• "A" motor neuron disease
• 50 Years Ago in TheJournalofPediatrics: Isolated Cortisol Deficiency due to ACTH Resistance: An Early Description of Familial Glucocorticoid Deficiency
• A corticotroph pituitary adenoma as the initial presentation of familial glucocorticoid deficiency
• A heterozygous variant of FGF13 caused X-linked developmental and epileptic encephalopathy 90 in a Chinese family
• A Novel Homozygous <em>MC2R</em> Variant Leading to Type-1 Familial Glucocorticoid Deficiency
• A Pediatric Patient With Type 1 Diabetes Mellitus With Poor Glycemic Control, Medication-Resistant Hypertension, and New-Onset Headache Diagnosed With Adrenocorticotropic Hormone (ACTH)-Secreting Pituitary Macroadenoma
• A polymorphic form of steroidogenic factor 1 associated with ACTH receptor deficiency in mouse adrenal cell mutants
• A polymorphic form of steroidogenic factor-1 is associated with adrenocorticotropin resistance in y1 mouse adrenocortical tumor cell mutants
• A rare and preventable aetiology of neurodevelopmental delay and epilepsy: familial glucocorticoid deficiency
• A rare genetic disorder causing persistent severe neonatal hypoglycaemia the diagnostic workup
• A rare homozygous variant of <em>MC2R</em> gene identified in a Chinese family with familial glucocorticoid deficiency type 1: A case report
• Abiraterone acetate for treatment of ectopic Cushing syndrome caused by ACTH-producing neuroendocrine tumor: a case report
• ACTH Resistance Syndrome: An Experience of Three Cases
• ACTH resistance syndromes
• ACTH resistance syndromes
• ACTH resistance: genes and mechanisms
• ACTH-receptor deficient mutants of the Y1 mouse adrenocortical tumor cell line
• Adrenal adenoma associated with raised metanephrine level: A case report
• Adrenocorticotropic hormone (ACTH) insensitivity syndrome: about a case
• Adrenocorticotropin receptor and adrenal disorders
• Adrenocorticotropin receptor gene mutations in familial glucocorticoid deficiency: relationships with clinical features in four families
• Adrenocorticotropin resistance syndromes
• Adrenocorticotropin-resistant mutants of the Y1 adrenal cell line fail to express the adrenocorticotropin receptor
• Allgrove (Triple A) Syndrome: A Case Report from the Kashmir Valley
• Allgrove Syndrome
• Allgrove syndrome (triple A). Finding of a mutation not described in the AAAS gene
• Allgrove syndrome and motor neuron disease
• Allgrove syndrome in the mainland of China: clinical report and mutation analysis
• Allgrove Syndrome: Adrenal Insufficiency with Hypertensive Encephalopathy
• Altered glucose-dependent secretion of glucagon and ACTH is associated with insulin resistance, assessed by population analysis
• Bioinactive ACTH causing glucocorticoid deficiency
• Clinical analysis of 78 patients with nonclassical 21-hydroxylase deficiency
• Clinical and genetic characterisation of a series of patients with triple A syndrome
• Clinical characteristics and genetic analysis of two children with Familial glucocorticoid deficiency type 1 due to variants of MC2R gene
• Clinical decision-making based on 11C-methionine PET in recurrent Cushing's disease with equivocal MRI findings
• Compound heterozygosity of a frameshift mutation in the coding region and a single base substitution in the promoter of the ACTH receptor gene in a family with isolated glucocorticoid deficiency
• Defects in G protein-coupled signal transduction in human disease
• Dietary Betaine Impacts Metabolic Responses to Moderate Heat Exposure in Sheep
• Different AHO phenotype in a Chinese family with a novel GNAS missense variant: a case report
• Differential Hypothalamic-pituitary-adrenal Response to Stress among Rat Strains: Methodological Considerations and Relevance for Neuropsychiatric Research
• Diminished adrenal androgen secretion in familial glucocorticoid deficiency implicates a significant role for ACTH in the induction of adrenarche
• Disorders of adrenal development
• Ectopic adrenocorticotrophic hormone syndrome secondary to treatment-related neuroendocrine differentiation of metastatic castrate-resistant prostate cancer
• Effect of mild intermittent cold stimulation on thymus immune function in broilers
• Effects of resistance training on bone mineral density and resting serum hormones in female collegiate distance runners: a randomized controlled pilot trial
• Emerging roles of melanocortin receptor accessory proteins (MRAP and MRAP2) in physiology and pathophysiology
• Endocrine characteristics and risk factors of type 2 diabetes complicated with gastrointestinal autonomic neuropathy: A single-center retrospective study
• Exclusion of the adrenocorticotropin (ACTH) receptor (MC2R) locus in some families with ACTH resistance but no mutations of the MC2R coding sequence (familial glucocorticoid deficiency type 2)
• Exogenous ACTH stimulus during the preovulatory period alters patterns of leukocyte recruitment in the ovary of dairy cows
• Expression of adenylyl cyclase-4 (AC-4) in Y1 and forskolin-resistant adrenal cells
• Familial glucocorticoid deficiency: a diagnostic challenge during acute illness
• Familial glucocorticoid deficiency: New genes and mechanisms
• Genetic adrenal diseases
• Genetic and phenotypic spectrum of non-21-hydroxylase-deficiency primary adrenal insufficiency in childhood: data from 111 Chinese patients
• Genetic disorders involving adrenal development
• Genetic heterogeneity of adrenocorticotropin (ACTH) resistance syndromes: identification of a novel mutation of the ACTH receptor gene in hereditary glucocorticoid deficiency
• Heterogeneity in the molecular basis of ACTH resistance syndrome
• Hypoaldosteronism
• Impaired Gonadotropin-Lowering Effects of Metformin in Postmenopausal Women with Autoimmune Thyroiditis: A Pilot Study
• Impaired steroidogenic factor 1 (NR5A1) activity in mutant Y1 mouse adrenocortical tumor cells
• Insight into Glyproline Peptides' Activity through the Modulation of the Inflammatory and Neurosignaling Genetic Response Following Cerebral Ischemia-Reperfusion
• Intact GR dimerization is critical for restraining plasma ACTH levels during chronic psychosocial stress
• Is ectopic Cushing's syndrome underdiagnosed in patients with small cell lung cancer?
