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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.
Revue Neurologique
|
January 29, 2005
[Parry-Romberg's syndrome and epilepsy]
M Chbicheb, A Gelot, F Rivier, 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
|
May 2, 2002
[The varied etiologies of childhood-onset dystonia]
A Roubertie, F Rivier, V Humbertclaude, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
March 29, 2001
[Acute myelitis of an unusual cause in a child: the lymphocytic choriomeningitis virus]
V Humbertclaude, S Tourtet, M Semprino, et al.
Brain & Development
|
November 27, 2001
Neurological presentation of three patients with 22q11 deletion (CATCH 22 syndrome)
A Roubertie, M Semprino, A M Chaze, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
March 1, 1997
[Ectopic intraspinal extradural anaplastic ependymoma in an infant]
A Roubertie, P Coubes, V Humbertclaude, et al.
Neuro-Chirurgie
|
August 17, 1999
[Treatment of early-onset generalized dystonia by chronic bilateral stimulation of the internal globus pallidus. Apropos of a case]
P Coubes, B Echenne, A Roubertie, et al.
Neuropediatrics
|
November 24, 1999
Recurrent episodes of coma: an unusual phenotype of familial hemiplegic migraine with linkage to chromosome 1
B Echenne, A Ducros, F Rivier, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
February 12, 1999
[Benign infantile convulsions. French collaborative study]
A Gautier, F Pouplard, N Bednarek, et al.
Page
of 3
Search research articles
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Showing results (11-20 of 23) with videos related to
Sort By:
Page
of 3
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.
Revue Neurologique
|
January 29, 2005
[Parry-Romberg's syndrome and epilepsy]
M Chbicheb, A Gelot, F Rivier, 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
|
May 2, 2002
[The varied etiologies of childhood-onset dystonia]
A Roubertie, F Rivier, V Humbertclaude, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
March 29, 2001
[Acute myelitis of an unusual cause in a child: the lymphocytic choriomeningitis virus]
V Humbertclaude, S Tourtet, M Semprino, et al.
Brain & Development
|
November 27, 2001
Neurological presentation of three patients with 22q11 deletion (CATCH 22 syndrome)
A Roubertie, M Semprino, A M Chaze, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
March 1, 1997
[Ectopic intraspinal extradural anaplastic ependymoma in an infant]
A Roubertie, P Coubes, V Humbertclaude, et al.
Neuro-Chirurgie
|
August 17, 1999
[Treatment of early-onset generalized dystonia by chronic bilateral stimulation of the internal globus pallidus. Apropos of a case]
P Coubes, B Echenne, A Roubertie, et al.
Neuropediatrics
|
November 24, 1999
Recurrent episodes of coma: an unusual phenotype of familial hemiplegic migraine with linkage to chromosome 1
B Echenne, A Ducros, F Rivier, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
February 12, 1999
[Benign infantile convulsions. French collaborative study]
A Gautier, F Pouplard, N Bednarek, et al.
Page
of 3