Elisabeth Steichen-Gersdorf

Innsbruck, 6020, Austria

Last Updated: 09/26/2026

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Found 15 publications

Migration background and diabetes technology use at diagnosis and follow-up in children and adolescents with type 1 diabetes: a single-centre study.

Migration background and diabetes technology use at diagnosis and follow-up in children and adolescents with type 1 diabetes: a single-centre study.

Journal: Acta diabetologica

Published: May 12, 2026

Author Correction: The human ciliopathy protein RSG1 links the CPLANE complex to transition zone architecture.

Author Correction: The human ciliopathy protein RSG1 links the CPLANE complex to transition zone architecture.

Journal: Nature communications

Published: February 02, 2026

The human ciliopathy protein RSG1 links the CPLANE complex to transition zone architecture.

The human ciliopathy protein RSG1 links the CPLANE complex to transition zone architecture.

Journal: bioRxiv : the preprint server for biology

Published: October 10, 2024

The human ciliopathy protein RSG1 links the CPLANE complex to transition zone architecture.

The human ciliopathy protein RSG1 links the CPLANE complex to transition zone architecture.

Journal: Nature communications

Published: September 23, 2024

The human ciliopathy protein RSG1 links the CPLANE complex to transition zone architecture.

The human ciliopathy protein RSG1 links the CPLANE complex to transition zone architecture.

Journal: Nature communications

Published: September 23, 2024

Pituitary Stalk Interruption Syndrome – clinical Presentation and Management of a Potentially Life-threatening Disease in Newborns

Pituitary Stalk Interruption Syndrome – clinical Presentation and Management of a Potentially Life-threatening Disease in Newborns

Journal: Journal of clinical research in pediatric endocrinology

Published: April 19, 2023

Author Correction: Mutations in PYCR1 cause cutis laxa with progeroid features.

Author Correction: Mutations in PYCR1 cause cutis laxa with progeroid features.

Journal: Nature genetics

Published: January 22, 2022

Frequency and Characteristics of MODY 1 (HNF4A Mutation) and MODY 5 (HNF1B Mutation): Analysis From the DPV Database.

Frequency and Characteristics of MODY 1 (HNF4A Mutation) and MODY 5 (HNF1B Mutation): Analysis From the DPV Database.

Journal: The Journal of clinical endocrinology and metabolism

Published: August 08, 2018

Genotyping of coeliac-specific human leucocyte antigen in children with type 1 diabetes: does this screening method make sense?

Genotyping of coeliac-specific human leucocyte antigen in children with type 1 diabetes: does this screening method make sense?

Journal: Archives of disease in childhood

Published: July 12, 2016

Needle detachment in a slim and physically active child with insulin pump treatment.

Needle detachment in a slim and physically active child with insulin pump treatment.

Journal: Pediatric diabetes

Published: March 31, 2015

ALG8-CDG: novel patients and review of the literature.

ALG8-CDG: novel patients and review of the literature.

Journal: Orphanet journal of rare diseases

Published: March 10, 2015

Phenotype and genotype in 103 patients with tricho-rhino-phalangeal syndrome.

Phenotype and genotype in 103 patients with tricho-rhino-phalangeal syndrome.

Journal: European journal of medical genetics

Published: February 04, 2015

Showing 1-12 of 15

Last Updated: 09/26/2026