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H H Jaspar

Showing results (11-20 of 21) with videos related to

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Clinical Neurology and Neurosurgery|January 1, 1977
Oculopharyngodistal myopathy with early onset and neurogenic featuresH H Jaspar, L A Bastiaensen, H J ter Laak, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|January 29, 1982
Kearns syndrome: a heterogeneous group of disorders with CPEO, or a nosological entity?L A Bastiaensen, C W Frenken, H J Ter Laak, et al.
Acta Neurologica Scandinavica|September 1, 1984
Defects in citric acid cycle and the electron transport chain in progressive poliodystrophyF J Gabreëls, M J Prick, J M Trijbels, et al.
European Journal of Pediatrics|September 1, 1983
A mitochondrial myopathy with a defective respiratory chain and carnitine deficiencyR C Sengers, J C Fischer, J M Trijbels, et al.
Clinical Neuropathology|January 1, 1987
Lafora disease: a quantitative morphological and biochemical study of the cerebral cortexH L Busard, W O Renier, F J Gabreëls, et al.
Helvetica Paediatrica Acta|February 1, 1978
Oculocutaneous albinism associated with motor neuron diseaseB C Hamel, R C Sengers, A M Stadhouders, et al.
Ophthalmologica. Journal International D'Ophtalmologie. International Journal of Ophthalmology. Zeitschrift Fur Augenheilkunde|January 1, 1982
Kearns syndrome or Kearns disease. Further evidence of a genuine entity in a case with uncommon featuresL A Bastiaensen, S L Notermans, C H Ramaekers, et al.
Clinical Neurology and Neurosurgery|January 1, 1981
Congenital fibre type disproportionH J ter Laak, H H Jaspar, F J Gabreëls, et al.
Acta Neuropathologica|January 1, 1981
Connatal Pelizaeus-Merzbacher disease with congenital stridor in two maternal cousinsW O Renier, F J Gabreëls, T W Hustinx, et al.
Clinical Neuropathology|March 1, 1991
Canavan disease: neuromorphological and biochemical analysis of a brain biopsy specimenI F de Coo, F J Gabreëls, W O Renier, et al.
Pageof 3

Showing results (11-20 of 21) with videos related to

Sort By:
Pageof 3
Clinical Neurology and Neurosurgery|January 1, 1977
Oculopharyngodistal myopathy with early onset and neurogenic featuresH H Jaspar, L A Bastiaensen, H J ter Laak, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|January 29, 1982
Kearns syndrome: a heterogeneous group of disorders with CPEO, or a nosological entity?L A Bastiaensen, C W Frenken, H J Ter Laak, et al.
Acta Neurologica Scandinavica|September 1, 1984
Defects in citric acid cycle and the electron transport chain in progressive poliodystrophyF J Gabreëls, M J Prick, J M Trijbels, et al.
European Journal of Pediatrics|September 1, 1983
A mitochondrial myopathy with a defective respiratory chain and carnitine deficiencyR C Sengers, J C Fischer, J M Trijbels, et al.
Clinical Neuropathology|January 1, 1987
Lafora disease: a quantitative morphological and biochemical study of the cerebral cortexH L Busard, W O Renier, F J Gabreëls, et al.
Helvetica Paediatrica Acta|February 1, 1978
Oculocutaneous albinism associated with motor neuron diseaseB C Hamel, R C Sengers, A M Stadhouders, et al.
Ophthalmologica. Journal International D'Ophtalmologie. International Journal of Ophthalmology. Zeitschrift Fur Augenheilkunde|January 1, 1982
Kearns syndrome or Kearns disease. Further evidence of a genuine entity in a case with uncommon featuresL A Bastiaensen, S L Notermans, C H Ramaekers, et al.
Clinical Neurology and Neurosurgery|January 1, 1981
Congenital fibre type disproportionH J ter Laak, H H Jaspar, F J Gabreëls, et al.
Acta Neuropathologica|January 1, 1981
Connatal Pelizaeus-Merzbacher disease with congenital stridor in two maternal cousinsW O Renier, F J Gabreëls, T W Hustinx, et al.
Clinical Neuropathology|March 1, 1991
Canavan disease: neuromorphological and biochemical analysis of a brain biopsy specimenI F de Coo, F J Gabreëls, W O Renier, et al.
Pageof 3