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Neurology|January 5, 2002
Late onset white matter disease in peroxisome biogenesis disorderP G Barth, J Gootjes, H Bode, et al.
Journal of Comparative Physiology. A, Neuroethology, Sensory, Neural, and Behavioral Physiology|March 30, 2011
Pheromone paths attached to the substrate in meliponine bees: helpful but not obligatory for recruitment successDirk Louis P Schorkopf, Linde Morawetz, José M S Bento, et al.
Journal of Computer Assisted Tomography|March 1, 1995
Central cortico-subcortical involvement: a distinct pattern of brain damage caused by perinatal and postnatal asphyxia in term infantsR P Rademakers, M S van der Knaap, B Verbeeten, et al.
Neuropadiatrie|May 1, 1980
Congenital muscular dystrophy and cerebral dysgenesis in a Dutch familyJ B Krijgsman, P G Barth, F C Stam, et al.
Journal of Inherited Metabolic Disease|July 17, 1999
X-linked cardioskeletal myopathy and neutropenia (Barth syndrome) (MIM 302060)P G Barth, R J Wanders, P Vreken, et al.
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.
Acta Biomaterialia|June 11, 2016
Micromechanical properties of strain-sensitive lyriform organs of a wandering spider (Cupiennius salei)Seth L Young, Marius Chyasnavichyus, Friedrich G Barth, 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.
The Journal of Biological Chemistry|August 22, 2003
Only one splice variant of the human TAZ gene encodes a functional protein with a role in cardiolipin metabolismFrédéric M Vaz, Riekelt H Houtkooper, Fredoen Valianpour, et al.
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