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Letter to the Editor from Berthon: "Cardiac Myxoma Caused by Fumarate Hydratase Gene Deletion in Patient With Cortisol-Secreting Adrenocortical Adenoma".
- Published in:
- 2020
- By:
- Publication type:
- Letter
The phenotype of the pediatric patient with Cushing syndrome but without obesity.
- Published in:
- European Journal of Endocrinology, 2024, v. 191, n. 4, p. 399, doi. 10.1093/ejendo/lvae114
- By:
- Publication type:
- Article
Diagnostic and management challenges in paediatric Cushing's syndrome.
- Published in:
- Clinical Endocrinology, 2024, v. 101, n. 6, p. 631, doi. 10.1111/cen.15096
- By:
- Publication type:
- Article
Clinical characteristics and outcomes of SDHB-related pheochromocytoma and paraganglioma in children and adolescents.
- Published in:
- Journal of Cancer Research & Clinical Oncology, 2020, v. 146, n. 4, p. 1051, doi. 10.1007/s00432-020-03138-5
- By:
- Publication type:
- Article
Altered amygdala and hippocampus function in adolescents with hypercortisolemia: A functional magnetic resonance imaging study of Cushing syndrome.
- Published in:
- Development & Psychopathology, 2008, v. 20, n. 4, p. 1177, doi. 10.1017/S0954579408000564
- By:
- Publication type:
- Article
Reversible posterior encephalopathy syndrome associated with micronodular adrenocortical disease and Cushing syndrome.
- Published in:
- 2010
- By:
- Publication type:
- Report
Cutaneous signs are important in the diagnosis of the rare neoplasia syndrome Carney complex.
- Published in:
- 2009
- By:
- Publication type:
- journal article
Complex Glycerol Kinase Deficiency and Adrenocortical Insufficiency in Two Neonates.
- Published in:
- Journal of Clinical Research in Pediatric Endocrinology, 2016, p. 468, doi. 10.4274/jcrpe.2539
- By:
- Publication type:
- Article
Whole-exome sequencing reveals insights into genetic susceptibility to Congenital Zika Syndrome.
- Published in:
- PLoS Neglected Tropical Diseases, 2021, v. 15, n. 6, p. 1, doi. 10.1371/journal.pntd.0009507
- By:
- Publication type:
- Article
Myxoma of the ear lobe in a 23-month-old girl with Carney complex.
- Published in:
- Journal of Cutaneous Pathology, 2012, v. 39, n. 1, p. 68, doi. 10.1111/j.1600-0560.2011.01786.x
- By:
- Publication type:
- Article
A variant of the cerebro-oculo-facio-skeletal syndrome with congenital ectropion and a case of lamellar ichthyosis in the same family.
- Published in:
- Clinical Genetics, 1994, v. 45, n. 3, p. 162, doi. 10.1111/j.1399-0004.1994.tb04014.x
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- Publication type:
- Article
FDG PET/CT Scan and Functional Adrenal Tumors: A Pilot Study for Lateralization.
- Published in:
- World Journal of Surgery, 2016, v. 40, n. 3, p. 683, doi. 10.1007/s00268-015-3242-y
- By:
- Publication type:
- Article
Genomic analysis, immunomodulation and deep phenotyping of patients with nodding syndrome.
- Published in:
- Brain: A Journal of Neurology, 2023, v. 146, n. 3, p. 968, doi. 10.1093/brain/awac357
- By:
- Publication type:
- Article
Cyclic AMP‐dependent protein kinase catalytic subunit A (PRKACA): the expected, the unexpected, and what might be next.
- Published in:
- Journal of Pathology, 2018, v. 244, n. 3, p. 257, doi. 10.1002/path.5014
- By:
- Publication type:
- Article
Diurnal Range and Intra-patient Variability of ACTH Is Restored With Remission in Cushing's Disease.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2023, v. 108, n. 11, p. 2812, doi. 10.1210/clinem/dgad309
- By:
- Publication type:
- Article
Cushing Syndrome in a Pediatric Patient With a KCNJ5 Variant and Successful Treatment With Low-dose Ketoconazole.
