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1. Mining the Plasma Proteome for Insights into the Molecular Pathology of Pulmonary Arterial Hypertension

2. On the role of the patella, ACL and joint contact forces in the extension of the knee.

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4. Oral examinations---equal opportunities, ethnicity, and fairness in the MRCGP Commentary: Oral exams---get them right or don't bother

5. An evaluation of a computer based education program for the diagnosis and management of dementia in primary care. An international study of the transcultural adaptations necessary for European dissemination

6. Renal ischemia induces tropomyosin dissociation-destabilizing microvilli microfilaments

7. ADF/cofilin mediates actin cytoskeletal alterations in LLC-PK cells during ATP depletion

8. Corridor consultations and the medical microbiological record: is patient safety at risk?

10. Does the MRCGP examination discriminate against Asian doctors?

12. General practitioners' views on quality specifications for 'outpatient referrals and care contracts'

16. Improving oral examinations: selecting, training, and monitoring examiners for the MRCGP. Royal College of General Practitioners

18. Primary care and public health. Differing roles create tension

20. Expression of an islet regenerating (reg) gene in isolated rat islets: effects of nutrient and non-nutrient growth factors

22. Authors' reply

23. Do clinical guidelines introduced with practice based education improve care of asthmatic and diabetic patients? A randomised controlled trial in general practices in east London.

24. On Various Attempts That Have Been Made to Record Extemporaneous Playing

25. Communication on the Ancient Egyptian Scale

26. Henry Littleton

27. The Treatment of Music by Novelists

30. Renal ischemia induces tropomyosin dissociation-destabilizing microvilli microfilaments.

31. Ready, set, co(produce): a co-operative inquiry into co-producing research to explore adolescent health and wellbeing in the Born in Bradford Age of Wonder project.

32. Defining the clinical validity of genes reported to cause pulmonary arterial hypertension.

33. Biallelic variants of ATP13A3 cause dose-dependent childhood-onset pulmonary arterial hypertension characterised by extreme morbidity and mortality.

34. Molecular genetics of pulmonary hypertension in children.

35. Extraction and high-throughput sequencing of oak heartwood DNA: Assessing the feasibility of genome-wide DNA methylation profiling.

37. Bayesian Inference Associates Rare KDR Variants with Specific Phenotypes in Pulmonary Arterial Hypertension.

38. Whole Exome Sequence Analysis Provides Novel Insights into the Genetic Framework of Childhood-Onset Pulmonary Arterial Hypertension.

39. Correction: A restricted spectrum of missense KMT2D variants cause a multiple malformations disorder distinct from Kabuki syndrome.

40. A restricted spectrum of missense KMT2D variants cause a multiple malformations disorder distinct from Kabuki syndrome.

41. Mendelian randomisation analysis of red cell distribution width in pulmonary arterial hypertension.

42. Identification of rare sequence variation underlying heritable pulmonary arterial hypertension.

43. Phenotypic Characterization of EIF2AK4 Mutation Carriers in a Large Cohort of Patients Diagnosed Clinically With Pulmonary Arterial Hypertension.

44. Heterozygous Loss-of-Function Mutations in DLL4 Cause Adams-Oliver Syndrome.

45. Assessment of a pulmonary origin for blood outgrowth endothelial cells by examination of identical twins harboring a BMPR2 mutation.

46. Gain-of-function mutations of ARHGAP31, a Cdc42/Rac1 GTPase regulator, cause syndromic cutis aplasia and limb anomalies.

47. Elevated levels of inflammatory cytokines predict survival in idiopathic and familial pulmonary arterial hypertension.

48. Corridor consultations and the medical microbiological record: is patient safety at risk?