Volume 472, Issue 7

Search all Pflügers Archiv - European Journal of Physiology articles

July 2020

Special Issue: Channelopathies: from mutation to diseases

Issue Editors:

Emilio Carbone,
Yasuo Mori

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18 articles in this issue

Ion channelopathies to bridge molecular lesions, channel function, and clinical therapies
Emilio Carbone
Yasuo Mori
Editorial 30 June 2020 Pages: 733 - 738
Skeletal muscle Ca_V1.1 channelopathies
Bernhard E. Flucher
Invited Review Open access 28 March 2020 Pages: 739 - 754
De novo CACAN1D Ca²⁺ channelopathies: clinical phenotypes and molecular mechanism
Nadine J. Ortner
Teresa Kaserer
Jörg Striessnig
Invited Review Open access 24 June 2020 Pages: 755 - 773
Cav1.2 channelopathies causing autism: new hallmarks on Timothy syndrome
Andrea Marcantoni
Chiara Calorio
Emilio Carbone
Invited Review 03 July 2020 Pages: 775 - 789
Rare CACNA1A mutations leading to congenital ataxia
Mercè Izquierdo-Serra
José M. Fernández-Fernández
Mercedes Serrano
Invited Review 26 May 2020 Pages: 791 - 809
Cav2.3 R-type calcium channels: from its discovery to pathogenic de novo CACNA1E variants: a historical perspective
T. Schneider
F. Neumaier
S. Alpdogan
Invited Review Open access 11 June 2020 Pages: 811 - 816
Channelopathies of voltage-gated L-type Cav1.3/α_1D and T-type Cav3.1/α_1G Ca²⁺ channels in dysfunction of heart automaticity
Angelo G. Torrente
Pietro Mesirca
Matteo E. Mangoni
Invited Review 29 June 2020 Pages: 817 - 830
Neuronal Cav3 channelopathies: recent progress and perspectives
Philippe Lory
Sophie Nicole
Arnaud Monteil
Invited Review Open access 07 July 2020 Pages: 831 - 844
Neuronal α₂δ proteins and brain disorders
Cornelia Ablinger
Stefanie M. Geisler
Gerald J. Obermair
Invited Review Open access 30 June 2020 Pages: 845 - 863
Painful and painless mutations of SCN9A and SCN11A voltage-gated sodium channels
Mark D. Baker
Mohammed A. Nassar
Invited Review Open access 29 June 2020 Pages: 865 - 880
Epileptic channelopathies caused by neuronal Kv7 (KCNQ) channel dysfunction
Piera Nappi
Francesco Miceli
Maurizio Taglialatela
Invited Review 06 June 2020 Pages: 881 - 898
Electromechanical coupling of the Kv1.1 voltage-gated K⁺ channel is fine-tuned by the simplest amino acid residue in the S4-S5 linker
Sonia Hasan
Alfredo Megaro
Maria Cristina D’Adamo
Original Article 23 June 2020 Pages: 899 - 909
TASK channels: channelopathies, trafficking, and receptor-mediated inhibition
Masumi Inoue
Hidetada Matsuoka
Masaki Kameyama
Invited Review 29 May 2020 Pages: 911 - 922
Altered functional properties of a missense variant in the TRESK K⁺ channel (KCNK18) associated with migraine and intellectual disability
Paola Imbrici
Ehsan Nematian-Ardestani
Maria Cristina D’Adamo
Original Article 12 May 2020 Pages: 923 - 930
Cardiac and neuronal HCN channelopathies
Ilaria Rivolta
Anna Binda
Jacopo C. DiFrancesco
Invited Review 18 May 2020 Pages: 931 - 951
TRPA1 gene variants hurting our feelings
Robbe Naert
Ariel Talavera
Karel Talavera
Invited Review 22 May 2020 Pages: 953 - 960
Skeletal muscle ClC-1 chloride channels in health and diseases
Concetta Altamura
Jean-Francois Desaphy
Paola Imbrici
Invited Review 02 May 2020 Pages: 961 - 975
Intracellular Cl⁻ dysregulation causing and caused by pathogenic neuronal activity
Tenpei Akita
Atsuo Fukuda
Invited Review 17 April 2020 Pages: 977 - 987

Volume 472, Issue 7

Ion channelopathies to bridge molecular lesions, channel function, and clinical therapies

Skeletal muscle Ca_V1.1 channelopathies

De novo CACAN1D Ca²⁺ channelopathies: clinical phenotypes and molecular mechanism

Cav1.2 channelopathies causing autism: new hallmarks on Timothy syndrome

Rare CACNA1A mutations leading to congenital ataxia

Cav2.3 R-type calcium channels: from its discovery to pathogenic de novo CACNA1E variants: a historical perspective

Channelopathies of voltage-gated L-type Cav1.3/α_1D and T-type Cav3.1/α_1G Ca²⁺ channels in dysfunction of heart automaticity

Neuronal Cav3 channelopathies: recent progress and perspectives

Neuronal α₂δ proteins and brain disorders

Painful and painless mutations of SCN9A and SCN11A voltage-gated sodium channels

Epileptic channelopathies caused by neuronal Kv7 (KCNQ) channel dysfunction

Electromechanical coupling of the Kv1.1 voltage-gated K⁺ channel is fine-tuned by the simplest amino acid residue in the S4-S5 linker

TASK channels: channelopathies, trafficking, and receptor-mediated inhibition

Altered functional properties of a missense variant in the TRESK K⁺ channel (KCNK18) associated with migraine and intellectual disability

Cardiac and neuronal HCN channelopathies

TRPA1 gene variants hurting our feelings

Skeletal muscle ClC-1 chloride channels in health and diseases

Intracellular Cl⁻ dysregulation causing and caused by pathogenic neuronal activity

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