Showing results (71-80 of 132) with videos related to

Sort By:
Pageof 14
Physical Chemistry Chemical Physics : PCCP|May 5, 2017
Can the tricyanomethanide anion improve CO<sub>2</sub> absorption by acetate-based ionic liquids?L F Lepre, J Szala-Bilnik, L Pison, et al.
Materials Science & Engineering. C, Materials for Biological Applications|February 4, 2016
Osteogenic effect of tricalcium phosphate substituted by magnesium associated with Genderm® membrane in rat calvarial defect modelNeusa M F Costa, Debora H Yassuda, Marcia S Sader, et al.
The Journal of Steroid Biochemistry and Molecular Biology|May 26, 2016
Steroid 5α-reductase 2 deficiencyBerenice B Mendonca, Rafael Loch Batista, Sorahia Domenice, et al.
The Journal of Steroid Biochemistry and Molecular Biology|November 16, 2016
Reprint of "Steroid 5α-reductase 2 deficiency"Berenice B Mendonca, Rafael Loch Batista, Sorahia Domenice, et al.
Arquivos Brasileiros De Endocrinologia E Metabologia|March 18, 2006
[Androgen insensitivity syndrome: clinical, hormonal and molecular analysis of 33 cases]Karla F S Melo, Berenice B Mendonça, Ana Elisa C Billerbeck, et al.
Brazilian Journal of Medical and Biological Research = Revista Brasileira De Pesquisas Medicas E Biologicas|December 23, 2003
Clinical and molecular analysis of human reproductive disorders in Brazilian patientsA C Latronico, E M F Costa, S Domenice, et al.
Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|November 2, 2006
Height and bone mineral density in androgen insensitivity syndrome with mutations in the androgen receptor geneD L S Danilovic, P H S Correa, E M F Costa, et al.
The Journal of Clinical Endocrinology and Metabolism|June 7, 2002
An unusual phenotype of Frasier syndrome due to IVS9 +4C>T mutation in the WT1 gene: predominantly male ambiguous genitalia and absence of gonadal dysgenesisKarla F S Melo, Regina M Martin, Elaine M F Costa, et al.
Pageof 14