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Research

Publications: Dr Paul Telfer

Frangoul H, Locatelli F, Sharma A, Bhatia M, Mapara MY, Molinari L, Wall DA, Liem R et al. ( 2024 ) . Elimination of Vaso-Occlusive Crises after Exagamglogene Autotemcel in Patients with Severe Sickle Cell Disease . Transplantation and Cellular Therapy vol. 30 , ( 2 ) s234 - s235 .
Frangoul H, Locatelli F, Sharma A, Bhatia M, Mapara M, Molinari L, Wall D, Liem RI et al. ( 2023 ) . Exagamglogene Autotemcel for Severe Sickle Cell Disease . Blood vol. 142 , ( Supplement 1 )
Achebe MO, Hassab HM, Al-Kindi S, Brown C, Telfer P, Biemond BJ, Lipato T, Davis M et al. ( 2023 ) . Over 4 Years of Safety and Efficacy with Voxelotor Treatment for Patients with Sickle Cell Disease: Updated Results from an Open-Label Extension of the Phase 3 HOPE Trial . Blood vol. 142 , ( Supplement 1 )
Summers K, Agrippa O, Lugthart S, Anie K, Telfer P ( 2023 ) . Predicting Vaso-Occlusive Crises in Sickle Cell Disease through Digital, Longitudinal Tracking of Wearable Metrics and Patient-Reported Outcomes . Blood vol. 142 , ( Supplement 1 )
Summers K, Agrippa O, Shastri O, Sharif S, Anie K, Telfer P, Lugthart S ( 2023 ) . Real-World Outcomes and Digitally Monitored Quality of Life in Voxelotor-Treated Patients with Sickle Cell Disease . Blood vol. 142 , ( Supplement 1 )
Gorur V, Kranc KR, Ganuza M, Telfer P ( 2023 ) . Haematopoietic stem cell health in sickle cell disease and its implications for stem cell therapies and secondary haematological disorders . Blood Reviews vol. 63 ,
Rankine-Mullings A, Keenan R, Chakravorty S, Inusa B, Telfer P, Velangi M, Ware RE, Moss JJ et al. ( 2023 ) . Efficacy, safety, and pharmacokinetics of a new, ready-to-use, liquid hydroxyurea in children with sickle cell anemia . Blood Advances vol. 7 , ( 16 ) 4319 - 4322 .
Ramalli M, Sangarappillai C, Kaya B, Barrosso F, Bennett S, Kafuko D, Bestwick JW, Telfer P ( 2023 ) . P1428: PREDICTORS OF VOC RATE DURING LONG-TERM FOLLOW-UP OF PATIENTS WITH HBSS IN A NEWBORN COHORT STUDY . HemaSphere vol. 7 , ( S3 )
Summers K, Agrippa O, Anie K, Telfer P, Lugthart S ( 2023 ) . P1441: REAL-WORLD OUTCOMES AND DIGITALLY MONITORED QUALITY OF LIFE IN CRIZANLIZUMAB-TREATED PATIENTS WITH SICKLE CELL DISEASE . HemaSphere vol. 7 , ( S3 )
Summers K, Agrippa O, Anie K, Telfer P, Lugthart S ( 2023 ) . P1448: CHARACTERISATION OF QUALITY OF LIFE-LINKED PATIENT-REPORTED OUTCOMES THROUGH A DIGITAL AND CONTINUOUS REMOTE MONITORING ECOSYSTEM IN SICKLE CELL DISEASE . HemaSphere vol. 7 , ( S3 )
Badat M, Ejaz A, Hua P, Rice S, Zhang W, Hentges LD, Fisher CA, Denny N et al. ( 2023 ) . Direct correction of haemoglobin E β-thalassaemia using base editors . Nature Communications vol. 14 , ( 1 )
Telfer PT, Carvalho SJC, Ruzangi JR, Arici MA, Binns MB, Beaubrun AB, Rice CTR, Were JJW ( 2023 ) . 5554869 ASSOCIATION BETWEEN HEMOGLOBIN LEVELS AND END‐ORGAN DAMAGE IN SICKLE CELL DISEASE: A RETROSPECTIVE LINKED PRIMARY AND SECONDARY CARE DATABASE ANALYSIS IN ENGLAND . HemaSphere vol. 7 , ( Suppl ) 9 - 9 .
