Search research articles
Contact Us
Filters
Showing results (31-40 of 53) with videos related to
Page
of 6
Sort By:
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
February 25, 2021
Diagnostic utility of fine needle aspiration cytology in pediatric thyroid nodules based on Bethesda Classification
Wen Jiang, Susan A Phillips, Robert O Newbury, et al.
International Journal of Pediatric Otorhinolaryngology
|
April 9, 2022
Mutational analysis using next generation sequencing in pediatric thyroid cancer reveals BRAF and fusion oncogenes are common
Ron S Newfield, Wen Jiang, Daniel X Sugganth, et al.
The Journal of Clinical Endocrinology and Metabolism
|
January 14, 2000
Normocortisolemic Cushing's syndrome initially presenting with increased glucocorticoid receptor numbers
R S Newfield, G Kalaitzoglou, T Licholai, et al.
Clinical Case Reports
|
December 3, 2019
Diagnosis and treatment of a boy with IPEX syndrome presenting with diabetes in early infancy
Sejal Kadakia, Lauge Farnaes, David Dimmock, et al.
Oxford Medical Case Reports
|
January 8, 2020
Undescended retropharyngeal parathyroid adenoma with adjacent thymic tissue in a 13-year-old boy with primary hyperparathyroidism
Anthony M Kordahi, Ron S Newfield, Stephen W Bickler, et al.
Journal of the Endocrine Society
|
June 19, 2026
Clinical burden of classic congenital adrenal hyperplasia and glucocorticoid-related complications: a claims analysis
Hyunwoo Kim, Vivian H Lin, Ron S Newfield, et al.
Pediatric Diabetes
|
November 24, 2018
Non-alcoholic fatty liver disease in pediatric type 2 diabetes: Metabolic and histologic characteristics in 38 subjects
Ron S Newfield, Carrie L Graves, Robert O Newbury, et al.
The Journal of Clinical Endocrinology and Metabolism
|
September 16, 1999
Prenatal diagnosis and treatment of 11beta-hydroxylase deficiency congenital adrenal hyperplasia resulting in normal female genitalia
B I Cerame, R S Newfield, L Pascoe, et al.
Pediatric Blood & Cancer
|
July 21, 2021
Improving vitamin D testing and supplementation in children with newly diagnosed cancer: A quality improvement initiative at Rady Children's Hospital San Diego
Ksenya Shliakhtsitsava, Erin Stucky Fisher, Erin M Trovillion, et al.
The Journal of Clinical Endocrinology and Metabolism
|
April 16, 2014
Codon Arg15 mutations of the AP2S1 gene: common occurrence in familial hypocalciuric hypercalcemia cases negative for calcium-sensing receptor (CASR) mutations
Geoffrey N Hendy, Lucie Canaff, Ron S Newfield, et al.
Page
of 6
Search research articles
Search
Showing results (31-40 of 53) with videos related to
Sort By:
Page
of 6
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
February 25, 2021
Diagnostic utility of fine needle aspiration cytology in pediatric thyroid nodules based on Bethesda Classification
Wen Jiang, Susan A Phillips, Robert O Newbury, et al.
International Journal of Pediatric Otorhinolaryngology
|
April 9, 2022
Mutational analysis using next generation sequencing in pediatric thyroid cancer reveals BRAF and fusion oncogenes are common
Ron S Newfield, Wen Jiang, Daniel X Sugganth, et al.
The Journal of Clinical Endocrinology and Metabolism
|
January 14, 2000
Normocortisolemic Cushing's syndrome initially presenting with increased glucocorticoid receptor numbers
R S Newfield, G Kalaitzoglou, T Licholai, et al.
Clinical Case Reports
|
December 3, 2019
Diagnosis and treatment of a boy with IPEX syndrome presenting with diabetes in early infancy
Sejal Kadakia, Lauge Farnaes, David Dimmock, et al.
Oxford Medical Case Reports
|
January 8, 2020
Undescended retropharyngeal parathyroid adenoma with adjacent thymic tissue in a 13-year-old boy with primary hyperparathyroidism
Anthony M Kordahi, Ron S Newfield, Stephen W Bickler, et al.
Journal of the Endocrine Society
|
June 19, 2026
Clinical burden of classic congenital adrenal hyperplasia and glucocorticoid-related complications: a claims analysis
Hyunwoo Kim, Vivian H Lin, Ron S Newfield, et al.
Pediatric Diabetes
|
November 24, 2018
Non-alcoholic fatty liver disease in pediatric type 2 diabetes: Metabolic and histologic characteristics in 38 subjects
Ron S Newfield, Carrie L Graves, Robert O Newbury, et al.
The Journal of Clinical Endocrinology and Metabolism
|
September 16, 1999
Prenatal diagnosis and treatment of 11beta-hydroxylase deficiency congenital adrenal hyperplasia resulting in normal female genitalia
B I Cerame, R S Newfield, L Pascoe, et al.
Pediatric Blood & Cancer
|
July 21, 2021
Improving vitamin D testing and supplementation in children with newly diagnosed cancer: A quality improvement initiative at Rady Children's Hospital San Diego
Ksenya Shliakhtsitsava, Erin Stucky Fisher, Erin M Trovillion, et al.
The Journal of Clinical Endocrinology and Metabolism
|
April 16, 2014
Codon Arg15 mutations of the AP2S1 gene: common occurrence in familial hypocalciuric hypercalcemia cases negative for calcium-sensing receptor (CASR) mutations
Geoffrey N Hendy, Lucie Canaff, Ron S Newfield, et al.
Page
of 6