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European Journal of Endocrinology
|
June 10, 2011
CDC73-related hereditary hyperparathyroidism: five new mutations and the clinical spectrum
Karin Frank-Raue, Christine Haag, Egbert Schulze, et al.
European Journal of Endocrinology
|
November 14, 2008
Clinical impact of two different intraoperative parathyroid hormone assays in primary and renal hyperparathyroidism
Sonja-Kerstin Meyer, Markus Zorn, Karin Frank-Raue, et al.
European Journal of Orthodontics
|
September 17, 2021
Intraoral scanning of neonates and infants with craniofacial disorders: feasibility, scanning duration, and clinical experience
Christina Weise, Karin Frank, Cornelia Wiechers, et al.
European Journal of Endocrinology
|
December 6, 2012
Molecular epidemiology of multiple endocrine neoplasia 2: implications for RET screening in the new millenium
Andreas Machens, Kerstin Lorenz, Carsten Sekulla, et al.
Plos One
|
June 5, 2013
Species-specific traits plus stabilizing processes best explain coexistence in biodiverse fire-prone plant communities
Jürgen Groeneveld, Neal J Enright, Byron B Lamont, et al.
Clinical Endocrinology
|
April 28, 2011
Inactivating calcium-sensing receptor mutations in patients with primary hyperparathyroidism
Karin Frank-Raue, Gudrun Leidig-Bruckner, Christine Haag, et al.
Plos One
|
December 16, 2014
Amino alcohol- (NPS-2143) and quinazolinone-derived calcilytics (ATF936 and AXT914) differentially mitigate excessive signalling of calcium-sensing receptor mutants causing Bartter syndrome Type 5 and autosomal dominant hypocalcemia
Saskia Letz, Christine Haag, Egbert Schulze, et al.
Thyroid : Official Journal of the American Thyroid Association
|
June 18, 2020
A Novel Double <i>RET</i> E768D/L790F Mutation Associated with a MEN2B-Like Phenotype
Annie Mathew, Soeren Latteyer, Karin Frank-Raue, et al.
The Journal of Clinical Endocrinology and Metabolism
|
February 20, 2020
Bone Metastases in Medullary Thyroid Carcinoma: High Morbidity and Poor Prognosis Associated With Osteolytic Morphology
Theresa Vogel, Julia Wendler, Karin Frank-Raue, et al.
European Journal of Endocrinology
|
June 12, 2004
Severe form of thyroid hormone resistance in a patient with homozygous/hemizygous mutation of T3 receptor gene
Karin Frank-Raue, Angela Lorenz, Christine Haag, et al.
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of 9
Search research articles
Search
Showing results (51-60 of 88) with videos related to
Sort By:
Page
of 9
European Journal of Endocrinology
|
June 10, 2011
CDC73-related hereditary hyperparathyroidism: five new mutations and the clinical spectrum
Karin Frank-Raue, Christine Haag, Egbert Schulze, et al.
European Journal of Endocrinology
|
November 14, 2008
Clinical impact of two different intraoperative parathyroid hormone assays in primary and renal hyperparathyroidism
Sonja-Kerstin Meyer, Markus Zorn, Karin Frank-Raue, et al.
European Journal of Orthodontics
|
September 17, 2021
Intraoral scanning of neonates and infants with craniofacial disorders: feasibility, scanning duration, and clinical experience
Christina Weise, Karin Frank, Cornelia Wiechers, et al.
European Journal of Endocrinology
|
December 6, 2012
Molecular epidemiology of multiple endocrine neoplasia 2: implications for RET screening in the new millenium
Andreas Machens, Kerstin Lorenz, Carsten Sekulla, et al.
Plos One
|
June 5, 2013
Species-specific traits plus stabilizing processes best explain coexistence in biodiverse fire-prone plant communities
Jürgen Groeneveld, Neal J Enright, Byron B Lamont, et al.
Clinical Endocrinology
|
April 28, 2011
Inactivating calcium-sensing receptor mutations in patients with primary hyperparathyroidism
Karin Frank-Raue, Gudrun Leidig-Bruckner, Christine Haag, et al.
Plos One
|
December 16, 2014
Amino alcohol- (NPS-2143) and quinazolinone-derived calcilytics (ATF936 and AXT914) differentially mitigate excessive signalling of calcium-sensing receptor mutants causing Bartter syndrome Type 5 and autosomal dominant hypocalcemia
Saskia Letz, Christine Haag, Egbert Schulze, et al.
Thyroid : Official Journal of the American Thyroid Association
|
June 18, 2020
A Novel Double <i>RET</i> E768D/L790F Mutation Associated with a MEN2B-Like Phenotype
Annie Mathew, Soeren Latteyer, Karin Frank-Raue, et al.
The Journal of Clinical Endocrinology and Metabolism
|
February 20, 2020
Bone Metastases in Medullary Thyroid Carcinoma: High Morbidity and Poor Prognosis Associated With Osteolytic Morphology
Theresa Vogel, Julia Wendler, Karin Frank-Raue, et al.
European Journal of Endocrinology
|
June 12, 2004
Severe form of thyroid hormone resistance in a patient with homozygous/hemizygous mutation of T3 receptor gene
Karin Frank-Raue, Angela Lorenz, Christine Haag, et al.
Page
of 9