Agrippa OA, Summers KZ, Anie KA, Telfer P, Lugthart S ( 2023 ) . 5609968 REAL‐WORLD PATIENT‐REPORTED OUTCOMES AND WEARABLE METRIC CORRELATIONS: REMOTE DAILY MONITORING FOR EXPLORATION OF QUALITY OF LIFE IN SICKLE CELL DISEASE . HemaSphere vol. 7 , ( Suppl ) 8 - 9 .
Agrippa OA, Summers KZ, Anie KA, Telfer P, Lugthart S ( 2023 ) . 5610107 LIVE OUTCOMES AND BIOMETRIC MONITORING: POTENTIAL IMPLICATIONS FOR PATIENT QUALITY OF LIFE IN SICKLE CELL DISEASE . HemaSphere vol. 7 , ( Suppl ) 54 - 54 .
Telfer P, Ruzangi J, Carvalho SJ, Barcelos G, Binns M, Beaubrun A, Rice C ( 2023 ) . 5613396 DIFFERENCE IN HOSPITALIZATIONS AND ANNUAL BED DAYS FOR PATIENTS WITH SICKLE CELL DISEASE BY VARYING LEVELS OF ANEMIA: A RETROSPECTIVE ANALYSIS OF LINKED PRIMARY AND SECONDARY CARE DATABASES IN ENGLAND . HemaSphere vol. 7 , ( Suppl ) 32 - 33 .
Sangarappillai C, Ramalli M, Kaya B, Barroso F, Bennett S, Kafuko D, Bestwick J, Telfer P ( 2023 ) . Incidence rates for acute complications in HbSS East London newborn sickle cell cohort (ELNSCS) . BRITISH JOURNAL OF HAEMATOLOGY . vol. 201 , 40 - 40 .
Eleftheriou P, Sharif J, Kesse-Adu R, Drasar E, de Kreuk A, Filian-Gloor M, Agrawal A, Barcelos G et al. ( 2023 ) . Treatment of sickle cell disease with Voxelotor through the UK early access to medicines scheme . BRITISH JOURNAL OF HAEMATOLOGY . vol. 201 , 5 - 6 .
Telfer P, Carvalho SJ, Ruzangi J, Cissé OA, Binns M, Beaubrun A, Rice C, Were J ( 2022 ) . Association entre le taux d’hémoglobine et les atteintes d’organes cibles dans la drépanocytose : analyse rétrospective d’une base de données de soins primaires et secondaires en Angleterre . La Revue de Médecine Interne vol. 43 ,
Telfer P, Carvalho S, Ruzangi J, Arici M, Binns M, Beaubrun A, Montealegre-Golcher F, Rice C et al. ( 2022 ) . ASSOCIATION BETWEEN HEMOGLOBIN LEVELS AND END-ORGAN DAMAGE IN SICKLE CELL DISEASE: A RETROSPECTIVE LINKED PRIMARY AND SECONDARY CARE DATABASE ANALYSIS IN ENGLAND . Hematology Transfusion and Cell Therapy vol. 44 , s10 - s11 .
O. A, K. S, K. A, P. T, J. J, E. L ( 2022 ) . P‐037: EXPLORATION OF THE REAL‐WORLD IMPACTS OF SLEEP UPON QUALITY OF LIFE IN PATIENTS WITH SICKLE CELL DISEASE . HemaSphere vol. 6 , ( Suppl ) 35 - 35 .
Telfer P, Carvalho S, Ruzangi J, Arici M, Binns M, Beaubrun A, Rice C, Were JJ ( 2022 ) . P1488: ASSOCIATION BETWEEN HEMOGLOBIN LEVELS AND END‐ORGAN DAMAGE IN SICKLE CELL DISEASE: A RETROSPECTIVE LINKED PRIMARY AND SECONDARY CARE DATABASE ANALYSIS IN ENGLAND . HemaSphere vol. 6 , ( Suppl ) 1370 - 1371 .
Sangarappillai C, Soriano M, Bestwick J, Kafuko D, Newell K, Kaya B, Bennett S, Barroso F et al. ( 2022 ) . P1493: CHRONIC COMPLICATIONS IN THE EAST LONDON SICKLE NEWBORN COHORT STUDY (ELSNCS) . HemaSphere vol. 6 , ( Suppl ) 1375 - 1376 .
