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M C Loonen

Showing results (11-20 of 37) with videos related to

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Clinical Genetics|April 1, 1976
beta-Galactosidase deficiency in an adult: a biochemical and somatic cell genetic study on a variant of GM1-gangliosidosisJ F Koster, M F Niermeijer, M C Loonen, et al.
Clinical Genetics|August 1, 1984
Combined sialidase (neuraminidase) and beta-galactosidase deficiency. Clinical, morphological and enzymological observations in a patientM C Loonen, A J Reuser, P Visser, et al.
Annals of Neurology|May 1, 1993
X-linked ataxia, weakness, deafness, and loss of vision in early childhood with a fatal courseW F Arts, M C Loonen, R C Sengers, et al.
Nederlands Tijdschrift Voor Geneeskunde|May 5, 1973
[The gangliosidoses]M C Loonen, K J Lamers, E D Schretlen, et al.
Neuropediatrics|December 1, 1993
Blind, deaf and mute after a status epilepticus caused by hyperpyrexia from shigellosis--a case report with a four-year follow-upH R van Dongen, M C Loonen, D J Heersema, et al.
Acta Neuropathologica|May 16, 1977
Ultrastructural study of the vacuoles in the peripheral lymphocytes in juvenile amaurotic idiocy. Juvenile form of generalized ceroid lipofuscinosisJ H Stekhoven, U J van Haelst, E M Joosten, et al.
Archives of Dermatology|September 1, 1994
Solomon's epidermal nevus syndrome (type: linear nevus sebaceus) and hypophosphatemic vitamin D-resistant ricketsA P Oranje, H Przyrembel, M Meradji, et al.
Zeitschrift Fur Kinder- Und Jugendpsychiatrie|March 1, 1989
[The Landau-Kleffner syndrome: a special form of acquired childhood aphasia]M Blouw-van Mourik, H R van Dongen, M C Loonen, et al.
Developmental Medicine and Child Neurology|August 1, 1990
Diagnostic features and clinical signs of 21 patients with lissencephaly type 1J F de Rijk-van Andel, W F Arts, P G Barth, et al.
Cephalalgia : an International Journal of Headache|May 1, 1996
A quality of life instrument for adolescents with chronic headacheJ H Langeveld, H M Koot, M C Loonen, et al.
Pageof 4

Showing results (11-20 of 37) with videos related to

Sort By:
Pageof 4
Clinical Genetics|April 1, 1976
beta-Galactosidase deficiency in an adult: a biochemical and somatic cell genetic study on a variant of GM1-gangliosidosisJ F Koster, M F Niermeijer, M C Loonen, et al.
Clinical Genetics|August 1, 1984
Combined sialidase (neuraminidase) and beta-galactosidase deficiency. Clinical, morphological and enzymological observations in a patientM C Loonen, A J Reuser, P Visser, et al.
Annals of Neurology|May 1, 1993
X-linked ataxia, weakness, deafness, and loss of vision in early childhood with a fatal courseW F Arts, M C Loonen, R C Sengers, et al.
Nederlands Tijdschrift Voor Geneeskunde|May 5, 1973
[The gangliosidoses]M C Loonen, K J Lamers, E D Schretlen, et al.
Neuropediatrics|December 1, 1993
Blind, deaf and mute after a status epilepticus caused by hyperpyrexia from shigellosis--a case report with a four-year follow-upH R van Dongen, M C Loonen, D J Heersema, et al.
Acta Neuropathologica|May 16, 1977
Ultrastructural study of the vacuoles in the peripheral lymphocytes in juvenile amaurotic idiocy. Juvenile form of generalized ceroid lipofuscinosisJ H Stekhoven, U J van Haelst, E M Joosten, et al.
Archives of Dermatology|September 1, 1994
Solomon's epidermal nevus syndrome (type: linear nevus sebaceus) and hypophosphatemic vitamin D-resistant ricketsA P Oranje, H Przyrembel, M Meradji, et al.
Zeitschrift Fur Kinder- Und Jugendpsychiatrie|March 1, 1989
[The Landau-Kleffner syndrome: a special form of acquired childhood aphasia]M Blouw-van Mourik, H R van Dongen, M C Loonen, et al.
Developmental Medicine and Child Neurology|August 1, 1990
Diagnostic features and clinical signs of 21 patients with lissencephaly type 1J F de Rijk-van Andel, W F Arts, P G Barth, et al.
Cephalalgia : an International Journal of Headache|May 1, 1996
A quality of life instrument for adolescents with chronic headacheJ H Langeveld, H M Koot, M C Loonen, et al.
Pageof 4