Chris Mühlhausen - Concepedia

Author

Chris Mühlhausen

University Medical Center Hamburg-Eppendorf ORCID

Also Known As

C Mühlhausen, C. Muhlhausen, C. MÜHlhausen, C. Mühlhausen, Chris Mühlhausen, Chris Mühlhausen, Pablo Mir

Publications

4.3K

Citations

H-Index

Concepts

All Affiliations

University Medical Center Hamburg-Eppendorf Universität Hamburg University Hospital Heidelberg Heidelberg University Heinrich Heine University Düsseldorf

About

Chris Mühlhausen is an author at University Medical Center Hamburg-Eppendorf specializing in medicine, metabolism, and physiology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	15	16	1.5K
2	Natural Sciences	5	5	992
3	Engineering	1	1	40
4	Health Sciences	1	1	20
5	Public Health	1	1	18

Chris Mühlhausen

Publications

3.4K

Citations

H-Index

Page 1

	Year	Citations
Lysine Glutarylation Is a Protein Posttranslational Modification Regulated by SIRT5 Minjia Tan, Chao Peng, Kristin A. Anderson, Cell Metabolism Protein FunctionSignal TransductionProtein ExpressionMolecular RegulationLysine Glutarylation	2014	860
The phenotypic spectrum of organic acidurias and urea cycle disorders. Part 1: the initial presentation Stefan Kölker, Ángeles García Cazorla, Vassili Valayannopoulos, Journal of Inherited Metabolic Disease	2015	242
The phenotypic spectrum of organic acidurias and urea cycle disorders. Part 2: the evolving clinical phenotype Stefan Kölker, Vassili Valayannopoulos, Alberto Burlina, Journal of Inherited Metabolic Disease	2015	229
Dynamic changes of striatal and extrastriatal abnormalities in glutaric aciduria type I Inga Harting, Eva Neumaier‐Probst, Angelika Seitz, Brain	2009	173
Use of guidelines improves the neurological outcome in glutaric aciduria type I Jana Herınger, S. P. Nikolas Boy, Regina Ensenauer, Annals of Neurology	2010	168
Intracerebral accumulation of glutaric and 3‐hydroxyglutaric acids secondary to limited flux across the blood–brain barrier constitute a biochemical risk factor for neurodegeneration in glutaryl‐CoA dehydrogenase deficiency Sven W. Sauer, Jürgen G. Okun, Gert Fricker, Journal of Neurochemistry	2006	162
Scoring Evaluation of the Natural Course of Mucopolysaccharidosis Type IIIA (Sanfilippo Syndrome Type A) Ann Meyer, Kai Kossow, Andreas Gal, PEDIATRICS	2007	112
Decline of Acute Encephalopathic Crises in Children with Glutaryl-CoA Dehydrogenase Deficiency Identified by Newborn Screening in Germany Stefan Kölker, Sven F. Garbade, Nikolas Boy, Pediatric Research Acute Encephalopathic CrisesNewborn ScreeningNeonatologyPediatric HydrocephalusPediatric Hematology	2007	111
Bi-allelic Truncating Mutations in TANGO2 Cause Infancy-Onset Recurrent Metabolic Crises with Encephalocardiomyopathy Laura S. Kremer, Felix Distelmaier, Bader Alhaddad, The American Journal of Human Genetics CardiomyopathyGenetic DisorderGeneticsMolecular GeneticsBi-allelic Truncating Mutations	2016	105
Newborn screening: A disease‐changing intervention for glutaric aciduria type 1 Nikolas Boy, Katharina Mengler, Eva Thimm, Annals of Neurology	2018	104

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