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Results of search for 'au:"Berthet, M"', page 2 of 2
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Authors
Baroudi, G
Bennaceur, M
Berthet, M
Cauchemez, B
Chahine, M
Cheav, T
Coumel, P
Denjoy, I
Donger, C
Guicheney, P
Hainque, B
Klug, D
Li, J Y
Lupoglazoff, J M
Neyroud, N
Pagesy, P
Peillon, F
Richard, P
Schwartz, K
Villain, E
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Topics
Adolescent
Adult
Amino Acid Sequence
Animals
Base Sequence
Cation Transport Proteins
Child
Child, Preschool
DNA-Binding Proteins
Electrocardiography
Female
Humans
Long QT Syndrome
Male
Middle Aged
Pedigree
Potassium Channels
Potassium Channels, Voltage-Gated
analysis
genetics
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English
French
Your search returned 24 results.
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21.
[Congenital long QT syndrome. The value of genetics in prognostic evaluation].
[electronic resource]
by
Denjoy, I
Lupoglazoff, J M
Donger, C
Berthet, M
Richard, P
Neyroud, N
Villain, E
Lucet, V
Coumel, P
Guicheney, P
Producer:
19990720
In:
Archives des maladies du coeur et des vaisseaux
vol. 92
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No items available.
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22.
[Neonatal forms of congenital long QT syndrome].
[electronic resource]
by
Lupoglazoff, J M
Denjoy, I
Villain, E
Fressart, V
Legall-Petit, I
Bozio, A
Berthet, M
Benammar, N
Hainque, B
Guicheney, P
Producer:
20041109
In:
Archives des maladies du coeur et des vaisseaux
vol. 97
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23.
C-terminal HERG mutations: the role of hypokalemia and a KCNQ1-associated mutation in cardiac event occurrence.
[electronic resource]
by
Berthet, M
Denjoy, I
Donger, C
Demay, L
Hammoude, H
Klug, D
Schulze-Bahr, E
Richard, P
Funke, H
Schwartz, K
Coumel, P
Hainque, B
Guicheney, P
Producer:
19990414
In:
Circulation
vol. 99
Online resources:
Available from publisher's website
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24.
Notched T waves on Holter recordings enhance detection of patients with LQt2 (HERG) mutations.
[electronic resource]
by
Lupoglazoff, J M
Denjoy, I
Berthet, M
Neyroud, N
Demay, L
Richard, P
Hainque, B
Vaksmann, G
Klug, D
Leenhardt, A
Maillard, G
Coumel, P
Guicheney, P
Producer:
20010614
In:
Circulation
vol. 103
Online resources:
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