- Published in:
- 2021
- By:
- Publication type:
- journal article
ARMC5 Alterations in Patients With Sporadic Neuroendocrine Tumors and Multiple Endocrine Neoplasia Type 1 (MEN1).
- Published in:
- 2020
- By:
- Publication type:
- journal article
The Association of ARMC5 with the Renin-Angiotensin-Aldosterone System, Blood Pressure, and Glycemia in African Americans.
- Published in:
- 2020
- By:
- Publication type:
- journal article
Germline CDKN1B Loss-of-Function Variants Cause Pediatric Cushing's Disease With or Without an MEN4 Phenotype.
- Published in:
- 2020
- By:
- Publication type:
- journal article
Letter to the Editor: "IGSF1 Deficiency Results in Human and Murine Somatotrope Neurosecretory Hyperfunction".
- Published in:
- 2020
- By:
- Publication type:
- Letter
Computerized Analysis of Brain MRI Parameter Dynamics in Young Patients With Cushing Syndrome-A Case-Control Study.
- Published in:
- 2019
- By:
- Publication type:
- journal article
Illicit Upregulation of Serotonin Signaling Pathway in Adrenals of Patients With High Plasma or Intra-Adrenal ACTH Levels.
- Published in:
- 2019
- By:
- Publication type:
- journal article
Genetics of Hypertension in African Americans and Others of African Descent.
- Published in:
- International Journal of Molecular Sciences, 2019, v. 20, n. 5, p. 1081, doi. 10.3390/ijms20051081
- By:
- Publication type:
- Article
Neuroendocrinology and Pathophysiology of the Stress System.
- Published in:
- Annals of the New York Academy of Sciences, 1995, v. 771, n. 1, p. 1, doi. 10.1111/j.1749-6632.1995.tb44666.x
- By:
- Publication type:
- Article
Glucocorticosteroid Resistance in Humans. Elucidation of the Molecular Mechanisms and Implications for Pathophysiology.
- Published in:
- Annals of the New York Academy of Sciences, 1994, v. 746, n. 1, p. 362, doi. 10.1111/j.1749-6632.1994.tb39257.x
- By:
- Publication type:
- Article
The Genetics of Pituitary Adenomas.
- Published in:
- Journal of Clinical Medicine, 2020, v. 9, n. 1, p. 30, doi. 10.3390/jcm9010030
- By:
- Publication type:
- Article
PRKAR1A deficiency impedes hypertrophy and reduces heart size.
- Published in:
- Physiological Reports, 2020, v. 8, n. 6, p. 1, doi. 10.14814/phy2.14405
- By:
- Publication type:
- Article
The Role of Protein Kinase A in Anxiety Behaviors.
- Published in:
- Neuroendocrinology, 2016, v. 103, n. 6, p. 625, doi. 10.1159/000444880
- By:
- Publication type:
- Article
MEN1, MEN4, and Carney Complex: Pathology and Molecular Genetics.
- Published in:
- Neuroendocrinology, 2016, v. 103, n. 1, p. 18, doi. 10.1159/000371819
- By:
- Publication type:
- Article
A novel AVPR2 splice site mutation leads to partial X-linked nephrogenic diabetes insipidus in two brothers.
- Published in:
- 2016
- By:
- Publication type:
- journal article
Death in pediatric Cushing syndrome is uncommon but still occurs.
- Published in:
- European Journal of Pediatrics, 2015, v. 174, n. 4, p. 501, doi. 10.1007/s00431-014-2427-y
- By:
- Publication type:
- Article
The complex of myxomas, spotty skin pigmentation and endocrine overactivity (Carney complex): imaging findings with clinical and pathological correlation.
- Published in:
- Insights into Imaging, 2013, v. 4, n. 1, p. 119, doi. 10.1007/s13244-012-0208-6
- By:
- Publication type:
- Article
Contralateral Suppression Index Does Not Predict Clinical Cure in Patients Undergoing Surgery for Primary Aldosteronism.
