Management of infertility in women with hypothalamic hypogonadotropic hypogonadism: an expert opinion.

Acquired transient vasopressin deficiency by cannabinoids and other substances.

GH Response to Glucagon in Transition: Role of BMI and Etiology in Childhood-Onset GH Deficiency.

Hypoprolactinemia: Biology, Clinical Relevance, and Diagnostic Challenges.

Primary adrenocortical insufficiency in patients with AIDS in Wuhan, China: 3 cases report and literature review.

Determinants of QTc Interval Prolongation in Patients with Hypopituitarism and Other Pituitary Disorders.

Exploring GHBP as a surrogate of GH activity in multimorbid older adults: A cross-sectional study.

Patients with langerhans cell histiocytosis and hypothalamic-pituitary involvement: insights from the HEROS study cohort.

Growth hormone deficiency after moderate traumatic brain injury with normal (or high) IGF-1; a case report demonstrating benefit of replacement therapy and clinical pearls for diagnosis.

Impact of traumatic brain injury severity on anterior pituitary function: A prospective study.

Management of acromegaly beyond primary surgery: efficacy and safety of repeat surgery and radiotherapy.

A Genetically-Engineered Thyroid Gland Built for Selective Triiodothyronine Secretion.

QT Prolongation and Torsades De Pointes Due to Undiagnosed Sheehan Syndrome: A Rare Cause of Lethal Arrhythmia.

Hypopituitarism: genetic, developmental, and acquired etiologies with a focus on the emerging concept of autoimmune hypophysitis.

Isolated adrenocorticotrophic hormone (ACTH) deficiency presenting with recurrent hypoglycemia and hyponatremia.

Pituitary dysfunction after cranial radiotherapy for brain tumor.

Central Hypothyroidism: Advances in Etiology, Diagnostic Challenges, Therapeutic Targets, and Associated Risks.

Growth hormone signaling and clinical implications: from molecular to therapeutic perspectives.

Clinical and genetic features of childhood-onset congenital combined pituitary hormone deficiency: a retrospective, single-center cohort study.

Central Adrenal Insufficiency: Etiology and Diagnostic Approach.

What Is Hidden Behind Growth Hormone Deficiency? The Neuroradiologist's Perspective.

A Case of Idiopathic Central Diabetes Insipidus and a Mosaic Form of Turner Syndrome.

An Update on Advances in Hypopituitarism: Etiology, Diagnosis, and Current Management.

The molecular basis of hypoprolactinaemia.

Acquired isolated ACTH deficiency co-occurrence with breast cancer irrespective of paraneoplastic syndrome: coincidence or inevitability.

Isolated hypoprolactinemia: The rarest of the rare?

Acquired hypoprolactinemia in men, possible phenotype.

Acquired thyroid-stimulating hormone, luteinizing hormone, and follicle-stimulating hormone deficiencies with circulating anti-glycoprotein hormones alpha chain-positive cell antibodies.

The somatotroph pituitary gland function in high-aged multimorbid hospitalized patients with IGF-I deficiency.

Long-term pituitary function and functional and patient-reported outcomes in severe acquired brain injury.

Acquiring Social Safety Engages Oxytocin Neurons in the Supraoptic Nucleus: Role of Magel2 Deficiency.

Diagnosis and management of congenital hypopituitarism in children.

Position statement on the diagnosis and management of congenital pituitary deficiency in adults: The French National Diagnosis and Treatment Protocol (NDTP).

Insights from an advisory board: Facilitating transition of care into adulthood in brain cancer survivors with acquired pediatric growth hormone deficiency.

Subclinical central hypothyroidism in patients with hypothalamic-pituitary disease: does it exist?

Idiopathic isolated adrenocorticotropic hormone deficiency: a systematic review of a heterogeneous and underreported disease.

Diagnosing and treating anterior pituitary hormone deficiency in pediatric patients.

Hypoglycaemia in adrenal insufficiency.

Clinical Characteristics of Children with Combined Pituitary Hormone Deficiency and the Effects of Growth Hormone Treatment.

Paraneoplastic isolated adrenocorticotropic hormone deficiency revealed after immune checkpoint inhibitors therapy: new insights into anti-corticotroph antibody.

Desmopressin Dose Requirements in Adults with Congenital and Acquired Central Diabetes Insipidus.

Successful pregnancy and delivery in a female with pituitary stalk interruption syndrome following in vitro fertilization and embryo transfer: A case report and literature review.

