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Pediatric Neurosurgery
|
January 1, 1995
Lesionectomy of MRI detected lesions in children with epilepsy
J L Montes, B Rosenblatt, J P Farmer, et al.
Pediatric Neurology
|
May 1, 1994
Encephaloduroarteriosynangiosis (EDAS) for the treatment of childhood moyamoya disease
I B Ross, M I Shevell, J L Montes, et al.
The New England Journal of Medicine
|
December 13, 1990
The sequelae of Haemophilus influenzae meningitis in school-age children
H G Taylor, E L Mills, A Ciampi, et al.
Annals of Neurology
|
October 1, 1988
Encephalitis among Cree children in northern Quebec
D N Black, G V Watters, E Andermann, et al.
American Journal of Medical Genetics
|
December 23, 1999
Knobloch syndrome involving midline scalp defect of the frontal region
L C Sniderman, R K Koenekoop, A M O'Gorman, et al.
Annals of Neurology
|
October 1, 1988
Leukoencephalopathy among native Indian infants in northern Quebec and Manitoba
D N Black, F Booth, G V Watters, et al.
Neuron
|
September 1, 1996
Clinical phenotypes of different MPZ (P0) mutations may include Charcot-Marie-Tooth type 1B, Dejerine-Sottas, and congenital hypomyelination
L E Warner, M J Hilz, S H Appel, et al.
Page
of 4
Search research articles
Search
Showing results (31-40 of 37) with videos related to
Sort By:
Page
of 4
You have reached the last page of results.
This site can display upto 37 results.
Pediatric Neurosurgery
|
January 1, 1995
Lesionectomy of MRI detected lesions in children with epilepsy
J L Montes, B Rosenblatt, J P Farmer, et al.
Pediatric Neurology
|
May 1, 1994
Encephaloduroarteriosynangiosis (EDAS) for the treatment of childhood moyamoya disease
I B Ross, M I Shevell, J L Montes, et al.
The New England Journal of Medicine
|
December 13, 1990
The sequelae of Haemophilus influenzae meningitis in school-age children
H G Taylor, E L Mills, A Ciampi, et al.
Annals of Neurology
|
October 1, 1988
Encephalitis among Cree children in northern Quebec
D N Black, G V Watters, E Andermann, et al.
American Journal of Medical Genetics
|
December 23, 1999
Knobloch syndrome involving midline scalp defect of the frontal region
L C Sniderman, R K Koenekoop, A M O'Gorman, et al.
Annals of Neurology
|
October 1, 1988
Leukoencephalopathy among native Indian infants in northern Quebec and Manitoba
D N Black, F Booth, G V Watters, et al.
Neuron
|
September 1, 1996
Clinical phenotypes of different MPZ (P0) mutations may include Charcot-Marie-Tooth type 1B, Dejerine-Sottas, and congenital hypomyelination
L E Warner, M J Hilz, S H Appel, et al.
Page
of 4