Disease: Anterior pituitary insufficiency- familial
- A Bayesian model to estimate the cutoff value of TSH for management of preterm birth
- A case of TSH-secreting pituitary adenoma with cyclic fluctuations in serum TSH levels
- A homozygous NOBOX truncating variant causes defective transcriptional activation and leads to primary ovarian insufficiency
- A mutation of the beta-domain in POU1F1 causes pituitary deficiency due to dominant PIT-1beta expression
- A mutation of the β-domain in POU1F1 causes pituitary deficiency due to dominant PIT-1β expression
- A novel <em>TBX19</em> gene mutation in patients with isolated ACTH deficiency from distinct families with a common geographical origin
- A Novel Mutation in the FSH Receptor (I423T) Affecting Receptor Activation and Leading to Primary Ovarian Failure
- A novel mutation in the NNT gene causing familial glucocorticoid deficiency, with a literature review
- A novel stop-loss DAX1 variant affecting its protein-interaction with SF1 precedes the adrenal hypoplasia congenital with rare spontaneous precocious puberty and elevated hypothalamic-pituitary-gonadal/adrenal axis responses
- A novel TBX19 gene mutation in patients with isolated ACTH deficiency from distinct families with a common geographical origin
- A novel variant in CDKN1C is associated with intrauterine growth restriction, short stature, and early-adulthood-onset diabetes
- A patient with novel mutations causing MEN1 and hereditary multiple osteochondroma
- A rare cause of neonatal hypoglycemia in two siblings: TBX19 gene mutation
- A review of renal GH/IGF1 family gene expression in chronic kidney diseases
- Abnormal Thyroid-Stimulating Hormone and Chronic Kidney Disease in Elderly Adults in Taipei City
- Allgrove Syndrome: Adrenal Insufficiency with Hypertensive Encephalopathy
- AMH in women with diminished ovarian reserve: potential differences by FMR1 CGG repeat level
- An Exploration of the Effects of Radiofrequency Radiation Emitted by Mobile Phones and Extremely Low Frequency Radiation on Thyroid Hormones and Thyroid Gland Histopathology
- Analysis of FMR1 gene premutation and X chromosome cytogenetic abnormalities in 100 Tunisian patients presenting premature ovarian failure
- Approach to growth hormone therapy in children with chronic kidney disease varies across North America: the Midwest Pediatric Nephrology Consortium report
- Are Prolactin Levels Linked to Suction Pressure?
- Association of TSH Elevation with All-Cause Mortality in Elderly Patients with Chronic Kidney Disease
- Beyond Premature Ovarian Insufficiency: Staging Reproductive Aging in Adolescent and Young Adult Cancer Survivors
- Biosimilar recombinant follitropin alfa preparations versus the reference product (Gonal-F®) in couples undergoing assisted reproductive technology treatment: a systematic review and meta-analysis
- Can Mild-to-Moderate Iodine Deficiency during Pregnancy Alter Thyroid Function? Lessons from a Mother-Newborn Cohort
- Case Report of Transgender Patient with Gonadotropic Dysfunction Secondary to Craniopharyngioma: Toward Improving Understanding of Biopsychosocial Dynamics of Gender Identity in Neurosurgical Care
- Childhood cerebral X-linked adrenoleukodystrophy with atypical neuroimaging abnormalities and a novel mutation
- Cholestasis and Hepatic Iron Deposition in an Infant With Complex Glycerol Kinase Deficiency
- Clinical and genetic characteristics of congenital isolated adrenocorticotropic hormone deficiency
- Clinical and molecular characterization of five Spanish kindreds with X-linked adrenal hypoplasia congenita: atypical findings and a novel mutation in NR0B1
- Clinical significance of elevated serum IL-36γ levels in patients with early-stage Hashimoto's thyroiditis
- Confirming the association between low serum 25OHD levels in girls with central precocious puberty and its severity
- Cortisol response patterns in depressed women and their healthy daughters at risk: Comparison with healthy women and their daughters
- Cytochrome P450 oxidoreductase deficiency caused by a novel mutation in the POR gene in two siblings: case report and literature review
- Delayed diagnosis of complex glycerol kinase deficiency in a Chinese male infant: a case report
- Delayed diagnosis of proopiomelanocortin (POMC) deficiency with type 1 diabetes in a 9-year-old girl and her infant sibling
- Diagnosing adrenal insufficiency using ACTH stimulation test
- Dietary minerals, reproductive hormone levels and sporadic anovulation: associations in healthy women with regular menstrual cycles
- Does Iodine Intake Modify the Effect of Maternal Dysglycemia on Birth Weight in Mild-to-Moderate Iodine-Deficient Populations? A Mother-Newborn Prospective Cohort Study
- Dysfunction of hypothalamic-pituitary-testicular axis in patients with adrenal hypoplasia congenita due to DAX-1 gene mutation
- Dysregulation of anti-Mullerian hormone expression levels in mural granulosa cells of FMR1 premutation carriers
- Early gestation screening of pregnant women for iodine deficiency disorders and iron deficiency in urban centre in Vadodara, Gujarat, India
- Effect of Low-Level Laser Therapy versus Electroacupuncture on Postnatal Scanty Milk Secretion: A Randomized Controlled Trial
- Effects of leukemia inhibitory receptor gene mutations on human hypothalamo-pituitary-adrenal function
- Emerging roles of melanocortin receptor accessory proteins (MRAP and MRAP2) in physiology and pathophysiology
- Evaluation of aldosterone concentrations in dogs with hypoadrenocorticism
- Falsely elevated plasma ACTH levels measured by the Elecsys assay related to heterophilic antibody in a case of secondary adrenocortical insufficiency
