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4. Eating Disorders Clinical Research Network (EDCRN)

5. Anti-viral Action Against Type 1 Diabetes Autoimmunity

9. Developing Allogeneic Musculoskeletal Therapies

12. Sedation and Weaning in Children Requiring Invasive Mechanical Ventilation (SANDWICH)

13. Ketogenic Diet in Infants With Epilepsy (KIWE) (KIWE)

15. A Multicentre randomiSed Controlled TRial of IntraVEnous Immunoglobulin Versus Standard Therapy for Transverse Myelitis (STRIVE)

17. Epidemiology of pre-existing multimorbidity in pregnant women in the UK in 2018: a population-based cross-sectional study

18. When Is a Critically Ill Cirrhotic Patient Too Sick to Transplant? Development of Consensus Criteria by a Multidisciplinary Panel of 35 International Experts

19. Placental Tissue Destruction and Insufficiency From COVID-19 Causes Stillbirth and Neonatal Death From Hypoxic-Ischemic Injury : A Study of 68 Cases With SARS-CoV-2 Placentitis From 12 Countries

20. Chronic Intestinal Failure in Children: An International Multicenter Cross-Sectional Survey

21. A Syndromic Neurodevelopmental Disorder Caused by Mutations in SMARCD1, a Core SWI/SNF Subunit Needed for Context-Dependent Neuronal Gene Regulation in Flies

22. Missense variants in DPYSL5 cause a neurodevelopmental disorder with corpus callosum agenesis and cerebellar abnormalities

23. Phase 1/2 Study of Lumasiran for Treatment of Primary Hyperoxaluria Type 1: A Placebo-Controlled Randomized Clinical Trial

24. Polygenic risk scores and breast and epithelial ovarian cancer risks for carriers of BRCA1 and BRCA2 pathogenic variants

25. Genome-wide association and Mendelian randomisation analysis provide insights into the pathogenesis of heart failure

26. New GJA8 variants and phenotypes highlight its critical role in a broad spectrum of eye anomalies

27. Heterozygous Variants in KMT2E Cause a Spectrum of Neurodevelopmental Disorders and Epilepsy

28. Genetics of anophthalmia and microphthalmia. Part 1: Non-syndromic anophthalmia/microphthalmia

29. The Influence of Number and Timing of Pregnancies on Breast Cancer Risk for Women With BRCA1 or BRCA2 Mutations

30. FOXE3 mutations: Genotype-phenotype correlations

31. FOXE3 mutations: Genotype-phenotype correlations

32. Mutations in the BAF-complex subunit DPF2 associated with Coffin-Siris syndrome

33. KLB , encoding β‐Klotho, is mutated in patients with congenital hypogonadotropic hypogonadism

34. Common variants at 12p11, 12q24, 9p21, 9q31.2 and in ZNF365 are associated with breast cancer risk for BRCA1 and/or BRCA2 mutation carriers

35. Common alleles at 6q25.1 and 1p11.2 are associated with breast cancer risk for BRCA1 and BRCA2 mutation carriers

36. Evidence for SMAD3 as a modifier of breast cancer risk in BRCA2 mutation carriers

37. Exploring the link between MORF4L1 and risk of breast cancer

38. "I'm quite proud of how we've handled it": health professionals' experiences of returning additional findings from the 100,000 genomes project.

39. Prophylaxis Options in Children With a History of Recurrent Urinary Tract Infections: A Systematic Review.

40. Revealing transparency gaps in publicly available COVID-19 datasets used for medical artificial intelligence development-a systematic review.

41. Inhaled methoxyflurane (Penthrox®) as a novel pain relief for outpatient hysteroscopy and other gynaecological procedures.

42. Prioritisation of early pregnancy risk factors for stillbirth: An international multistakeholder modified e-Delphi consensus study.

43. Clinical Consensus Statement on the Use of Indocyanine Green Fluorescence-guided Surgery in Pediatric Patients.

44. Placental architectural characteristics following laser ablation within monochorionic twins complicated by twin-twin transfusion syndrome: A systematic review and meta-analysis of outcomes.

45. Diagnosis and management of selective fetal growth restriction in monochorionic twin pregnancies: A cross-sectional international survey.

46. Acute generalized exanthematous pustulosis: European expert consensus for diagnosis and management.

47. The potential clinical utility of Whole Genome Sequencing for patients with cancer: evaluation of a regional implementation of the 100,000 Genomes Project.

48. Elevated hospital floor-based HDU (POPUP-HDU): a new safe alternative to PICU for high-risk neuromuscular and syndromic children undergoing scoliosis surgery.

49. Deletion upstream of MAB21L2 highlights the importance of evolutionarily conserved non-coding sequences for eye development.

50. Trends in Pediatric Hospital Admissions Caused or Contributed by SARS-CoV-2 Infection in England.

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