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P G Barth

Showing results (51-60 of 177) with videos related to

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Nederlands Tijdschrift Voor Geneeskunde|May 1, 1993
[3 examples of fetal genetic neuromuscular disorders which lead to hydramnion]A H Teeuw, P G Barth, L van Sonderen, et al.
Neuropediatrics|October 1, 1996
Lissencephaly with extreme cerebral and cerebellar hypoplasia. A magnetic resonance imaging studyA A Kroon, B J Smit, P G Barth, et al.
Clinical Genetics|January 1, 1987
A male infant with holoprosencephaly, associated with ring chromosome 21D C Aronson, M C Jansweijer, J M Hoovers, et al.
Neurology|December 1, 1994
Predominance of the adrenomyeloneuropathy phenotype of X-linked adrenoleukodystrophy in The Netherlands: a survey of 30 kindredsB M van Geel, J Assies, G J Weverling, et al.
Brain : a Journal of Neurology|April 29, 1999
Bethlem myopathy: a slowly progressive congenital muscular dystrophy with contracturesG J Jöbsis, J M Boers, P G Barth, et al.
Brain & Development|March 1, 1995
Epidermal nevus syndrome with isolated enlargement of one temporal lobe: a case reportV I Kwa, J H Smitt, B W Verbeeten, et al.
American Journal of Medical Genetics|March 15, 1996
Variant rhizomelic chondrodysplasia punctata (RCDP) with normal plasma phytanic acid: clinico-biochemical delineation of a subtype and complementation studiesP G Barth, R J Wanders, R B Schutgens, et al.
European Journal of Pediatrics|January 1, 1994
Clinical and biochemical characteristics of peroxisomal disorders: an updateR J Wanders, P G Barth, R B Schutgens, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|July 1, 1997
X linked adrenoleukodystrophy: clinical presentation, diagnosis, and therapyB M van Geel, J Assies, R J Wanders, et al.
Tijdschrift Voor Kindergeneeskunde|April 1, 1982
[The Aicardi syndrome]P G Barth, R F Oosterkamp, T N Boen-Tan, et al.
Pageof 18

Showing results (51-60 of 177) with videos related to

Sort By:
Pageof 18
Nederlands Tijdschrift Voor Geneeskunde|May 1, 1993
[3 examples of fetal genetic neuromuscular disorders which lead to hydramnion]A H Teeuw, P G Barth, L van Sonderen, et al.
Neuropediatrics|October 1, 1996
Lissencephaly with extreme cerebral and cerebellar hypoplasia. A magnetic resonance imaging studyA A Kroon, B J Smit, P G Barth, et al.
Clinical Genetics|January 1, 1987
A male infant with holoprosencephaly, associated with ring chromosome 21D C Aronson, M C Jansweijer, J M Hoovers, et al.
Neurology|December 1, 1994
Predominance of the adrenomyeloneuropathy phenotype of X-linked adrenoleukodystrophy in The Netherlands: a survey of 30 kindredsB M van Geel, J Assies, G J Weverling, et al.
Brain : a Journal of Neurology|April 29, 1999
Bethlem myopathy: a slowly progressive congenital muscular dystrophy with contracturesG J Jöbsis, J M Boers, P G Barth, et al.
Brain & Development|March 1, 1995
Epidermal nevus syndrome with isolated enlargement of one temporal lobe: a case reportV I Kwa, J H Smitt, B W Verbeeten, et al.
American Journal of Medical Genetics|March 15, 1996
Variant rhizomelic chondrodysplasia punctata (RCDP) with normal plasma phytanic acid: clinico-biochemical delineation of a subtype and complementation studiesP G Barth, R J Wanders, R B Schutgens, et al.
European Journal of Pediatrics|January 1, 1994
Clinical and biochemical characteristics of peroxisomal disorders: an updateR J Wanders, P G Barth, R B Schutgens, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|July 1, 1997
X linked adrenoleukodystrophy: clinical presentation, diagnosis, and therapyB M van Geel, J Assies, R J Wanders, et al.
Tijdschrift Voor Kindergeneeskunde|April 1, 1982
[The Aicardi syndrome]P G Barth, R F Oosterkamp, T N Boen-Tan, et al.
Pageof 18