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Nav1.4 mutations cause hypokalaemic periodic paralysis by disrupting IIIS4 movement during recovery

Brain (London, England : 1878), 2014-04, Vol.137 (Pt 4), p.998-1008

2014

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German cooperation-network ‘equity in health’—health promotion in settings

Health promotion international, 2018-04, Vol.33 (2), p.318-324

2018

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Systematic Analysis of the Impact of Diagnostic Delay on Bowel Damage in Paediatric Versus Adult Onset Crohn's Disease

Journal of Crohn's and colitis, 2019-09, Vol.13 (10), p.1334-1342

2019

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Enhanced inactivation and pH sensitivity of Na+ channel mutations causing hypokalaemic periodic paralysis type II

Brain (London, England : 1878), 2002-04, Vol.125 (Pt 4), p.835-843

2002

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A spectrum of histopathologic findings in autoimmune liver disease

American journal of clinical pathology, 2000-11, Vol.114 (5), p.705-711

2000

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German cooperation-network ‘equity in health’—health promotion in settings: Table 1

Health promotion international, 2016-09, p.daw069

2016

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Quality of Life in Swiss Paediatric Inflammatory Bowel Disease Patients: Do Patients and Their Parents Experience Disease in the Same Way?

Journal of Crohn's and colitis, 2016-03, Vol.10 (3), p.269-276

2016

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Transient compartment-like syndrome and normokalaemic periodic paralysis due to a Cav1.1 mutation

Brain (London, England : 1878), 2013-12, Vol.136 (12), p.3775-3786

2013

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Transient compartment-like syndrome and normokalaemic periodic paralysis due to a Ca(v)1.1 mutation

Brain (London, England : 1878), 2013-12, Vol.136 (Pt 12), p.3775-3786

2013

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Prognostic value of cell cycle and apoptosis regulatory proteins in mismatch repair-proficient colorectal cancer : A tissue microarray-based approach

American journal of clinical pathology, 2007, Vol.127 (1), p.114-123

2007

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Na sub(V)1.4 mutations cause hypokalaemic periodic paralysis by disrupting IIIS4 movement during recovery

Brain (London, England : 1878), 2014-04, Vol.137 (4), p.998-1008

2014

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Calretinin as a marker for cardiac myxoma : Diagnostic and histogenetic considerations

American journal of clinical pathology, 2000-11, Vol.114 (5), p.754-759

2000

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Transient compartment-like syndrome and normokalaemic periodic paralysis due to a Ca sub(v)1.1 mutation

Brain (London, England : 1878), 2013-12, Vol.136 (12), p.3775-3786

2013

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Hypokalaemic periodic paralysis type 2 caused by mutations at codon 672 in the muscle sodium channel gene SCN4A

Brain (London, England : 1878), 2001-06, Vol.124 (6), p.1091-1099

2001

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Identification of four novel mutations in the C-terminal membrane spanning domain of the ryanodine receptor 1: association with central core disease and alteration of calcium homeostasis

Human molecular genetics, 2001-12, Vol.10 (25), p.2879-2887

2001

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Screening of the Ryanodine Receptor Gene in 105 Malignant Hyperthermia Families: Novel Mutations and Concordance with the in Vitro Contracture Test

Human molecular genetics, 1999-10, Vol.8 (11), p.2055-2062

1999

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A calcium channel mutation causing hypokalemic periodic paralysis

Human molecular genetics, 1994-08, Vol.3 (8), p.1415-1419

1994

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Sight: automating genomic data-mining without programming skills

Bioinformatics, 2004-07, Vol.20 (11), p.1718-1720

2004

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A novel SCN4A mutation causing myotonia aggravated by cold and potassium

Human molecular genetics, 1993-09, Vol.2 (9), p.1349-1353

1993

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Calretinin as a Marker for Cardiac Myxoma

American journal of clinical pathology, 2000-11, Vol.114 (5), p.754-759

2000

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Myotonia levior is a chloride channel disorder

Human molecular genetics, 1995-08, Vol.4 (8), p.1397-1402

1995

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Mutant channels contribute <50% to Na+ current in paramyotonia congenita muscle

Brain (London, England : 1878), 1999-06, Vol.122 (6), p.1085-1092

1999

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Proof of a non-functional muscle chloride channel in recessive myotonia congenita (Becker) by detection of a 4 base pair deletion

Human molecular genetics, 1994-07, Vol.3 (7), p.1123-1128

1994

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Catalase and NO CATALASE ACTIVITY1 Promote Autophagy-Dependent Cell Death in Arabidopsis

The Plant cell, 2013-11, Vol.25 (11), p.4616-4626

2013

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Running: the risk of coronary events : Prevalence and prognostic relevance of coronary atherosclerosis in marathon runners

European heart journal, 2008-08, Vol.29 (15), p.1903-1910

2008

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Nav1.4 mutations cause hypokalaemic periodic paralysis by disrupting IIIS4 movement during recovery

German cooperation-network ‘equity in health’—health promotion in settings

Systematic Analysis of the Impact of Diagnostic Delay on Bowel Damage in Paediatric Versus Adult Onset Crohn's Disease

Enhanced inactivation and pH sensitivity of Na+ channel mutations causing hypokalaemic periodic paralysis type II

A spectrum of histopathologic findings in autoimmune liver disease

German cooperation-network ‘equity in health’—health promotion in settings: Table 1

Quality of Life in Swiss Paediatric Inflammatory Bowel Disease Patients: Do Patients and Their Parents Experience Disease in the Same Way?

Transient compartment-like syndrome and normokalaemic periodic paralysis due to a Cav1.1 mutation

Transient compartment-like syndrome and normokalaemic periodic paralysis due to a Ca(v)1.1 mutation

Prognostic value of cell cycle and apoptosis regulatory proteins in mismatch repair-proficient colorectal cancer : A tissue microarray-based approach

Na sub(V)1.4 mutations cause hypokalaemic periodic paralysis by disrupting IIIS4 movement during recovery

Calretinin as a marker for cardiac myxoma : Diagnostic and histogenetic considerations

Transient compartment-like syndrome and normokalaemic periodic paralysis due to a Ca sub(v)1.1 mutation

Hypokalaemic periodic paralysis type 2 caused by mutations at codon 672 in the muscle sodium channel gene SCN4A

Identification of four novel mutations in the C-terminal membrane spanning domain of the ryanodine receptor 1: association with central core disease and alteration of calcium homeostasis

Screening of the Ryanodine Receptor Gene in 105 Malignant Hyperthermia Families: Novel Mutations and Concordance with the in Vitro Contracture Test

A calcium channel mutation causing hypokalemic periodic paralysis

Sight: automating genomic data-mining without programming skills

A novel SCN4A mutation causing myotonia aggravated by cold and potassium

Calretinin as a Marker for Cardiac Myxoma

Myotonia levior is a chloride channel disorder

Mutant channels contribute <50% to Na+ current in paramyotonia congenita muscle

Proof of a non-functional muscle chloride channel in recessive myotonia congenita (Becker) by detection of a 4 base pair deletion

Catalase and NO CATALASE ACTIVITY1 Promote Autophagy-Dependent Cell Death in Arabidopsis

Running: the risk of coronary events : Prevalence and prognostic relevance of coronary atherosclerosis in marathon runners

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