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Clinica Chimica Acta; International Journal of Clinical Chemistry
|
October 31, 1983
Thin-layer chromatography of oligosaccharides in urine as a rapid indication for the diagnosis of lysosomal acid maltase deficiency (Pompe's disease)
W Blom, J C Luteyn, H H Kelholt-Dijkman, et al.
Neuropediatrics
|
August 1, 1985
Late-onset globoid cell leucodystrophy (Krabbe's disease). Clinical and genetic delineation of two forms and their relation to the early-infantile form
M C Loonen, O P Van Diggelen, H C Janse, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
July 1, 1989
The natural history of the Guillain-Barré syndrome in 18 children and 50 adults
R P Kleyweg, F G van der Meché, M C Loonen, et al.
Nederlands Tijdschrift Voor Geneeskunde
|
April 28, 1984
[Incontinentia pigmenti (Bloch-Sulzberger syndrome)]
A P Oranje, W F Arts, M C Loonen, et al.
Pediatric Research
|
July 1, 1988
Receptor-mediated uptake of acid alpha-glucosidase corrects lysosomal glycogen storage in cultured skeletal muscle
A T Van der Ploeg, M C Loonen, P A Bolhuis, et al.
Journal of the Neurological Sciences
|
January 1, 1987
Cytochrome c oxidase deficiency in subacute necrotizing encephalomyelopathy
W F Arts, H R Scholte, M C Loonen, et al.
Muscle & Nerve
|
March 5, 1998
Muscle computed tomography in adult-onset acid maltase deficiency
A E de Jager, T M van der Vliet, T C van der Ree, et al.
Epilepsia
|
May 1, 1988
Follow-up of 146 children with epilepsy after withdrawal of antiepileptic therapy
W F Arts, L H Visser, M C Loonen, et al.
Biochemical and Biophysical Research Communications
|
December 16, 1983
Two genetically different MU-NANA neuraminidases in human leucocytes
F W Verheijen, H C Janse, O P van Diggelen, et al.
Lancet (London, England)
|
September 6, 2000
Recombinant human alpha-glucosidase from rabbit milk in Pompe patients
H Van den Hout, A J Reuser, A G Vulto, et al.
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of 4
Search research articles
Search
Showing results (21-30 of 37) with videos related to
Sort By:
Page
of 4
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
October 31, 1983
Thin-layer chromatography of oligosaccharides in urine as a rapid indication for the diagnosis of lysosomal acid maltase deficiency (Pompe's disease)
W Blom, J C Luteyn, H H Kelholt-Dijkman, et al.
Neuropediatrics
|
August 1, 1985
Late-onset globoid cell leucodystrophy (Krabbe's disease). Clinical and genetic delineation of two forms and their relation to the early-infantile form
M C Loonen, O P Van Diggelen, H C Janse, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
July 1, 1989
The natural history of the Guillain-Barré syndrome in 18 children and 50 adults
R P Kleyweg, F G van der Meché, M C Loonen, et al.
Nederlands Tijdschrift Voor Geneeskunde
|
April 28, 1984
[Incontinentia pigmenti (Bloch-Sulzberger syndrome)]
A P Oranje, W F Arts, M C Loonen, et al.
Pediatric Research
|
July 1, 1988
Receptor-mediated uptake of acid alpha-glucosidase corrects lysosomal glycogen storage in cultured skeletal muscle
A T Van der Ploeg, M C Loonen, P A Bolhuis, et al.
Journal of the Neurological Sciences
|
January 1, 1987
Cytochrome c oxidase deficiency in subacute necrotizing encephalomyelopathy
W F Arts, H R Scholte, M C Loonen, et al.
Muscle & Nerve
|
March 5, 1998
Muscle computed tomography in adult-onset acid maltase deficiency
A E de Jager, T M van der Vliet, T C van der Ree, et al.
Epilepsia
|
May 1, 1988
Follow-up of 146 children with epilepsy after withdrawal of antiepileptic therapy
W F Arts, L H Visser, M C Loonen, et al.
Biochemical and Biophysical Research Communications
|
December 16, 1983
Two genetically different MU-NANA neuraminidases in human leucocytes
F W Verheijen, H C Janse, O P van Diggelen, et al.
Lancet (London, England)
|
September 6, 2000
Recombinant human alpha-glucosidase from rabbit milk in Pompe patients
H Van den Hout, A J Reuser, A G Vulto, et al.
Page
of 4