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Authors: Magnus R. Dias da Silva
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Journal Article

The Natural History of a Man With Ovotesticular 46,XX DSD Caused by a Novel 3-Mb 15q26.2 Deletion Containing NR2F2 Gene Open Access

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Gianna Carvalheira and others
Journal of the Endocrine Society, Volume 3, Issue 11, November 2019, Pages 2107–2113, https://doi.org/10.1210/js.2019-00241
Published: 28 August 2019
Journal Article

DUOX2 Mutations Are Associated With Congenital Hypothyroidism With Ectopic Thyroid Gland Free

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Marina M L Kizys and others
The Journal of Clinical Endocrinology & Metabolism, Volume 102, Issue 11, 1 November 2017, Pages 4060–4071, https://doi.org/10.1210/jc.2017-00832
Published: 28 June 2017
Journal Article

Gender Affirmation Process in Brazilian Public Health System: Challenges to Integral Care Get access

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Ana Luiza Fanganiello and others
The Journal of Sexual Medicine, Volume 14, Issue Supplement_4b, May 2017, Page e343, https://doi.org/10.1016/j.jsxm.2017.04.619
Published: 01 May 2017
Journal Article

Evidence for the founder effect of RET533 as the common Greek and Brazilian ancestor spreading multiple endocrine neoplasia 2A Get access

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Lucas L Cunha and others
European Journal of Endocrinology, Volume 176, Issue 5, May 2017, Pages 515–519, https://doi.org/10.1530/EJE-16-1021
Published: 01 May 2017
Journal Article

Experience Report on Setting Up a Transdisciplinary Outpatient Unit for Transgender Health Get access

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Denise Leite Vieira and others
The Journal of Sexual Medicine, Volume 14, Issue Supplement_4b, May 2017, Page e267, https://doi.org/10.1016/j.jsxm.2017.04.302
Published: 01 May 2017
Journal Article

Novel lincRNA Susceptibility Gene and Its Role in Etiopathogenesis of Thyrotoxic Periodic Paralysis Open Access

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Maria Clara C. Melo and others
Journal of the Endocrine Society, Volume 1, Issue 7, 1 July 2017, Pages 809–815, https://doi.org/10.1210/js.2017-00015
Published: 28 February 2017
Journal Article

Macrocalcitonin Is a Novel Pitfall in the Routine of Serum Calcitonin Immunoassay Free

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Thalita G. Alves and others
The Journal of Clinical Endocrinology & Metabolism, Volume 101, Issue 2, 1 February 2016, Pages 653–658, https://doi.org/10.1210/jc.2015-3137
Published: 01 February 2016
Journal Article

A Novel Germ-Line Point Mutation in RET Exon 8 (Gly533Cys) in a Large Kindred with Familial Medullary Thyroid Carcinoma Get access

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Adriana M. Álvares Da Silva and others
The Journal of Clinical Endocrinology & Metabolism, Volume 88, Issue 11, 1 November 2003, Pages 5438–5443, https://doi.org/10.1210/jc.2003-030997
Published: 01 November 2003
Journal Article

Familial Combined Pituitary Hormone Deficiency due to a Novel Mutation R99Q in the Hot Spot Region of Prophet of Pit-1 Presenting as Constitutional Growth Delay Get access

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Teresa C. Vieira and others
The Journal of Clinical Endocrinology & Metabolism, Volume 88, Issue 1, 1 January 2003, Pages 38–44, https://doi.org/10.1210/jc.2001-011872
Published: 01 January 2003
Journal Article

A Mutation in the KCNE3 Potassium Channel Gene Is Associated with Susceptibility to Thyrotoxic Hypokalemic Periodic Paralysis Get access

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Magnus R. Dias Da Silva and others
The Journal of Clinical Endocrinology & Metabolism, Volume 87, Issue 11, 1 November 2002, Pages 4881–4884, https://doi.org/10.1210/jc.2002-020698
Published: 01 November 2002