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An Uncommon Association of Familial Partial Lipodystrophy, Dilated Cardiomyopathy, and Conduction System Disease

JIM - high impact case reports, 2016-07, Vol.4 (3), p.2324709616658495-2324709616658495

2016

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High prevalence of non-thyroidal illness syndrome in patients at long-term care facilities

Endocrine, 2020-11, Vol.70 (2), p.348-355

2020

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Mutations in SECISBP2 result in abnormal thyroid hormone metabolism

Nature genetics, 2005-11, Vol.37 (11), p.1247-1252

2005

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The effect of growth hormone replacement on the thyroid axis in patients with hypopituitarism: in vivo and ex vivo studies

Clinical endocrinology (Oxford), 2017-05, Vol.86 (5), p.747-754

2017

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Prevalence and functional analysis of the S107P polymorphism (rs6647476) of the monocarboxylate transporter 8 (SLC16A2) gene in the male population of north-west Spain (Galicia)

Clinical endocrinology (Oxford), 2009-04, Vol.70 (4), p.636-643

2009

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Lipopolysaccharide (LPS)-induced septic shock causes profound changes in myocardial energy metabolites in pigs

Metabolomics, 2018-10, Vol.14 (10), p.131-12, Article 131

2018

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Identification of molecular mechanisms related to nonthyroidal illness syndrome in skeletal muscle and adipose tissue from patients with septic shock

Clinical endocrinology (Oxford), 2008-05, Vol.68 (5), p.821-827

2008

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Non-thyroidal illness syndrome, the hidden player in the septic shock induced myocardial contractile depression

Medical hypotheses, 2020-09, Vol.142, p.109775-109775, Article 109775

Lado-Abeal, Joaquin

2020

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Thyroid Cancer Prevalence, Risk Exposure, and Clinical Features Among Transgender Female Veterans

Journal of the Endocrine Society, 2024-04, Vol.8 (6), p.bvae060-bvae060

2024

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Primary and Secondary Endocrinopathies Found in a Patient With Craniopharyngioma

The American journal of the medical sciences, 2014-12, Vol.348 (6), p.534-535

2014

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Diffuse Idiopathic Skeletal Hyperostosis and Familial Hypocalciuric Hypercalcemia: A Unique Association in a Young Female

The American journal of the medical sciences, 2013-09, Vol.346 (3), p.247-249

2013

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A novel phenotypic expression associated with a new mutation in LMNA gene, characterized by partial lipodystrophy, insulin resistance, aortic stenosis and hypertrophic cardiomyopathy

Clinical endocrinology (Oxford), 2008-07, Vol.69 (1), p.61-68

2008

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Thyroid hormones are needed to sustain "inappropriately" normal TSH during non-thyroidal illness syndrome: a clinical observation in severely ill patients with primary hypothyroidism

Neuro-endocrinology letters, 2015, Vol.36 (1), p.41-47

Lado-Abeal, Joaquin

2015

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Pendred syndrome

Expert Review of Endocrinology & Metabolism, 2008-09, Vol.3 (5), p.635-643

Lado Abeal, Joaquin

2008

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Unfavorable Socioeconomic Factors Underlie High Rates of Hospitalization for Complicated Thyrotoxicosis in Some Regions of the United States

Thyroid (New York, N.Y.), 2019-01, Vol.29 (1), p.27

2019

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Thyroid Hormone Resistance and Its Management

Proceedings - Baylor University. Medical Center, 2016-04, Vol.29 (2), p.209-211

2016

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Adrenal Medullary Hyperplasia: An Under the Radar Cause of Endocrine Hypertension

The American journal of the medical sciences, 2022-01, Vol.363 (1), p.64-68

2022

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BILATERAL ADRENAL MYELOLIPOMAS PRESENTING AS ACUTE ADRENAL INSUFFICIENCY IN AN ADULT WITH CONGENITAL ADRENAL HYPERPLASIA

AACE clinical case reports, 2018-04, Article ACCR-2017-0262

2018

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Thyrotoxic Periodic Paralysis and Complicated Thyrotoxicosis, Two Presentations of Hyperthyroidism with Notable Differences in their Clinical Manifestations: An Experience from a Tertiary Care Hospital in the United States

Endocrine practice, 2020-07, Vol.26 (7), p.699

2020

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ADRENAL MEDULLARY HYPERPLASIA AS A CAUSE OF SECONDARY HYPERTENSION AND METANEPHRINES EXCESS

Endocrine practice, 2018-04, Vol.24, p.15-15

2018

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Abstract #124 Adrenal Medullary Hyperplasia as a Cause of Secondary Hypertension and Metanephrines Excess

