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Primary Adrenal Insufficiency Due to Bilateral Adrenal Infarction in COVID-19

The journal of clinical endocrinology and metabolism, 2022-01, Vol.107 (1), p.e394-e400

2022

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Applying precision medicine to the diagnosis and management of endocrine disorders

Endocrine Connections, 2022-10, Vol.11 (10), p.1-12

2022

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Causes, diagnosis, and treatment of central precocious puberty

The lancet. Diabetes & endocrinology, 2016-03, Vol.4 (3), p.265-274

2016

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Central Precocious Puberty Caused by a Heterozygous Deletion in the MKRN3 Promoter Region

Neuroendocrinology, 2018-01, Vol.107 (2), p.127-132

2018

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Expression of Insulin-Like Growth Factor-II and Its Receptor in Pediatric and Adult Adrenocortical Tumors

The journal of clinical endocrinology and metabolism, 2008-09, Vol.93 (9), p.3524-3531

2008

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Loss-of-Function Mutations in the Genes Encoding Prokineticin-2 or Prokineticin Receptor-2 Cause Autosomal Recessive Kallmann Syndrome

The journal of clinical endocrinology and metabolism, 2008-10, Vol.93 (10), p.4113-4118

2008

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KISS1R Intracellular Trafficking and Degradation: Effect of the Arg386Pro Disease-Associated Mutation

Endocrinology (Philadelphia), 2011-04, Vol.152 (4), p.1616-1626

2011

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Challenges in monitoring GnRH analog treatment in central precocious puberty

Archives of endocrinology and metabolism, 2020-04, Vol.64 (2), p.103

Latronico, Ana Claudia

2020

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Novel inactivating mutations in the GH secretagogue receptor gene in patients with constitutional delay of growth and puberty

European journal of endocrinology, 2011-08, Vol.165 (2), p.233

2011

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Central Precocious Puberty Caused by Mutations in the Imprinted Gene MKRN3

The New England journal of medicine, 2013-06, Vol.368 (26), p.2467-2475

2013

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MKRN3 inhibits the reproductive axis through actions in kisspeptin-expressing neurons

The Journal of clinical investigation, 2020-08, Vol.130 (8), p.4486-4500

2020

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The Congenital and Acquired Mechanisms Implicated in the Etiology of Central Precocious Puberty

Endocrine reviews, 2023-04, Vol.44 (2), p.193-221

2023

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A new pathway in the control of the initiation of puberty: the MKRN3 gene

Journal of molecular endocrinology, 2015-06, Vol.54 (3), p.R131-R139

2015

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New genetic findings in a large cohort of congenital hypogonadotropic hypogonadism

European journal of endocrinology, 2019-08, Vol.181 (2), p.103

2019

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Pioneering studies on monogenic central precocious puberty

Archives of Endocrinology and Metabolism, 2019-08, Vol.63 (4), p.438-444

2019

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KCNJ5 Somatic Mutation Is a Predictor of Hypertension Remission After Adrenalectomy for Unilateral Primary Aldosteronism

The journal of clinical endocrinology and metabolism, 2019-10, Vol.104 (10), p.4695-4702

2019

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Genotype–Phenotype Correlations in Central Precocious Puberty Caused by MKRN3 Mutations

The journal of clinical endocrinology and metabolism, 2021-04, Vol.106 (4), p.1041-1050

2021

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TAC3/TACR3 Mutations Reveal Preferential Activation of Gonadotropin-Releasing Hormone Release by Neurokinin B in Neonatal Life Followed by Reversal in Adulthood

The journal of clinical endocrinology and metabolism, 2010-06, Vol.95 (6), p.2857-2867

2010

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Underdiagnosis of central precocious puberty in boys with loss-of function mutations of MKRN3

The Journal of pediatrics, 2017-04, Vol.183, p.202-203

2017

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High Frequency of MKRN3 Mutations in Male Central Precocious Puberty Previously Classified as Idiopathic

Neuroendocrinology, 2017-01, Vol.105 (1), p.17-25

2017

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Outcomes of Patients with Central Precocious Puberty Due to Loss-of-Function Mutations in the MKRN3 Gene after Treatment with Gonadotropin-Releasing Hormone Analog

Neuroendocrinology, 2020-07, Vol.110 (7-8), p.705-713

2020

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Clinical and Genetic Characterization of a Constitutional Delay of Growth and Puberty Cohort

Neuroendocrinology, 2020-10, Vol.110 (11-12), p.959-966

2020

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Molecular and Genetic Aspects of Congenital Isolated Hypogonadotropic Hypogonadism

Endocrinology and metabolism clinics of North America, 2017-06, Vol.46 (2), p.283-303

2017

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MKRN3 Mutations in Central Precocious Puberty: A Systematic Review and Meta-Analysis

Journal of the Endocrine Society, 2019-05, Vol.3 (5), p.979-995

2019

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Primary malignant tumors of the adrenal glands

Clinics (São Paulo, Brazil), 2018-01, Vol.73 (suppl 1), p.e756s-e756s, Article e756s

2018

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Primary Adrenal Insufficiency Due to Bilateral Adrenal Infarction in COVID-19

Applying precision medicine to the diagnosis and management of endocrine disorders

Causes, diagnosis, and treatment of central precocious puberty

Central Precocious Puberty Caused by a Heterozygous Deletion in the MKRN3 Promoter Region

Expression of Insulin-Like Growth Factor-II and Its Receptor in Pediatric and Adult Adrenocortical Tumors

Loss-of-Function Mutations in the Genes Encoding Prokineticin-2 or Prokineticin Receptor-2 Cause Autosomal Recessive Kallmann Syndrome

KISS1R Intracellular Trafficking and Degradation: Effect of the Arg386Pro Disease-Associated Mutation

Challenges in monitoring GnRH analog treatment in central precocious puberty

Novel inactivating mutations in the GH secretagogue receptor gene in patients with constitutional delay of growth and puberty

Central Precocious Puberty Caused by Mutations in the Imprinted Gene MKRN3

MKRN3 inhibits the reproductive axis through actions in kisspeptin-expressing neurons

The Congenital and Acquired Mechanisms Implicated in the Etiology of Central Precocious Puberty

A new pathway in the control of the initiation of puberty: the MKRN3 gene

New genetic findings in a large cohort of congenital hypogonadotropic hypogonadism

Pioneering studies on monogenic central precocious puberty

KCNJ5 Somatic Mutation Is a Predictor of Hypertension Remission After Adrenalectomy for Unilateral Primary Aldosteronism

Genotype–Phenotype Correlations in Central Precocious Puberty Caused by MKRN3 Mutations

TAC3/TACR3 Mutations Reveal Preferential Activation of Gonadotropin-Releasing Hormone Release by Neurokinin B in Neonatal Life Followed by Reversal in Adulthood

Underdiagnosis of central precocious puberty in boys with loss-of function mutations of MKRN3

High Frequency of MKRN3 Mutations in Male Central Precocious Puberty Previously Classified as Idiopathic

Outcomes of Patients with Central Precocious Puberty Due to Loss-of-Function Mutations in the MKRN3 Gene after Treatment with Gonadotropin-Releasing Hormone Analog

Clinical and Genetic Characterization of a Constitutional Delay of Growth and Puberty Cohort

Molecular and Genetic Aspects of Congenital Isolated Hypogonadotropic Hypogonadism

MKRN3 Mutations in Central Precocious Puberty: A Systematic Review and Meta-Analysis

Primary malignant tumors of the adrenal glands

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