Search research articles
Contact Us
Filters
Showing results (41-50 of 51) with videos related to
Page
of 6
Sort By:
Acta Neurologica Scandinavica
|
January 19, 2010
Intraoperative hyperventilation vs remifentanil during electrocorticography for epilepsy surgery - a case report
T W Kjaer, F F Madsen, F B Moltke, et al.
Peritoneal Dialysis International : Journal of the International Society for Peritoneal Dialysis
|
January 1, 1993
Pruritus in continuous ambulatory peritoneal dialysis and hemodialysis patients
E V Balaskas, M Chu, R P Uldall, et al.
BJOG : an International Journal of Obstetrics and Gynaecology
|
November 28, 2008
Asphyxia-related risk factors and their timing in spastic cerebral palsy
L F Nielsen, D Schendel, J Grove, et al.
Human Reproduction (Oxford, England)
|
June 18, 2010
Multiplicity and early gestational age contribute to an increased risk of cerebral palsy from assisted conception: a population-based cohort study
D Hvidtjørn, J Grove, D Schendel, et al.
Ugeskrift for Laeger
|
April 28, 1980
[Rapid diagnosis of respiratory virus infections in children. Respiratory syncytial virus demonstrated by the immunofluorescent technic]
A Hornsleth, B Friis, C H Mordhorst, et al.
Ugeskrift for Laeger
|
January 4, 1982
[Social pediatrics in Denmark today]
K K Ibsen, B Hansen, J Jensen, et al.
Archives of Disease in Childhood
|
November 1, 1984
Antibiotic treatment of pneumonia and bronchiolitis. A prospective randomised study
B Friis, P Andersen, E Brenøe, et al.
European Journal of Neurology
|
May 12, 2018
Ictal and interictal electric source imaging in pre-surgical evaluation: a prospective study
P Sharma, M Scherg, L H Pinborg, et al.
American Journal of Human Genetics
|
May 20, 1999
Mutational analysis of the defective protease in classic late-infantile neuronal ceroid lipofuscinosis, a neurodegenerative lysosomal storage disorder
D E Sleat, R M Gin, I Sohar, et al.
Nature Genetics
|
March 1, 1997
Unstable insertion in the 5' flanking region of the cystatin B gene is the most common mutation in progressive myoclonus epilepsy type 1, EPM1
R G Lafrenière, D L Rochefort, N Chrétien, et al.
Page
of 6
Search research articles
Search
Showing results (41-50 of 51) with videos related to
Sort By:
Page
of 6
Acta Neurologica Scandinavica
|
January 19, 2010
Intraoperative hyperventilation vs remifentanil during electrocorticography for epilepsy surgery - a case report
T W Kjaer, F F Madsen, F B Moltke, et al.
Peritoneal Dialysis International : Journal of the International Society for Peritoneal Dialysis
|
January 1, 1993
Pruritus in continuous ambulatory peritoneal dialysis and hemodialysis patients
E V Balaskas, M Chu, R P Uldall, et al.
BJOG : an International Journal of Obstetrics and Gynaecology
|
November 28, 2008
Asphyxia-related risk factors and their timing in spastic cerebral palsy
L F Nielsen, D Schendel, J Grove, et al.
Human Reproduction (Oxford, England)
|
June 18, 2010
Multiplicity and early gestational age contribute to an increased risk of cerebral palsy from assisted conception: a population-based cohort study
D Hvidtjørn, J Grove, D Schendel, et al.
Ugeskrift for Laeger
|
April 28, 1980
[Rapid diagnosis of respiratory virus infections in children. Respiratory syncytial virus demonstrated by the immunofluorescent technic]
A Hornsleth, B Friis, C H Mordhorst, et al.
Ugeskrift for Laeger
|
January 4, 1982
[Social pediatrics in Denmark today]
K K Ibsen, B Hansen, J Jensen, et al.
Archives of Disease in Childhood
|
November 1, 1984
Antibiotic treatment of pneumonia and bronchiolitis. A prospective randomised study
B Friis, P Andersen, E Brenøe, et al.
European Journal of Neurology
|
May 12, 2018
Ictal and interictal electric source imaging in pre-surgical evaluation: a prospective study
P Sharma, M Scherg, L H Pinborg, et al.
American Journal of Human Genetics
|
May 20, 1999
Mutational analysis of the defective protease in classic late-infantile neuronal ceroid lipofuscinosis, a neurodegenerative lysosomal storage disorder
D E Sleat, R M Gin, I Sohar, et al.
Nature Genetics
|
March 1, 1997
Unstable insertion in the 5' flanking region of the cystatin B gene is the most common mutation in progressive myoclonus epilepsy type 1, EPM1
R G Lafrenière, D L Rochefort, N Chrétien, et al.
Page
of 6