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Muggenthaler, M.
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1

Whole exome sequence analysis reveals a homozygous mutation..:

Muggenthaler, M. ; Petropoulou, E. ; Omer, S....
International Journal of Cardiology.  210 (2016)  - p. 41-44 , 2016
Link: https://doi.org/10.1016/..
 
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2

Prätherapeutische Ablaufanalyse bei einem Massenanfall von ..:

Mück, F. ; Wirth, K. ; Muggenthaler, M....
Der Unfallchirurg.  119 (2016)  8 - p. 632-641 , 2016
Link: https://doi.org/10.1007/..
 
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3

16 * Ethnicity and phenotype in the SCN5A E1784K mutation:

Wijeyeratne, Y. D. ; Muggenthaler, M. ; Batchvarov, V....
Europace.  16 (2014)  suppl 3 - p. iii7-iii7 , 2014
Link: https://doi.org/10.1093/..
 
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4

Brugada syndrome and atrial fibrillation: pathophysiology a..:

Muggenthaler, M. ; Behr, E. R.
Europace.  13 (2011)  7 - p. 913-915 , 2011
Link: https://doi.org/10.1093/..
 
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5

MNS1 variant associated with situs inversus and male infert..:

Leslie, Joseph S. ; Rawlins, Lettie E. ; Chioza, Barry A....
European Journal of Human Genetics.  28 (2019)  1 - p. 50-55 , 2019
Link: https://doi.org/10.1038/..
 
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6

Mutations in HYAL2, Encoding Hyaluronidase 2, Cause a Syndr..:

Muggenthaler, Martina M. A. ; Chowdhury, Biswajit ; Hasan, S. Naimul...
PLOS Genetics.  13 (2017)  1 - p. e1006470 , 2017
Link: https://doi.org/10.1371/..
 
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7

Scn5a mutation type and a genetic risk score associate vari..:

Wijeyeratne, Y.D ; Tanck, M.W ; Mizusawa, Y...
info:eu-repo/semantics/altIdentifier/doi/10.1161/CIRCGEN.120.002911.  , 2020
Link: https://push-zb.helmholt..
 
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8

SCN5A mutation type and a genetic risk score associate vari..:

Wijeyeratne Y. D ; Tanck M. W ; Mizusawa Y...
info:eu-repo/semantics/altIdentifier/pmid/33164571.  , 2020
Link: http://hdl.handle.net/10..
 
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9

SCN5A Mutation Type and a Genetic Risk Score Associate Vari..:

Wijeyeratne, YD ; Tanck, MW ; Mizusawa, Y...
https://openaccess.sgul.ac.uk/id/eprint/112608/1/CIRCGEN.120.002911.pdf.  , 2020
Link: https://openaccess.sgul...
 
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10

Whole exome sequence analysis reveals a homozygous mutation..:

Muggenthaler, M ; Petropoulou, E ; Omer, S...
https://openaccess.sgul.ac.uk/id/eprint/107736/7/IJC-D-15-05769R1.pdf.  , 2016
Link: https://openaccess.sgul...
 
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11

MNS1 variant associated with situs inversus and male infert..:

Rawlins, Lettie E ; Fasham, James ; Muggenthaler, Martina M A..
http://dx.doi.org/10.1038/s41431-019-0489-z.  , 2020
Link: https://doi.org/10.1038/..
 
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12

MNS1 variant associated with situs inversus and male infert..:

Leslie, Joseph S ; Rawlins, Lettie E ; Chioza, Barry A...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6906318/.  , 2019
Link: http://www.ncbi.nlm.nih...
 
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13

Mutations in HYAL2, Encoding Hyaluronidase 2, Cause a Syndr..:

Muggenthaler, Martina M. A ; Chowdhury, Biswajit ; Hasan, S. Naimul...
http://dx.plos.org/10.1371/journal.pgen.1006470.  , 2017
Link: http://hdl.handle.net/10..
 
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14

Mutations in HYAL2, Encoding Hyaluronidase 2, Cause a Syndr..:

Martina M A Muggenthaler ; Biswajit Chowdhury ; S Naimul Hasan...
http://europepmc.org/articles/PMC5230738?pdf=render.  , 2017
Link: https://doi.org/10.1371/..
 
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15

Abhängigkeit der Stichkraft von der Klingenform – Entwicklu..:

Hunold, T. ; Spieß, R. ; Wissenbach, D. K....
Rechtsmedizin.  33 (2023)  4 - p. 269-274 , 2023
Link: https://doi.org/10.1007/..
 
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