Achebe M, Hassab H, Alkindi S, Brown C, Telfer P, Biemond B, Gordeuk V, Lipato T et al. ( 2022 ) . Sécurité et efficacité à long terme du voxelotor chez des patients atteints de drépanocytose : résultats d’une étude d’extension en ouvert de l’essai de phase 3 HOPE . La Revue de Médecine Interne vol. 43 ,
Agrippa O, Summers K, Anie K, Telfer P, James J, Low E ( 2022 ) . P131: REAL‐TIME VACCINATION IMPACTS IN SICKLE CELL DISEASE: A REAL‐WORLD PATIENT CASE STUDY FOR INFLUENZA AND COVID‐19 VACCINATION . HemaSphere vol. 6 , ( Suppl ) 32 - 33 .
Lugthart S, Kotsiopoulou S, Luqmani A, Eleftheriou P, Drasar E, Brown R, Webster A, Chakravorty S et al. ( 2022 ) . S110: ACUTE AND CHRONIC PAIN MANAGEMENT IN SICKLE CELL DISEASE: OUTCOMES OF AN ENGLISH NATIONAL AUDIT . HemaSphere vol. 6 , ( Suppl ) 6 - 6 .
Achebe M, Nduba V, Hassab H, Alkindi S, Brown R, Telfer P, Biemond B, Gordeuk V et al. ( 2022 ) . S118: LONG‐TERM SAFETY AND EFFICACY OF VOXELOTOR FOR PATIENTS WITH SICKLE CELL DISEASE: RESULTS FROM AN OPEN‐LABEL EXTENSION OF THE PHASE 3 HOPE TRIAL . HemaSphere vol. 6 , ( Suppl ) 9 - 10 .
Oyesanya F, Gorur V, Awe E, Barroso F, Bennett S, Kaya B, De Michele C-A, Newell K et al. ( 2022 ) . A retrospective comparative study of the effect of automated exchange transfusion <i>versus</i> other treatment modalities on vaso-occlusive crisis admission rates in patients with sickle cell disease . BRITISH JOURNAL OF HAEMATOLOGY . vol. 197 , 138 - 139 .
Lugthart S, Kotsiopoulou S, Luqmani A, Eleftheriou P, Drasar E, Brown R, Webster A, Chakravorty S et al. ( 2022 ) . Challenges of acute and chronic pain management in sickle cell disease: Outcomes of an English national audit . BRITISH JOURNAL OF HAEMATOLOGY . vol. 197 , 11 - 12 .
Achebe M, Hassab H, Alkindi S, Brown RCC, Telfer P, Biemond BJ, Gordeuk VR, Lipato T et al. ( 2021 ) . Long-Term Safety and Efficacy of Voxelotor for Patients with Sickle Cell Disease: Results from an Open-Label Extension of the Phase 3 HOPE Trial . Blood vol. 138 , ( Supplement 1 )
Colombatti R, Sangarappillai C, Soriano M, Bestwick J, Hann W, Wieczorek K, Munaretto V, Coppadoro B et al. ( 2021 ) . Severe Acute Complications of Sickle Cell Disease in Two Expert Referral Centers (UK and Italy): Natural History Studies Highlight Ongoing Unmet Need for Effective Disease Modifying or Curative Therapies . Blood vol. 138 , ( Supplement 1 )
Shah F, Telfer P, Velangi M, Pancham S, Wynn R, Pollard S, Chalmers E, Kell J et al. ( 2021 ) . Routine management, healthcare resource use and patient and carer‐reported outcomes of patients with transfusion‐dependent β‐thalassaemia in the United Kingdom: A mixed methods observational study . eJHaem vol. 2 , ( 4 ) 738 - 749 .
Telfer P, Bestwick J, Elander J, Osias A, Khalid N, Skene I, Nzouakou R, Challands J et al. ( 2021 ) . A non-injected opioid analgesia protocol for acute pain crisis in adolescents and adults with sickle cell disease . British Journal of Pain vol. 16 , ( 2 ) 179 - 190 .
Hossain MS, Mahbub Hasan M, Petrou M, Telfer P, Mosabbir AA ( 2021 ) . The parental perspective of thalassaemia in Bangladesh: lack of knowledge, regret, and barriers . Orphanet Journal of Rare Diseases vol. 16 , ( 1 )
Chen F, Booth C, Barroso F, Bennett S, Kaya B, Win N, Telfer P ( 2021 ) . Salvage of refractory post‐transfusion hyperhaemolysis by targeting hyperinflammation and macrophage activation with tocilizumab . Transfusion Medicine vol. 32 , ( 5 ) 437 - 440 .
de la Fuente J, Gluckman E, Makani J, Telfer P, Faulkner L, Corbacioglu S, Transplantation PDWPOTESFBAM, Amrolia P et al. ( 2020 ) . The role of haematopoietic stem cell transplantation for sickle cell disease in the era of targeted disease-modifying therapies and gene editing . The Lancet Haematology vol. 7 , ( 12 ) e902 - e911 .
