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W Mortier

Showing results (41-50 of 61) with videos related to

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Human Mutation|December 29, 1999
Novel mutation in the RYR1 gene (R2454C) in a patient with malignant hyperthermiaM Gencik, A Gencik, W Mortier, et al.
Brain & Development|January 1, 1982
Lymphocyte capping in muscular dystrophiesC R Bartram, J Serwinski, D Reinhardt, et al.
Annals of Neurology|January 1, 1982
Value of C26:O fatty acid determination for the diagnosis of atypical adrenoleukodystrophyM Philippart, M R Nuwer, W Mortier, et al.
Neuropediatrics|November 1, 1982
The slit-ventricle syndrome after shunting in hydrocephalic childrenR Kiekens, W Mortier, R Pothmann, et al.
European Journal of Pediatrics|March 1, 1982
Subacute sclerosing panencephalitis in a brother and sister. Therapeutic trial of fibroblast interferonC R Bartram, J Henke, J Treuner, et al.
Neurology|May 5, 1999
Phenotypic variability in rippling muscle diseaseM Vorgerd, H Bolz, T Patzold, et al.
Muscle & Nerve|May 16, 2001
Isolated loss of gamma-sarcoglycan: diagnostic implications in autosomal recessive limb-girdle muscular dystrophiesM Vorgerd, M Gencik, J Mortier, et al.
European Journal of Pediatrics|July 31, 2001
Alpha-sarcoglycanopathy previously misdiagnosed as Duchenne muscular dystrophy: implications for current diagnostics and patient careU Schara, M Gencik, J Mortier, et al.
Acta Paediatrica (Oslo, Norway : 1992)|March 25, 1999
Short stature in Duchenne muscular dystrophy: a study of 34 patientsB H Nagel, W Mortier, M Elmlinger, et al.
European Journal of Medical Research|March 14, 1998
Congenital myasthenic syndromes: clinical and genetic analysis of 18 patientsA Abicht, W Müller-Felber, P Fischer, et al.
Pageof 7

Showing results (41-50 of 61) with videos related to

Sort By:
Pageof 7
Human Mutation|December 29, 1999
Novel mutation in the RYR1 gene (R2454C) in a patient with malignant hyperthermiaM Gencik, A Gencik, W Mortier, et al.
Brain & Development|January 1, 1982
Lymphocyte capping in muscular dystrophiesC R Bartram, J Serwinski, D Reinhardt, et al.
Annals of Neurology|January 1, 1982
Value of C26:O fatty acid determination for the diagnosis of atypical adrenoleukodystrophyM Philippart, M R Nuwer, W Mortier, et al.
Neuropediatrics|November 1, 1982
The slit-ventricle syndrome after shunting in hydrocephalic childrenR Kiekens, W Mortier, R Pothmann, et al.
European Journal of Pediatrics|March 1, 1982
Subacute sclerosing panencephalitis in a brother and sister. Therapeutic trial of fibroblast interferonC R Bartram, J Henke, J Treuner, et al.
Neurology|May 5, 1999
Phenotypic variability in rippling muscle diseaseM Vorgerd, H Bolz, T Patzold, et al.
Muscle & Nerve|May 16, 2001
Isolated loss of gamma-sarcoglycan: diagnostic implications in autosomal recessive limb-girdle muscular dystrophiesM Vorgerd, M Gencik, J Mortier, et al.
European Journal of Pediatrics|July 31, 2001
Alpha-sarcoglycanopathy previously misdiagnosed as Duchenne muscular dystrophy: implications for current diagnostics and patient careU Schara, M Gencik, J Mortier, et al.
Acta Paediatrica (Oslo, Norway : 1992)|March 25, 1999
Short stature in Duchenne muscular dystrophy: a study of 34 patientsB H Nagel, W Mortier, M Elmlinger, et al.
European Journal of Medical Research|March 14, 1998
Congenital myasthenic syndromes: clinical and genetic analysis of 18 patientsA Abicht, W Müller-Felber, P Fischer, et al.
Pageof 7