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Min Ae Lee-Kirsch

Ärztin

Name	Min Ae Lee-Kirsch
Profession	Ärztin (characteristic profession) Kinderärztin
Variant	Min Ae Lee- Kirsch
Record type	Person
GND-Identifier	136595715
Record ID	136595715
Involved in show all Variable Syndromic Immunodeficiency in Patients with Biallelic PRIM1 Mutations Die Aktivität der Cytochrom-c-Oxidase bei Morbus Wilson-Patient*innen unter kupfersenkender Therapie Etablierung eines reprogrammierten humanen neuronalen Modells zur Untersuchung einer entzündlichen Leukodystrophie Intrazelluläre Stressmechanismen in Fibroblasten von Patienten mit myotoner Dystrophie Using CRISPR-Cas9 Techniques to Model Type I Interferonopathies Variable syndromic immunodeficiency in patients with Biallelic PRIM1 mutations The role of Samhd1 in controlling DNA damage and tumour development in in vivo models Der klinische Versorgungspfad zur multiprofessionellen Versorgung seltener Erkrankungen in der Pädiatrie – Ergebnisse aus dem Projekt TRANSLATE-NAMSE An Integrated clinical pathway for diagnosis, treatment and care of rare diseases: model, operating procedures, and results of the project TRANSLATE-NAMSE funded by the German Federal Joint Committee Curative Treatment of POMP-Related Autoinflammation and Immune Dysregulation (PRAID) by Hematopoietic Stem Cell Transplantation Curative treatment of POMP-related autoinflammation and immune dysregulation (PRAID) by hematopoietic stem cell transplantation Development of a human in-vitro pathophysiological model of FUS-ALS based on the induced pluripotent stem-cell technique and translation to patient phenotypes Genetische Ursachen und ein neuer therapeutischer Ansatz für einen monogenetischen systemischen Lupus erythematodes The role of molecular mimicry between GAD65 and coxsackievirus B4 in the pathogenesis of type 1 diabetes The status quo of rare diseases centres for the development of a clinical decision support system - a cross-sectional study Assignment of the human homeobox 11-like 2 gene (HOX11L2) to chromosome 5q34→q35 by radiation hybrid mapping Familial Chilblain Lupus – A Monogenic Form of Cutaneous Lupus Erythematosus due to a Heterozygous Mutation in TREX1 Phenotypic Variability in a Family with Aicardi-Goutières Syndrome Due to the Common A177T RNASEH2B Mutation Molekulargenetische Analyse multifaktorieller Krankheiten

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Katalog der Deutschen Nationalbibliothek

Min Ae Lee-Kirsch

Variable Syndromic Immunodeficiency in Patients with Biallelic PRIM1 Mutations

Die Aktivität der Cytochrom-c-Oxidase bei Morbus Wilson-Patient*innen unter kupfersenkender Therapie

Etablierung eines reprogrammierten humanen neuronalen Modells zur Untersuchung einer entzündlichen Leukodystrophie

Intrazelluläre Stressmechanismen in Fibroblasten von Patienten mit myotoner Dystrophie

Using CRISPR-Cas9 Techniques to Model Type I Interferonopathies

Variable syndromic immunodeficiency in patients with Biallelic PRIM1 mutations

The role of Samhd1 in controlling DNA damage and tumour development in in vivo models

Der klinische Versorgungspfad zur multiprofessionellen Versorgung seltener Erkrankungen in der Pädiatrie – Ergebnisse aus dem Projekt TRANSLATE-NAMSE

An Integrated clinical pathway for diagnosis, treatment and care of rare diseases: model, operating procedures, and results of the project TRANSLATE-NAMSE funded by the German Federal Joint Committee

Curative Treatment of POMP-Related Autoinflammation and Immune Dysregulation (PRAID) by Hematopoietic Stem Cell Transplantation

Curative treatment of POMP-related autoinflammation and immune dysregulation (PRAID) by hematopoietic stem cell transplantation

Development of a human in-vitro pathophysiological model of FUS-ALS based on the induced pluripotent stem-cell technique and translation to patient phenotypes

Genetische Ursachen und ein neuer therapeutischer Ansatz für einen monogenetischen systemischen Lupus erythematodes

The role of molecular mimicry between GAD65 and coxsackievirus B4 in the pathogenesis of type 1 diabetes

The status quo of rare diseases centres for the development of a clinical decision support system - a cross-sectional study

Assignment of the human homeobox 11-like 2 gene (HOX11L2) to chromosome 5q34→q35 by radiation hybrid mapping

Familial Chilblain Lupus – A Monogenic Form of Cutaneous Lupus Erythematosus due to a Heterozygous Mutation in TREX1

Phenotypic Variability in a Family with Aicardi-Goutières Syndrome Due to the Common A177T RNASEH2B Mutation

Molekulargenetische Analyse multifaktorieller Krankheiten