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Neuromuscular Disorders : NMD
|
May 1, 1997
Merosin positive congenital muscular dystrophy with mental deficiency, epilepsy and MRI changes in the cerebral white matter
B Echenne, F Rivier, A J Jellali, et al.
Pediatrie
|
October 1, 1982
[Type II fucosidosis. 2 cases]
B Echenne, P Baldet, I Maire, et al.
Revue D'Electroencephalographie Et De Neurophysiologie Clinique
|
December 1, 1981
[All-night polygraphic recordings in the child with suspected epileptic seizures, in spite of normal routine and post-sleep deprivation EEGs (author's transl)]
M Billiard, B Echenne, A Besset, et al.
Muscle & Nerve
|
September 15, 1998
Mosaic expression of two dystrophins in a boy with progressive muscular dystrophy
F Rivier, S Tuffery, A J Jellali, et al.
Journal of Child Neurology
|
August 21, 2001
Is hyperprolinemia type I actually a benign trait? Report of a case with severe neurologic involvement and vigabatrin intolerance
V Humbertclaude, F Rivier, A Roubertie, et al.
Pediatrie
|
January 1, 1976
[Nosologic problems of essential polycythemia in children. Apropos of a case]
B Echenne, D Brunel, J Astruc, et al.
Epilepsia
|
August 1, 1996
Treatment with vigabatrin may mimic alpha-aminoadipic aciduria
C Vallat, F Rivier, H Bellet, et al.
Neuromuscular Disorders : NMD
|
March 21, 2001
A standardized method for the evaluation of respiratory muscle endurance in patients with Duchenne muscular dystrophy
S Matecki, N Topin, M Hayot, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
November 14, 2003
[Movement disorders in childhood: classification and genetic update]
A Roubertie, F Rivier, S Tuffery-Giraud, et al.
Revue Neurologique
|
January 29, 2005
[Parry-Romberg's syndrome and epilepsy]
M Chbicheb, A Gelot, F Rivier, et al.
Page
of 13
Search research articles
Search
Showing results (71-80 of 121) with videos related to
Sort By:
Page
of 13
Neuromuscular Disorders : NMD
|
May 1, 1997
Merosin positive congenital muscular dystrophy with mental deficiency, epilepsy and MRI changes in the cerebral white matter
B Echenne, F Rivier, A J Jellali, et al.
Pediatrie
|
October 1, 1982
[Type II fucosidosis. 2 cases]
B Echenne, P Baldet, I Maire, et al.
Revue D'Electroencephalographie Et De Neurophysiologie Clinique
|
December 1, 1981
[All-night polygraphic recordings in the child with suspected epileptic seizures, in spite of normal routine and post-sleep deprivation EEGs (author's transl)]
M Billiard, B Echenne, A Besset, et al.
Muscle & Nerve
|
September 15, 1998
Mosaic expression of two dystrophins in a boy with progressive muscular dystrophy
F Rivier, S Tuffery, A J Jellali, et al.
Journal of Child Neurology
|
August 21, 2001
Is hyperprolinemia type I actually a benign trait? Report of a case with severe neurologic involvement and vigabatrin intolerance
V Humbertclaude, F Rivier, A Roubertie, et al.
Pediatrie
|
January 1, 1976
[Nosologic problems of essential polycythemia in children. Apropos of a case]
B Echenne, D Brunel, J Astruc, et al.
Epilepsia
|
August 1, 1996
Treatment with vigabatrin may mimic alpha-aminoadipic aciduria
C Vallat, F Rivier, H Bellet, et al.
Neuromuscular Disorders : NMD
|
March 21, 2001
A standardized method for the evaluation of respiratory muscle endurance in patients with Duchenne muscular dystrophy
S Matecki, N Topin, M Hayot, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
November 14, 2003
[Movement disorders in childhood: classification and genetic update]
A Roubertie, F Rivier, S Tuffery-Giraud, et al.
Revue Neurologique
|
January 29, 2005
[Parry-Romberg's syndrome and epilepsy]
M Chbicheb, A Gelot, F Rivier, et al.
Page
of 13