Unusual and lesser-known rare causes of adult growth hormone deficiency.

Mild traumatic brain injury as a cause of adult growth hormone deficiency: Diagnosis and treatment.

Autoantibodies to selenoprotein P in chronic fatigue syndrome suggest selenium transport impairment and acquired resistance to thyroid hormone.

Acquired Hypothyroidism in Children.

Acquired idiopathic isolated ACTH deficiency with associated autoimmune thyroiditis in pediatrics: case report and review of the literature.

Neuroendocrine Disruptions Following Head Injury.

Paraneoplastic autoimmune hypophysitis: a novel form of paraneoplastic endocrine syndrome.

Short Stature: Think About the Pituitary Stalk Interruption Syndrome.

New developments and concepts in the diagnosis and management of diabetes insipidus (AVP-deficiency and resistance).

Downregulation of ACAN is Associated with the Growth hormone pathway and Induces short stature.

Analysis of ProP1 Gene in a Cohort of Tunisian Patients with Congenital Combined Pituitary Hormone Deficiency.

Pituitary Abscess Causing Hypopituitarism in a Patient With Acquired Immunodeficiency Syndrome.

Combining metabolomics and machine learning models as a tool to distinguish non-classic 21-hydroxylase deficiency from polycystic ovary syndrome without adrenocorticotropic hormone testing.

Menorrhagia as main presentation sign of severe hypothyroidism in a pediatric patient: a case report.

PEGylated Recombinant Human Growth Hormone Jintrolong® Exhibits Good Long-Term Safety in Cynomolgus Monkeys and Human Pediatric Growth Hormone Deficiency Patients.

Presentation and diagnosis of childhood-onset combined pituitary hormone deficiency: A single center experience from over 30 years.

Case Report: Acquired Generalized Anhidrosis Caused by Brain Tumor: Review of the Literature.

Adding T2-Weighted Images to FAST1 Protocol to Evaluate the Anatomy of the Hypothalamic-Pituitary Region.

Camurati-Engelmann Disease Complicated by Hypopituitarism: Management Challenges and Literature Review of Outcomes With Bisphosphonates.

Dental arches in inherited severe isolated growth hormone deficiency.

Gonadotropin-releasing hormone-secreting neuron development and function: an update.

Approach to the Pediatric Patient: Central Diabetes Insipidus.

Is treated hypopituitarism associated with increased left ventricular strains?-detailed analysis from the three-dimensional speckle-tracking echocardiographic MAGYAR-Path Study.

Acquired growth hormone deficiency in Fanconi-Bickel syndrome.

Fetal and Neonatal Thyroid Dysfunction.

Short and Long-Term Effects of Growth Hormone in Children and Adolescents With GH Deficiency.

Variability in Oral Desmopressin Dose Requirements in Children with Central Diabetes Insipidus.

Advances in differential diagnosis and management of growth hormone deficiency in children.

Nuclear Receptor CoRepressors, NCOR1 and SMRT, are required for maintaining systemic metabolic homeostasis.

Design and synthesis of polyacrylic acid/deoxycholic acid-modified chitosan copolymer and a close inspection of human growth hormone-copolymer interactions: An experimental and computational study.

Differential Diagnosis of the Short IGF-I-Deficient Child with Apparently Normal Growth Hormone Secretion.

Prevalence of growth hormone deficiency in patients with unexplained chronic fatigue after undergoing bone marrow transplantation in adulthood.

Aetiologies and clinical patterns of hypopituitarism in Sudanese children.

Individuals with isolated congenital GH deficiency due to a GHRH receptor gene mutation appear to cope better with SARS-CoV-2 infection than controls.

Premature Ejaculation and Endocrine Disorders: A Literature Review.

Clinical Heterogeneity of Acquired Idiopathic Isolated Adrenocorticotropic Hormone Deficiency.

Two Cases of anti-PIT-1 Hypophysitis Exhibited as a Form of Paraneoplastic Syndrome not Associated With Thymoma.

Paediatric hypopituitarism: a case report and management challenges in a resource poor setting.

The phenotypic spectrum of X-linked, infantile onset ALG13-related developmental and epileptic encephalopathy.

[Rathke's cleft cyst in a middle-aged man with chief complaint of depression : A case report and literature review].

HPG-Dependent Peri-Pubertal Regulation of Adult Neurogenesis in Mice.

Evolving pituitary hormone deficits in primarily isolated GHD: a review and experts' consensus.

