Cobalamin deficiency in elderly patients

par Ray, Joel G., Cole, David E.C.
Publié 2005

Vitamin B(12) and homocysteine

par Ray, Joel G., Cole, David E.C.
Publié 2005

Ruling in a Suspect: The Role of AP2S1 Mutations in Familial Hypocalciuric Hypercalcemia Type 3

par Hendy, Geoffrey N., Cole, David E. C.
Publié 2013

Maternal ethnicity and risk of neural tube defects: a population-based study

par Ray, Joel G., Vermeulen, Marian J., Meier, Chris, Cole, David E.C., Wyatt, Philip R.
Publié 2004

Predictors of 25-Hydroxyvitamin D Concentration Measured at Multiple Time Points in a Multiethnic Population

par Knight, Julia A, Wong, Jody, Cole, David E C, Lee, Tim K, Parra, Esteban J
Publié dans Am J Epidemiol (2017)

Topiramate Treatment May Interfere With Urinary Cortisol Measurement By Radioimmunoassay (RIA) – A Case Report

par Chan, Pak Cheung R., Silverberg, Jay, Cole, David E. C., Lem-Ragosnig, Bonny, Recknagel, Frank
Publié dans EJIFCC (2005)

Low wintertime vitamin D levels in a sample of healthy young adults of diverse ancestry living in the Toronto area: associations with vitamin D intake and skin pigmentation

par Gozdzik, Agnes, Barta, Jodi Lynn, Wu, Hongyu, Wagner, Dennis, Cole, David E, Vieth, Reinhold, Whiting, Susan, Parra, Esteban J
Publié 2008

Common variants of the vitamin D binding protein gene and adverse health outcomes

par Malik, Suneil, Fu, Lei, Juras, David James, Karmali, Mohamed, Wong, Betty Y. L., Gozdzik, Agnes, Cole, David E. C.
Publié 2013

Genetic Defect in CYP24A1, the Vitamin D 24-Hydroxylase Gene, in a Patient with Severe Infantile Hypercalcemia

par Dauber, Andrew, Nguyen, Thutrang T., Sochett, Etienne, Cole, David E. C., Horst, Ronald, Abrams, Steven A., Carpenter, Thomas O., Hirschhorn, Joel N.
Publié 2012

Relationship of Total and Free 25-Hydroxyvitamin D to Biomarkers and Metabolic Indices in Healthy Children

par Simpson, Christine A, Zhang, Jane H, Vanderschueren, Dirk, Fu, Lei, Pennestri, Teresita C, Bouillon, Roger, Cole, David E C, Carpenter, Thomas O
Publié dans J Clin Endocrinol Metab (2019)

25-OHD response to vitamin D supplementation in children: effect of dose but not GC haplotype

par Simpson, Christine A., Zhang, Jane H., Vanderschueren, Dirk, Fu, Lei, Pennestri, Teresita C., Bouillon, Roger, Cole, David E.C., Carpenter, Thomas O.
Publié dans Eur J Endocrinol (2021)

Vitamin D Binding Protein is a key determinant of 25-hydroxyvitamin D levels in infants and toddlers

par Carpenter, Thomas O., Zhang, Jane H., Parra, Esteban, Ellis, Bruce K., Simpson, Christine, Lee, William M., Balko, Jody, Fu, Lei, Wong, Betty Y-L, Cole, David E. C.
Publié 2013

Large intragenic deletion of CDC73 (exons 4–10) in a three-generation hyperparathyroidism-jaw tumor (HPT-JT) syndrome family

par Guarnieri, Vito, Seaberg, Raewyn M., Kelly, Catherine, Jean Davidson, M., Raphael, Simon, Shuen, Andrew Y., Baorda, Filomena, Palumbo, Orazio, Scillitani, Alfredo, Hendy, Geoffrey N., Cole, David E. C.
Publié dans BMC Med Genet (2017)

Erratum to: Large intragenic deletion of CDC73 (exons 4–10) in a three-generation hyperparathyroidism-jaw tumor (HPT-JT) syndrome family

par Guarnieri, Vito, Seaberg, Raewyn M., Kelly, Catherine, Jean Davidson, M., Raphael, Simon, Shuen, Andrew Y., Baorda, Filomena, Palumbo, Orazio, Scillitani, Alfredo, Hendy, Geoffrey N., Cole, David E.C.
Publié dans BMC Med Genet (2017)

Haplotypes in the Dystrophin DNA Segment Point to a Mosaic Origin of Modern Human Diversity

par Ziętkiewicz, Ewa, Yotova, Vania, Gehl, Dominik, Wambach, Tina, Arrieta, Isabel, Batzer, Mark, Cole, David E. C., Hechtman, Peter, Kaplan, Feige, Modiano, David, Moisan, Jean-Paul, Michalski, Roman, Labuda, Damian
Publié 2003

Traditional foods and 25(OH)D concentrations in a subarctic First Nations community

par Mansuri, Sudaba, Badawi, Alaa, Kayaniyil, Sheena, Cole, David E., Harris, Stewart B., Mamakeesick, Mary, Wolever, Thomas, Gittelsohn, Joel, Maguire, Jonathon L., Connelly, Philip W., Zinman, Bernard, Hanley, Anthony J.
Publié dans Int J Circumpolar Health (2016)

Vitamin D in adult health and disease: a review and guideline statement from Osteoporosis Canada

par Hanley, David A., Cranney, Ann, Jones, Glenville, Whiting, Susan J., Leslie, William D., Cole, David E.C., Atkinson, Stephanie A., Josse, Robert G., Feldman, Sidney, Kline, Gregory A., Rosen, Cheryl
Publié 2010

Association of Directly Measured Plasma Free 25(OH)D With Insulin Sensitivity and Secretion: The IRAS Family Study

par Lee, C. Christine, Young, Kendra A., Norris, Jill M., Rotter, Jerome I., Liu, Yeheng, Lorenzo, Carlos, Wagenknecht, Lynne E., Cole, David E., Haffner, Steven M., Chen, Yii-Der I., Hanley, Anthony J.
Publié dans J Clin Endocrinol Metab (2017)

MEN1 gene mutation with parathyroid carcinoma: first report of a familial case

par Cinque, Luigia, Sparaneo, Angelo, Salcuni, Antonio S, de Martino, Danilo, Battista, Claudia, Logoluso, Francesco, Palumbo, Orazio, Cocchi, Roberto, Maiello, Evaristo, Graziano, Paolo, Hendy, Geoffrey N, Cole, David E C, Scillitani, Alfredo, Guarnieri, Vito
Publié dans Endocr Connect (2017)

Stage Dependence, Cell-Origin Independence, and Prognostic Capacity of Serum Glycan Fucosylation, β1–4 Branching, β1–6 Branching, and α2–6 Sialylation in Cancer

par Ferdosi, Shadi, Rehder, Douglas S., Maranian, Paul, Castle, Erik P., Ho, Thai H., Pass, Harvey I., Cramer, Daniel W., Anderson, Karen S., Fu, Lei, Cole, David E. C., Le, Tao, Wu, Xifeng, Borges, Chad R.
Publié dans J Proteome Res (2017)