Endocrine practice, 2018-04, Vol.24, p.15

2018

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THYROTOXIC PERIODIC PARALYSIS AND COMPLICATED THYROTOXICOSIS, TWO PRESENTATIONS OF HYPERTHYROIDISM WITH NOTABLE DIFFERENCES IN THEIR CLINICAL MANIFESTATIONS. AN EXPERIENCE FROM A TERTIARY CARE HOSPITAL IN THE UNITED STATES

Endocrine practice, 2020-07, Vol.26 (7), p.699-706

2020

Volltextzugriff (PDF)

Partial thyroxine-binding globulin (TBG) deficiency in a family with no detectable mutation of the TBG gene

Clinical endocrinology (Oxford), 2003-12, Vol.59 (6), p.824-825

2003

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Usefulness of plasmapheresis in patients with severe complicated thyrotoxicosis

Proceedings - Baylor University. Medical Center, 2020-12, Vol.34 (2), p.279-282

2020

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Septic shock non-thyroidal illness syndrome causes hypothyroidism and conditions for reduced sensitivity to thyroid hormone

Journal of molecular endocrinology, 2013-04, Vol.50 (2), p.255-266

2013

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An Uncommon Association of Familial Partial Lipodystrophy, Dilated Cardiomyopathy, and Conduction System Disease

High prevalence of non-thyroidal illness syndrome in patients at long-term care facilities

Mutations in SECISBP2 result in abnormal thyroid hormone metabolism

The effect of growth hormone replacement on the thyroid axis in patients with hypopituitarism: in vivo and ex vivo studies

Prevalence and functional analysis of the S107P polymorphism (rs6647476) of the monocarboxylate transporter 8 (SLC16A2) gene in the male population of north-west Spain (Galicia)

Lipopolysaccharide (LPS)-induced septic shock causes profound changes in myocardial energy metabolites in pigs

Identification of molecular mechanisms related to nonthyroidal illness syndrome in skeletal muscle and adipose tissue from patients with septic shock

Non-thyroidal illness syndrome, the hidden player in the septic shock induced myocardial contractile depression

Thyroid Cancer Prevalence, Risk Exposure, and Clinical Features Among Transgender Female Veterans

Primary and Secondary Endocrinopathies Found in a Patient With Craniopharyngioma

Diffuse Idiopathic Skeletal Hyperostosis and Familial Hypocalciuric Hypercalcemia: A Unique Association in a Young Female

A novel phenotypic expression associated with a new mutation in LMNA gene, characterized by partial lipodystrophy, insulin resistance, aortic stenosis and hypertrophic cardiomyopathy

Thyroid hormones are needed to sustain "inappropriately" normal TSH during non-thyroidal illness syndrome: a clinical observation in severely ill patients with primary hypothyroidism

Pendred syndrome

Unfavorable Socioeconomic Factors Underlie High Rates of Hospitalization for Complicated Thyrotoxicosis in Some Regions of the United States

Thyroid Hormone Resistance and Its Management

Adrenal Medullary Hyperplasia: An Under the Radar Cause of Endocrine Hypertension

BILATERAL ADRENAL MYELOLIPOMAS PRESENTING AS ACUTE ADRENAL INSUFFICIENCY IN AN ADULT WITH CONGENITAL ADRENAL HYPERPLASIA

Thyrotoxic Periodic Paralysis and Complicated Thyrotoxicosis, Two Presentations of Hyperthyroidism with Notable Differences in their Clinical Manifestations: An Experience from a Tertiary Care Hospital in the United States

ADRENAL MEDULLARY HYPERPLASIA AS A CAUSE OF SECONDARY HYPERTENSION AND METANEPHRINES EXCESS

Abstract #124 Adrenal Medullary Hyperplasia as a Cause of Secondary Hypertension and Metanephrines Excess

THYROTOXIC PERIODIC PARALYSIS AND COMPLICATED THYROTOXICOSIS, TWO PRESENTATIONS OF HYPERTHYROIDISM WITH NOTABLE DIFFERENCES IN THEIR CLINICAL MANIFESTATIONS. AN EXPERIENCE FROM A TERTIARY CARE HOSPITAL IN THE UNITED STATES

Partial thyroxine-binding globulin (TBG) deficiency in a family with no detectable mutation of the TBG gene

Usefulness of plasmapheresis in patients with severe complicated thyrotoxicosis

Septic shock non-thyroidal illness syndrome causes hypothyroidism and conditions for reduced sensitivity to thyroid hormone

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