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P G Barth

Showing results (81-90 of 177) with videos related to

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Journal of Neurology|February 1, 1992
Hereditary protein S deficiency presenting with cerebral sinus thrombosis in an adolescent girlJ H Koelman, C M Bakker, W C Plandsoen, et al.
Journal of the Neurological Sciences|June 1, 1990
Inherited syndrome of microcephaly, dyskinesia and pontocerebellar hypoplasia: a systemic atrophy with early onsetP G Barth, G F Vrensen, H B Uylings, et al.
Neuropadiatrie|February 1, 1980
On the relationship between germinal layer haemorrhage and telencephalic leucoencephalopathy in the preterm infantP G Barth, F C Stam, R F Oosterkamp, et al.
Acta Neuropathologica|January 1, 1984
Axonal dystrophy in a case of connatal thalamic and brain stem degenerationF G Jennekens, P G Barth, P Fleury, et al.
European Journal of Pediatrics|July 1, 1991
A family with severe X-linked arthrogryposisR C Hennekam, P G Barth, W Van Lookeren Campagne, et al.
European Journal of Pediatrics|July 1, 1990
Peroxisomal beta-oxidation defect with detectable peroxisomes: a case with neonatal onset and progressive courseP G Barth, R J Wanders, R B Schutgens, et al.
European Journal of Obstetrics, Gynecology, and Reproductive Biology|September 1, 1985
Intra-uterine tachycardia associated with multicystic encephalomalacia (MCE)M C van Doornik, B P Cats, P G Barth, et al.
Biochimie|January 1, 1993
Postnatal diagnosis of peroxisomal disorders: a biochemical approachR J Wanders, R B Schutgens, P G Barth, et al.
The Journal of Pediatrics|March 4, 2000
Carbohydrate-deficient glycoprotein syndrome type 1a: a variant phenotype with borderline cognitive dysfunction, cerebellar hypoplasia, and coagulation disturbancesC H van Ommen, M Peters, P G Barth, et al.
Journal of Inherited Metabolic Disease|August 2, 2003
The eye as a window to inborn errors of metabolismB T Poll-The, L J Maillette de Buy Wenniger-Prick, P G Barth, et al.
Pageof 18

Showing results (81-90 of 177) with videos related to

Sort By:
Pageof 18
Journal of Neurology|February 1, 1992
Hereditary protein S deficiency presenting with cerebral sinus thrombosis in an adolescent girlJ H Koelman, C M Bakker, W C Plandsoen, et al.
Journal of the Neurological Sciences|June 1, 1990
Inherited syndrome of microcephaly, dyskinesia and pontocerebellar hypoplasia: a systemic atrophy with early onsetP G Barth, G F Vrensen, H B Uylings, et al.
Neuropadiatrie|February 1, 1980
On the relationship between germinal layer haemorrhage and telencephalic leucoencephalopathy in the preterm infantP G Barth, F C Stam, R F Oosterkamp, et al.
Acta Neuropathologica|January 1, 1984
Axonal dystrophy in a case of connatal thalamic and brain stem degenerationF G Jennekens, P G Barth, P Fleury, et al.
European Journal of Pediatrics|July 1, 1991
A family with severe X-linked arthrogryposisR C Hennekam, P G Barth, W Van Lookeren Campagne, et al.
European Journal of Pediatrics|July 1, 1990
Peroxisomal beta-oxidation defect with detectable peroxisomes: a case with neonatal onset and progressive courseP G Barth, R J Wanders, R B Schutgens, et al.
European Journal of Obstetrics, Gynecology, and Reproductive Biology|September 1, 1985
Intra-uterine tachycardia associated with multicystic encephalomalacia (MCE)M C van Doornik, B P Cats, P G Barth, et al.
Biochimie|January 1, 1993
Postnatal diagnosis of peroxisomal disorders: a biochemical approachR J Wanders, R B Schutgens, P G Barth, et al.
The Journal of Pediatrics|March 4, 2000
Carbohydrate-deficient glycoprotein syndrome type 1a: a variant phenotype with borderline cognitive dysfunction, cerebellar hypoplasia, and coagulation disturbancesC H van Ommen, M Peters, P G Barth, et al.
Journal of Inherited Metabolic Disease|August 2, 2003
The eye as a window to inborn errors of metabolismB T Poll-The, L J Maillette de Buy Wenniger-Prick, P G Barth, et al.
Pageof 18