E-LIB Suche - Ergebnisse für: Bittner, Reginald E.

1

Overlapping and Distinct Features of Cardiac Pathology in I..:

Dorninger, Fabian ; Kiss, Attila ; Rothauer, Peter...
International Journal of Molecular Sciences. 24 (2023) 3 - p. 1884 , 2023

Link: https://doi.org/10.3390/..

2

Proteins implicated in muscular dystrophy and cancer are fu..:

Winter, Lilli ; Kustermann, Monika ; Ernhofer, Büsra...
Life Science Alliance. 5 (2022) 11 - p. e202201367 , 2022

Link: https://doi.org/10.26508..

3

Diagnostik von Myopathien bei Kindern und Jugendlichen; Dia..:

Bernert, Günther ; Ille, Alexandra ; Bittner, Reginald E..
Monatsschrift Kinderheilkunde. 169 (2021) 11 - p. 1093-1103 , 2021

Link: https://doi.org/10.1007/..

4

The bradycardic agent ivabradine decreases conduction veloc..:

Amstetter, Daniel ; Badt, Florian ; Rubi, Lena...
European Journal of Pharmacology. 893 (2021) - p. 173818 , 2021

Link: https://doi.org/10.1016/..

5

Impaired muscle spindle function in murine models of muscul..:

Gerwin, Laura ; Rossmanith, Sarah ; Haupt, Corinna...
The Journal of Physiology. 598 (2020) 8 - p. 1591-1609 , 2020

Link: https://doi.org/10.1113/..

6

Biallelic loss-of-function P4HTM gene variants cause hypoto..:

Rahikkala, Elisa ; Myllykoski, Matti ; Hinttala, Reetta...
Genetics in Medicine. 21 (2019) 10 - p. 2355-2363 , 2019

Link: https://doi.org/10.1038/..

7

Long‐term outcomes in a 25‐year‐old female affected with li..:

Stepien, Karolina M. ; Schmidt, Wolfgang M. ; Bittner, Reginald E....
JIMD Reports. 46 (2019) 1 - p. 4-10 , 2019

Link: https://doi.org/10.1002/..

8

Evidence of mild founderLMOD3mutations causing nemaline myo..:

Schatz, Ulrich A. ; Weiss, Simone ; Wenninger, Stephan...
Neurology. 91 (2018) 18 - p. , 2018

Link: https://doi.org/10.1212/..

9

Acute decompensated heart failure associated with a heterop..:

Auer, Johann ; Wallner, Manfred ; Windpessl, Martin...
European Heart Journal. 37 (2016) 21 - p. 1707-1707 , 2016

Link: https://doi.org/10.1093/..

10

Homozygous SYNE1 mutation causes congenital onset of muscul..:

Baumann, Matthias ; Steichen-Gersdorf, Elisabeth ; Krabichler, Birgit...
European Journal of Human Genetics. 25 (2016) 2 - p. 262-266 , 2016

Link: https://doi.org/10.1038/..

11

A novel therapeutic approach for LPIN1 mutation-associated ..:

Pichler, Karin ; Scholl-Buergi, Sabine ; Birnbacher, Robert...
Muscle & Nerve. 52 (2015) 3 - p. 437-439 , 2015

Link: https://doi.org/10.1002/..

12

Targeted disruption of Hspa4 gene leads to cardiac hypertro..:

Mohamed, Belal A. ; Barakat, Amal Z. ; Zimmermann, Wolfram-Hubertus...
Journal of Molecular and Cellular Cardiology. 53 (2012) 4 - p. 459-468 , 2012

Link: https://doi.org/10.1016/..

13

Impaired L-type Ca2+ channel function in the dystrophic hea..:

Koenig, Xaver ; Dang, Xuan B ; Rubi, Lena...
BMC Pharmacology and Toxicology. 13 (2012) S1 - p. , 2012

Link: https://doi.org/10.1186/..

14

SNP-array based whole genome homozygosity mapping: A quick ..:

Papić, Lea ; Fischer, Dirk ; Trajanoski, Slave...
European Journal of Medical Genetics. 54 (2011) 3 - p. 214-219 , 2011

Link: https://doi.org/10.1016/..

15

DNA Damage, Somatic Aneuploidy, and Malignant Sarcoma Susce..:

Schmidt, Wolfgang M. ; Uddin, Mohammed H. ; Dysek, Sandra...
PLoS Genetics. 7 (2011) 4 - p. e1002042 , 2011

Link: https://doi.org/10.1371/..