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Archives of Neurology
|
August 1, 1995
Correlations between triplet repeat expansion and clinical features in Huntington's disease
S Claes, K Van Zand, E Legius, et al.
Annals of Neurology
|
June 1, 1994
Deletion in the CMT1A locus on chromosome 17p11.2 in hereditary neuropathy with liability to pressure palsies
D Verhalle, A Löfgren, E Nelis, et al.
Journal of Medical Genetics
|
December 14, 1999
Psychological functioning before predictive testing for Huntington's disease: the role of the parental disease, risk perception, and subjective proximity of the disease
M Decruyenaere, G Evers-Kiebooms, A Boogaerts, et al.
Clinical Neurology and Neurosurgery
|
January 1, 1985
Early onset myophosphorylase deficiency (Mc Ardle's disease) with absence of myophosphorylase protein on SDS electrophoresis. The role of the ischemic forearm test
W van Riet, J de Meirsman, J de Saedeleer, et al.
Acta Neurologica Belgica
|
November 2, 1999
Methodological issues in a cost-of-dementia study in Belgium: the NAtional Dementia Economic Study (NADES)
X Kurz, M Broers, J Scuvée-Moreau, et al.
European Journal of Epidemiology
|
September 15, 1999
A retrospective study of Creutzfeldt-Jakob disease in Belgium
P Pals, B Van Everbroeck, R Sciot, et al.
Disability and Rehabilitation
|
July 1, 2006
The use of rhythmic auditory cues to influence gait in patients with Parkinson's disease, the differential effect for freezers and non-freezers, an explorative study
A M Willems, A Nieuwboer, F Chavret, et al.
Journal Belge De Radiologie
|
January 1, 1987
Bilateral paramedian thalamic infarction: CT and anatomopathological confrontation
P Lefêre, P Van de Voorde, G Pattyn, et al.
Acta Neuropathologica
|
April 29, 2000
Retrospective study of Creutzfeldt-Jakob disease in Belgium: neuropathological findings
B Van Everbroeck, P Pals, T Dziedzic, et al.
Annals of Neurology
|
November 1, 1996
Clinical and molecular genetic features of congenital spinal muscular atrophy
K Devriendt, M Lammens, E Schollen, et al.
Page
of 14
Search research articles
Search
Showing results (111-120 of 131) with videos related to
Sort By:
Page
of 14
Archives of Neurology
|
August 1, 1995
Correlations between triplet repeat expansion and clinical features in Huntington's disease
S Claes, K Van Zand, E Legius, et al.
Annals of Neurology
|
June 1, 1994
Deletion in the CMT1A locus on chromosome 17p11.2 in hereditary neuropathy with liability to pressure palsies
D Verhalle, A Löfgren, E Nelis, et al.
Journal of Medical Genetics
|
December 14, 1999
Psychological functioning before predictive testing for Huntington's disease: the role of the parental disease, risk perception, and subjective proximity of the disease
M Decruyenaere, G Evers-Kiebooms, A Boogaerts, et al.
Clinical Neurology and Neurosurgery
|
January 1, 1985
Early onset myophosphorylase deficiency (Mc Ardle's disease) with absence of myophosphorylase protein on SDS electrophoresis. The role of the ischemic forearm test
W van Riet, J de Meirsman, J de Saedeleer, et al.
Acta Neurologica Belgica
|
November 2, 1999
Methodological issues in a cost-of-dementia study in Belgium: the NAtional Dementia Economic Study (NADES)
X Kurz, M Broers, J Scuvée-Moreau, et al.
European Journal of Epidemiology
|
September 15, 1999
A retrospective study of Creutzfeldt-Jakob disease in Belgium
P Pals, B Van Everbroeck, R Sciot, et al.
Disability and Rehabilitation
|
July 1, 2006
The use of rhythmic auditory cues to influence gait in patients with Parkinson's disease, the differential effect for freezers and non-freezers, an explorative study
A M Willems, A Nieuwboer, F Chavret, et al.
Journal Belge De Radiologie
|
January 1, 1987
Bilateral paramedian thalamic infarction: CT and anatomopathological confrontation
P Lefêre, P Van de Voorde, G Pattyn, et al.
Acta Neuropathologica
|
April 29, 2000
Retrospective study of Creutzfeldt-Jakob disease in Belgium: neuropathological findings
B Van Everbroeck, P Pals, T Dziedzic, et al.
Annals of Neurology
|
November 1, 1996
Clinical and molecular genetic features of congenital spinal muscular atrophy
K Devriendt, M Lammens, E Schollen, et al.
Page
of 14