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The Journal of Pediatrics
|
July 22, 1998
Bone marrow transplantation in metachromatic leukodystrophy caused by saposin-B deficiency: a case report with a 3-year follow-up period
P Landrieu, S Blanche, M T Vanier, et al.
Neuropediatrics
|
August 1, 1987
Paralytic poliomyelitis in vaccinated children
E Dussaix, G Huault, P Landrieu, et al.
Revue Neurologique
|
January 1, 1992
[Cerebral complications of incontinentia pigmenti. A clinicopathological study of a case]
C Triki, D Devictor, S Kah, et al.
Journal of Medical Genetics
|
June 3, 2004
Screening of MECP2 coding sequence in patients with phenotypes of decreasing likelihood for Rett syndrome: a cohort of 171 cases
F Kammoun, N de Roux, O Boespflug-Tanguy, et al.
Journal of Neurology
|
May 1, 1993
Central nervous system lesions in hypomelanosis of Ito: an MRI and pathological study
V Malherbe, D Pariente, M Tardieu, et al.
Lancet (London, England)
|
July 29, 1995
SMN gene deletion in variant of infantile spinal muscular atrophy
L Bürglen, R Spiegel, J Ignatius, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
August 1, 1997
[Ischemic cerebral vascular accident caused by vertebral artery dissection]
B Tabarki, A el Madani, H Alvarez, et al.
Neurology
|
May 1, 1996
Extensive brain calcifications, leukodystrophy, and formation of parenchymal cysts: a new progressive disorder due to diffuse cerebral microangiopathy
P Labrune, C Lacroix, F Goutières, et al.
Annals of Neurology
|
October 12, 2000
Peripheral neuropathy with hypomyelination, chronic intestinal pseudo-obstruction and deafness: a developmental "neural crest syndrome" related to a SOX10 mutation
V Pingault, A Guiochon-Mantel, N Bondurand, et al.
Cell Motility and the Cytoskeleton
|
January 1, 1996
Aggregation of a subpopulation of vimentin filaments in cultured human skin fibroblasts derived from patients with giant axonal neuropathy
O Bousquet, M Basseville, E Vila-Porcile, et al.
Page
of 13
Search research articles
Search
Showing results (101-110 of 126) with videos related to
Sort By:
Page
of 13
The Journal of Pediatrics
|
July 22, 1998
Bone marrow transplantation in metachromatic leukodystrophy caused by saposin-B deficiency: a case report with a 3-year follow-up period
P Landrieu, S Blanche, M T Vanier, et al.
Neuropediatrics
|
August 1, 1987
Paralytic poliomyelitis in vaccinated children
E Dussaix, G Huault, P Landrieu, et al.
Revue Neurologique
|
January 1, 1992
[Cerebral complications of incontinentia pigmenti. A clinicopathological study of a case]
C Triki, D Devictor, S Kah, et al.
Journal of Medical Genetics
|
June 3, 2004
Screening of MECP2 coding sequence in patients with phenotypes of decreasing likelihood for Rett syndrome: a cohort of 171 cases
F Kammoun, N de Roux, O Boespflug-Tanguy, et al.
Journal of Neurology
|
May 1, 1993
Central nervous system lesions in hypomelanosis of Ito: an MRI and pathological study
V Malherbe, D Pariente, M Tardieu, et al.
Lancet (London, England)
|
July 29, 1995
SMN gene deletion in variant of infantile spinal muscular atrophy
L Bürglen, R Spiegel, J Ignatius, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
August 1, 1997
[Ischemic cerebral vascular accident caused by vertebral artery dissection]
B Tabarki, A el Madani, H Alvarez, et al.
Neurology
|
May 1, 1996
Extensive brain calcifications, leukodystrophy, and formation of parenchymal cysts: a new progressive disorder due to diffuse cerebral microangiopathy
P Labrune, C Lacroix, F Goutières, et al.
Annals of Neurology
|
October 12, 2000
Peripheral neuropathy with hypomyelination, chronic intestinal pseudo-obstruction and deafness: a developmental "neural crest syndrome" related to a SOX10 mutation
V Pingault, A Guiochon-Mantel, N Bondurand, et al.
Cell Motility and the Cytoskeleton
|
January 1, 1996
Aggregation of a subpopulation of vimentin filaments in cultured human skin fibroblasts derived from patients with giant axonal neuropathy
O Bousquet, M Basseville, E Vila-Porcile, et al.
Page
of 13