| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Altered functional properties of a missense variant in the TRESK K+ channel (KCNK18) associated with migraine and intellectual disability
|
Imbrici, Paola
|
|
|
472 |
7 |
p. 923-930
|
artikel
|
| 2 |
Cardiac and neuronal HCN channelopathies
|
Rivolta, Ilaria
|
|
|
472 |
7 |
p. 931-951
|
artikel
|
| 3 |
Cav1.2 channelopathies causing autism: new hallmarks on Timothy syndrome
|
Marcantoni, Andrea
|
|
|
472 |
7 |
p. 775-789
|
artikel
|
| 4 |
Cav2.3 R-type calcium channels: from its discovery to pathogenic de novo CACNA1E variants: a historical perspective
|
Schneider, T.
|
|
|
472 |
7 |
p. 811-816
|
artikel
|
| 5 |
Channelopathies of voltage-gated L-type Cav1.3/α1D and T-type Cav3.1/α1G Ca2+ channels in dysfunction of heart automaticity
|
Torrente, Angelo G.
|
|
|
472 |
7 |
p. 817-830
|
artikel
|
| 6 |
De novo CACAN1D Ca2+ channelopathies: clinical phenotypes and molecular mechanism
|
Ortner, Nadine J.
|
|
|
472 |
7 |
p. 755-773
|
artikel
|
| 7 |
Electromechanical coupling of the Kv1.1 voltage-gated K+ channel is fine-tuned by the simplest amino acid residue in the S4-S5 linker
|
Hasan, Sonia
|
|
|
472 |
7 |
p. 899-909
|
artikel
|
| 8 |
Epileptic channelopathies caused by neuronal Kv7 (KCNQ) channel dysfunction
|
Nappi, Piera
|
|
|
472 |
7 |
p. 881-898
|
artikel
|
| 9 |
Intracellular Cl− dysregulation causing and caused by pathogenic neuronal activity
|
Akita, Tenpei
|
|
|
472 |
7 |
p. 977-987
|
artikel
|
| 10 |
Ion channelopathies to bridge molecular lesions, channel function, and clinical therapies
|
Carbone, Emilio
|
|
|
472 |
7 |
p. 733-738
|
artikel
|
| 11 |
Neuronal Cav3 channelopathies: recent progress and perspectives
|
Lory, Philippe
|
|
|
472 |
7 |
p. 831-844
|
artikel
|
| 12 |
Neuronal α2δ proteins and brain disorders
|
Ablinger, Cornelia
|
|
|
472 |
7 |
p. 845-863
|
artikel
|
| 13 |
Painful and painless mutations of SCN9A and SCN11A voltage-gated sodium channels
|
Baker, Mark D.
|
|
|
472 |
7 |
p. 865-880
|
artikel
|
| 14 |
Rare CACNA1A mutations leading to congenital ataxia
|
Izquierdo-Serra, Mercè
|
|
|
472 |
7 |
p. 791-809
|
artikel
|
| 15 |
Skeletal muscle CaV1.1 channelopathies
|
Flucher, Bernhard E.
|
|
|
472 |
7 |
p. 739-754
|
artikel
|
| 16 |
Skeletal muscle ClC-1 chloride channels in health and diseases
|
Altamura, Concetta
|
|
|
472 |
7 |
p. 961-975
|
artikel
|
| 17 |
TASK channels: channelopathies, trafficking, and receptor-mediated inhibition
|
Inoue, Masumi
|
|
|
472 |
7 |
p. 911-922
|
artikel
|
| 18 |
TRPA1 gene variants hurting our feelings
|
Naert, Robbe
|
|
|
472 |
7 |
p. 953-960
|
artikel
|
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