Disease: Familial hypopituitarism
- <em>PROKR2</em> Mutations in Patients with Short Stature Who Have Isolated Growth Hormone Deficiency and Multiple Pituitary Hormone Deficiency
- A GHRHR founder mutation causes isolated growth hormone deficiency type IV in a consanguineous Pakistani family
- A Novel RNPC3 Gene Variant Expands the Phenotype in Patients with Congenital Hypopituitarism and Neuropathy
- Approach of Acromegaly during Pregnancy
- Association of Homozygous <em>PROP1</em> Mutation in a Saudi Family with Combined Pituitary Hormone Deficiency
- Association of Homozygous PROP1 Mutation in a Saudi Family with Combined Pituitary Hormone Deficiency
- Asymptomatic trigger of adrenal crisis in a patient with Sheehan syndrome: importance of timely recognition and intervention
- Caregiver-based perception of disease burden in Schaaf-Yang syndrome
- Caregiving burden and special needs of parents in the care of their short-statured children - a qualitative approach
- Clinical and genetic analysis of a child with Schaaf-Yang syndrome
- Clinical, radiological, and molecular diagnosis of congenital pituitary diseases causing short stature
- Congenital hypopituitarism and multiple midline defects in a newborn with non-familial Cat Eye syndrome
- Copy number variation in pituitary stalk interruption syndrome: A large case series of sporadic non-syndromic patients and literature review
- Correction of In-Patient Severe Hypernatremia in an 81-Year-Old Female With Hypopituitarism
- Early onset critically ill infants with Schaaf-Yang syndrome: a retrospective study from the China neonatal genomes project and literature review
- Exome sequencing (ES) of a pediatric cohort with chronic endocrine diseases: a single-center study (within the framework of the TRANSLATE-NAMSE project)
- Genetic diagnosis of congenital hypopituitarism in Turkish patients by a target gene panel: novel pathogenic variants in GHRHR, GLI2, LHX4 and POU1F1 genes
- Growth hormone treatment in children with short stature: impact of the diagnosis on parents
- Hemochromatosis: Ferroptosis, ROS, Gut Microbiome, and Clinical Challenges with Alcohol as Confounding Variable
- Hypopituitarism Presenting as Recurrent Episodes of Hypoglycemia: Houssay Phenomenon
- Identification of genetic variants and phenotypic characterization of a large cohort of patients with congenital hypopituitarism and related disorders
- Isolated growth hormone deficiency in children with vertically transmitted short stature: What do the genes tell us?
- Long-term safety of growth hormone replacement therapy in survivors of cancer and tumors of the pituitary region
- Lymphocytic Hypophysitis in a Patient With Suspected Syndrome of Inappropriate Antidiuretic Hormone Secretion (SIADH)
- Neurodevelopmental impairments in children with septo-optic dysplasia spectrum conditions: a systematic review
- Neuropathy, ataxia, retinitis pigmentosa: a case of a mother and two siblings
- Oxytocin-based therapies for treatment of Prader-Willi and Schaaf-Yang syndromes: evidence, disappointments, and future research strategies
- Phenotype-Genotype Correlations of GH1 Gene Variants in Patients with Isolated Growth Hormone Deficiency or Multiple Pituitary Hormone Deficiency
- Position statement on the diagnosis and management of acromegaly: The French National Diagnosis and Treatment Protocol (NDTP)
- Preimplantation Genetic Testing (PGT) and Prenatal Diagnosis of Schaaf-Yang Syndrome: A Report of Three Families and a Research on Genotype-Phenotype Correlations
- SALL4 Phenotype in Four Generations of One Family: An Interplay of the Upper Limb, Kidneys, and the Pituitary
- Short Stature due to Bioinactive Growth Hormone (Kowarski Syndrome)
- The Genetic Pathophysiology and Clinical Management of the TADopathy, X-Linked Acrogigantism
- The Treatment of Growth Disorders in Childhood and Adolescence