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Genomics|September 6, 2002
A new gene family (FAM9) of low-copy repeats in Xp22.3 expressed exclusively in testis: implications for recombinations in this regionIsabel Martinez-Garay, Sibylle Jablonka, Marketa Sutajova, et al.Journal of Neurology|March 3, 2010
Female carriers of X-chromosomal adrenoleukodystrophy: a major differential diagnosis in progressive myelopathyAnne-Katrin Guettsches, Alma Kuechler, Andreas Gal, et al.Journal of Proteome Research|March 8, 2013
The identification of new biomarkers for identifying and monitoring kidney disease and their translation into a rapid mass spectrometry-based test: evidence of presymptomatic kidney disease in pediatric Fabry and type-I diabetic patientsVictoria Manwaring, Wendy E Heywood, Robert Clayton, et al.Psychiatrische Praxis|February 16, 2005
[Is there a connection between right-wing extremism and social distancing from mentally ill people? Results from a representative survey among the adult German population]Michael Beck, Matthias C Angermeyer, Elmar BrählerCanadian Journal of Psychiatry. Revue Canadienne De Psychiatrie|December 17, 2003
Determinants of the public's preference for social distance from people with schizophreniaMatthias C Angermeyer, Michael Beck, Herbert MatschingerJournal of Marital and Family Therapy|August 29, 2006
Three perspectives on clients' experiences of the therapeutic alliance: a discovery-oriented investigationMichael Beck, Myrna L Friedlander, Valentín EscuderoGeneral Dentistry|March 19, 2003
Anesthetic efficacy of different volumes of lidocaine with epinephrine for inferior alveolar nerve blocksJohn Nusstein, Al Reader, F Michael BeckSocial Psychiatry and Psychiatric Epidemiology|September 25, 2003
Social representations of major depression in West and East Germany--do differences still persist 11 years after reunification?Michael Beck, Herbert Matschinger, Matthias C AngermeyerPediatrics|October 17, 2007
Scoring evaluation of the natural course of mucopolysaccharidosis type IIIA (Sanfilippo syndrome type A)Ann Meyer, Kai Kossow, Andreas Gal, et al.Human Mutation|August 10, 2004
Impaired calmodulin binding of myosin-7A causes autosomal dominant hearing loss (DFNA11)Hanno Bolz, Steffen-Sebastian Bolz, Götz Schade, et al.Pageof 31