All Stories

  1. Transient gonadotropin suppression by exogenous testosterone decreases INSL3 in early puberty in boys with constitutional delay of growth and puberty
  2. Finnish-Enriched SLC26A7 Variant in Congenital Hypothyroidism: Clinical Spectrum, Thyroid Histopathology, and Expression Analysis
  3. Puberty‐Promoting Treatment and Psychosocial Well‐Being in Boys With Constitutional Delay of Puberty: A Randomized Controlled Trial
  4. Impact of Aromatase Inhibition on Bone Mineral Density and Structure: A Randomized Controlled Trial in Boys With Delayed Puberty
  5. RFX6 haploinsufficiency predisposes to diabetes through impaired beta cell function
  6. Prenatal, newborn and childhood factors and the timing of puberty in boys and girls
  7. During an 18‐month course of automated insulin delivery treatment, children aged 2 to 6 years achieve and maintain a higher time in tight range
  8. Health-related quality of life and self-reported health status in adolescents with chronic health conditions before transfer of care to adult health care: an international cohort study
  9. Central precocious puberty in boys: secular trend and clinical features
  10. Mechanisms of thyrotropin receptor–mediated phenotype variability deciphered by gene mutations and M453T-knockin model
  11. Congenital hypogonadotropic hypogonadism in a patient with a de novoPOGZmutation
  12. Residual insulin secretion in individuals with type 1 diabetes in Finland: longitudinal and cross-sectional analyses
  13. Pancreatic imaging in MEN1—comparison of conventional and somatostatin receptor positron emission tomography/computed tomography imaging in real-life setting
  14. Disease control and psychiatric comorbidity among adolescents with chronic medical conditions: a single-centre retrospective study
  15. MiniMed 780G™ in 2- to 6-Year-Old Children: Safety and Clinical Outcomes After the First 12 Weeks
  16. Health-related quality of life in boys with constitutional delay of growth and puberty
  17. Identification of monogenic variants in more than ten per cent of children without type 1 diabetes-related autoantibodies at diagnosis in the Finnish Pediatric Diabetes Register
  18. Presentation and diagnosis of childhood-onset combined pituitary hormone deficiency: A single center experience from over 30 years
  19. Timing of puberty and school performance: A population-based study
  20. Circulating Liver-enriched Antimicrobial Peptide-2 Decreases During Male Puberty
  21. The effect of COVID-19 lockdown on the glycemic control of children with type 1 diabetes
  22. A multigenerational study on phenotypic consequences of the most common causal variant of HNF1A-MODY
  23. Gut microbiota develop towards an adult profile in a sex-specific manner during puberty
  24. The aetiology of extreme tall stature in a screened Finnish paediatric population
  25. Cytosolic phosphoenolpyruvate carboxykinase deficiency: Expanding the clinical phenotype and novel laboratory findings
  26. Serum testosterone and oestradiol predict the growth response during puberty promoting treatment
  27. Onset and progression of puberty in Klinefelter syndrome
  28. Bridge study protocol: an international, observational cohort study on the transition of healthcare for adolescents with chronic conditions
  29. First year on commercial hybrid closed‐loop system—experience on 111 children and adolescents with type 1 diabetes
  30. New-onset type 1 diabetes in Finnish children during the COVID-19 pandemic
  31. Circulating miR-30b levels increase during male puberty
  32. Impact of SARS-CoV-2 Pandemic and Strategies for Resumption of Activities During the Second Wave of the Pandemic: A Report From Eight Paediatric Hospitals From the ECHO Network
  33. Bone structure assessed with pQCT in prepubertal males with delayed puberty or congenital hypogonadotropic hypogonadism
  34. Motivational Interviewing and Glycemic Control in Adolescents With Poorly Controlled Type 1 Diabetes: A Randomized Controlled Pilot Trial
  35. Familial central precocious puberty: two novel MKRN3 mutations
  36. Etiology of severe short stature below −3 SDS in a screened Finnish population
  37. Androgen deprivation and SARS-CoV-2 in men with prostate cancer
  38. Loss-of-Function Variants in TBC1D32 Underlie Syndromic Hypopituitarism
  39. Anti-Müllerian hormone and letrozole levels in boys with constitutional delay of growth and puberty treated with letrozole or testosterone
  40. Constitutional delay of puberty versus congenital hypogonadotropic hypogonadism: Genetics, management and updates