Vichinsky E, Gordeuk VR, Telfer P, Inati A, Tonda M, Gray S, Agodoa I, Ataga KI ( 2020 ) . Higher Hemoglobin Levels Achieved with Voxelotor Are Associated with Lower Vaso-occlusive Crisis Incidence: 72-Week Analysis from the HOPE Study . Blood vol. 136 , ( Supplement 1 ) 31 - 32 .
Smith WR, Hankins JS, Abboud MR, Cong Z, Sorof J, Gray S, Hoppe C, Telfer P ( 2020 ) . Improvement in the Clinical Global Impression of Change with Voxelotor in Patients with Sickle Cell Disease in the Phase 3 HOPE Trial . Blood vol. 136 , ( Supplement 1 ) 5 - 6 .
Jobanputra M, Paramore C, Laird SG, McGahan M, Telfer P ( 2020 ) . Co‐morbidities and mortality associated with transfusion‐dependent beta‐thalassaemia in patients in England: a 10‐year retrospective cohort analysis . British Journal of Haematology vol. 191 , ( 5 ) 897 - 905 .
Telfer P, De la Fuente J, Sohal M, Brown R, Eleftheriou P, Roy N, Piel FB, Chakravorty S et al. ( 2020 ) . Real-time national survey of COVID-19 in hemoglobinopathy and rare inherited anemia patients . Haematologica vol. 105 , ( 11 ) 2651 - 2654 .
Kountouris P, Michailidou K, Christou S, Hadjigavriel M, Sitarou M, Kolnagou A, Kleanthous M, Telfer P ( 2020 ) . Effect of HBB genotype on survival in a cohort of transfusion-dependent thalassemia patients in Cyprus . Haematologica vol. 106 , ( 9 ) 2458 - 2468 .
Maggio A, Kattamis A, Felisi M, Reggiardo G, El-Beshlawy A, Bejaoui M, Sherief L, Christou S et al. ( 2020 ) . Evaluation of the efficacy and safety of deferiprone compared with deferasirox in paediatric patients with transfusion-dependent haemoglobinopathies (DEEP-2): a multicentre, randomised, open-label, non-inferiority, phase 3 trial . The Lancet Haematology vol. 7 , ( 6 ) e469 - e478 .
Roy NBA, Telfer P, Eleftheriou P, de la Fuente J, Drasar E, Shah F, Roberts D, Atoyebi W et al. ( 2020 ) . Protecting vulnerable patients with inherited anaemias from unnecessary death during the COVID‐19 pandemic . British Journal of Haematology vol. 189 , ( 4 ) 635 - 639 .
Oakley LL, Awogbade M, Brien S, Briley A, Chorozoglou M, Drasar E, Johns J, Rhodes E et al. ( 2020 ) . Serial prophylactic exchange blood transfusion in pregnant women with sickle cell disease (TAPS-2): study protocol for a randomised controlled feasibility trial . Trials vol. 21 , ( 1 )
DeBaun MR, Jordan LC, King AA, Schatz J, Vichinsky E, Fox CK, McKinstry RC, Telfer P et al. ( 2020 ) . American Society of Hematology 2020 guidelines for sickle cell disease: prevention, diagnosis, and treatment of cerebrovascular disease in children and adults . Blood Advances vol. 4 , ( 8 ) 1554 - 1588 .
Hossain MS, Hasan MM, Raheem E, Islam MS, Al Mosabbir A, Petrou M, Telfer P, Siddiqee MH ( 2020 ) . Lack of knowledge and misperceptions about thalassaemia among college students in Bangladesh: a cross-sectional baseline study . Orphanet Journal of Rare Diseases vol. 15 , ( 1 )
Sangarappillai C, Soriano M, Telfer P, Newell K, Amoh I, Halbert J, Ndifor N, Kaya B et al. ( 2020 ) . Hydroxyurea therapy does not impact TCD velocity in the East London sickle cell newborn cohort study . BRITISH JOURNAL OF HAEMATOLOGY . vol. 189 , 146 - 147 .
