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Publications by Lisbeth Tranebjaerg

3-Methylglutaconic Aciduria—lessons From 50 Genes and 977 Patients

Journal of Inherited Metabolic Disease
Genetics
2013English

Effects of Human Deafness Γ-Actin Mutations (DFNA20/26) on Actin Function

Journal of Biological Chemistry
BiochemistryCell BiologyMolecular Biology
2006English

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Iron‐sulfur Cluster ISD11 Deficiency ( LYRM4 Gene) Presenting as Cardiorespiratory Arrest and 3‐methylglutaconic Aciduria

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2019English

Leucine Loading Test Is Only Discriminative for 3-Methylglutaconic Aciduria Due to AUH Defect

JIMD Reports
Internal MedicineGeneticsMolecular BiologyBiochemistryEndocrinologyMetabolismDiabetes
2014English

CLPB Mutations Cause 3-Methylglutaconic Aciduria, Progressive Brain Atrophy, Intellectual Disability, Congenital Neutropenia, Cataracts, Movement Disorder

American Journal of Human Genetics
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2015English

3-Hydroxy-3-Methylglutaric Aciduria

2020English

CDC's First 50 Years: Lessons Learned and Relearned.

American Journal of Public Health
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1996English

Rare Disease Genes—Lessons and Challenges

Genome Research
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1997English

CDC at 50: Lessons to Be Learned.

American Journal of Public Health
EnvironmentalPublic HealthOccupational Health
1998English

Newly Identified Genes Linked to Endometrial Receptiveness: Lessons From IVF

Biomarkers in Medicine
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2009English

3-Hydroxy-3-Methylglutaric Aciduria With Bilateral Basal Ganglia Lesion: A Case Report

Experimental and Therapeutic Medicine
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2016English

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