- Published in:
- Annals of Surgical Oncology: An Oncology Journal for Surgeons, 2021, v. 28, n. 12, p. 7487, doi. 10.1245/s10434-021-09692-7
- By:
- Publication type:
- Article
Long-Term Outcome of Bilateral Laparoscopic Adrenalectomy Measured by Disease-Specific Questionnaire in a Unique Group of Patients with Cushing's Syndrome.
- Published in:
- Annals of Surgical Oncology: An Oncology Journal for Surgeons, 2015, v. 22, p. 699, doi. 10.1245/s10434-015-4605-1
- By:
- Publication type:
- Article
Adrenal Histologic Findings Show No Difference in Clinical Presentation and Outcome in Primary Hyperaldosteronism.
- Published in:
- Annals of Surgical Oncology: An Oncology Journal for Surgeons, 2013, v. 20, n. 3, p. 753, doi. 10.1245/s10434-012-2670-2
- By:
- Publication type:
- Article
What is the Best Criterion for the Interpretation of Adrenal Vein Sample Results in Patients with Primary Hyperaldosteronism?
- Published in:
- Annals of Surgical Oncology: An Oncology Journal for Surgeons, 2012, v. 19, n. 6, p. 1881, doi. 10.1245/s10434-011-2121-5
- By:
- Publication type:
- Article
Adrenal function in Smith-Lemli-Opitz syndrome.
- Published in:
- American Journal of Medical Genetics. Part A, 2011, v. 155A, n. 11, p. 2732, doi. 10.1002/ajmg.a.34271
- By:
- Publication type:
- Article
Scoping review of COVID-19-related systematic reviews and meta-analyses: can we really have confidence in their results?
- Published in:
- 2022
- By:
- Publication type:
- Journal Article
The Human Vitamin D Receptor Gene ( VDR) Is Localized to Region 12cen-q12 by Fluorescent In Situ Hybridization and Radiation Hybrid Mapping: Genetic and Physical VDR Map.
- Published in:
- Journal of Bone & Mineral Research, 1999, v. 14, n. 7, p. 1163, doi. 10.1359/jbmr.1999.14.7.1163
- By:
- Publication type:
- Article
Mutations of the gene encoding the protein kinase A type I-α regulatory subunit in patients with the Carney complex.
- Published in:
- Nature Genetics, 2000, v. 26, n. 1, p. 89, doi. 10.1038/79238
- By:
- Publication type:
- Article
Somatic USP8 Gene Mutations Are a Common Cause of Pediatric Cushing Disease.
- Published in:
- 2017
- By:
- Publication type:
- journal article
Normalized Early Postoperative Cortisol and ACTH Values Predict Nonremission After Surgery for Cushing Disease.
- Published in:
- 2017
- By:
- Publication type:
- journal article
Characteristics of Pediatric vs Adult Pheochromocytomas and Paragangliomas.
- Published in:
- 2017
- By:
- Publication type:
- journal article
Bilateral Adrenal Hyperplasia as a Possible Mechanism for Hyperandrogenism in Women With Polycystic Ovary Syndrome.
- Published in:
- 2016
- By:
- Publication type:
- journal article
Diagnosis and Treatment of Primary Adrenal Insufficiency: An Endocrine Society Clinical Practice Guideline.
- Published in:
- 2016
- By:
- Publication type:
- journal article
Facial Plethora: Modern Technology for Quantifying an Ancient Clinical Sign and Its Use in Cushing Syndrome.
- Published in:
- 2015
- By:
- Publication type:
- journal article
Cholesterol Biosynthesis and Trafficking in Cortisol-Producing Lesions of the Adrenal Cortex.
- Published in:
- 2015
- By:
- Publication type:
- journal article
The Gene of the Ubiquitin-Specific Protease 8 Is Frequently Mutated in Adenomas Causing Cushing's Disease.
- Published in:
- 2015
- By:
- Publication type:
- journal article
ARMC5 Mutations in a Large Cohort of Primary Macronodular Adrenal Hyperplasia: Clinical and Functional Consequences.
- Published in:
- 2015
- By:
- Publication type:
- journal article
Endocrine disorders in Fanconi anemia: recommendations for screening and treatment.
- Published in:
- 2015
- By:
- Publication type:
- journal article