Booth CS, Barroso F, Bennett S, Kafuko D, Telfer P, Kaya B ( 2020 ) . Rh antibodies in patients with sickle cell disease - an on-going challenge . BRITISH JOURNAL OF HAEMATOLOGY . vol. 189 , 166 - 166 .
Renedo A, Miles S, Chakravorty S, Leigh A, Telfer P, Warner JO, Marston C ( 2019 ) . Not being heard: barriers to high quality unplanned hospital care during young people’s transition to adult services – evidence from ‘this sickle cell life’ research . BMC Health Services Research vol. 19 , ( 1 )
Vichinsky EP, Telfer P, Inati A, Tonda M, Tong B, Agodoa I, Lehrer-Graiwer J, Ataga KI ( 2019 ) . Incidence of Vaso-Occlusive Crisis Does Not Increase with Achieving Higher Hemoglobin Levels on Voxelotor Treatment or after Discontinuation: Analyses of the HOPE Study . Blood vol. 134 , ( Supplement_1 )
Shah F, Telfer P, Velangi M, Pancham S, Wynn R, Pollard S, Chalmers E, Kell J et al. ( 2019 ) . Routine Management, Healthcare Resource Use and Patient/Caregiver-Reported Outcomes of Patients with Transfusion-Dependent β-Thalassaemia in the United Kingdom: A Mixed Methods Observational Study . Blood vol. 134 , ( Supplement_1 )
Ryan K, Pancham S, Telfer P, Shah F, Kell J, Pollard S, Wynn R, Velangi M et al. ( 2019 ) . PRO146 HEALTH-RELATED QUALITY OF LIFE AND PRODUCTIVITY/ACTIVITY IMPAIRMENT IN PATIENTS WITH TRANSFUSION DEPENDENT B-THALASSAEMIA IN THE UK NHS: DATA FROM A UK MULTICENTRE OBSERVATIONAL STUDY . Value in Health vol. 22 , s868 - s869 .
Telfer P, Barroso F, Newell K, Challands J, Kaya B ( 2019 ) . Evaluation of a Non-Parenteral Opioid Analgesia Protocol for Acute Sickle Cell Pain Episodes in Children . Journal of Clinical Medicine vol. 8 , ( 10 )
Downes M, de Haan M, Telfer PT, Kirkham FJ ( 2019 ) . The Role of Family Functioning in the Development of Executive Functions in Preschool Children with Sickle Cell Anemia . Developmental Neuropsychology vol. 44 , ( 6 ) 452 - 467 .
Telfer PT ( 2019 ) . Management of sickle cell disease: management of acute episodes in the community and in hospital . Paediatrics and Child Health vol. 29 , ( Br J Haematol 120 2003 ) 345 - 351 .
Kaya B, Telfer PT ( 2019 ) . Management of sickle cell disease: outpatient and community aspects . Paediatrics and Child Health vol. 29 , ( N Engl J Med 339 1998 Jul 2 ) 352 - 358 .
Telfer P, Kountouris P, Christou S, Hadjigavriel M, Sitarou M, Kolnagou A, Kleanthous M ( 2019 ) . PF785 CHANGING CAUSES OF MORTALITY IN TDT DURING THE ERA OF ORAL CHELATION THERAPY FROM 2000 TO 2018 . HemaSphere vol. 3 , ( S1 ) 346 - 347 .
Kattamis A, Felisi M, Reggiardo G, El‐Beshlawy A, Bejaoui M, Sherief L, Christou S, Cosmi C et al. ( 2019 ) . S144 A MULTICENTRE, RANDOMIZED, NON‐INFERIORITY TRIAL COMPARING THE EFFICACY OF DEFERIPRONE VERSUS DEFERASIROX IN PEDIATRIC PATIENTS AFFECTED BY TRANSFUSION‐DEPENDENT HEMOGLOBINOPATHIES (DEEP‐2 TRIAL) . HemaSphere vol. 3 , ( S1 ) 23 - 24 .
Vichinsky E, Hoppe CC, Ataga KI, Ware RE, Nduba V, Beshlawy AE, Hassab H, Achebe MM et al. ( 2019 ) . S147 RESULTS FROM THE RANDOMIZED PLACEBO‐CONTROLLED PHASE 3 HOPE TRIAL OF VOXELOTOR IN ADULTS AND ADOLESCENTS WITH SICKLE CELL DISEASE . HemaSphere vol. 3 , ( S1 ) 25 - 26 .
