Showing results (101-110 of 295) with videos related to
Sort By:
Pageof 30
Clinical Neurology and Neurosurgery|August 1, 1994
Limb girdle muscular dystrophy: reappraisal of a rejected entityA J van der Kooi, M de Visser, P G BarthJournal of Neurology, Neurosurgery, and Psychiatry|October 1, 1984
Paucity of secondary synaptic clefts in a case of congenital myasthenia with multiple contractures: ultrastructural morphology of a developmental disorderL M Smit, F G Jennekens, H Veldman, et al.International Journal of Andrology|September 1, 2005
Signs of testicular insufficiency in adrenomyeloneuropathy and neurologically asymptomatic X-linked adrenoleukodystrophy: a retrospective studyJ Assies, L J Gooren, B Van Geel, et al.European Journal of Pediatrics|August 1, 1980
The Joubert syndrome associated with bilateral chorioretinal colobomaD Lindhout, P G Barth, J Valk, et al.Orphanet Journal of Rare Diseases|July 14, 2011
Classification, diagnosis and potential mechanisms in pontocerebellar hypoplasiaYasmin Namavar, Peter G Barth, Bwee Tien Poll-The, et al.Journal of Vascular Surgery|April 1, 1994
The role of circulating cells in the healing of vascular prosthesesS M Scott, M G Barth, L R Gaddy, et al.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.Journal of Comparative Physiology. A, Sensory, Neural, and Behavioral Physiology|July 27, 2001
Arthropod touch reception: spider hair sensilla as rapid touch detectorsJ T Albert, O C Friedrich, H E Dechant, 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.Pageof 30