- Familial Central Hypothyroidism Caused by a Novel IGSF1 Gene Mutation
- Genetic analysis of novel pathogenic gene <em>HROB</em> in a family with primary ovarian insufficiency
- Genetic analysis of novel pathogenic gene HROB in a family with primary ovarian insufficiency
- Gonadotropins and their receptors: coevolution, genetic variants, receptor imaging, and functional antagonists
- Growth pattern in children with X-linked hypophosphatemia treated with burosumab and growth hormone
- Growth retardation in children with chronic renal disease
- HFpEF and HFrEF Display Different Phenotypes as Assessed by IGF-1 and IGFBP-1
- Holoprosencephaly: ZIC2 mutation in a case with panhypopituitarism
- Hypopituitarism in a neonate with hyperbilirubinemia and decreased level of consciousness: a case report study
- Impact of short stature on quality of life: A systematic literature review
- Isolated glucocorticoid deficiency: Genetic causes and animal models
- Late-onset isolated adrenocorticotropic hormone deficiency caused by nivolumab: a case report
- LCZ696 (sacubitril/valsartan) mitigates cyclophosphamide-induced premature ovarian failure in rats; the role of TLR4/NF-κB/NLRP3/Caspase-1 signaling pathway
- Management of Short Stature: Use of Growth Hormone in GH-Deficient and non-GH-Deficient Conditions
- Maternal prolactin during late pregnancy is important in generating nurturing behavior in the offspring
- Minipuberty in Sons of Women with Low Vitamin D Status during Pregnancy
- New-Onset Primary Adrenal Insufficiency and Autoimmune Hypothyroidism in a Pediatric Patient Presenting with MIS-C
- Newly diagnosed autoimmune Addison's disease in a patient with COVID-19 with autoimmune disseminated encephalomyelitis
- Novel mutation points to a hot spot in CDKN1C causing Silver-Russell syndrome
- Novel nonsense gain-of-function <em>NFKB2</em> mutations associated with a combined immunodeficiency phenotype
- Outcomes of random start versus clomiphene citrate and gonadotropin cycles in occult premature ovarian insufficiency patients, refusing oocyte donation: a retrospective cohort study
- Pituitary stalk interruption syndrome: A rare case report and literature review
- Plasma-derived from human umbilical cord blood restores ovarian function and improves serum reproductive hormones levels in mice with premature ovarian insufficiency (POI) through cytokines and growth factors
- Pleomorphism of the HPG axis with <em>NR0B1</em> gene mutation - a case report of longitudinal follow-up of a proband with central precocious puberty
- Presence of aberrant adrenocorticotropic hormone precursors in two cases of McCune-Albright syndrome
- Primary adrenal insufficiency due to hereditary apolipoprotein AI amyloidosis: endocrine involvement beyond hypogonadism
- Primary adrenal insufficiency in children: Diagnosis and management
- Primary lymphocytic hypophysitis: Clinical characteristics and treatment of 50 cases in a single centre in China over 18 years
- Prolidase as a marker of fibrogenesis in idiopathic primary ovarian insufficiency
- Rare deleterious BUB1B variants induce premature ovarian insufficiency and early menopause
- Reassessment of predictive values of ACTH-stimulated serum 21-deoxycortisol and 17-hydroxyprogesterone to identify CYP21A2 heterozygote carriers and nonclassic subjects
- Rehabilitation of anterior pituitary dysfunction combined with extrapontine myelinolysis: A case report
- Retrospective analysis of 19 patients with 6-Pyruvoyl Tetrahydropterin Synthase Deficiency: Prolactin levels inversely correlate with growth
- Salivary Cortisol Based Early ACTH Test for Identifying Adrenal Insufficiency in Low Birth Weight Infants
- Severe ovarian hyperstimulation syndrome after combined GnRH-agonist and low-dose human chorionic gonadotropin trigger in a patient with a single kidney
- STAR mutations causing non-classical lipoid adrenal hyperplasia manifested as familial glucocorticoid deficiency
- STAR mutations causing non‑classical lipoid adrenal hyperplasia manifested as familial glucocorticoid deficiency
- The copper content in the blood plasma of children with different types of short stature
- The Effects of Myo-Inositol and D-Chiro-Inositol in a Ratio 40:1 on Hormonal and Metabolic Profile in Women with Polycystic Ovary Syndrome Classified as Phenotype A by the Rotterdam Criteria and EMS-Type 1 by the EGOI Criteria
- The gonadotropin system, lessons from animal models and clinical cases
- The natural history of autoimmune Addison's disease with a non-classical presentation: a case report and review of literature
- The role of acid-labile subunit (ALS) in the modulation of GH-IGF-I action
- The role of Hippo pathway signaling and A-kinase anchoring protein 13 in primordial follicle activation and inhibition
- The Treatment of Growth Disorders in Childhood and Adolescence
- The Use of Human Induced Pluripotent Stem Cells for Testing Neuroprotective Activity of Pharmacological Compounds
- Thyroid and Parathyroid Conditions: Hypothyroidism
- Thyroid Function and Nutrient Status in the Athlete
- Treatment Adherence to Injectable Treatments in Pediatric Growth Hormone Deficiency Compared With Injectable Treatments in Other Chronic Pediatric Conditions: A Systematic Literature Review
- Triple-A syndrome: a wide spectrum of adrenal dysfunction
- Use of recombinant Human Growth Hormone (rHGH)
- Uterine Notch2 facilitates pregnancy recognition and corpus luteum maintenance via upregulating decidual Prl8a2
- Very low doses of heavy oxygen ion radiation induce premature ovarian failure
- Whole-exome sequencing identifies homozygous GPR161 mutation in a family with pituitary stalk interruption syndrome