143 results on '"Badminton M"'
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2. Key Terms and Definitions in Acute Porphyrias: Results of an International Delphi Consensus Led by the European Porphyria Network
3. Acute hepatic porphyria and anaesthesia:a practical approach to the prevention and management of acute neurovisceral attacks
4. EXPLORE: A Prospective, Multinational, Natural History Study of Patients with Acute Hepatic Porphyria with Recurrent Attacks
5. Molecular mechanisms of dominant expression in porphyria
6. A Novel Molecular Mechanism Causing Acute Intermittent Porphyria: OC30
7. Congenital erythropoietic porphyria: a single-observer clinical study of 29 cases
8. A management algorithm for congenital erythropoietic porphyria derived from a study of 29 cases
9. Liver transplantation in acute intermittent porphyria provides novel insights into the pathogenesis of acute attacks: O28
10. Proposed management algorithm for congenital erythropoietic porphyria: O25
11. X-linked dominant protoporphyria in the U.K.: O22
12. Investigation of ferrochelatase mRNA in ‘mutation-negative’ erythropoietic protoporphyria patients: O19
13. An unusual case of porphyric neuropathy with atypical clinical and electrodiagnostic features: O05cc
14. Molecular epidemiology of erythropoietic protoporphyria in the U.K.
15. A homozygous mutation in the ferrochelatase gene underlies erythropoietic protoporphyria associated with palmar keratoderma – reply
16. Metabolic basis of protoporphyrin accumulation in Erythropoietic Protoporphyria: Ferrochelatase deficiency versus Ala Synthase 2 gain of function: IL 3.2-1
17. Hereditary erythropoietic protoporphyria (EPP) presenting in old age with an unexpected genotype: lessons for the pathogenesis of symptoms in EPP: PD-3
18. X-linked dominant protoporphyria: a new form of porphyria caused by a gain of function mutation in aminolaevulinic acid synthase: O-12
19. Sclerodermatous changes of face, neck and scalp associated with familial porphyria cutanea tarda
20. Serum 25-hydroxyvitamin D in erythropoietic protoporphyria
21. Congenital erythropoietic porphyria: a genotype/phenotype correlation and health-related quality of life study of 27 unrelated cases: O-14
22. Congenital erythropoietic porphyria: a novel mutation: PD-3
23. Multiple nutritional deficiencies mimicking erythro-poietic protoporphyria: PA-14
24. The history of congenital erythropoietic porphyria (Giintherʼs disease): H-9
25. New mutation identified in adult onset erythropoietic protoporphyria: O-10
26. Allogeneic bone marrow transplantation in a 7-year-old girl with congenital erythropoietic porphyria: a treatment dilemma
27. Late-onset erythropoietic protoporphyria in association with haematological malignancy
28. Erythropoietic protoporphyria in the U.K.: clinical features and effect on quality of life
29. Treatment of an acute attack of porphyria during pregnancy
30. Autosomal recessive erythropoietic protoporphyria in the United Kingdom: prevalence and relationship to liver disease
31. Autosomal recessive erythropoietic protoporphy- ria associated with liver dysfunction
32. Urinary catecholamines and metabolites in the immediate postoperative period following major surgery
33. Myeloproliferative disease complicated by late-onset erythropoietic protoporphyria and liver disease
34. Clinical experience of trainees in chemical pathology: a survey of junior medical staff in the United Kingdom
35. Imaging bioluminescent indicators shows Ca2+ and ATP permeability thresholds in live cells attacked by complement
36. An Analysis of Healthcare Utilization and Costs Associated with Patients with Acute Hepatic Porphyrias (AHPS) with Recurrent Attacks in Explore: A Prospective, Multinational Natural History Study of Patients with AHP
37. Trends in healthcare utilization in the United States and Europe associated with patient with acute hepatic porphyria with recurrent attacks in EXPLORE: A prospective, multinational natural history study of patients with acute hepatic porphyria
38. EXPLORE: A prospective, multinational natural history study of patients with acute hepatic porphyria with recurrent attacks
39. Impact of acute hepatic porphyrias on quality of life and work loss: An analysis of EXPLORE natural history study
40. PHS39 - An Analysis of Healthcare Utilization and Costs Associated with Patients with Acute Hepatic Porphyrias (AHPS) with Recurrent Attacks in Explore: A Prospective, Multinational Natural History Study of Patients with AHP
41. SAT-041 - Trends in healthcare utilization in the United States and Europe associated with patient with acute hepatic porphyria with recurrent attacks in EXPLORE: A prospective, multinational natural history study of patients with acute hepatic porphyria
42. SAT-040 - Impact of acute hepatic porphyrias on quality of life and work loss: An analysis of EXPLORE natural history study
43. PS-143 - EXPLORE: A prospective, multinational natural history study of patients with acute hepatic porphyria with recurrent attacks
44. Role of genetic testing in the management of patients with inherited porphyria and their families
45. European porphyria initiative (EPI): a platform to develop a common approach to the management of porphyrias and to promote research in the field
46. John ("Jack") Parsons Shillingford Robert Michael Badminton Terry Coates Christopher Charles Crampton Richard Michael Dean Desmond Stopford Mulock Enraght-Moony Eric Glyn Hughes Alfred Cecil Victor Maltby Gisela ("Gilli") Oppenheim Fredrick Shepherd Eleanor Mary Singer Barry Leonard Stone Brian Ponsford Webber Henry John ("Jack") Weldon Giles Martin James Woolley
47. Mefenamic acid prevents assessment of drug abuse with EMIT assays
48. Evaluation of a New Rapid Immunometric Method for the Measurement of the MB Isoenzyme of Creatine Kinase in Serum
49. Use of a Non-Extraction HPLC Technique for Measuring Angiotensin-Converting Enzyme under Optimum Conditions
50. Luteinizing hormone-releasing hormone (LH-RH) binding to purified rat pituitary nuclei
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