Clinical lessons learned in constitutional hypopituitarism from two decades of experience in a large international cohort.

ACQUIRED ECTOPIC POSTERIOR PITUITARY BRIGHT SPOT DUE TO VASCULOTOXIC SNAKEBITE.

Morphological changes of the cerebral cortex between children with isolated growth hormone deficiency and idiopathic short stature.

A case report of glucose transporter 1 deficiency syndrome with growth hormone deficiency diagnosed before starting ketogenic diet.

Acquired forms of central diabetes insipidus: Mechanisms of disease.

Clinical and Biochemical Characteristics of Severe Hypothyroidism Due to Autoimmune Thyroiditis in Children.

Central hypothyroidism or subclinical hyperthyroidism: can they be confused with each other?

Diagnosis and Treatment of Growth Hormone Deficiency: A Position Statement from Korean Endocrine Society and Korean Society of Pediatric Endocrinology.

How I treat gastrointestinal bleeding in congenital and acquired von Willebrand disease.

The Optimized Calculation Method for Insulin Dosage in an Insulin Tolerance Test (ITT): A Randomized Parallel Control Study.

Potential applications for rhIGF-I: Bone disease and IGFI.

Therapeutic senescence via GPCR activation in synovial fibroblasts facilitates resolution of arthritis.

Geographical influences on the iodine status in pregnant women, neonates, and school-age children in China.

A Rare SPRY4 Gene Mutation Is Associated With Anosmia and Adult-Onset Isolated Hypogonadotropic Hypogonadism.

Pathogenesis of Anti-PIT-1 Antibody Syndrome: PIT-1 Presentation by HLA Class I on Anterior Pituitary Cells.

Autoimmune Pituitary Disease: New Concepts With Clinical Implications.

Systematic profiling of clinical missence mutation effects on the intermolecular interaction between human growth hormone and its receptor in isolated growth hormone deficiency.

Growth hormone treatment and health-related quality of life in children and adolescents: A national, prospective, one-year controlled study.

Limited Utility of Biochemical Screening for Pituitary Deficiencies and Adverse Effects in Idiopathic GH Deficiency.

Identification of a Novel PROP1 Mutation in a Patient with Combined Pituitary Hormone Deficiency and Enlarged Pituitary.

Androgen potentiates the expression of FSH receptor and supports preantral follicle development in mice.

Clinical and Immunological Phenotype of Patients With Primary Immunodeficiency Due to Damaging Mutations in NFKB2.

Pituitary deficiency and precocious puberty after childhood severe traumatic brain injury: a long-term follow-up prospective study.

Evaluation and management of the child with hypothyroidism.

Differences in the functional connectivity density of the brain between individuals with growth hormone deficiency and idiopathic short stature.

Limited Adherence to Growth Hormone Replacement in Patients with Traumatic Brain Injury.

Less known aspects of central hypothyroidism: Part 1 - Acquired etiologies.

Basal characteristics and first year responses to human growth hormone (GH) vary according to diagnostic criteria in children with non-acquired GH deficiency (naGHD): observations from a single center over a period of five decades.

Phase 2 Randomized, Placebo-Controlled Clinical Trial of Recombinant Human Growth Hormone (rhGH) During Rehabilitation From Traumatic Brain Injury.

Racial/Ethnic Disparities in US Pediatric Growth Hormone Treatment.

National Program of Severe Growth Hormone Deficiency Treatment in Adults and Adolescents after Completion of Growth Promoting Therapy.

Central adrenal insufficiency in children and adolescents.

IMPORTANCE OF ISOLATED GESTATIONAL HYPOTHYROXINEMIA IN THE DEVELOPMENT OF OBSTETRIC AND SOMATIC PATHOLOGIES.

The aryl hydrocarbon receptor is indispensable for dioxin-induced defects in sexually-dimorphic behaviors due to the reduction in fetal steroidogenesis of the pituitary-gonadal axis in rats.

Pituitary dysfunction and association with fatigue in stroke and other acute brain injury.

Transcriptomics and machine learning predict diagnosis and severity of growth hormone deficiency.

Semen quality in patients with pituitary disease and adult-onset hypogonadotropic hypogonadism.

Low FT4 Concentrations around the Start of Recombinant Human Growth Hormone Treatment: Predictor of Congenital Structural Hypothalamic-Pituitary Abnormalities?

