Works matching IS 00316768 AND DT 2020 AND VI 472 AND IP 7
Results: 18
Painful and painless mutations of SCN9A and SCN11A voltage-gated sodium channels.
- Published in:
- Pflügers Archiv: European Journal of Physiology, 2020, v. 472, n. 7, p. 865, doi. 10.1007/s00424-020-02419-9
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- Publication type:
- Article
Rare CACNA1A mutations leading to congenital ataxia.
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- Pflügers Archiv: European Journal of Physiology, 2020, v. 472, n. 7, p. 791, doi. 10.1007/s00424-020-02396-z
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- Publication type:
- Article
Cav1.2 channelopathies causing autism: new hallmarks on Timothy syndrome.
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- Pflügers Archiv: European Journal of Physiology, 2020, v. 472, n. 7, p. 775, doi. 10.1007/s00424-020-02430-0
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- Publication type:
- Article
Neuronal Cav3 channelopathies: recent progress and perspectives.
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- Pflügers Archiv: European Journal of Physiology, 2020, v. 472, n. 7, p. 831, doi. 10.1007/s00424-020-02429-7
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- Article
Ion channelopathies to bridge molecular lesions, channel function, and clinical therapies.
- Published in:
- 2020
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- Publication type:
- Editorial
Neuronal α2δ proteins and brain disorders.
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- Pflügers Archiv: European Journal of Physiology, 2020, v. 472, n. 7, p. 845, doi. 10.1007/s00424-020-02420-2
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- Publication type:
- Article
Channelopathies of voltage-gated L-type Cav1.3/α1D and T-type Cav3.1/α1G Ca2+ channels in dysfunction of heart automaticity.
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- Pflügers Archiv: European Journal of Physiology, 2020, v. 472, n. 7, p. 817, doi. 10.1007/s00424-020-02421-1
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- Publication type:
- Article
Cav2.3 R-type calcium channels: from its discovery to pathogenic de novo CACNA1E variants: a historical perspective.
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- Pflügers Archiv: European Journal of Physiology, 2020, v. 472, n. 7, p. 811, doi. 10.1007/s00424-020-02395-0
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- Publication type:
- Article
De novo CACAN1D Ca2+ channelopathies: clinical phenotypes and molecular mechanism.
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- Pflügers Archiv: European Journal of Physiology, 2020, v. 472, n. 7, p. 755, doi. 10.1007/s00424-020-02418-w
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- Publication type:
- Article
Electromechanical coupling of the Kv1.1 voltage-gated K+ channel is fine-tuned by the simplest amino acid residue in the S4-S5 linker.
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- Pflügers Archiv: European Journal of Physiology, 2020, v. 472, n. 7, p. 899, doi. 10.1007/s00424-020-02414-0
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- Publication type:
- Article
TASK channels: channelopathies, trafficking, and receptor-mediated inhibition.
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- Pflügers Archiv: European Journal of Physiology, 2020, v. 472, n. 7, p. 911, doi. 10.1007/s00424-020-02403-3
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- Publication type:
- Article
Epileptic channelopathies caused by neuronal Kv7 (KCNQ) channel dysfunction.
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- Pflügers Archiv: European Journal of Physiology, 2020, v. 472, n. 7, p. 881, doi. 10.1007/s00424-020-02404-2
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- Publication type:
- Article
TRPA1 gene variants hurting our feelings.
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- Pflügers Archiv: European Journal of Physiology, 2020, v. 472, n. 7, p. 953, doi. 10.1007/s00424-020-02397-y
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- Publication type:
- Article
Cardiac and neuronal HCN channelopathies.
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- Pflügers Archiv: European Journal of Physiology, 2020, v. 472, n. 7, p. 931, doi. 10.1007/s00424-020-02384-3
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- Publication type:
- Article
Altered functional properties of a missense variant in the TRESK K+ channel (KCNK18) associated with migraine and intellectual disability.
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- Pflügers Archiv: European Journal of Physiology, 2020, v. 472, n. 7, p. 923, doi. 10.1007/s00424-020-02382-5
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- Publication type:
- Article
Skeletal muscle ClC-1 chloride channels in health and diseases.
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- Pflügers Archiv: European Journal of Physiology, 2020, v. 472, n. 7, p. 961, doi. 10.1007/s00424-020-02376-3
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- Publication type:
- Article
Intracellular Cl− dysregulation causing and caused by pathogenic neuronal activity.
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- Pflügers Archiv: European Journal of Physiology, 2020, v. 472, n. 7, p. 977, doi. 10.1007/s00424-020-02375-4
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- Publication type:
- Article
Skeletal muscle CaV1.1 channelopathies.
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- Pflügers Archiv: European Journal of Physiology, 2020, v. 472, n. 7, p. 739, doi. 10.1007/s00424-020-02368-3
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- Publication type:
- Article