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Annals of Neurology|September 8, 2000
Familial Alzheimer's disease: site of mutation influences clinical phenotypeC F Lippa, J M Swearer, K J Kane, et al.
Annals of Neurology|June 1, 1996
Molecular basis of phenotypic variability in sporadic Creutzfeldt-Jakob diseaseP Parchi, R Castellani, S Capellari, et al.
The Journal of Allergy and Clinical Immunology|February 11, 2018
New mechanism underlying IL-31-induced atopic dermatitisJianghui Meng, Masaki Moriyama, Micha Feld, et al.
Journal of Women'S Health Physical Therapy|August 9, 2021
Hip and Pelvic Floor Muscle Strength in Women with and without Urgency and Frequency Predominant Lower Urinary Tract SymptomsStefanie N Foster, Theresa M Spitznagle, Lori J Tuttle, et al.
Scientific Reports|January 17, 2017
Novel strain properties distinguishing sporadic prion diseases sharing prion protein genotype and prion typeLaura Cracco, Silvio Notari, Ignazio Cali, et al.
International Psychogeriatrics|June 30, 2006
Performance on MMSE sub-items and education level in presenilin-1 mutation carriers without dementiaJohn M Ringman, Yaneth Rodriguez, Claudia Diaz-Olavarrieta, et al.
Scandinavian Journal of Medicine & Science in Sports|May 13, 2010
Changes in exercise capacity induced by heart transplantation: prognostic and therapeutic implicationsF Grigioni, S Specchia, P Maietta, et al.
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