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Showing results (141-150 of 160) with videos related to

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Transplantation|September 24, 2005
Thromboembolism in heart transplantation: role of prothrombin G20210A and factor V LeidenSantiago G Miriuka, Loralie J Langman, Jovan Evrovski, et al.
The Journal of Clinical Endocrinology and Metabolism|February 19, 2010
Calcium-sensing receptor (CASR) mutations in hypercalcemic states: studies from a single endocrine clinic over three yearsVito Guarnieri, Lucie Canaff, Francisco H J Yun, et al.
European Journal of Endocrinology|June 27, 2014
Factors associated with vertebral fracture risk in patients with primary hyperparathyroidismCristina Eller-Vainicher, Claudia Battista, Vito Guarnieri, et al.
Endocrine Connections|November 4, 2017
<i>MEN1</i> gene mutation with parathyroid carcinoma: first report of a familial caseLuigia Cinque, Angelo Sparaneo, Antonio S Salcuni, et al.
American Journal of Medical Genetics. Part A|June 26, 2010
Hyperphosphatasia with seizures, neurologic deficit, and characteristic facial features: Five new patients with Mabry syndromeMiles D Thompson, Marjan M Nezarati, Gabriele Gillessen-Kaesbach, et al.
European Journal of Endocrinology|January 17, 2022
Novel Glial Cells Missing-2 (GCM2) variants in parathyroid disordersLucie Canaff, Vito Guarnieri, Yoojung Kim, et al.
Journal of Proteome Research|November 14, 2017
Stage Dependence, Cell-Origin Independence, and Prognostic Capacity of Serum Glycan Fucosylation, β1-4 Branching, β1-6 Branching, and α2-6 Sialylation in CancerShadi Ferdosi, Douglas S Rehder, Paul Maranian, et al.
Plos Medicine|October 29, 2014
The causal effect of vitamin D binding protein (DBP) levels on calcemic and cardiometabolic diseases: a Mendelian randomization studyAaron Leong, Waheed Rehman, Zari Dastani, et al.
Oncology Letters|July 12, 2017
Novel association of <i>MEN1</i> gene mutations with parathyroid carcinomaLuigia Cinque, Angelo Sparaneo, Filomena Cetani, et al.
Endocrine|November 19, 2011
A rare S33C mutation of CTNNB1 encoding β-catenin in a parathyroid adenoma found in an Italian primary hyperparathyroid cohortVito Guarnieri, Filomena Baorda, Claudia Battista, et al.
Pageof 16

Showing results (141-150 of 160) with videos related to

Sort By:
Pageof 16
Transplantation|September 24, 2005
Thromboembolism in heart transplantation: role of prothrombin G20210A and factor V LeidenSantiago G Miriuka, Loralie J Langman, Jovan Evrovski, et al.
The Journal of Clinical Endocrinology and Metabolism|February 19, 2010
Calcium-sensing receptor (CASR) mutations in hypercalcemic states: studies from a single endocrine clinic over three yearsVito Guarnieri, Lucie Canaff, Francisco H J Yun, et al.
European Journal of Endocrinology|June 27, 2014
Factors associated with vertebral fracture risk in patients with primary hyperparathyroidismCristina Eller-Vainicher, Claudia Battista, Vito Guarnieri, et al.
Endocrine Connections|November 4, 2017
<i>MEN1</i> gene mutation with parathyroid carcinoma: first report of a familial caseLuigia Cinque, Angelo Sparaneo, Antonio S Salcuni, et al.
American Journal of Medical Genetics. Part A|June 26, 2010
Hyperphosphatasia with seizures, neurologic deficit, and characteristic facial features: Five new patients with Mabry syndromeMiles D Thompson, Marjan M Nezarati, Gabriele Gillessen-Kaesbach, et al.
European Journal of Endocrinology|January 17, 2022
Novel Glial Cells Missing-2 (GCM2) variants in parathyroid disordersLucie Canaff, Vito Guarnieri, Yoojung Kim, et al.
Journal of Proteome Research|November 14, 2017
Stage Dependence, Cell-Origin Independence, and Prognostic Capacity of Serum Glycan Fucosylation, β1-4 Branching, β1-6 Branching, and α2-6 Sialylation in CancerShadi Ferdosi, Douglas S Rehder, Paul Maranian, et al.
Plos Medicine|October 29, 2014
The causal effect of vitamin D binding protein (DBP) levels on calcemic and cardiometabolic diseases: a Mendelian randomization studyAaron Leong, Waheed Rehman, Zari Dastani, et al.
Oncology Letters|July 12, 2017
Novel association of <i>MEN1</i> gene mutations with parathyroid carcinomaLuigia Cinque, Angelo Sparaneo, Filomena Cetani, et al.
Endocrine|November 19, 2011
A rare S33C mutation of CTNNB1 encoding β-catenin in a parathyroid adenoma found in an Italian primary hyperparathyroid cohortVito Guarnieri, Filomena Baorda, Claudia Battista, et al.
Pageof 16