• <em>Nf1</em> deficiency modulates the stromal environment in the pretumorigenic rat mammary gland
• 2023 American College of Rheumatology (ACR)/American College of Chest Physicians (CHEST) Guideline for the Screening and Monitoring of Interstitial Lung Disease in People with Systemic Autoimmune Rheumatic Diseases
• A 10-YEAR STUDY OF CHILDREN WITH GONADAL TUMORS AND DISORDERS OF SEX DIFFERENTIATION, IN ROMANIA
• A Diagnosis of Turner Syndrome in the Eighth Decade of Life
• A prognostic model for use before elective surgery to estimate the risk of postoperative pulmonary complications (GSU-Pulmonary Score): a development and validation study in three international cohorts
• A Systematic Review and Meta-analysis of 24 Month Patency After Endovenous Stenting of Superior Vena Cava, Subclavian, and Brachiocephalic Vein Stenosis
• An unusual case of 17-hydroxylase deficiency presenting with short stature
• Analysis of copy number variants detected by sequencing in spontaneous abortion
• Are Young People with Turner Syndrome Who Have Undergone Treatment with Growth and Sex Hormones at Higher Risk of Metabolic Syndrome and Its Complications?
• Assessment of aortic dilatation in Chinese children and adolescents with Turner syndrome: a single center experience
• Biomarkers for Radiation Biodosimetry and Correlation with Hematopoietic Injury in a Humanized Mouse Model
• Bone mineral density: comparison between women under hormone replacement therapy with Turner syndrome or idiopathic premature ovarian insufficiency
• Capture rates of Eptesicus fuscus increase following white-nose syndrome across the eastern US
• Cardiovascular Disease and Inpatient Complications in Turner Syndrome: A Propensity Score Analysis
• Carotid Intima-Media Thickness and Cardiometabolic Profile in Turner Syndrome: A Cross-Sectional Study
• CD4⁺ T cells exhibit distinct transcriptional phenotypes in the lymph nodes and blood following mRNA vaccination in humans
• Cell Cycle Kinetics and Sister Chromatid Exchange in Mosaic Turner Syndrome
• Cephalometric Evaluation of Children with Short Stature of Genetic Etiology: A Review
• Changes in body proportions and body fat content in GH-deficient and non-GH-deficient children during the first year of growth hormone treatment
• Characterization of Turner Syndrome-associated diabetes mellitus
• Clinical and genetic characteristics of disorders of sex development in Sudanese patients
• Clinical decision aids and computed tomography coronary angiography in patients with suspected acute coronary syndrome
• Clinical dilemmas in ovarian tissue cryopreservation
• Clinical practice guidelines for the care of girls and women with Turner syndrome
• Clinical, Electrodiagnostic, and Ultrasound Findings in 87 Patients With Finger Drop
• Cognitive and psychiatric symptom trajectories 2-3 years after hospital admission for COVID-19: a longitudinal, prospective cohort study in the UK
• Combined Application of Multiple Techniques in Prenatal Diagnosis of a Fetus with Turner Syndrome
• COVID-19 Vaccine Related Cervical Radiculitis and Parsonage-Turner Syndrome: Comment
• Description and Cross-Sectional Analyses of 25,880 Adults and Children in the UK National Registry of Rare Kidney Diseases Cohort
• Early trajectories of virological and immunological biomarkers and clinical outcomes in patients admitted to hospital for COVID-19: an international, prospective cohort study
• Editorial Comment on "Turner Syndrome With Y Chromosome and Germ Cells: A Case Report Highlighting the Need to Prioritize Individualized Care"
• Editorial: Transition to adulthood in Turner syndrome
• Erratum: Correction of Text in the Article "Effects of Hormone Replacement Therapy on Bone Mineral Density in Korean Adults With Turner Syndrome"
• Exploring the impact of a KCNH2 missense variant on Long QT syndrome: insights into a novel gender-selective, incomplete penetrance inheritance mode
• Fertility and pregnancy outcomes in women with Turner syndrome: A single centre experience
• First Successful Ovarian Cortex Allotransplant To A Turner Syndrome Patient Requiring Immunosuppression: Wide Implications
• From chromosomal aberrations to mutations in individual genes - the significance of genetic studies of chorions after miscarriage in the search for causes of miscarriages
• Genetic analysis of a child with mos 46,X,psu idic(X)(q21.3)[40]/45,X[3]
• Genetic predisposition to porto-sinusoidal vascular disorder
• Growth Hormone treatment in children with Growth Hormone deficiency, idiopathic short stature, SHOX gene mutation, small for gestational age and Turner syndrome
• Heart rate vARiability and physical activity in inpatient treatMent of burnOut and DepressIon (HARMODI): protocol of a cross-sectional study with up to 8-week follow up
• Histologic analysis of gonadal tissue in patients with Turner syndrome and Y chromosome material
• Human Genetics of Hypoplastic Left Heart Syndrome
• Human Genetics of Semilunar Valve and Aortic Arch Anomalies
• If SARS-CoV-2 vaccination is blamed for Parsonage-Turner syndrome, neurosurgical neurolysis is not indicated
• In vitro fertilization and pregnancy outcomes of women with X chromosome abnormality: A case series
• Increased acquired melanocytic nevi in Turner syndrome associated with use of growth hormone: An observational study
• Infant Feeding and Weight Trajectories in the Eat, Sleep, Console Trial: A Secondary Analysis of a Randomized Clinical Trial
• Influence of Solvent Selection on the Crystallizability and Polymorphic Selectivity Associated with the Formation of the "Disappeared" Form I Polymorph of Ritonavir
• Iodine deficiency hypothyroidism in children in recent years: a re-emerging issue?
