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Publications by Daniela Karall

Bi-Allelic ADPRHL2 Mutations Cause Neurodegeneration With Developmental Delay, Ataxia, and Axonal Neuropathy

American Journal of Human Genetics

English

KCNC1 ‐related Disorders: New De Novo Variants Expand the Phenotypic Spectrum

Annals of Clinical and Translational Neurology

English

Very Long-/ and Long Chain-3-Hydroxy Acyl CoA Dehydrogenase Deficiency Correlates With Deregulation of the Mitochondrial Fusion/Fission Machinery

Scientific Reports

Multidisciplinary

English

Reducing Complexity: Explaining Inborn Errors of Metabolism and Their Treatment to Children and Adolescents

Orphanet Journal of Rare Diseases

English

Three New Cases of Late-Onset cblC Defect and Review of the Literature Illustrating When to Consider Inborn Errors of Metabolism Beyond Infancy

Orphanet Journal of Rare Diseases

English

Frenotomy for Tongue‐tie (Frenulum Linguae Breve) Showed Improved Symptoms in the Short and Long Term Follow‐up

Acta Paediatrica, International Journal of Paediatrics

English

MNGIE Syndrome: Liver Cirrhosis Should Be Ruled Out Prior to Bone Marrow Transplantation

Internal Medicine

Molecular Biology

English

Versorgung Von Kindern Und Jugendlichen Mit Diabetes an Österreichs Schulen

Monatsschrift fur Kinderheilkunde

English