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)

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

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

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)

Prevalence and Penetrance of Germline BRCA1 and BRCA2 Mutations in a Population Series of 649 Women with Ovarian Cancer

par Risch, Harvey A., McLaughlin, John R., Cole, David E. C., Rosen, Barry, Bradley, Linda, Kwan, Elaine, Jack, Elaine, Vesprini, Danny J., Kuperstein, Graciela, Abrahamson, John L. A., Fan, Isabel, Wong, Betty, Narod, Steven A.
Publié 2001

The Causal Effect of Vitamin D Binding Protein (DBP) Levels on Calcemic and Cardiometabolic Diseases: A Mendelian Randomization Study

par Leong, Aaron, Rehman, Waheed, Dastani, Zari, Greenwood, Celia, Timpson, Nicholas, Langsetmo, Lisa, Berger, Claudie, Fu, Lei, Wong, Betty Y. L., Malik, Suneil, Malik, Rainer, Hanley, David A., Cole, David E. C., Goltzman, David, Richards, J. Brent
Publié 2014

Novel association of MEN1 gene mutations with parathyroid carcinoma

par Cinque, Luigia, Sparaneo, Angelo, Cetani, Filomena, Coco, Michelina, Clemente, Celeste, Chetta, Massimiliano, Balsamo, Teresa, Battista, Claudia, Sanpaolo, Eliana, Pardi, Elena, D'Agruma, Leonardo, Marcocci, Claudio, Maiello, Evaristo, Hendy, Geoffrey N., Cole, David E.C., Scillitani, Alfredo, Guarnieri, Vito
Publié dans Oncol Lett (2017)