• Leveraging real-world data to predict cancer cachexia stage, quality of life, and survival in a racially and ethnically diverse multi-institutional cohort of treatment-naïve patients with pancreatic ductal adenocarcinoma
• Lifelong medical challenges and immunogenetics of turner syndrome
• Longitudinal Quantitative MRI Changes of Muscle Denervation in Parsonage-Turner Syndrome
• Lymphedema in Turner syndrome: correlations with phenotype and karyotype
• Malignant hypertension in a patient with Turner syndrome: A case report
• Markers of Fertility in Adolescents With Chronic Endocrinopathies at Transition From Paediatric to Adult Care
• Maternal cardiovascular morbidity and mortality associated with pregnancy in individuals with Turner syndrome: a committee opinion
• Monocentric Study on the Performance of Noninvasive Prenatal Testing on Cell-Free DNA for the Detection of Monosomy X
• Multiple aneuploidy: first report of a patient presenting with a karyotype 45,X/48,XXX,+21
• Neurodevelopmental Disorders Associated with Gut Microbiome Dysbiosis in Children
• Non-Cirrhotic Portal Hypertension in Turner's Syndrome: A Case Report
• Oral Hormone Replacement Therapy and Uterine Volume in Korean Adolescents with Turner Syndrome: A Retrospective Case-Control Study
• Parsonage Turner syndrome after needle electromyography: a needle in a haystack
• Parsonage-Turner Syndrome and SARS-CoV-2 Infection: A Literature Review With Case Presentation
• Parsonage-Turner syndrome, affecting suprascapular nerve and especially to infraspinatus muscles after COVID-19 vaccination in a professional wrestler, a case report and literature review of causes and treatments
• Performance of Tumor Surveillance for Children With Cancer Predisposition
• Phylogeny, envenomation syndrome, and membrane permeabilising venom produced by Australia's electric caterpillar Comana monomorpha
• Population pharmacokinetics and CD20 binding dynamics for mosunetuzumab in relapsed/refractory B-cell non-Hodgkin lymphoma
• Prenatal diagnosis and genetic analysis of small supernumerary marker chromosomes in the eastern chinese han population: A retrospective study of 36 cases
• Prenatal diagnosis and genetic counseling of 45,X/46,XX low-level mosaicism with a favorable outcome
• Presentation of Rare Phenotypes Associated with the <em>FKBP10</em> Gene
• Prevalence, diagnostic features, and medical outcomes of females with Turner syndrome with a trisomy X cell line (45,X/47,XXX): Results from the InsighTS Registry
• Primary immune thrombocytopenic purpura with exuberant oral manifestations in a patient with Turner syndrome
• Proteomic analysis of lung responses to SARS-CoV-2 infection in aged non-human primates: clinical and research relevance
• Rare Turner syndrome and lupus coexistence with insights from DNA methylation patterns
• Refractory hypertension complicated with Turner syndrome: A case report
• Reply letter to: If SARS-CoV-2 vaccination is blamed for Parsonage-Turner syndrome, neurosurgical neurolysis is not indicated
• Reply to Editorial Comment on "Turner Syndrome With Y Chromosome and Germ Cells: A Case Report Highlighting the Need to Prioritize Individualized Care"
• Satisfaction with a new patient education program for children, adolescents, and young adults with differences of sex development (DSD) and their parents
• Sequential Infection with Influenza A Virus Followed by Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) Leads to More Severe Disease and Encephalitis in a Mouse Model of COVID-19
• Skeletal abnormalities, pediatric-onset severe osteoporosis, and multiple fragility fractures in a patient with a novel <em>CTNNB1 de novo</em> variant
• Society for endocrinology guideline for understanding, diagnosing and treating female hypogonadism
• SRY-positive 45,X/46,XY karyotype in a phenotypically Turner-like Chinese adolescent female with ovarian dysgerminoma and gonadoblastoma
• Successful management of pregnancy in Turner syndrome (Monosomy X): A rare condition-based learning experience from Vietnam
• Surprising Course of a Pregnant Patient With Mosaic Turner Syndrome
• Survival to Young Adulthood Among Individuals With Congenital Heart Defects and Genetic Syndromes: Congenital Heart Survey to Recognize Outcomes, Needs, and Well-Being
• Systemic Inflammatory Indices and Liver Dysfunction in Turner Syndrome Patients: A Retrospective Case-control Study
• The antimicrobial susceptibility patterns of diabetic foot ulcers in the South African public healthcare sector
• The importance of genetic counselling for turner syndrome transition
• The lysosomal trafficking regulator "LYST": an 80-year traffic jam
• Treatment of prolonged drug reaction with eosinophilia and systemic symptoms syndrome with dupilumab using a molecularly-guided approach
• Turner syndrome and metabolic syndrome: A case study
• Turner syndrome with isochromosome Xq as a cause of granulomatous hepatitis: a case report
• Turner Syndrome With Y Chromosome and Germ Cells: A Case Report Highlighting the Need to Prioritize Individualized Care
• Turner Syndrome: Pitfalls of Transition from Paediatric to Adult Health Care
• Turner's syndrome, glucagon-like peptide 1, and glucose-dependent insulinotropic polypeptide agents: Silver bullets?
• Using a new analytic approach for genotyping and phenotyping chromosome 9p deletion syndrome
• Valvulopathies and Genetics: Where are We?
• Vosoritide treatment for children with hypochondroplasia: a phase 2 trial
• William Aldren Turner (1864-1945)