Martin Munteanu
Essen, NW, Germany
Last Updated: 09/26/2026
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Found 10 publications
Author Correction: Next-generation phenotyping integrated in a national framework for patients with ultrarare disorders improves genetic diagnostics and yields new molecular findings.
Journal: Nature genetics
Published: June 24, 2025
Autosomal recessive hypophosphatemic rickets type 2 (ARHR2): Is phosphate supplementation safe?
Journal: Bone
Published: April 16, 2025
The Endocrine Chameleon: Expanding the Phenotype of Pseudohypoparathyroidism 1A in Infancy.
Journal: Hormone research in paediatrics
Published: August 16, 2024
Next-generation phenotyping integrated in a national framework for patients with ultrarare disorders improves genetic diagnostics and yields new molecular findings.
Journal: Nature genetics
Published: July 19, 2023
Prevalence of osteopathologies in a single center cohort of survivors of childhood primary brain tumor.
Journal: Frontiers in pediatrics
Published: April 05, 2022
Clinical relevance of postzygotic mosaicism in Cornelia de Lange syndrome and purifying selection of NIPBL variants in blood.
Journal: Scientific reports
Published: May 27, 2021
Increased Prevalence of Subclinical Hypothyroidism and Thyroid Autoimmunity in Depressed Adolescents: Results From a Clinical Cross-Sectional Study in Comparison to the General Pediatric Population.
Journal: The Journal of clinical psychiatry
Published: May 14, 2021
Biallelic PI4KA variants cause neurological, intestinal and immunological disease.
Journal: Brain : a journal of neurology
Published: January 26, 2021
Prevalence of Osteopathologies in Children and Adolescents After Diagnosis of Acute Lymphoblastic Leukemia.
Journal: Frontiers in pediatrics
Published: May 12, 2020
Resistance to GHRH but Not to PTH in a 15-Year-Old Boy With Pseudohypoparathyroidism 1A.
Journal: Journal of the Endocrine Society
Published: February 25, 2019
Showing 1-10 of 10
Last Updated: 09/26/2026