Disease: Laron-type dwarfism
- A 42-Year-Old Woman with Untreated Growth Hormone Insensitivity, Diabetic Retinopathy, and Gene Sequencing Identifies a Variant of Laron Syndrome
- A common human missense mutation of vesicle coat protein SEC23B leads to growth restriction and chronic pancreatitis in mice
- A novel heterozygous STAT5B variant in a patient with short stature and partial growth hormone insensitivity (GHI)
- A Novel, Heterozygous, de novo Splicing Variant Affecting the Intracellular Domain of the Growth Hormone Receptor, and Causing a Mild Short Stature
- A Recurrent Mutation in Growth Hormone Receptor (<em>GHR</em>) Gene Underlying Laron-type Dwarfism in a Pakistani Family
- A Recurrent Mutation in Growth Hormone Receptor (GHR) Gene Underlying Laron-type Dwarfism in a Pakistani Family
- A zebrafish model of growth hormone insensitivity syndrome with immune dysregulation 1 (GHISID1)
- About a Suggestive Association Between Fanconi Anemia and Laron Syndrome
- Adult patients with Laron syndrome tend to develop the metabolic syndrome
- Alterations in Stem Cell Populations in IGF-1 Deficient Pediatric Patients Subjected to Mecasermin (Increlex) Treatment
- An unusual brain lesion in a patient with Laron Syndrome
- Anti-Müllerian Hormone, Growth Hormone, and Insulin-Like Growth Factor 1 Modulate the Migratory and Secretory Patterns of GnRH Neurons
- Assessing insulin sensitivity and resistance in syndromes of severe short stature
- Branding of subjects affected with genetic syndromes of severe short stature in developing countries
- Cancer in Ecuadorian subjects with Laron syndrome (ELS)
- Cancer in GH excess and GH deficit
- Cancer in growth hormone excess and growth hormone deficit
- Cardiac examination in children with Laron syndrome undergoing mecasermin therapy
- Challenges in the care of individuals with severe primary insulin-like growth factor-I deficiency (SPIGFD): an international, multi-stakeholder perspective
- Changes in plasma amino acids metabolites, caused by long-term IGF-I deficiency, are reversed by IGF-I treatment - A pilot study
- Clinical profile of Laron dwarfism - experience from a tertiary care institute in Chennai
- Congenital IGF-1 deficiency protects from cancer: lessons from Laron syndrome
- Diagnosis of Laron syndrome using monoplex-polymerase chain reaction technology with a whole-genome amplification template: A case report
- Divergent metabolic phenotypes in two genetic syndromes of low insulin secretion
- Dominant-negative STAT5B mutations cause growth hormone insensitivity with short stature and mild immune dysregulation
- Effect of Growth Hormone Receptor Deficiency on Androgen-Associated Gene Expression of Hepatic Drug Metabolizing Enzymes and Drug Transporters in Pigs
- Effectiveness and safety of rhIGF1 therapy in patients with or without Laron syndrome
- Effects of GHR Deficiency and Juvenile Hypoglycemia on Immune Cells of a Porcine Model for Laron Syndrome
- Erratum: Laron syndrome
- Fanconi's anaemia & Laron syndrome: An enigma
- Fanconi's anaemia & Laron syndrome: An enigma
- First use of gene therapy to treat growth hormone resistant dwarfism in a mouse model
- Focal Epilepsy in Individuals with Laron Syndrome
- Frequency and Predictive Factors of Hypoglycemia in Patients Treated With rhIGF-1: Data From the Eu-IGFD Registry
- From Churchill to Elephants: The Role of Protective Genes against Cancer
- From dwarves to giants: South American's contribution to the history of growth hormone and related disorders
- Functional changes of the liver in the absence of growth hormone (GH) action - Proteomic and metabolomic insights from a GH receptor deficient pig model
- Further Clinical Evidence for the Effect of IGF-1 on Hair Growth and Alopecia
- Genetic causes of growth hormone insensitivity beyond GHR
- Genetic Characterization of Short Stature Patients With Overlapping Features of Growth Hormone Insensitivity Syndromes
- Genetic Competencies for Effective Pediatric Endocrine Nursing Practice
- Genome-Wide Profiling of Laron Syndrome Patients Identifies Novel Cancer Protection Pathways
- GH-dependent growth of experimentally induced carcinomas in vivo
- Growth Hormone and the Human Hair Follicle
- Growth Hormone Deficiency: Health and Longevity
- Growth Hormone insensitivity (Laron syndrome): Report of a new family and review of Brazilian patients
- Growth hormone insensitivity and adipose tissue: tissue morphology and transcriptome analyses in pigs and humans
- Growth hormone modulates Trypanosoma cruzi infection in vitro
- Growth Hormone Receptor (GHR) 6Ω Pseudoexon Activation: a Novel Cause of Severe Growth Hormone Insensitivity
- Growth Hormone Receptor (Ghr) 6ω Pseudoexon Activation: A Novel Cause Of Severe Growth Hormone Insensitivity (Ghi)