Elander J, Bij D, Kapadi R, Schofield MB, Osias A, Khalid N, Kaya B, Telfer P ( 2019 ) . Development and validation of the Satisfaction with Treatment for Pain Questionnaire (STPQ) among patients with sickle cell disease . British Journal of Haematology . vol. 187 , 105 - 116 .
Vichinsky E, Hoppe CC, Ataga KI, Ware RE, Nduba V, El-Beshlawy A, Hassab H, Achebe MM et al. ( 2019 ) . A Phase 3 Randomized Trial of Voxelotor in Sickle Cell Disease . New England Journal of Medicine vol. 381 , ( 6 ) 509 - 519 .
Cooper O, McBain H, Tangayi S, Telfer P, Tsitsikas D, Yardumian A, Mulligan K ( 2019 ) . Psychometric analysis of the adult sickle cell quality of life measurement information system (ACSQ-Me) in a UK population . Health and Quality of Life Outcomes vol. 17 , ( 1 )
Mecci J, Maxan M-E, Kemos P, Telfer P, Barroso F, Foster G, Banu K ( 2019 ) . FRI-437-Diagnosis of sickle cell liver disease may be aided by non-invasive tests . Journal of Hepatology . vol. 70 , e586 - e587 .
Brown RA, Moon JC, Telfer PT, Khanji MY ( 2019 ) . Extreme cardiac iron loading in transfusion-dependent thalassaemia major: cardiac T2* and T1 mapping guiding treatment . European Heart Journal vol. 40 , ( 43 )
Howard J, Hemmaway CJ, Telfer P, Layton DM, Porter J, Awogbade M, Mant T, Gretler DD et al. ( 2019 ) . A phase 1/2 ascending dose study and open-label extension study of voxelotor in patients with sickle cell disease . Blood vol. 133 , ( 17 ) 1865 - 1875 .
Telfer P, Kaya B, Barroso F, Nzouakou R, Osias A, Bloom B, Skene I, Boulton O et al. ( 2019 ) . A Phase 1 study to determine maximum tolerated dose of sublingual fentanyl in combination with oral oxycodone for hospital management of an acute painful crisis in adolescents and adults with sickle cell disease . BRITISH JOURNAL OF HAEMATOLOGY . vol. 185 , 113 - 114 .
Ryan K, Pancham S, Telfer P, Shah F, Kell J, Pollard S, Wynn R, Velangi M et al. ( 2019 ) . An observational study to evaluate the routine management, healthcare resource use and outcomes for patients with transfusion-dependent β-thalassaemia treated in the United Kingdom: an interim analysis . BRITISH JOURNAL OF HAEMATOLOGY . vol. 185 , 114 - 115 .
Mckinnon K, Telfer P, Kaya B ( 2019 ) . Causes, management and outcomes of extreme paediatric thrombocytosis . BRITISH JOURNAL OF HAEMATOLOGY . vol. 185 , 108 - 108 .
Ryan K, Pancham S, Telfer P, Shah F, Kell J, Pollard S, Wynn R, Velangi M et al. ( 2019 ) . HEALTH-RELATED QUALITY OF LIFE AND PRODUCTIVITY/ACTIVITY IMPAIRMENT IN PATIENTS WITH TRANSFUSION DEPENDENT B-THALASSAEMIA IN THE UK NHS: DATA FROM A UK MULTICENTRE OBSERVATIONAL STUDY . VALUE IN HEALTH . vol. 22 , S868 - S869 .
Sangarappillai C, Kaya B, Barroso F, Telfer P ( 2019 ) . Patients lost to follow-up in the East London Newborn Sickle Cell Cohort Study . BRITISH JOURNAL OF HAEMATOLOGY . vol. 185 , 123 - 124 .
Okochi J, Tsiagbe M, Joseph W, James J, Osmond-Joseph K, Telfer P, Barroso F, Kaya B ( 2019 ) . Peer to peer mentoring for patients with Sickle Cell Disease - interim analysis of results from a pilot programme in East London . BRITISH JOURNAL OF HAEMATOLOGY . vol. 185 , 116 - 116 .
Downes M, de Haan M, O’Leary T, Telfer PT, Kirkham FJ ( 2018 ) . Temperament in preschool children with sickle cell anaemia . Archives of Disease in Childhood vol. 105 , ( 9 ) 900 - 902 .
