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Triparésie spastique «ammoniacale» réversible

Acta neurologica Belgica, 1992, Vol.92 (1), p.41-44

1992

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Encéphalopathie mitochondriale avec atteinte exclusive du système nerveux central

Revue neurologique (Paris), 1991, Vol.147 (6-7), p.538-541

1991

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Mitochondrial myopathy of childhood associated with depletion of mitochondrial DNA

Neurology, 1992-01, Vol.42 (1), p.209-209

1992

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Infantile spinal muscular atrophy variant with congenital fractures in a female neonate: evidence for autosomal recessive inheritance

Journal of medical genetics, 2002-01, Vol.39 (1), p.74-77

2002

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Migraine (author's transl)

Revue médicale de Bruxelles, 1980-02, Vol.1 (2), p.113

Telerman-Toppet, N

1980

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Modifications des unités motrices chez des malades atteints de paraplégie traumatique

Revue neurologique, 1983, Vol.139 (11), p.635-642

1983

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Fatal cytochrome c oxidase-deficient myopathy of infancy associated with mtDNA depletion. Differential involvement of skeletal muscle and cultured fibroblasts

Journal of inherited metabolic disease, 1992-01, Vol.15 (3), p.323-326

1992

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Unusual occurrence of cervical myelopathy in a case of Stickler's syndrome

Journal of medical genetics, 1992-03, Vol.29 (3), p.200-202

1992

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Avitaminosis D in the adult: pathogenesis and physiopathology

Annales d'endocrinologie, 1960-12, Vol.21, p.878-898

1960

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Auriculo-ventricular block and distal myopathy with rimmed vacuoles and desmin storage

Clinical neuropathology, 1991-03, Vol.10 (2), p.61

1991

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Type 2 fiber predominance in muscle cramp and exertional myalgia

Muscle & nerve, 1985-09, Vol.8 (7), p.563-567

1985

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Orthostatic hypotension with lower brain stem glioma

Journal of neurology, neurosurgery and psychiatry, 1982-12, Vol.45 (12), p.1147-1150

1982

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Urinary excretion of phosphates. Hormonal control and pathological deviations

Maroc médical, 1962-11, Vol.41, p.1074

1962

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Motor innervation and fiber type pattern in amyotrophic lateral sclerosis and in Charcot-Marie-Tooth disease

Muscle & nerve, 1978-03, Vol.1 (2), p.133-139

1978

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Cimetidine interaction with carbamazepine

Annals of internal medicine, 1981-04, Vol.94 (4 pt 1), p.544

1981

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Rhinocerebral mucormycosis in haemodialysis patients treated with desferrioxamine: possible role of recent surgery as an additional risk factor

Nephrology, dialysis, transplantation, 1991, Vol.6 (9), p.656-658

1991

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Complications of anaesthesia in dystrophia myotonica

Acta neurologica Belgica, 1970-09, Vol.70 (5), p.551-560

Telerman-Toppet, N

1970

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MORPHOLOGICAL AND HISTOCHEMICAL CHANGES OF MOTOR UNITS IN MYASTHENIA

Annals of the New York Academy of Sciences, 1976-05, Vol.274 (1), p.6-19

1976

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Differential diagnosis of limb-girdle muscular dystrophy and spinal muscular atrophy

Neurology, 1979-07, Vol.29 (7), p.957-957

1979

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Myopathie sporadique du disque Z avec accumulation de bâtonnets et corps cytoplasmiques

Revue neurologique, 1991, Vol.147 (2), p.144-147

1991

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Polycystic kidneys & cerebral aneurysms: reference to 3 personal cases

Acta clinica belgica (English ed. Online), 1957-09, Vol.12 (5), p.462-476

1957

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Familial myopathies with restricted distribution, facial weakness and inflammatory changes in affected muscles

Journal of neurology, 1985, Vol.231 (6), p.295-300

1985

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Central core disease: A study of clinically unaffected muscle

Journal of the neurological sciences, 1973-01, Vol.19 (2), p.207-223

1973

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Acute renal insufficiency and ischemic neuromyopathy during toxic coma: apropos of 2 cases

Journal d'urologie et de nephrologie, 1975-04, Vol.81 (4-5), p.306

1975

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Pathogenicity and treatment of cerebral edema

Bruxelles medical, 1974-06, Vol.54 (6), p.371

1974

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Triparésie spastique «ammoniacale» réversible

Encéphalopathie mitochondriale avec atteinte exclusive du système nerveux central

Mitochondrial myopathy of childhood associated with depletion of mitochondrial DNA

Infantile spinal muscular atrophy variant with congenital fractures in a female neonate: evidence for autosomal recessive inheritance

Migraine (author's transl)

Modifications des unités motrices chez des malades atteints de paraplégie traumatique

Fatal cytochrome c oxidase-deficient myopathy of infancy associated with mtDNA depletion. Differential involvement of skeletal muscle and cultured fibroblasts

Unusual occurrence of cervical myelopathy in a case of Stickler's syndrome

Avitaminosis D in the adult: pathogenesis and physiopathology

Auriculo-ventricular block and distal myopathy with rimmed vacuoles and desmin storage

Type 2 fiber predominance in muscle cramp and exertional myalgia

Orthostatic hypotension with lower brain stem glioma

Urinary excretion of phosphates. Hormonal control and pathological deviations

Motor innervation and fiber type pattern in amyotrophic lateral sclerosis and in Charcot-Marie-Tooth disease

Cimetidine interaction with carbamazepine

Rhinocerebral mucormycosis in haemodialysis patients treated with desferrioxamine: possible role of recent surgery as an additional risk factor

Complications of anaesthesia in dystrophia myotonica

MORPHOLOGICAL AND HISTOCHEMICAL CHANGES OF MOTOR UNITS IN MYASTHENIA

Differential diagnosis of limb-girdle muscular dystrophy and spinal muscular atrophy

Myopathie sporadique du disque Z avec accumulation de bâtonnets et corps cytoplasmiques

Polycystic kidneys & cerebral aneurysms: reference to 3 personal cases

Familial myopathies with restricted distribution, facial weakness and inflammatory changes in affected muscles

Central core disease: A study of clinically unaffected muscle

Acute renal insufficiency and ischemic neuromyopathy during toxic coma: apropos of 2 cases

Pathogenicity and treatment of cerebral edema

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