- Growth hormone receptor deficiency in humans associates to obesity, increased body fat percentage, a healthy brain and a coordinated insulin sensitivity
- Growth hormone receptor knockout: Relevance to xenotransplantation
- Growth Hormone's Links to Cancer
- High growth hormone serum partially protects mice against Trypanosoma cruzi infection
- Hormone resistance in children: what primary care physicians need to know
- Identification and <em>In Vitro</em> Functional Verification of Two Novel Mutations of <em>GHR</em> Gene in the Chinese Children with Laron Syndrome
- Identification and In Vitro Functional Verification of Two Novel Mutations of GHR Gene in the Chinese Children with Laron Syndrome
- Identification of nephronectin as a new target for IGF1 action
- Identification of UDP-Glucuronosyltransferase 2B15 (UGT2B15) as a Target for IGF1 and Insulin Action
- Identification of ZYG11A as a candidate IGF1-dependent proto-oncogene in endometrial cancer
- In Reference to Fanconi Anemia and Laron Syndrome
- Insights from the clinical phenotype of subjects with Laron syndrome in Ecuador
- Insulin-like growth factors and aging: lessons from Laron syndrome
- Invaluable Role of Consanguinity in Providing Insight into Paediatric Endocrine Conditions: Lessons Learnt from Congenital Hyperinsulinism, Monogenic Diabetes, and Short Stature
- Laron syndrome - A historical perspective
- Laron syndrome in three female siblings with the development of subclinical hypothyroidism and dyslipidemia in one case: first report of a Syrian family
- Laron syndrome related to homozygous growth hormone receptor c.784>C mutation in a patient with hypoplastic pulmonary arteries
- Laron syndrome related to homozygous growth hormone receptor c.784>C mutation in a patient with hypoplastic pulmonary arteries
- Laron Syndrome Research Paves the Way for New Insights in Oncological Investigation
- Laron Syndrome: A Tale of Two Siblings
- Letters to the Editor: Why are Children with Klinefelter Syndrome Tall?
- Long-Term IGF1 Stimulation Leads to Cellular Senescence via Functional Interaction with the Thioredoxin-Interacting Protein, TXNIP
- Marjolin's Ulcer in Laron Syndrome - an Unexpected Combination: A Case Report
- MECHANISMS IN ENDOCRINOLOGY: Transient juvenile hypoglycemia in growth hormone receptor deficiency - mechanistic insights from Laron syndrome and tailored animal models
- Mesenchymal growth hormone receptor deficiency leads to failure of alveolar progenitor cell function and severe pulmonary fibrosis
- Metabolomics changes in patients with PAPP-A2 deficiency in response to rhIGF1 treatment
- MicroRNA 132-3p Is Upregulated in Laron Syndrome Patients and Controls Longevity Gene Expression
- Mild phenotype in two siblings with a missense GHR variant
- Mitochondrial Function Is Compromised in Cortical Bone Osteocytes of Long-Lived Growth Hormone Receptor Null Mice
- Mouse models of growth hormone insensitivity
- Musculoskeletal Effects of Altered GH Action
- Mutations of uncertain significance in heterozygous variants as a possible cause of severe short stature: a case report
- Normal or improved cardiovascular risk factors in IGF-I-deficient adults with growth hormone receptor deficiency
- Prevalence of diabetes among children treated with growth hormone in Israel
- Reporting a novel growth hormone receptor gene variant in an Iranian consanguineous pedigree with Laron syndrome: a case report
- Role of the GH-IGF1 axis on the hypothalamus-pituitary-testicular axis function: lessons from Laron syndrome
- Role of the GH-IGF1 system in progression of cancer
- Same Phenotype in Children with Growth Hormone Deficiency and Resistance
- Sequential measurements of IGF-I serum concentrations in adolescents with Laron syndrome treated with recombinant human IGF-I (rhIGF-I)
- Severe growth failure associated with a novel heterozygous nonsense mutation in the GHR transmembrane domain leading to elevated growth hormone binding protein
- Short stature related to Growth Hormone Insensitivity (GHI) in childhood
- Structural and proteomic repercussions of growth hormone receptor deficiency on the pituitary gland: Lessons from a translational pig model
- Systemic Deficiency of GHR in Pigs leads to Hepatic Steatosis via Negative Regulation of AHR Signaling
- The History of the Insulin-Like Growth Factor System
- The Olfactory Receptor Gene Product, OR5H2, Modulates Endometrial Cancer Cells Proliferation via Interaction with the IGF1 Signaling Pathway
- Therapeutic application of Sertoli cells for treatment of various diseases
- Therapy with recombinant human IGF-1 for children with primary insulin-like growth factor-I deficiency
- Tmem263 deletion disrupts the GH/IGF-1 axis and causes dwarfism and impairs skeletal acquisition
- Toward gene therapy of Laron syndrome
- Treatment for Infertility in Laron Syndrome: A Case Report