Telfer P, Kaya B, Tsitsikas DA, Barroso F, Sangarappillai C ( 2018 ) . Hydroxyurea Therapy Does Not Impact Current Survival Estimates in the East London Sickle Cell Newborn Cohort Study . Blood vol. 132 , ( Supplement 1 )
Vichinsky E, Hoppe C, Howard J, Ataga KI, Nduba V, El-Beshlawy A, Diuguid DL, Al-Kindi S et al. ( 2018 ) . Results from Part A of the Hemoglobin Oxygen Affinity Modulation to Inhibit HbS Polymerization (HOPE) Trial (GBT440-031), a Placebo-Controlled Randomized Study Evaluating Voxelotor (GBT440) in Adults and Adolescents with Sickle Cell Disease . Blood . vol. 132 ,
Casella JF, Adams RJ, Brambilla DJ, Strouse JJ, Maier P, Dlugash R, Avadhani R, Vermillion K et al. ( 2018 ) . Developing a risk-based composite neurologic outcome for a trial of hydroxyurea in young children with sickle cell disease . Clinical Trials vol. 16 , ( 1 ) 20 - 31 .
Lobitz S, Telfer P, Cela E, Allaf B, Angastiniotis M, Johansson CB, Badens C, Bento C et al. ( 2018 ) . Newborn screening for sickle cell disease in Europe: recommendations from a Pan‐European Consensus Conference . British Journal of Haematology vol. 183 , ( 4 ) 648 - 660 .
Telfer PT, Devereux H, Savage K, Scott F, Dhillon AP, Dusheiko G, Lee CA ( 2018 ) . Chronic Hepatitis C Virus Infection in Haemophilic Patients: Clinical Significance of Viral Genotype . Thrombosis and Haemostasis vol. 74 , ( 05 ) 1259 - 1264 .
Downes M, Kirkham FJ, Berg C, Telfer P, de Haan M ( 2018 ) . Executive performance on the preschool executive task assessment in children with sickle cell anemia and matched controls . Child Neuropsychology vol. 25 , ( 2 ) 278 - 285 .
Downes M, Kirkham FJ, Telfer PT, de Haan M ( 2018 ) . Assessment of Executive Functions in Preschool Children With Sickle Cell Anemia . Journal of the International Neuropsychological Society vol. 24 , ( 9 ) 949 - 954 .
Telfer P, Agodoa I, Fox KM, Burke L, Mant T, Jurek M, Tonda M, Lehrer-Graiwer J ( 2018 ) . Impact of voxelotor (GBT440) on unconjugated bilirubin and jaundice in sickle cell disease . Hematology Reports vol. 10 , ( 2 )
Yeo JH, Islam A, Cavenagh J, Smith M, Telfer P, Kaya B ( 2018 ) . A Case Report of Dehydrated Hereditary Stomatocytosis and Spherocytosis . BRITISH JOURNAL OF HAEMATOLOGY . vol. 181 , 125 - 125 .
Nzouakou R, Kaya B, Koomson E, Barroso F, Telfer P ( 2018 ) . Cross-over study comparing manual exchange transfusion versus automated erythrocytapheresis. Experience of a single centre . BRITISH JOURNAL OF HAEMATOLOGY . vol. 181 , 122 - 122 .
Smith C, Kawadler J, Kirkham F, Hogan A, Telfer P, Stotesbury H ( 2018 ) . Residential proximity to major roads and cognitive function in asymptomatic children with Sickle Cell Anaemia: a longitudinal study . BRITISH JOURNAL OF HAEMATOLOGY . vol. 181 , 117 - 117 .
Telfer P, Kaya B ( 2017 ) . Optimizing the care model for an uncomplicated acute pain episode in sickle cell disease . Hematology vol. 2017 , ( 1 ) 525 - 533 .
de Montalembert M, Brousse V, Chakravorty S, Pagliuca A, Porter J, Telfer P, Vora A, Rees DC ( 2017 ) . Are the risks of treatment to cure a child with severe sickle cell disease too high? . The BMJ vol. 359 ,
Downes M, Kirkham FJ, Telfer PT, de Haan M ( 2017 ) . Altered Neurophysiological Processing of Auditory Attention in Preschool Children With Sickle Cell Disease . Journal of Pediatric Psychology vol. 43 , ( 8 ) 856 - 869 .
