about
FGF-2 protects small cell lung cancer cells from apoptosis through a complex involving PKCepsilon, B-Raf and S6K2Membranoproliferative glomerulonephritis associated with a mutation in Wilms' tumour suppressor gene 1DCDC2 mutations cause a renal-hepatic ciliopathy by disrupting Wnt signalingA molecular map of mesenchymal tumors.Imaging Invasion: Micro-CT imaging of adamantinomatous craniopharyngioma highlights cell type specific spatial relationships of tissue invasionOptimization of Liver Decellularization Maintains Extracellular Matrix Micro-Architecture and Composition Predisposing to Effective Cell SeedingWilms’ Tumour – Histology and Differential DiagnosisNormal perinatal and paediatric postmortem magnetic resonance imaging appearancesIdiopathic restrictive cardiomyopathy in children is caused by mutations in cardiac sarcomere protein genesLin28 sustains early renal progenitors and induces Wilms tumorOutcome for children born after in utero laser ablation therapy for severe twin-to-twin transfusion syndrome.EVERREST prospective study: a 6-year prospective study to define the clinical and biological characteristics of pregnancies affected by severe early onset fetal growth restriction.Diagnostic accuracy of post-mortem magnetic resonance imaging in fetuses, children and adults: a systematic review.Risks of miscarriage and early preterm birth in trichorionic triplet pregnancies with embryo reduction versus expectant management: new data and systematic review.Endoscopic laser coagulation in the management of severe twin-to-twin transfusion syndrome.A semi-automated method for non-invasive internal organ weight estimation by post-mortem magnetic resonance imaging in fetuses, newborns and children.Successful renal transplantation in factor H autoantibody associated HUS with CFHR1 and 3 deficiency and CFH variant G2850T.Thymus transplantation for complete DiGeorge syndrome: European experience.Extrarenal rhabdoid tumours outside the central nervous system in infancy.Ultrastructural features of neuroblastic tumours in relation to morphological, and molecular findings; a retrospective review study.A pathogenic mosaic TP53 mutation in two germ layers detected by next generation sequencing.Reference ranges for organ weights of infants at autopsy: results of >1,000 consecutive cases from a single centre.Vaginal progesterone prophylaxis for preterm birth (the OPPTIMUM study): a multicentre, randomised, double-blind trial.Melanoma in congenital melanocytic naevi.Perineal lipoma with accessory labioscrotal fold and penis-like phallus in a female infant with unilateral renal agenesis.Gain of 1q As a Prognostic Biomarker in Wilms Tumors (WTs) Treated With Preoperative Chemotherapy in the International Society of Paediatric Oncology (SIOP) WT 2001 Trial: A SIOP Renal Tumours Biology Consortium Study.Pathogenetics of alveolar capillary dysplasia with misalignment of pulmonary veinsBrain lipid-binding protein: a marker of differentiation in neuroblastic tumors.Post mortem magnetic resonance imaging in the fetus, infant and child: a comparative study with conventional autopsy (MaRIAS Protocol).Gestational trophoblastic disease.Outcome of twin pregnancies with complete hydatidiform mole and healthy co-twin.DICER1 syndrome: clarifying the diagnosis, clinical features and management implications of a pleiotropic tumour predisposition syndrome.Human male infertility associated with mutations in NR5A1 encoding steroidogenic factor 1Clinico-pathological correlations of congenital and infantile nephrotic syndrome over twenty years.Diagnostic accuracy of post-mortem MRI for thoracic abnormalities in fetuses and children.The impact of article titles on citation hits: an analysis of general and specialist medical journalsTP53 mutational status is a potential marker for risk stratification in Wilms tumour with diffuse anaplasia.Trial protocol OPPTIMUM-- does progesterone prophylaxis for the prevention of preterm labour improve outcome?The lambda sign at 10-14 weeks of gestation as a predictor of chorionicity in twin pregnancies.Interleukin-8 (CXCL8) production is a signatory T cell effector function of human newborn infants.
P50
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Neil J. Sebire
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Neil J. Sebire
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Neil J. Sebire
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Neil J. Sebire
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