N. Telerman‐Toppet

发表

[Vasculitis of the central nervous system].

E. Cogan, S. Noël, N. Telerman‐Toppet, 1992, Revue medicale de Bruxelles.

Central core disease. A study of clinically unaffected muscle.

C. Coërs, J. Gérard, N. Telerman‐Toppet, 1973, Journal of the neurological sciences.

[Mitochondrial encephalopathy affecting only the central nervous system].

P. Davous, P. Tric, N. Telerman‐Toppet, 1991, Revue neurologique.

Oculocraniosomatic neuromuscular disease with hypoparathyroidism.

H. Szliwowski, C. Coërs, M. Toppet, 1977, American journal of diseases of children.

Acute quadriparesis with mucle spasms related to electrolyte disturbances in steatorrhea. Clinical and biochemical data.

C. Coërs, N. Telerman‐Toppet, M. Cremer, 1972, The American journal of medicine.

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

C. Coërs, N. Telerman‐Toppet, M. Bacq, 2004, Journal of Neurology.

Terminal motor innervation in myopathic hamsters

G. Jasmin, C. Coërs, N. Telerman‐Toppet, 1980, Journal of the Neurological Sciences.

Orthostatic hypotension with lower brain stem glioma

J. Vanderhaeghen, N. Telerman‐Toppet, M. Warszawski, 1982, Journal of neurology, neurosurgery, and psychiatry.

Charcot-Marie-Tooth disease associated with retinal pigment dystrophy and protanopia. Neurological, ophthalmological and genetic study of a family.

N. van Regemorter, D. Toussaint, C. Coërs, 1979, Journal of neurology.

Changes in motor innervation and histochemical pattern of muscle fibers in some congenital myopathies

H. Szliwowski, J. Bethlem, C. Coërs, 1976, Neurology.

Adult from of basal cell navevus syndrome: A family study

D. Balériaux, D. Toussaint, C. Coërs, 2004, Journal of Neurology.

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

D. Balériaux, S. Noël, N. Telerman‐Toppet, 1992, Journal of medical genetics.

MORPHOLOGICAL AND HISTOCHEMICAL CHANGES OF MOTOR UNITS IN MYASTHENIA *

C. Coërs, N. Telerman‐Toppet, 1976, Annals of the New York Academy of Sciences.

Mitochondrial myopathy of childhood associated with depletion of mitochondrial DNA

S. Dimauro, E. Schon, H. Tritschler, 1992, Neurology.

Regressive vacuolar myopathy in steatorrhea. Electrophysiological and histological study.

C. Coërs, N. Telerman‐Toppet, M. Cremer, 1971, Archives of neurology.

[Complications of anaesthesia in dystrophia myotonica].

N. Telerman‐Toppet, 1970, Acta neurologica Belgica.

Terminal Innervation Ratio in Neuromuscular Disease: II. Disorders of Lower Motor Neuron, Peripheral Nerve, and Muscle

C. Coërs, J. Gérard, N. Telerman‐Toppet, 1973 .

Motor innervation in Type II atrophy of skeletal muscle

C. Coërs, N. Telerman‐Toppet, 1975, Journal of the Neurological Sciences.

Intraventricular administration of rifampin for tuberculous meningitis

W. Vincken, J. Noterman, N. Telerman‐Toppet, 1981, Journal of Neurology.

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

S. Noël, N. Telerman‐Toppet, G. Bauherz, 1991, Clinical neuropathology.

Charcot-Marie-Tooth disease associated with retinal pigment dystrophy and protanopia

D. Toussaint, C. Coërs, N. Regemorter, 2004, Journal of Neurology.

Familial focal loss of cross striations

K. Dingemans, J. Bethlem, C. Coërs, 1977, Journal of Neurology.

Terminal Innervation Ratio in Neuromuscular Disease: I. Methods and Controls

C. Coërs, J. Gérard, N. Telerman‐Toppet, 1973 .

Benign monoclonal gammopathy and relapsing polymyositis.

M. Wittek, C. Coërs, N. Telerman‐Toppet, 1982, Muscle & nerve.

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

H. Scheffer, F. Avni, B. Dachy, 2002, Journal of medical genetics.

Neurogenic benign fasciculations, pseudomyotonia, and pseudotetany. A disease in search of a name.

C. Coërs, N. Telerman‐Toppet, J. Durdu, 1981, Archives of neurology.

The early stages of neuromuscular regeneration after crushing the sciatic nerve in the rat Electrophysiological and histological study

C. Coërs, G. Graff, N. Telerman‐Toppet, 1975, Journal of the Neurological Sciences.

Cimetidine interaction with carbamazepine.

C. Coërs, M. Duret, N. Telerman‐Toppet, 1981, Annals of internal medicine.

Morphological changes of motor units in Duchenne's muscular dystrophy.

C Coërs, N Telerman-Toppet, C. Coërs, 1977, Archives of neurology.

Type 2 fiber predominance in muscle cramp and exertional myalgia

C. Coërs, N. Telerman‐Toppet, P. Khoubesserian, 1985, Muscle & nerve.

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

N. Telerman‐Toppet, C. Goërs, 1979, Neurology.

Type 2 fiber predominance in muscle cramp and exertional myalgia

C. Coërs, N. Telerman‐Toppet, P. Khoubesserian, 1985, Muscle & nerve.

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

C. Coërs, N. Telerman‐Toppet, 1978, Muscle & nerve.

Toxoplasma encephalitis in a HIV patient: unusual involvement of the corpus callosum

Nicole Hermanus, Frederic Supiot, Marie-Paule Guillaume, 1997, Clinical Neurology and Neurosurgery.

FACT AND FANCY IN THE HISTOLOGICAL DIAGNOSIS OF DENERVATION

C. Coërs, N. Telerman‐Toppet, 1978 .

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

S. Dimauro, D. Biarent, E. Vamos, 1992, Journal of Inherited Metabolic Disease.