  41. Treatment of gonadotropin deficiency during the first year of life: long-term observation and outcome in five boys
  42. Letrozole versus testosterone for promotion of endogenous puberty in boys with constitutional delay of growth and puberty: a randomised controlled phase 3 trial
  43. Recombinant Human FSH Treatment Outcomes in Five Boys With Severe Congenital Hypogonadotropic Hypogonadism
  44. The Role of KCNQ1 Mutations and Maternal Beta Blocker Use During Pregnancy in the Growth of Children With Long QT Syndrome
  45. Disorders of sex development: timing of diagnosis and management in a single large tertiary center
  46. GnRH receptor gene mutations in adolescents and young adults presenting with signs of partial gonadotropin deficiency
  47. Heterozygous RFX6 protein truncating variants are associated with MODY with reduced penetrance
  48. Precocious Puberty or Premature Thelarche: Analysis of a Large Patient Series in a Single Tertiary Center with Special Emphasis on 6- to 8-Year-Old Girls
  49. Biliary Anomalies in Patients With HNF1B Diabetes
  50. Congenital hypogonadotropic hypogonadism, functional hypogonadotropism or constitutional delay of growth and puberty? An analysis of a large patient series from a single tertiary center
  51. Detection of Novel Gene Variants Associated with Congenital Hypothyroidism in a Finnish Patient Cohort
  52. Fundus Photography as a Screening Method for Diabetic Retinopathy in Children With Type 1 Diabetes: Outcome of the Initial Photography
  53. Clinical, Genetic, and Biochemical Characteristics of Early-Onset Diabetes in the Finnish Population
  54. Circulating makorin ring finger protein 3 levels decline in boys before the clinical onset of puberty
  55. Childhood growth in boys with congenital hypogonadotropic hypogonadism
  56. Early-Onset Diabetic E1-DN Mice Develop Albuminuria and Glomerular Injury Typical of Diabetic Nephropathy
  57. EGFR Signaling Promotes β-Cell Proliferation and Survivin Expression during Pregnancy
  58. In vivo activation of the PI3K–Akt pathway in mouse beta cells by the EGFR mutation L858R protects against diabetes
  59. Use of Electronic Health Records for Automated Screening of Growth Disorders in Primary Care
  60. Gender Identity and Gender Role Orientation in Female Assigned Patients with Disorders of Sex Development
  61. Prevalence and characteristics of diabetes among Somali children and adolescents living in Helsinki, Finland
  62. Sexual Function and Attitudes Toward Surgery After Feminizing Genitoplasty
  63. Epidermal growth factor (EGF)-receptor signalling is needed for murine beta cell mass expansion in response to high-fat diet and pregnancy but not after pancreatic duct ligation
  64. Sexual Function and Attitudes towards Surgery After Feminizing Genitoplasty
  65. Transcription factor AP-1 promotes growth and radioresistance in prostate cancer cells
  66. EGF-receptor regulates salivary gland branching morphogenesis by supporting proliferation and maturation of epithelial cells and survival of mesenchymal cells
  67. EGF receptor in pancreatic β-cell mass regulation
  68. ERBB receptors in developing, dysplastic and malignant oral epithelia
  69. Hydrocortisone and Indomethacin Negatively Modulate EGF-R Signaling in Human Fetal Intestine
  70. EGF-R regulates MMP function in fibroblasts through MAPK and AP-1 pathways
  71. Downregulation of EGF Receptor Signaling in Pancreatic Islets Causes Diabetes Due to Impaired Postnatal  -Cell Growth
  72. Effects of epidermal growth factor receptor deficiency and 2,3,7,8-tetrachlorodibenzo-p-dioxin on fetal development in mice
  73. Novel splice site CACNA1A mutation causing episodic ataxia type 2
  74. Different Mechanisms of Syndecan-1 Activation through a Fibroblast-growth-factor-inducible Response Element (FiRE) in Mucosal and Cutaneous Wounds
  75. ErbB Signaling Regulates Lineage Determination of Developing Pancreatic Islet Cells in Embryonic Organ Culture
  76. Abnormal astrocyte development and neuronal death in mice lacking the epidermal growth factor receptor
  77. Uterine and Vaginal Organ Growth Requires Epidermal Growth Factor Receptor Signaling from Stroma1
  78. Impaired Lung Branching Morphogenesis in the Absence of Functional EGF Receptor
  79. A WD-domain protein that is associated with and phosphorylated by the type II TGF-β receptor
  80. Epithelial immaturity and multiorgan failure in mice lacking epidermal growth factor receptor
  81. Transforming Growth Factor-α and Epidermal Growth Factor Expression in Human Fetal Gastrointestinal Tract
  82. EGF- and TGF-α-Like Peptides in Human Fetal Gut