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HEREDITARY MOTOR AND SENSORY NEUROPATHY OF NEURONAL TYPE WITH ONSET IN EARLY CHILDHOOD

Brain (London, England : 1878), 1991-08, Vol.114 (4), p.1855-1870

1991

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CONGENITAL DEMYELINATING MOTOR AND SENSORY NEUROPATHY WITH FOCALLY FOLDED MYELIN SHEATHS

Brain (London, England : 1878), 1990-12, Vol.113 (6), p.1629-1643

1990

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Muscle fatigue in McArdle's disease : muscle fibre conduction velocity and surface EMG frequency spectrum during ischaemic exercise

Brain (London, England : 1878), 1990-12, Vol.113 (6), p.1779-1793

1990

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Hereditary neuropathy with liability to pressure palsies in childhood

Neuropediatrics, 1992-06, Vol.23 (3), p.138-143

1992

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Muscle cramp : main theories as to aetiology

European Archives of Psychiatry and Neurological Sciences, 1990-01, Vol.239 (5), p.337-342

1990

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THE SECOND WIND PHENOMENON IN McARDLE'S DISEASE

Brain (London, England : 1878), 1986-12, Vol.109 (6), p.1087-1101

1986

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Variability and interrelationships of surface EMG parameters during local muscle fatigue

Muscle & nerve, 1993-08, Vol.16 (8), p.849-856

1993

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Polyglucosan bodies in intramuscular motor nerves

Acta neuropathologica, 1989-01, Vol.77 (6), p.629-633

1989

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Myotonic dystrophy : predictive value of normal results on clinical examination

Brain (London, England : 1878), 1991-10, Vol.114 (5), p.2303-2311

1991

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Hereditary neuropathy with liability to pressure palsies: A clinical, electroneurophysiological and morphological study

Journal of the neurological sciences, 1993-06, Vol.116 (2), p.176-184

1993

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AMP deaminase deficiency: study of the human skeletal muscle purine metabolism during ischaemic isometric exercise

Clinical science (1979), 1987-04, Vol.72 (4), p.475-482

1987

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Early morphological features in dominantly inherited demyelinating motor and sensory neuropathy (HMSN type I)

Journal of the neurological sciences, 1992-02, Vol.107 (2), p.145-154

1992

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A rapidly progressive autosomal dominant scapulohumeral form of spinal muscular atrophy

Annals of neurology, 1986-10, Vol.20 (4), p.538-540

1986

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Ischaemic exercise test in myoadenylate deaminase deficiency and McArdle's disease: measurement of plasma adenosine, inosine and hypoxanthine

Clinical science (1979), 1986-04, Vol.70 (4), p.399-401

1986

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Prevention of recurrent exertional rhabdomyolysis by dantrolene sodium

Muscle & nerve, 1987-01, Vol.10 (1), p.45-46

1987

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Autosomal recessive form of hereditary motor and sensory neuropathy type I

Neurology, 1992-09, Vol.42 (9), p.1755-1755

1992

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Allelic heterogeneity in hereditary motor and sensory neuropathy type Ia (Charcot-Marie-Tooth disease type 1a)

Neurology, 1993-05, Vol.43 (5), p.1010

1993

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Exertional rhabdomyolysis in a patient with calcium adenosine triphosphatase deficiency

Journal of neurology, neurosurgery and psychiatry, 1993-07, Vol.56 (7), p.823-826

1993

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Familial progressive vestibulocochlear dysfunction

Archives of neurology (Chicago), 1988-07, Vol.45 (7), p.766-768

1988

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FORCE AND FATIGUE IN HUMAN TYPE I MUSCLE FIBRES: A SURFACE EMG STUDY IN PATIENTS WITH CONGENITAL MYOPATHY AND TYPE I FIBRE PREDOMINANCE

Brain (London, England : 1878), 1991-10, Vol.114 (5), p.2123-2132

1991

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Persistent periodic hiccups following brain abscess: a case report

Journal of neurology, neurosurgery and psychiatry, 1990-01, Vol.53 (1), p.83-84

1990

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Adult polyglucosan body disease: The diagnostic value of axilla skin biopsy

Annals of neurology, 1991-04, Vol.29 (4), p.448-451

1991

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Update on Prevalence of Pain in Patients with Cancer: Systematic Review and Meta-Analysis

Journal of pain and symptom management, 2016-06, Vol.51 (6), p.1070-1090.e9

2016

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Hereditary vestibulo-cochlear dysfunction and vascular disorders

Journal of the neurological sciences, 1989-08, Vol.92 (1), p.55-63

1989

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Respiratory failure as initial symptom of acid maltase deficiency

Journal of neurology, neurosurgery and psychiatry, 1984-05, Vol.47 (5), p.549-552

1984

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HEREDITARY MOTOR AND SENSORY NEUROPATHY OF NEURONAL TYPE WITH ONSET IN EARLY CHILDHOOD

CONGENITAL DEMYELINATING MOTOR AND SENSORY NEUROPATHY WITH FOCALLY FOLDED MYELIN SHEATHS

Muscle fatigue in McArdle's disease : muscle fibre conduction velocity and surface EMG frequency spectrum during ischaemic exercise

Hereditary neuropathy with liability to pressure palsies in childhood

Muscle cramp : main theories as to aetiology

THE SECOND WIND PHENOMENON IN McARDLE'S DISEASE

Variability and interrelationships of surface EMG parameters during local muscle fatigue

Polyglucosan bodies in intramuscular motor nerves

Myotonic dystrophy : predictive value of normal results on clinical examination

Hereditary neuropathy with liability to pressure palsies: A clinical, electroneurophysiological and morphological study

AMP deaminase deficiency: study of the human skeletal muscle purine metabolism during ischaemic isometric exercise

Early morphological features in dominantly inherited demyelinating motor and sensory neuropathy (HMSN type I)

A rapidly progressive autosomal dominant scapulohumeral form of spinal muscular atrophy

Ischaemic exercise test in myoadenylate deaminase deficiency and McArdle's disease: measurement of plasma adenosine, inosine and hypoxanthine

Prevention of recurrent exertional rhabdomyolysis by dantrolene sodium

Autosomal recessive form of hereditary motor and sensory neuropathy type I

Allelic heterogeneity in hereditary motor and sensory neuropathy type Ia (Charcot-Marie-Tooth disease type 1a)

Exertional rhabdomyolysis in a patient with calcium adenosine triphosphatase deficiency

Familial progressive vestibulocochlear dysfunction

FORCE AND FATIGUE IN HUMAN TYPE I MUSCLE FIBRES: A SURFACE EMG STUDY IN PATIENTS WITH CONGENITAL MYOPATHY AND TYPE I FIBRE PREDOMINANCE

Persistent periodic hiccups following brain abscess: a case report

Adult polyglucosan body disease: The diagnostic value of axilla skin biopsy

Update on Prevalence of Pain in Patients with Cancer: Systematic Review and Meta-Analysis

Hereditary vestibulo-cochlear dysfunction and vascular disorders

Respiratory failure as initial symptom of acid maltase deficiency

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