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Christiane Kehrer Selected Research

AB Variant Tay-Sachs Disease

4/2017Rare Variant of GM2 Gangliosidosis through Activator-Protein Deficiency.

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Christiane Kehrer Research Topics

Disease

5Metachromatic Leukodystrophy (Sulfatide Lipidosis)
01/2022 - 01/2016
2Neurodegenerative Diseases (Neurodegenerative Disease)
03/2021 - 10/2020
2Disease Progression
11/2020 - 09/2020
1Deglutition Disorders (Dysphagia)
12/2021
1Dysostoses
03/2021
1Ichthyosis (Xeroderma)
03/2021
1Lysosomal Storage Diseases (Lysosomal Storage Disease)
03/2021
1Multiple Sulfatase Deficiency Disease (Mucosulfatidosis)
03/2021
1Mucopolysaccharidoses
11/2020
1Chondrodysplasia Punctata (Stippled Epiphyses)
11/2020
1X-Linked Ichthyosis (Ichthyosis, X Linked)
11/2020
1Globoid Cell Leukodystrophy (Krabbe Disease)
10/2020
1Seizures (Absence Seizure)
10/2020
1GM2 Gangliosidoses (GM2 Gangliosidosis)
04/2017
1AB Variant Tay-Sachs Disease
04/2017

Drug/Important Bio-Agent (IBA)

2Cerebroside-Sulfatase (Arylsulfatase A)IBA
01/2022 - 03/2021
2SulfatasesIBA
03/2021 - 11/2020
2EnzymesIBA
03/2021 - 10/2020
1N-formylglycineIBA
03/2021
1Sulfoglycosphingolipids (Sulfatides)IBA
03/2021
1GalactosylceramidaseIBA
10/2020
1Hexosaminidase BIBA
04/2017
1Hexosaminidase A (Hex A)IBA
04/2017
1G(M2) Activator ProteinIBA
04/2017

Therapy/Procedure

3Hematopoietic Stem Cell Transplantation
01/2022 - 01/2016
2Enteral Nutrition (Feeding, Tube)
12/2021 - 10/2020
1Transplantation
09/2020