Tobias Linden

Oldenburg, NI, Germany

Last Updated: 09/26/2026

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Found 14 publications

Rehabilitation in a child with Chiari II malformation, lumbosacral meningomyelocele, achondroplasia and impaired respiratory regulation - a case report and literature review.

Rehabilitation in a child with Chiari II malformation, lumbosacral meningomyelocele, achondroplasia and impaired respiratory regulation - a case report and literature review.

Journal: Journal of pediatric rehabilitation medicine
Published: June 16, 2025

Tyrosine supplementation with high-protein diet as a therapeutic strategy for YARS1 deficiency.

Tyrosine supplementation with high-protein diet as a therapeutic strategy for YARS1 deficiency.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: May 27, 2025

Loss-of-function variants in the CAPN1 activator CD99L2 cause X-linked spastic ataxia.

Loss-of-function variants in the CAPN1 activator CD99L2 cause X-linked spastic ataxia.

Journal: Nature communications
Published: March 31, 2025

PIEZO1 mechanical insensitivity in generalized lymphatic dysplasia with the potential for pharmacological rescue.

PIEZO1 mechanical insensitivity in generalized lymphatic dysplasia with the potential for pharmacological rescue.

Journal: iScience
Published: December 09, 2024

Further delineation of the SCAF4-associated neurodevelopmental disorder.

Further delineation of the SCAF4-associated neurodevelopmental disorder.

Journal: European journal of human genetics : EJHG
Published: April 23, 2024

Natural History and Developmental Trajectories of Individuals With Disease-Causing Variants in STXBP1.

Natural History and Developmental Trajectories of Individuals With Disease-Causing Variants in STXBP1.

Journal: Neurology
Published: December 14, 2022

Interaction between fat- and muscle development in children and adolescents.

Interaction between fat- and muscle development in children and adolescents.

Journal: Anthropologischer Anzeiger; Bericht uber die biologisch-anthropologische Literatur
Published: January 11, 2022

Diagnostic Evaluation of the Functional Muscle-Bone Unit in Children With Cerebral Palsy With and Without Low Trauma Fractures.

Diagnostic Evaluation of the Functional Muscle-Bone Unit in Children With Cerebral Palsy With and Without Low Trauma Fractures.

Journal: Journal of clinical densitometry : the official journal of the International Society for Clinical Densitometry
Published: July 31, 2021

Primary haemophagocytic lymphohistiocytosis (Chédiak-Higashi Syndrome) triggered by acute SARS-CoV-2 infection in a six-week-old infant.

Primary haemophagocytic lymphohistiocytosis (Chédiak-Higashi Syndrome) triggered by acute SARS-CoV-2 infection in a six-week-old infant.

Journal: British journal of haematology
Published: June 16, 2021

Pediatric Reference Centiles of Bone Mineral Density and Body Composition of Lower Limbs.

Pediatric Reference Centiles of Bone Mineral Density and Body Composition of Lower Limbs.

Journal: Journal of clinical densitometry : the official journal of the International Society for Clinical Densitometry
Published: February 18, 2021

Correction: A new microdeletion syndrome involving TBC1D24, ATP6V0C, and PDPK1 causes epilepsy, microcephaly, and developmental delay.

Correction: A new microdeletion syndrome involving TBC1D24, ATP6V0C, and PDPK1 causes epilepsy, microcephaly, and developmental delay.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: January 16, 2019

A new microdeletion syndrome involving TBC1D24, ATP6V0C, and PDPK1 causes epilepsy, microcephaly, and developmental delay.

A new microdeletion syndrome involving TBC1D24, ATP6V0C, and PDPK1 causes epilepsy, microcephaly, and developmental delay.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: June 05, 2018
Showing 1-12 of 14

Last Updated: 09/26/2026