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Clinical, genetic, and expression studies of mutations in the potassium channel gene KCNA1 reveal new phenotypic variability

Annals of neurology, 2000-10, Vol.48 (4), p.647-656

2000

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A novel mutation in the human voltage-gated potassium channel gene (Kv1.1) associates with episodic ataxia type 1 and sometimes with partial epilepsy

Brain (London, England : 1878), 1999-05, Vol.122 (5), p.817-825

1999

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Human epilepsy associated with dysfunction of the brain P/Q-type calcium channel

The Lancet (British edition), 2001-09, Vol.358 (9284), p.801-807

2001

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Hauptsache trocken! Reicht das? Der „Qualifizierte Entzug“, eine suchtmedizinische Errungenschaft

Suchttherapie, 2012, Vol.13 (4)

Spauschus, A

2012

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Variable K+ channel subunit dysfunction in inherited mutations of KCNA1

The Journal of physiology, 2002-01, Vol.538 (1), p.5-23

2002

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The molecular biology of the autosomal-dominant cerebellar ataxias

Movement disorders, 2000-07, Vol.15 (4), p.604-612

2000

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The origin of ocular microtremor in man

Experimental brain research, 1999-06, Vol.126 (4), p.556-562

1999

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A G-protein-activated inwardly rectifying K+ channel (GIRK4) from human hippocampus associates with other GIRK channels

The Journal of neuroscience, 1996-02, Vol.16 (3), p.930-938

1996

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Position statement: Are urban dwellers more depressed and anxious than the rural population? Results of a representative survey

Psychotherapie, Psychosomatik, medizinische Psychologie, 2013-11, Vol.63 (11), p.455

2013

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Subunit Interactions in the Assembly of Neuronal Kir3.0 Inwardly Rectifying K+Channels

Molecular and cellular neuroscience, 1997, Vol.9 (3), p.194-206

1997

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Functional Characterization of a Novel Mutation in KCNA1 in Episodic Ataxia Type 1 Associated with Epilepsy

Annals of the New York Academy of Sciences, 1999-04, Vol.868 (1), p.442-446

1999

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The Inherited Episodic Ataxias: How Well Do We Understand the Disease Mechanisms?

The Neuroscientist (Baltimore, Md.), 2001-02, Vol.7 (1), p.80-88

2001

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Episodic-ataxia-type-1-mutation in Kv1.1 reduces the current amplitude and alters the biophysical properties

Aktuelle Neurologie, 2004, Vol.31 (S 1)

2004

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A Hyperprostaglandin E Syndrome Mutation in Kir1.1 (Renal Outer Medullary Potassium) Channels Reveals a Crucial Residue for Channel Function in Kir1.3 Channels

The Journal of biological chemistry, 1998-09, Vol.273 (37), p.23884-23891

1998

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Intensivierte ambulante Disulfiram-gestützte Nachbehandlung alkoholabhängiger Patienten: erste Erfahrungen aus Hamburg

Suchttherapie, 2010-05, Vol.11 (2), p.85-88

2010

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Functional Expression and Cellular mRNA Localization of a G Protein-Activated K+inward Rectifier Isolated from Rat Brain

Biochemical and biophysical research communications, 1996-06, Vol.223 (2), p.474-479

1996

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Recanalization of an a. lusoria occlusion with PTA and stent

RöFo : Fortschritte auf dem Gebiet der Röntgenstrahlen und der bildgebende Verfahren, 2003-02, Vol.175 (2), p.289

2003

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Rekanalisation eines A. lusoria-Verschlusses mittels PTA und Stent

RöFo : Fortschritte auf dem Gebiet der Röntgenstrahlen und der bildgebende Verfahren, 2003-02, Vol.175 (2), p.289-290

2003

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Subunit interactions in the assembly of neuronal Kir3.0 inwardly rectifying K super(+) channels

Molecular and cellular neuroscience, 1997-01, Vol.9 (3), p.194-206

1997

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A G-protein-activated inwardly rectifying K super(+) channel (GIRK4) from human hippocampus associates with other GIRK channels

The Journal of neuroscience, 1996-01, Vol.16 (3), p.930-938

1996

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042 Familial generalized myokymia: A new potassium channelopathy

European journal of paediatric neurology, 1999, Vol.3 (6), p.A123-A124

1999

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Moschcowitz syndrome mimicking basilar pathology

Aktuelle Neurologie, 2004, Vol.31 (S 1)

2004

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Are urban dwellers more depressed and anxious than the rural population? Results of a representative survey

Psychotherapie, Psychosomatik, medizinische Psychologie, 2013-11, Vol.63 (11), p.445

2013

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Acute, Non-Lethal Marchiafava-Bignami Disease With Reversible Posterior Leucoencephalopathy and Split-Brain Syndrome

The journal of neuropsychiatry and clinical neurosciences, 2011-10, Vol.23 (4), p.E27-E28

2011

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Potassium channel dysfunction and depolarized resting membrane potential in a cell model of SCA3

Experimental neurology, 2006-09, Vol.201 (1), p.182-192

2006

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Clinical, genetic, and expression studies of mutations in the potassium channel gene KCNA1 reveal new phenotypic variability

A novel mutation in the human voltage-gated potassium channel gene (Kv1.1) associates with episodic ataxia type 1 and sometimes with partial epilepsy

Human epilepsy associated with dysfunction of the brain P/Q-type calcium channel

Hauptsache trocken! Reicht das? Der „Qualifizierte Entzug“, eine suchtmedizinische Errungenschaft

Variable K+ channel subunit dysfunction in inherited mutations of KCNA1

The molecular biology of the autosomal-dominant cerebellar ataxias

The origin of ocular microtremor in man

A G-protein-activated inwardly rectifying K+ channel (GIRK4) from human hippocampus associates with other GIRK channels

Position statement: Are urban dwellers more depressed and anxious than the rural population? Results of a representative survey

Subunit Interactions in the Assembly of Neuronal Kir3.0 Inwardly Rectifying K+Channels

Functional Characterization of a Novel Mutation in KCNA1 in Episodic Ataxia Type 1 Associated with Epilepsy

The Inherited Episodic Ataxias: How Well Do We Understand the Disease Mechanisms?

Episodic-ataxia-type-1-mutation in Kv1.1 reduces the current amplitude and alters the biophysical properties

A Hyperprostaglandin E Syndrome Mutation in Kir1.1 (Renal Outer Medullary Potassium) Channels Reveals a Crucial Residue for Channel Function in Kir1.3 Channels

Intensivierte ambulante Disulfiram-gestützte Nachbehandlung alkoholabhängiger Patienten: erste Erfahrungen aus Hamburg

Functional Expression and Cellular mRNA Localization of a G Protein-Activated K+inward Rectifier Isolated from Rat Brain

Recanalization of an a. lusoria occlusion with PTA and stent

Rekanalisation eines A. lusoria-Verschlusses mittels PTA und Stent

Subunit interactions in the assembly of neuronal Kir3.0 inwardly rectifying K super(+) channels

A G-protein-activated inwardly rectifying K super(+) channel (GIRK4) from human hippocampus associates with other GIRK channels

042 Familial generalized myokymia: A new potassium channelopathy

Moschcowitz syndrome mimicking basilar pathology

Are urban dwellers more depressed and anxious than the rural population? Results of a representative survey

Acute, Non-Lethal Marchiafava-Bignami Disease With Reversible Posterior Leucoencephalopathy and Split-Brain Syndrome

Potassium channel dysfunction and depolarized resting membrane potential in a cell model of SCA3

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