Social prescribing for dementia by Gallacher, J, Burns, A

THE USE OF NEXT-GENERATION SEQUENCING TO SCREEN FOR MUTATIONS IN 16 GENES INVOLVED IN IRON HOMEOSTASIS AS AN AID TO GENETIC DIAGNOSIS FOR PATIENTS WITH IRON OVERLOAD OR IRON DEFICI... by Bignell, P, Burns, A, Schuh, A, Robson, K

The subunit structure of chick lens crystallins and its relationship to their antigenic properties by Truman D.E.S, Clayton R, Burns A.T.H, Campbell J

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Bright light therapy for agitation in dementia: a randomized controlled trial. by Burns, A, Allen, H, Tomenson, B, Duignan, D, Byrne, J

Multiphase '97 : How deep? How far? How soon? / by International Conference on Multiphase '97 (8th: 1997: Cannes,France), Burns, A. P.

Targeted Gene Profiling Identifies Differential Genetic Make-up Depending On Chronic Lymphocytic Leukaemia Subtype by Burns, A, Clifford, R, Dreau, H, Hatton, C, Henderson, S, Taylor, J, Schuh, A

Targeted Gene Profiling Identifies Differential Genetic Make-up Depending On Chronic Lymphocytic Leukaemia Subtype by Burns, A, Clifford, R, Dreau, H, Hatton, C, Henderson, S, Taylor, J, Schuh, A

Diagnosing Burkitt lymphoma in sub-saharan Africa by sequencing of circulating tumour DNA: a comparative microcosting study by Morrell, L, Burns, A, Dreau, H, Leonte, M, El Mouden, C, Schuh, A, Wordsworth, S

The normalisation of disrupted attentional processing of infant distress in depressed pregnant women following Cognitive Behavioural Therapy. by Pearson, R, O'Mahen, H, Burns, A, Bennert, K, Shepherd, C, Baxter, H, Chauhan, D, Evans, J

The normalisation of disrupted attentional processing of infant distress in depressed pregnant women following Cognitive Behavioural Therapy by Pearson, R, O'Mahen, H, Burns, A, Bennert, K, Shepherd, C, Baxter, H, Chauhan, D, Evans, J

Assessment of petrophysical parameters of clastics using well logs: The Upper Miocene in El-Wastani gas field, onshore Nile Delta, Egypt by Ezz S El-Din, Maher A Mesbah, Mohamed A Kassab, Ibtehal F Mohamed, Burns A Cheadle, Mostafa A Teama

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Whole-exome sequencing in del(5q) myelodysplastic syndromes in transformation to acute myeloid leukemia by Pellagatti, A, Fernandez-Mercado, M, Di Genua, C, Larrayoz, M, Killick, S, Dolatshad, H, Burns, A, Calasanz, M, Schuh, A, Boultwood, J

Whole-exome sequencing in del(5q) myelodysplastic syndromes in transformation to acute myeloid leukemia. by Pellagatti, A, Fernandez-Mercado, M, Di Genua, C, Larrayoz, M, Killick, S, Dolatshad, H, Burns, A, Calasanz, M, Schuh, A, Boultwood, J

A pilot randomised controlled trial of cognitive behavioural therapy for antenatal depression. by Burns, A, O'Mahen, H, Baxter, H, Bennert, K, Wiles, N, Ramchandani, P, Turner, K, Sharp, D, Thorn, J, Noble, S, Evans, J

Quantitative Whole Genome Analysis of Sequential Samples From Patients with B-CLL Identifies Novel Recurrent Copy Number Alterations Involving Critical B-Cell Transcription Factors by Timbs, A, Knight, S, SadighiAkha, E, Burns, A, Dreau, H, Hewitt, A, Hatton, C, Yau, C, Holmes, C, Taylor, J, Schuh, A

Quantitative Whole Genome Analysis of Sequential Samples From Patients with B CLL Identifies Novel Recurrent Copy Number Alterations Involving Critical B Cell Transcription Factors by Timbs, A, Knight, S, SadighiAkha, E, Burns, A, Dreau, H, Hewitt, A, Hatton, C, Yau, C, Holmes, C, Taylor, J, Schuh, A

Targeted re-sequencing analysis of 25 genes commonly mutated in myeloid disorders in del(5q) myelodysplastic syndromes. by Fernandez-Mercado, M, Burns, A, Pellagatti, A, Giagounidis, A, Germing, U, Agirre, X, Prosper, F, Aul, C, Killick, S, Wainscoat, J, Schuh, A, Boultwood, J

Immunomodulatory effect of a decellularized skeletal muscle scaffold in a discordant xenotransplantation model. by Fishman, J, Lowdell, M, Urbani, L, Ansari, T, Burns, A, Turmaine, M, North, J, Sibbons, P, Seifalian, A, Wood, K, Birchall, M, De Coppi, P

Mutations in SETBP1 are recurrent in myelodysplastic syndromes and often coexist with cytogenetic markers associated with disease progression. by Fernandez-Mercado, M, Pellagatti, A, Di Genua, C, Larrayoz, M, Winkelmann, N, Aranaz, P, Burns, A, Schuh, A, Calasanz, M, Cross, N, Boultwood, J

Mutations in SETBP1 are recurrent in myelodysplastic syndromes and often coexist with cytogenetic markers associated with disease progression by Fernandez-Mercado, M, Pellagatti, A, Di Genua, C, Larrayoz, M, Winkelmann, N, Aranaz, P, Burns, A, Schuh, A, Calasanz, M, Cross, N, Boultwood, J