Functional Roles of Sex-Biased, Growth Hormone-Regulated MicroRNAs miR-1948 and miR-802 in Young Adult Mouse Liver.

Iatrogenic Creutzfeldt-Jakob disease with Amyloid-β pathology: an international study.

Hypothalamic abnormalities: Growth failure due to defects of the GHRH receptor.

Acute development of Cushing syndrome in an HIV-infected child on atazanavir/ritonavir based antiretroviral therapy.

Progression from isolated growth hormone deficiency to combined pituitary hormone deficiency.

Impact of the underlying etiology of growth hormone deficiency on serum IGF-I SDS levels during GH treatment in children.

Long-Standing Isolated Autoimmune Hypothalamitis Diagnosed with Endoscopic Transventricular Biopsy.

Hypopituitarism is associated with lower oxytocin concentrations and reduced empathic ability.

Opioid-induced hyponatremia in a patient with central diabetes insipidus: independence from ADH.

Central hypothyroidism - a neglected thyroid disorder.

Stem cell therapy and its potential role in pituitary disorders.

Growth hormone deficiency and human immunodeficiency virus.

Classical and non-classical causes of GH deficiency in adults.

Pattern of Thyroid Disorders in Children and Adolescents Seen at the Lagos University Teaching Hospital, Nigeria, Over a 10-year Period.

Cholestasis caused by panhypopituitarism and acquired cytomegalovirus infection in a 2-month-old male infant: A case report.

A Novel Clinical Entity of Autoimmune Endocrinopathy: Anti-PIT-1 Antibody Syndrome.

CENTRAL DIABETES INSIPIDUS: CLINICAL CHARACTERISTICS AND LONG-TERM COURSE IN A LARGE COHORT OF ADULTS.

A novel thymoma-associated autoimmune disease: Anti-PIT-1 antibody syndrome.

Untangling the Gordian knot of HIV, stress, and cognitive impairment.

Baseline Characteristics and Gender Differences in Prepubertal Children Treated with Growth Hormone in Europe, USA, and Japan: 25 Years' KIGS® Experience (1987-2012) and Review.

UK Iatrogenic Creutzfeldt-Jakob disease: investigating human prion transmission across genotypic barriers using human tissue-based and molecular approaches.

Long-term safety of growth hormone replacement therapy after childhood medulloblastoma and PNET: it is time to set aside old concerns.

Clinical Applications of Gonadotropins in the Male.

Hypogonadotropic Hypogonadism and Short Stature in Patients with Diabetes Due to Neurogenin 3 Deficiency.

Hypopituitarism patterns among adult males with prolactinomas.

The physiology of functional hypothalamic amenorrhea associated with energy deficiency in exercising women and in women with anorexia nervosa.

Burden of Growth Hormone Deficiency and Excess in Children.

Compensated reduction in Leydig cell function is associated with lower semen quality variables: a study of 8182 European young men.

Reversible growth failure and complete GH deficiency in a 4-year-old girl with very early Hashimoto's thyroiditis and subsequent hyperplasia of pituitary thyrotroph cells.

Causes of hypogonadotropic hypogonadism predict response to gonadotropin substitution in adults.

[Endocrine consequences in young adult survivors of childhood cancer treatment].

Acquired Hypogonadotropic Hypogonadism (AHH) in Thalassaemia Major Patients: An Underdiagnosed Condition?

Atypical defects resulting in growth hormone insensitivity.

Hypotestosteronaemia in the aging male: should we treat it?

[A Novel Clinical Entity "Anti-PIT-1 Antibody Syndrome"--Autoimmunity against a Transcription Factor].

The practical management of testosterone deficiency in men.

Autosomal Dominant Growth Hormone Deficiency (Type II).

Subjects with isolated GH deficiency due to a null GHRHR mutation eat proportionally more, but healthier than controls.

Age-related testosterone decline is due to waning of both testicular and hypothalamic-pituitary function.

Treatment situation of male hypogonadotropic hypogonadism in pediatrics and proposal of testosterone and gonadotropins replacement therapy protocols.

Anti-PIT-1 antibody syndrome; a novel clinical entity leading to hypopituitarism.

Natural history of growth hormone deficiency in a pediatric cohort.

Secondary IGF-I deficiency as a prognostic factor of growth hormone (GH) therapy effectiveness in children with isolated, non-acquired GH deficiency.

Reversal of idiopathic hypogonadotropic hypogonadism: a cohort study in Chinese patients.