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Journal of Orofacial Pain|January 1, 1994
Management of craniomandibular disorders. Part II: Clinical assessment of patients with craniocervical dysfunctionC Wallace, I J KlinebergJournal of Orofacial Pain|January 1, 1993
Management of craniomandibular disorders. Part 1: A craniocervical dysfunction indexC Wallace, I J KlinebergChild: Care, Health and Development|November 1, 1995
Establishing a district palliative care team for childrenA C Wallace, S JacksonGenetics in Medicine : Official Journal of the American College of Medical Genetics|August 21, 2007
The pharmacology of multiple regimens of agalsidase alfa enzyme replacement therapy for Fabry diseaseJoe T R Clarke, Michael L West, Jan Bultas, et al.DNA and Cell Biology|May 1, 1996
Isolation and characterization of several members of the murine Hsd3b gene familyT R Clarke, P A Bain, M Burmeister, et al.Endocrinology|May 1, 1993
Enzyme characteristics of two distinct forms of mouse 3 beta-hydroxysteroid dehydrogenase/delta 5-delta 4-isomerase complementary deoxyribonucleic acids expressed in COS-1 cellsT R Clarke, P A Bain, L Sha, et al.Journal of Inherited Metabolic Disease|January 27, 2005
Gaucher disease: variability in phenotype among siblingsD Amato, T Stachiw, J T R Clarke, et al.Journal of Inherited Metabolic Disease|October 26, 2007
Unsuccessful treatment attempt: cord blood stem cell transplantation in a patient with Niemann-Pick disease type AC F Morel, A Gassas, J Doyle, et al.The West Indian Medical Journal|March 2, 2011
Response to first line HAART using CD4 cell counts experience in a university hospital in KingstonT R Clarke, G Barrow, D Thompson, et al.Journal of Inherited Metabolic Disease|June 10, 2010
Childhood onset of Scheie syndrome, the attenuated form of mucopolysaccharidosis IJanet A Thomas, Michael Beck, Joe T R Clarke, et al.Pageof 157