Detail page

Knowledge Web

Person

Johannes Krämer (1986-)

Arzt

Name	Johannes Krämer
Time	1986- (Date of birth and death)
Place	Ulm (Wirkungsort) Deutschland
Gender	männlich
Academic degree	Dr.
Profession	Arzt (characteristic profession)
Related	Kinderklinik und Poliklinik (Ulm)
Further information	Dissertation an der Medizinischen Fakultät der Universität Würzburg (2015); seit August 2014 Kinderklinik der Universität Ulm (Assistenzarzt in Facharztweiterbildung Pädiatrie)
Source	Dissertation
Record type	Person
GND-Identifier	1077198787
Record ID	1077198787
Involved in show all Parental and child's psychosocial and financial burden living with an inherited metabolic disease identified by newborn screening Outcomes after newborn screening for propionic and methylmalonic acidemia and homocystinurias Collaborative evaluation study on 18 candidate diseases for newborn screening in 1.77 million samples Isovaleric aciduria identified by newborn screening: strategies to predict disease severity and stratify treatment Long‐term anthropometric development of individuals with inherited metabolic diseases identified by newborn screening Publisher correction: The biochemical subtype is a predictor for cognitive function in glutaric aciduria type 1: a national prospective follow-up study The biochemical subtype is a predictor for cognitive function in glutaric aciduria type 1: a national prospective follow-up study Myokardiale Fibrose bei der Fabry-Kardiomyopathie : systematische nicht-invasive Quantifizierung der Fibrose und deren Bedeutung für die Langzeitprognose

Please note

The beta version does not yet contain all functions and information of the DNB portal catalogue. If you are missing information or want to order a medium, please visit the page in the DNB portal catalogue via the following link:

Katalog der Deutschen Nationalbibliothek

Johannes Krämer (1986-)

Parental and child's psychosocial and financial burden living with an inherited metabolic disease identified by newborn screening

Outcomes after newborn screening for propionic and methylmalonic acidemia and homocystinurias

Collaborative evaluation study on 18 candidate diseases for newborn screening in 1.77 million samples

Isovaleric aciduria identified by newborn screening: strategies to predict disease severity and stratify treatment

Long‐term anthropometric development of individuals with inherited metabolic diseases identified by newborn screening

Publisher correction: The biochemical subtype is a predictor for cognitive function in glutaric aciduria type 1: a national prospective follow-up study

The biochemical subtype is a predictor for cognitive function in glutaric aciduria type 1: a national prospective follow-up study

Myokardiale Fibrose bei der Fabry-Kardiomyopathie : systematische nicht-invasive Quantifizierung der Fibrose und deren Bedeutung für die Langzeitprognose