Lehrer-Graiwer J, Howard J, Hemmaway CJ, Awogbade M, Telfer P, Layton M, Porter JB, Mant T et al. ( 2016 ) . Long-Term Dosing in Sickle Cell Disease Subjects with GBT440, a Novel HbS Polymerization Inhibitor . Blood . vol. 128 ,
Piel FB, Tewari S, Brousse V, Analitis A, Font A, Menzel S, Chakravorty S, Thein SL et al. ( 2016 ) . Associations between environmental factors and hospital admissions for sickle cell disease . Haematologica vol. 102 , ( 4 ) 666 - 675 .
Downes M, de Haan M, Kirkham FJ, Telfer PT ( 2016 ) . Parent reported sleep problems in preschool children with sickle cell anemia and controls in East London . Pediatric Blood & Cancer vol. 64 , ( 6 )
Telfer P, Dwan K, Simmons A, Evanson J, Gadong N, Newell K, Tangayi S, Leigh A et al. ( 2016 ) . Transcranial Doppler Screening in a Regional Care Network for Sickle Cell Disease in the United Kingdom . Journal of Pediatric Hematology/Oncology vol. 38 , ( 7 ) 517 - 524 .
Fisher AE, Oduro AKY, Adzaku F, Telfer P ( 2016 ) . Presentations of sickle cell disease patients to hospital in Ghana: key findings from a preliminary study at Volta Regional Hospital . British Journal of Haematology vol. 178 , ( 3 ) 489 - 491 .
Tewari S, Piel F, Brousse V, Analitis A, Ghersi V, Menzel S, Chakravorty S, Inusa B et al. ( 2016 ) . ASSOCIATION BETWEEN ENVIRONMENTAL FACTORS AND HOSPITAL ADMISSIONS FOR SICKLE CELL DISEASE: A RETROSPECTIVE TIME SERIES ANALYSIS . HAEMATOLOGICA . vol. 101 , 127 - 128 .
Nzouakou R, Newell K, Barroso F, Telfer P, Kaya B ( 2016 ) . Annual review of transfusion targets in regularly transfused paediatric and adult sickle cell patients. Experiences from Bart's Health NHS Trust . BRITISH JOURNAL OF HAEMATOLOGY . vol. 173 , 153 - 154 .
Lehrer-Graiwer J, Hemmaway C, Howard J, Telfer P, Layton M, Awogbade M, Porter J, Roberts-Harewood M et al. ( 2016 ) . GBT440, A NOVEL HBS POLYMERIZATION INHIBITOR, INCREASES HB OXYGEN AFFINITY AND RESULTS IN A RAPID IMPROVEMENT IN HEMOLYSIS AND ANEMIA . HAEMATOLOGICA . vol. 101 , 125 - 125 .
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Tsouana E, Kaya B, Gadong N, Hemmaway C, Newell H, Simmons A, Whitmarsh S, Telfer P ( 2013 ) . Inadequate Long-Term Control Of Transfusion Iron Overload In Children With Sickle Cell Disease Chelated With Deferasirox . Blood vol. 122 , ( 21 )
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King MJ, Telfer P, MacKinnon H, Langabeer L, McMahon C, Darbyshire P, Dhermy D ( 2008 ) . Using the eosin-5-maleimide binding test in the differential diagnosis of hereditary spherocytosis and hereditary pyropoikilocytosis . CYTOM PART B-CLIN CY vol. 74B , ( 4 ) 244 - 250 .
Kirkham J, Baird J, Telfer P, Khatura J, Sahota TP, Wilkey O, Robins A, Morgan MA et al. ( 2008 ) . HEIGHT AND WEIGHT IN A UK POPULATION OF CHILDREN WITH SICKLE CELL DISEASE . HAEMATOLOGICA-THE HEMATOLOGY JOURNAL . vol. 93 , 448 - 448 .
Kirkham J, Telfer P, Bucks RS, Hewes DKM, Kaya B, Prengler M, Dundas I, Lane R et al. ( 2008 ) . OVERNIGHT OXYHAEMOGLOBIN DESATURATION PREDICTS ABNORMAL TRANSCRANIAL DOPPLER IN SICKLE CELL ANAEMIA . HAEMATOLOGICA-THE HEMATOLOGY JOURNAL . vol. 93 , 252 - 252 .
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Hogan AM, Telfer P, Prengler M, Saunders D, Wade AM, Vargha-Khadem F, Kirkham FJ ( 2008 ) . Intellectual function in children with sickle cell anemia: longitudinal data from the East London cohort . BRITISH JOURNAL OF HAEMATOLOGY . vol. 141 , 111 - 111 .
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