Biancalana, V
63  Ergebnisse:
Personensuche X
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1

New mutations identified in a case of Glycogenin-1 deficien..:

Pruvost, R ; Csanyi, M ; Lefebvre, G...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10792954/.  , 2024
 
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2

Electromagnetic induction imaging: Signal detection based o..:

Bevilacqua G ; Biancalana V ; Dancheva Y...
info:eu-repo/semantics/altIdentifier/wos/WOS:000716468800007.  , 2021
 
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3

Studying and applying magnetic dressing with a Bell and Blo..:

Bevilacqua, G ; Biancalana, V ; Dancheva, Y.
info:eu-repo/semantics/altIdentifier/wos/WOS:000700377600018.  , 2021
 
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4

Homozygous C-terminal loss-of-function NaV1.4 variant in a ..:

Echaniz-Laguna, A ; Biancalana, V ; Nadaj-Pakleza, A...
https://discovery.ucl.ac.uk/id/eprint/10107087/1/Homozygous%20C-terminal%20loss-of-function%20NaV1.4%20variant%20in%20a%20patient%20with%20congenital%20myasthenic%20syndrome%20.pdf.  , 2020
 
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7

Forty years after the first dark resonance experiment: An o..:

Mariotti, E ; Bevilacqua, G ; Biancalana, V...
https://discovery.ucl.ac.uk/id/eprint/1534645/1/Marmugi_Forty%20years%20after%20the%20first%20dark%20resonance%20experiment%20-%20An%20overview%20of%20the%20COSMA%20project%20results.pdf.  , 2017
 
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9

Dihydropyridine receptor (DHPR, CACNA1S) congenital myopath:

Schartner, V ; Romero, NB ; Donkervoort, S...
https://discovery.ucl.ac.uk/id/eprint/10051648/1/Matthews%20161207DHPRmanuscript%20post%20revisions.pdf.  , 2016
 
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