• Isolated Addison's disease is unlikely to be caused by mutations in MC2R, MRAP or STAR, three genes responsible for familial glucocorticoid deficiency
• Isolated glucocorticoid deficiency: Genetic causes and animal models
• Ketogenic Diet Initially Masks Symptoms of Hypercortisolism in Cushing's Disease
• Medical Therapies in Functioning Pituitary Neuroendocrine Tumors(PitNETs)
• Medical treatment of Cushing's disease with concurrent diabetes mellitus
• Metasilicate-based alkaline mineral water confers diarrhea resistance in maternally separated piglets via the microbiota-gut interaction
• Missense mutations in the melanocortin 2 receptor accessory protein that lead to late onset familial glucocorticoid deficiency type 2
• Myo-Inositol Enhances the Inhibitory Effect of Metformin on Gonadotropin Levels in Postmenopausal Women
• Myo-Inositol Potentiates the Inhibitory Effect of Metformin on Prolactin Levels
• Myocardiopathy and isolated glucocorticoid deficit with ACTH resistance: a fortuitous association?
• Neonatal hyperpigmentation: diagnosis of familial glucocorticoid deficiency with a novel mutation in the melanocortin-2 receptor gene
• Neonatal presentation of familial glucocorticoid deficiency with a MRAP mutation: A case report
• Novel polymorphisms and lack of mutations in the ACD gene in patients with ACTH resistance syndromes
• Periodic hypoxia, intermittent pain, and caffeine in male and female neonatal rats: corticosterone, insulin resistance, and hepatic gene expression
• Pituitary tumors and the risk of other malignancies: is the relationship coincidental or causal?
• Prenatal Hypoxia-Induced Adverse Reaction to Mild Stress is Associated with Depressive-Like Changes in the Glucocorticoid System of Rats
• Presentation of primary adrenal insufficiency in childhood
• Primary hypothyroidism revealing pseudohypoparathyroidism without hypocalcemia and hyperphosphoremia
• Rare monogenic causes of primary adrenal insufficiency
• Real-word adrenocorticotropic hormone treatment for childhood-onset nephrotic syndrome
• Recurrent pulmonary infection leads to the diagnosis of triple A syndrome: a case report
• SCARB1 downregulation in adrenal insufficiency with Allgrove syndrome
• SF1 polymorphisms in the mouse and steroidogenic potential
• Spectrum of mutations of the AAAS gene in Allgrove syndrome: lack of mutations in six kindreds with isolated resistance to corticotropin
• Tall stature in familial glucocorticoid deficiency
• The Effect of Metformin on Plasma Prolactin Levels in Young Women with Autoimmune Thyroiditis
• The Effects of Peptide Receptor Radionuclide Therapy on the Neoplastic and Normal Pituitary
• The Entity of Connshing Syndrome: Primary Aldosteronism with Autonomous Cortisol Secretion
• The genetics of ACTH resistance syndromes
• The Hypothalamus-Pituitary-Adrenocortical response to critical illness: a concept in need of revision
• The molecular basis of adrenocorticotrophin resistance syndrome
• Thioredoxin Reductase 2 (TXNRD2) mutation associated with familial glucocorticoid deficiency (FGD)
• Triple A (Allgrove) syndrome due to AAAS gene mutation with a rare association of amyotrophy
• Triple A syndrome-related achalasia treated by per-oral endoscopic myotomy: Three case reports
• Uncommon neonatal case of hypoglycemia: ACTH resistance syndrome
• Vitamin D Status Determines the Impact of Metformin on Gonadotropin Levels in Postmenopausal Women
• Yeast hydrolysate attenuates lipopolysaccharide-induced inflammatory responses and intestinal barrier damage in weaned piglets