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Maria I New

Showing results (71-80 of 104) with videos related to

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The Journal of Molecular Diagnostics : JMD|April 29, 2005
Validation and clinical application of a locus-specific polymerase chain reaction- and minisequencing-based assay for congenital adrenal hyperplasia (21-hydroxylase deficiency)Dianne Keen-Kim, Joy B Redman, Reno U Alanes, et al.
The Journal of Clinical Endocrinology and Metabolism|November 15, 2007
Report of fertility in a woman with a predominantly 46,XY karyotype in a family with multiple disorders of sexual developmentMiroslav Dumic, Karen Lin-Su, Natasha I Leibel, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|April 2, 2004
Nonclassic 21-hydroxylase deficiency in CroatiaMiroslav Dumic, Jasenka Ille, Renata Zunec, et al.
The Journal of Steroid Biochemistry and Molecular Biology|April 5, 2016
Molecular genetic analysis in 93 patients and 193 family members with classical congenital adrenal hyperplasia due to 21-hydroxylase deficiency in CroatiaKatja K Dumic, Zorana Grubic, Tony Yuen, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 14, 2014
RNAi-mediated silencing of hepatic Alas1 effectively prevents and treats the induced acute attacks in acute intermittent porphyria miceMakiko Yasuda, Lin Gan, Brenden Chen, et al.
The Journal of Endocrinology|March 21, 2018
Actions of pituitary hormones beyond traditional targetsMone Zaidi, Maria I New, Harry C Blair, et al.
Journal of Clinical Research in Pediatric Endocrinology|January 29, 2011
CYP21A2 gene mutations in congenital adrenal hyperplasia: genotype-phenotype correlation in Turkish childrenFirdevs Baş, Hülya Kayserili, Feyza Darendeliler, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 5, 2018
FSIP1 regulates autophagy in breast cancerCaigang Liu, Lisha Sun, Jie Yang, et al.
Annals of the New York Academy of Sciences|August 16, 2016
A novel mutation in HSD11B2 causes apparent mineralocorticoid excess in an Omani kindredMabel Yau, Hanan Said Al Azkawi, Shozeb Haider, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 30, 2013
Genetic confirmation for a central role for TNFα in the direct action of thyroid stimulating hormone on the skeletonLi Sun, Ling-Ling Zhu, Ping Lu, et al.
Pageof 11

Showing results (71-80 of 104) with videos related to

Sort By:
Pageof 11
The Journal of Molecular Diagnostics : JMD|April 29, 2005
Validation and clinical application of a locus-specific polymerase chain reaction- and minisequencing-based assay for congenital adrenal hyperplasia (21-hydroxylase deficiency)Dianne Keen-Kim, Joy B Redman, Reno U Alanes, et al.
The Journal of Clinical Endocrinology and Metabolism|November 15, 2007
Report of fertility in a woman with a predominantly 46,XY karyotype in a family with multiple disorders of sexual developmentMiroslav Dumic, Karen Lin-Su, Natasha I Leibel, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|April 2, 2004
Nonclassic 21-hydroxylase deficiency in CroatiaMiroslav Dumic, Jasenka Ille, Renata Zunec, et al.
The Journal of Steroid Biochemistry and Molecular Biology|April 5, 2016
Molecular genetic analysis in 93 patients and 193 family members with classical congenital adrenal hyperplasia due to 21-hydroxylase deficiency in CroatiaKatja K Dumic, Zorana Grubic, Tony Yuen, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 14, 2014
RNAi-mediated silencing of hepatic Alas1 effectively prevents and treats the induced acute attacks in acute intermittent porphyria miceMakiko Yasuda, Lin Gan, Brenden Chen, et al.
The Journal of Endocrinology|March 21, 2018
Actions of pituitary hormones beyond traditional targetsMone Zaidi, Maria I New, Harry C Blair, et al.
Journal of Clinical Research in Pediatric Endocrinology|January 29, 2011
CYP21A2 gene mutations in congenital adrenal hyperplasia: genotype-phenotype correlation in Turkish childrenFirdevs Baş, Hülya Kayserili, Feyza Darendeliler, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 5, 2018
FSIP1 regulates autophagy in breast cancerCaigang Liu, Lisha Sun, Jie Yang, et al.
Annals of the New York Academy of Sciences|August 16, 2016
A novel mutation in HSD11B2 causes apparent mineralocorticoid excess in an Omani kindredMabel Yau, Hanan Said Al Azkawi, Shozeb Haider, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 30, 2013
Genetic confirmation for a central role for TNFα in the direct action of thyroid stimulating hormone on the skeletonLi Sun, Ling-Ling Zhu, Ping Lu, et al.
Pageof 11