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Olaf Hiort

Showing results (131-140 of 195) with videos related to

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Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|June 20, 2014
46,XY disorder of sex development in a sudanese patient caused by a novel mutation in the HSD17B3 geneMona Ellaithi, Ralf Werner, Felix G Riepe, et al.
Endocrine Pathology|January 1, 1995
Molecular Diagnosis of Multiple Endocrine Neoplasia (MEN) in Paraffin-Embedded SpecimensPaul Komminoth, Seraina Muletta-Feurer, Parvin Saremaslani, et al.
Journal of Medical Genetics|October 13, 2022
Disruption of the topologically associated domain at Xp21.2 is related to 46,XY gonadal dysgenesisJakob A Meinel, Verónica Yumiceba, Axel Künstner, et al.
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|December 10, 2019
Clinical Findings and Follow-Up of 46,XY and 45,X/46,XY Testicular DysgenesisJuliana G R Andrade, Helena Fabbri-Scallet, Ana P Dos Santos, et al.
BMJ Paediatrics Open|April 12, 2018
Understanding the needs of professionals who provide psychosocial care for children and adults with disorders of sex developmentArianne Dessens, Guilherme Guaragna-Filho, Andreas Kyriakou, et al.
Endocrine|March 8, 2022
Metabolic effects of estradiol versus testosterone in complete androgen insensitivity syndromeMatthias K Auer, Wiebke Birnbaum, Michaela F Hartmann, et al.
Orphanet Journal of Rare Diseases|June 10, 2020
Genetic testing in inherited endocrine disorders: joint position paper of the European reference network on rare endocrine conditions (Endo-ERN)Thomas Eggermann, Miriam Elbracht, Ingo Kurth, et al.
BMC Genomics|October 20, 2007
Intrinsic androgen-dependent gene expression patterns revealed by comparison of genital fibroblasts from normal males and individuals with complete and partial androgen insensitivity syndromePaul-Martin Holterhus, Uta Deppe, Ralf Werner, et al.
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|June 28, 2022
Can Non-Coding NR5A1 Gene Variants Explain Phenotypes of Disorders of Sex Development?Helena Fabbri-Scallet, Ralf Werner, Mara S Guaragna, et al.
European Journal of Endocrinology|September 21, 2019
Standardised data collection for clinical follow-up and assessment of outcomes in differences of sex development (DSD): recommendations from the COST action DSDnetChrista Flück, Anna Nordenström, S Faisal Ahmed, et al.
Pageof 20

Showing results (131-140 of 195) with videos related to

Sort By:
Pageof 20
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|June 20, 2014
46,XY disorder of sex development in a sudanese patient caused by a novel mutation in the HSD17B3 geneMona Ellaithi, Ralf Werner, Felix G Riepe, et al.
Endocrine Pathology|January 1, 1995
Molecular Diagnosis of Multiple Endocrine Neoplasia (MEN) in Paraffin-Embedded SpecimensPaul Komminoth, Seraina Muletta-Feurer, Parvin Saremaslani, et al.
Journal of Medical Genetics|October 13, 2022
Disruption of the topologically associated domain at Xp21.2 is related to 46,XY gonadal dysgenesisJakob A Meinel, Verónica Yumiceba, Axel Künstner, et al.
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|December 10, 2019
Clinical Findings and Follow-Up of 46,XY and 45,X/46,XY Testicular DysgenesisJuliana G R Andrade, Helena Fabbri-Scallet, Ana P Dos Santos, et al.
BMJ Paediatrics Open|April 12, 2018
Understanding the needs of professionals who provide psychosocial care for children and adults with disorders of sex developmentArianne Dessens, Guilherme Guaragna-Filho, Andreas Kyriakou, et al.
Endocrine|March 8, 2022
Metabolic effects of estradiol versus testosterone in complete androgen insensitivity syndromeMatthias K Auer, Wiebke Birnbaum, Michaela F Hartmann, et al.
Orphanet Journal of Rare Diseases|June 10, 2020
Genetic testing in inherited endocrine disorders: joint position paper of the European reference network on rare endocrine conditions (Endo-ERN)Thomas Eggermann, Miriam Elbracht, Ingo Kurth, et al.
BMC Genomics|October 20, 2007
Intrinsic androgen-dependent gene expression patterns revealed by comparison of genital fibroblasts from normal males and individuals with complete and partial androgen insensitivity syndromePaul-Martin Holterhus, Uta Deppe, Ralf Werner, et al.
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|June 28, 2022
Can Non-Coding NR5A1 Gene Variants Explain Phenotypes of Disorders of Sex Development?Helena Fabbri-Scallet, Ralf Werner, Mara S Guaragna, et al.
European Journal of Endocrinology|September 21, 2019
Standardised data collection for clinical follow-up and assessment of outcomes in differences of sex development (DSD): recommendations from the COST action DSDnetChrista Flück, Anna Nordenström, S Faisal Ahmed, et al.
Pageof 20