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M S Damian

Showing results (11-20 of 23) with videos related to

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American Journal of Medical Genetics|April 24, 1996
VACTERL with the mitochondrial np 3243 point mutationM S Damian, P Seibel, W Schachenmayr, et al.
European Journal of Neurology|October 18, 2019
Admission patterns and survival from status epilepticus in critical care in the UK: an analysis of the Intensive Care National Audit and Research Centre Case Mix Programme databaseM S Damian, Y Ben-Shlomo, R Howard, et al.
Journal of Neurology|April 1, 1991
Stroke-like episodes in familial mitochondrial encephalomyopathy: clinical and biochemical aspectsM S Damian, H Reichmann, H J Schütz, et al.
Deutsche Medizinische Wochenschrift (1946)|December 9, 1994
[Polyneuritis and myositis in Trypanosoma gambiense infection]M S Damian, W Dorndorf, H Burkardt, et al.
European Radiology|February 5, 1999
Degenerative joint disease on MRI and physical activity: a clinical study of the knee joint in 320 patientsG F Bachmann, E Basad, K Rauber, et al.
Der Nervenarzt|April 1, 1994
[MELAS syndrome. Clinical aspects, MRI, biochemistry and molecular genetics]M S Damian, H Reichmann, P Seibel, et al.
Acta Neurologica Scandinavica|December 1, 1994
White matter lesions and cognitive deficits: relevance of lesion pattern?M S Damian, G Schilling, G Bachmann, et al.
Neuroradiology|October 1, 1996
The clinical and genetic correlates of MRI findings in myotonic dystrophyG Bachmann, M S Damian, M Koch, et al.
Neuroreport|December 20, 1994
Brain disease and molecular analysis in myotonic dystrophyM S Damian, G Bachmann, M C Koch, et al.
European Neurology|February 26, 1998
Follow-up in carriers of the 'MELAS' mutation without strokesM S Damian, A Hertel, P Seibel, et al.
Pageof 3

Showing results (11-20 of 23) with videos related to

Sort By:
Pageof 3
American Journal of Medical Genetics|April 24, 1996
VACTERL with the mitochondrial np 3243 point mutationM S Damian, P Seibel, W Schachenmayr, et al.
European Journal of Neurology|October 18, 2019
Admission patterns and survival from status epilepticus in critical care in the UK: an analysis of the Intensive Care National Audit and Research Centre Case Mix Programme databaseM S Damian, Y Ben-Shlomo, R Howard, et al.
Journal of Neurology|April 1, 1991
Stroke-like episodes in familial mitochondrial encephalomyopathy: clinical and biochemical aspectsM S Damian, H Reichmann, H J Schütz, et al.
Deutsche Medizinische Wochenschrift (1946)|December 9, 1994
[Polyneuritis and myositis in Trypanosoma gambiense infection]M S Damian, W Dorndorf, H Burkardt, et al.
European Radiology|February 5, 1999
Degenerative joint disease on MRI and physical activity: a clinical study of the knee joint in 320 patientsG F Bachmann, E Basad, K Rauber, et al.
Der Nervenarzt|April 1, 1994
[MELAS syndrome. Clinical aspects, MRI, biochemistry and molecular genetics]M S Damian, H Reichmann, P Seibel, et al.
Acta Neurologica Scandinavica|December 1, 1994
White matter lesions and cognitive deficits: relevance of lesion pattern?M S Damian, G Schilling, G Bachmann, et al.
Neuroradiology|October 1, 1996
The clinical and genetic correlates of MRI findings in myotonic dystrophyG Bachmann, M S Damian, M Koch, et al.
Neuroreport|December 20, 1994
Brain disease and molecular analysis in myotonic dystrophyM S Damian, G Bachmann, M C Koch, et al.
European Neurology|February 26, 1998
Follow-up in carriers of the 'MELAS' mutation without strokesM S Damian, A Hertel, P Seibel, et al.
Pageof 3