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Heiko Krude

Showing results (1-10 of 130) with videos related to

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Deutsches Arzteblatt International|May 24, 2023
In ReplyHeiko Krude
Endocrine Development|September 19, 2014
Evolution, child development and the thyroid: a phylogenetic and ontogenetic introduction to normal thyroid functionHeiko Krude
Archives of Disease in Childhood|July 8, 2010
Treating patients not numbers: the benefit and burden of lowering TSH newborn screening cut-offsHeiko Krude, Oliver Blankenstein
Deutsches Arzteblatt International|February 10, 2022
Target Diseases for Neonatal Screening in GermanyUte Spiekerkoetter, Heiko Krude
Hormone Research|February 7, 2008
Update on the management of congenital hypothyroidismAnnette Grüters, Heiko Krude
Mobile Genetic Elements|October 23, 2012
Alu elements and human common diseases like obesityPeter Kuehnen, Heiko Krude
Nature Reviews. Endocrinology|October 20, 2011
Detection and treatment of congenital hypothyroidismAnnette Grüters, Heiko Krude
European Journal of Pediatrics|January 21, 2011
A novel mutation of LHX3 is associated with combined pituitary hormone deficiency including ACTH deficiency, sensorineural hearing loss, and short neck-a case report and review of the literatureWalter Bonfig, Heiko Krude, Heinrich Schmidt
Cell Metabolism|August 4, 2021
Melanocortin 4 receptor mutations become commonPeter Kühnen, Heike Biebermann, Heiko Krude
Hormone Research|February 5, 2003
Neonatal thyroid disordersAnnette Grüters, Heike Biebermann, Heiko Krude
Pageof 13

Showing results (1-10 of 130) with videos related to

Sort By:
Pageof 13
Deutsches Arzteblatt International|May 24, 2023
In ReplyHeiko Krude
Endocrine Development|September 19, 2014
Evolution, child development and the thyroid: a phylogenetic and ontogenetic introduction to normal thyroid functionHeiko Krude
Archives of Disease in Childhood|July 8, 2010
Treating patients not numbers: the benefit and burden of lowering TSH newborn screening cut-offsHeiko Krude, Oliver Blankenstein
Deutsches Arzteblatt International|February 10, 2022
Target Diseases for Neonatal Screening in GermanyUte Spiekerkoetter, Heiko Krude
Hormone Research|February 7, 2008
Update on the management of congenital hypothyroidismAnnette Grüters, Heiko Krude
Mobile Genetic Elements|October 23, 2012
Alu elements and human common diseases like obesityPeter Kuehnen, Heiko Krude
Nature Reviews. Endocrinology|October 20, 2011
Detection and treatment of congenital hypothyroidismAnnette Grüters, Heiko Krude
European Journal of Pediatrics|January 21, 2011
A novel mutation of LHX3 is associated with combined pituitary hormone deficiency including ACTH deficiency, sensorineural hearing loss, and short neck-a case report and review of the literatureWalter Bonfig, Heiko Krude, Heinrich Schmidt
Cell Metabolism|August 4, 2021
Melanocortin 4 receptor mutations become commonPeter Kühnen, Heike Biebermann, Heiko Krude
Hormone Research|February 5, 2003
Neonatal thyroid disordersAnnette Grüters, Heike Biebermann, Heiko Krude
Pageof 13