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Maria I New

Showing results (61-70 of 104) with videos related to

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Journal of Hypertension|July 9, 2005
Familial hyperaldosteronism type II is linked to the chromosome 7p22 region but also shows predicted heterogeneityAlbertina So, David L Duffy, Richard D Gordon, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 11, 2018
Human hydroxymethylbilane synthase: Molecular dynamics of the pyrrole chain elongation identifies step-specific residues that cause AIPNavneet Bung, Arijit Roy, Brenden Chen, et al.
Gynecological Endocrinology : the Official Journal of the International Society of Gynecological Endocrinology|January 11, 2011
Isolated mild clitoral hypertrophy may reveal 46,XY disorders of sex development in infancy due to 17βHSD-3 defect confirmed by molecular analysisMinu M George, Sunil Sinha, Irene Mamkin, et al.
Annals of the New York Academy of Sciences|June 23, 2017
Linking the degree of virilization in females with congenital adrenal hyperplasia to genotypeSemyon Gurgov, Kerlly J Bernabé, John Stites, et al.
The Journal of Clinical Endocrinology and Metabolism|March 31, 2005
Treatment with growth hormone and luteinizing hormone releasing hormone analog improves final adult height in children with congenital adrenal hyperplasiaKaren Lin-Su, Maria G Vogiatzi, Ian Marshall, et al.
Molecular Genetics and Metabolism|February 6, 2007
Ethnic-specific distribution of mutations in 716 patients with congenital adrenal hyperplasia owing to 21-hydroxylase deficiencyRobert C Wilson, Saroj Nimkarn, Miro Dumic, et al.
Annals of the New York Academy of Sciences|August 21, 2015
A rare CYP21A2 mutation in a congenital adrenal hyperplasia kindred displaying genotype-phenotype nonconcordanceAhmed Khattab, Tony Yuen, Sultan Al-Malki, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 30, 2013
Genotype-phenotype correlation in 1,507 families with congenital adrenal hyperplasia owing to 21-hydroxylase deficiencyMaria I New, Moolamannil Abraham, Brian Gonzalez, et al.
The Journal of Steroid Biochemistry and Molecular Biology|April 30, 2016
Long term outcomes in 46, XX adult patients with congenital adrenal hyperplasia reared as malesA Khattab, M Yau, A Qamar, et al.
The Journal of Clinical Endocrinology and Metabolism|July 11, 2002
Adrenomedullary function may predict phenotype and genotype in classic 21-hydroxylase deficiencyEvangelia Charmandari, Graeme Eisenhofer, Sarah L Mehlinger, et al.
Pageof 11

Showing results (61-70 of 104) with videos related to

Sort By:
Pageof 11
Journal of Hypertension|July 9, 2005
Familial hyperaldosteronism type II is linked to the chromosome 7p22 region but also shows predicted heterogeneityAlbertina So, David L Duffy, Richard D Gordon, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 11, 2018
Human hydroxymethylbilane synthase: Molecular dynamics of the pyrrole chain elongation identifies step-specific residues that cause AIPNavneet Bung, Arijit Roy, Brenden Chen, et al.
Gynecological Endocrinology : the Official Journal of the International Society of Gynecological Endocrinology|January 11, 2011
Isolated mild clitoral hypertrophy may reveal 46,XY disorders of sex development in infancy due to 17βHSD-3 defect confirmed by molecular analysisMinu M George, Sunil Sinha, Irene Mamkin, et al.
Annals of the New York Academy of Sciences|June 23, 2017
Linking the degree of virilization in females with congenital adrenal hyperplasia to genotypeSemyon Gurgov, Kerlly J Bernabé, John Stites, et al.
The Journal of Clinical Endocrinology and Metabolism|March 31, 2005
Treatment with growth hormone and luteinizing hormone releasing hormone analog improves final adult height in children with congenital adrenal hyperplasiaKaren Lin-Su, Maria G Vogiatzi, Ian Marshall, et al.
Molecular Genetics and Metabolism|February 6, 2007
Ethnic-specific distribution of mutations in 716 patients with congenital adrenal hyperplasia owing to 21-hydroxylase deficiencyRobert C Wilson, Saroj Nimkarn, Miro Dumic, et al.
Annals of the New York Academy of Sciences|August 21, 2015
A rare CYP21A2 mutation in a congenital adrenal hyperplasia kindred displaying genotype-phenotype nonconcordanceAhmed Khattab, Tony Yuen, Sultan Al-Malki, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 30, 2013
Genotype-phenotype correlation in 1,507 families with congenital adrenal hyperplasia owing to 21-hydroxylase deficiencyMaria I New, Moolamannil Abraham, Brian Gonzalez, et al.
The Journal of Steroid Biochemistry and Molecular Biology|April 30, 2016
Long term outcomes in 46, XX adult patients with congenital adrenal hyperplasia reared as malesA Khattab, M Yau, A Qamar, et al.
The Journal of Clinical Endocrinology and Metabolism|July 11, 2002
Adrenomedullary function may predict phenotype and genotype in classic 21-hydroxylase deficiencyEvangelia Charmandari, Graeme Eisenhofer, Sarah L Mehlinger, et al.
Pageof 11