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Christine Haag

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Hormone Research in Paediatrics|June 1, 2011
Diagnosis of glucocorticoid-remediable aldosteronism in hypertensive childrenClemens Kamrath, Christiane Maser-Gluth, Christine Haag, et al.
Brain Sciences|July 27, 2024
Changes in Spatiotemporal Dynamics of Default Network Oscillations between 19 and 29 Years of AgeThorsten Fehr, Sophia Mehrens, Marie-Christine Haag, et al.
Journal of Neurochemistry|December 24, 2003
The localisation of the extraneuronal monoamine transporter (EMT) in rat brainChristine Haag, Reinhard Berkels, Dirk Gründemann, et al.
British Journal of Pharmacology|November 2, 2002
Activation of the extraneuronal monoamine transporter (EMT) from rat expressed in 293 cellsDirk Gründemann, Ann-Cathrin Koschker, Christine Haag, et al.
Psychiatrische Praxis|June 21, 2008
[Diagnostic procedure and antidementive therapy of dementia patients in primary care: an urban-rural comparison]Carolin Donath, Elmar Grassel, Maria Grossfeld-Schmitz, et al.
Hormone Research|June 10, 2006
Screening for Pax8 mutations in patients with congenital hypothyroidism in South-West GermanyKirsten Lanzerath, Markus Bettendorf, Christine Haag, et al.
European Journal of Endocrinology|June 10, 2011
CDC73-related hereditary hyperparathyroidism: five new mutations and the clinical spectrumKarin Frank-Raue, Christine Haag, Egbert Schulze, et al.
Clinical Endocrinology|April 28, 2011
Inactivating calcium-sensing receptor mutations in patients with primary hyperparathyroidismKarin 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 hypocalcemiaSaskia Letz, Christine Haag, Egbert Schulze, 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 geneKarin Frank-Raue, Angela Lorenz, Christine Haag, et al.
Pageof 2

Showing results (1-10 of 16) with videos related to

Sort By:
Pageof 2
Hormone Research in Paediatrics|June 1, 2011
Diagnosis of glucocorticoid-remediable aldosteronism in hypertensive childrenClemens Kamrath, Christiane Maser-Gluth, Christine Haag, et al.
Brain Sciences|July 27, 2024
Changes in Spatiotemporal Dynamics of Default Network Oscillations between 19 and 29 Years of AgeThorsten Fehr, Sophia Mehrens, Marie-Christine Haag, et al.
Journal of Neurochemistry|December 24, 2003
The localisation of the extraneuronal monoamine transporter (EMT) in rat brainChristine Haag, Reinhard Berkels, Dirk Gründemann, et al.
British Journal of Pharmacology|November 2, 2002
Activation of the extraneuronal monoamine transporter (EMT) from rat expressed in 293 cellsDirk Gründemann, Ann-Cathrin Koschker, Christine Haag, et al.
Psychiatrische Praxis|June 21, 2008
[Diagnostic procedure and antidementive therapy of dementia patients in primary care: an urban-rural comparison]Carolin Donath, Elmar Grassel, Maria Grossfeld-Schmitz, et al.
Hormone Research|June 10, 2006
Screening for Pax8 mutations in patients with congenital hypothyroidism in South-West GermanyKirsten Lanzerath, Markus Bettendorf, Christine Haag, et al.
European Journal of Endocrinology|June 10, 2011
CDC73-related hereditary hyperparathyroidism: five new mutations and the clinical spectrumKarin Frank-Raue, Christine Haag, Egbert Schulze, et al.
Clinical Endocrinology|April 28, 2011
Inactivating calcium-sensing receptor mutations in patients with primary hyperparathyroidismKarin 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 hypocalcemiaSaskia Letz, Christine Haag, Egbert Schulze, 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 geneKarin Frank-Raue, Angela Lorenz, Christine Haag, et al.
Pageof 2