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Primary episodic ataxias: diagnosis, pathogenesis and treatment

Brain (London, England : 1878), 2007-10, Vol.130 (10), p.2484-2493

2007

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3. Value of the exercise compound muscle action potential study and provocative tests in possible periodic paralysis

Clinical neurophysiology, 2012-06, Vol.123 (6), p.e18-e18

2012

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P25 Double-blind, placebo-controlled, parallel group, phase III study comparing dichlorphenamide vs. placebo for the treatment of periodic paralysis (HYP HOP trial)

Neuromuscular disorders : NMD, 2011, Vol.21, p.S13-S13

2011

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P29 Genotype-phenotype correlation and longitudinal study of Andersen-Tawil Syndrome in the UK

Neuromuscular disorders : NMD, 2011, Vol.21, p.S14-S14

2011

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P27 Genotype-phenotype correlation and longitudinal three year natural history study in the non-dystrophic myotonias in the UK

Neuromuscular disorders : NMD, 2011, Vol.21, p.S14-S14

2011

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P44 The genetic skeletal muscle channelopathies: genotype–phenotype correlation and longitudinal studies

Neuromuscular disorders : NMD, 2010, Vol.20, p.S16-S17

2010

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IN75-FR-02 Neuromuscular channelopathies: diagnosis and treatment

Journal of the neurological sciences, 2009, Vol.285, p.S54-S54

Griggs, R.C

2009

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Acetazolamide efficacy in hypokalemic periodic paralysis and the predictive role of genotype

Neurology, 2011-11, Vol.77 (22), p.1960-1964

2011

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Randomized, double-blind six-month trial of prednisone in Duchenne's muscular dystrophy

The New England journal of medicine, 1989-06, Vol.320 (24), p.1592-1597

1989

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T.P.5.03 Equipoise concerning corticosteroid use in boys with Duchenne muscular dystrophy: persistent wide variations in practice

Neuromuscular disorders : NMD, 2008-10, Vol.18 (9), p.824-824

2008

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Identification of two new KCNA1 mutations in episodic ataxia/myokymia families

Human molecular genetics, 1995-09, Vol.4 (9), p.1671-1672

1995

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Genotype-phenotype correlations of DHP receptor α1-subunit gene mutations causing hypokalemic periodic paralysis

Neuromuscular disorders : NMD, 1997, Vol.7 (1), p.33-38

1997

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American Academy of Neurology policy on pharmaceutical and device industry support

Neurology, 2012-03, Vol.78 (10), p.750-754

2012

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Mapping the facioscapulohumeral muscular dystrophy gene is complicated by chromosome 4q35 recombination events

Nature genetics, 1993-06, Vol.4 (2), p.165-169

1993

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Hypothyroidism unmasking proximal myotonic myopathy

Neuromuscular disorders : NMD, 2000-03, Vol.10 (3), p.165-172

2000

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Leucine incorporation into mixed skeletal muscle protein in humans

American journal of physiology: endocrinology and metabolism, 1988-02, Vol.254 (2), p.E208-E213

1988

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Channelopathies; Clinical Manifestations

Encyclopedia of the Neurological Sciences, 2014, p.743-749

Second Edition, 2014

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Hereditary myokymia and periodic ataxia

Journal of the neurological sciences, 1975-01, Vol.25 (1), p.109-118

1975

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O.83 Forearm leucine metabolism studied by stable isotope technology

Clinical nutrition (Edinburgh, Scotland), 1983, Vol.2, p.44-44

1983

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Investigation of chronic endemic nephropathy in Yugoslavia

The American journal of medicine, 1965-08, Vol.39 (2), p.210-217

1965

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Investigation of chronic endemic nephropathy in Yugoslavia: II. Renal pathology

The American journal of medicine, 1965-08, Vol.39 (2), p.210-217

1965

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Primary episodic ataxias: diagnosis, pathogenesis and treatment

3. Value of the exercise compound muscle action potential study and provocative tests in possible periodic paralysis

P25 Double-blind, placebo-controlled, parallel group, phase III study comparing dichlorphenamide vs. placebo for the treatment of periodic paralysis (HYP HOP trial)

P29 Genotype-phenotype correlation and longitudinal study of Andersen-Tawil Syndrome in the UK

P27 Genotype-phenotype correlation and longitudinal three year natural history study in the non-dystrophic myotonias in the UK

P44 The genetic skeletal muscle channelopathies: genotype–phenotype correlation and longitudinal studies

IN75-FR-02 Neuromuscular channelopathies: diagnosis and treatment

Acetazolamide efficacy in hypokalemic periodic paralysis and the predictive role of genotype

Randomized, double-blind six-month trial of prednisone in Duchenne's muscular dystrophy

T.P.5.03 Equipoise concerning corticosteroid use in boys with Duchenne muscular dystrophy: persistent wide variations in practice

Identification of two new KCNA1 mutations in episodic ataxia/myokymia families

Genotype-phenotype correlations of DHP receptor α1-subunit gene mutations causing hypokalemic periodic paralysis

American Academy of Neurology policy on pharmaceutical and device industry support

Mapping the facioscapulohumeral muscular dystrophy gene is complicated by chromosome 4q35 recombination events

Hypothyroidism unmasking proximal myotonic myopathy

Leucine incorporation into mixed skeletal muscle protein in humans

Channelopathies; Clinical Manifestations

Hereditary myokymia and periodic ataxia

O.83 Forearm leucine metabolism studied by stable isotope technology

Investigation of chronic endemic nephropathy in Yugoslavia

Investigation of chronic endemic nephropathy in Yugoslavia: II. Renal pathology

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