376V.

A New Multisystem Disorder Caused by the Gαs Mutation p.F376V.

Journal: The Journal of clinical endocrinology and metabolism

Published: June 08, 2018

A New Multisystem Disorder Caused by the Gαs Mutation p.F376V.

A New Multisystem Disorder Caused by the Gαs Mutation p.F376V.

Journal: The Journal of clinical endocrinology and metabolism

Published: June 08, 2018

2018 European Thyroid Association (ETA) Guidelines on the Diagnosis and Management of Central Hypothyroidism.

2018 European Thyroid Association (ETA) Guidelines on the Diagnosis and Management of Central Hypothyroidism.

Journal: European thyroid journal

Published: May 28, 2018

MC4R agonism promotes durable weight loss in patients with leptin receptor deficiency.

MC4R agonism promotes durable weight loss in patients with leptin receptor deficiency.

Journal: Nature medicine

Published: December 09, 2017

Mean High-Dose l-Thyroxine Treatment Is Efficient and Safe to Achieve a Normal IQ in Young Adult Patients With Congenital Hypothyroidism.

Mean High-Dose l-Thyroxine Treatment Is Efficient and Safe to Achieve a Normal IQ in Young Adult Patients With Congenital Hypothyroidism.

Journal: The Journal of clinical endocrinology and metabolism

Published: August 31, 2017

Investigation of Naturally Occurring Single-Nucleotide Variants in Human TAAR1.

Investigation of Naturally Occurring Single-Nucleotide Variants in Human TAAR1.

Journal: Frontiers in pharmacology

Published: August 18, 2017

Somatic mutations and progressive monosomy modify SAMD9-related phenotypes in humans.

Somatic mutations and progressive monosomy modify SAMD9-related phenotypes in humans.

Journal: The Journal of clinical investigation

Published: November 28, 2016

Showing 1-12 of 30

Last Updated: 09/26/2026