Result Number | Material Type | Add to My Shelf Action | Record Details and Options |
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11 |
Material Type: Artigo
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Chromidrosis And Iodide Of PotashTemple, G. H.British medical journal, 1891-08, Vol.2 (1600), p.477-477British Medical AssociationTexto completo disponível |
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12 |
Material Type: Artigo
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Combination of cimetidine and alginic acid : an improvement in the treatment of oesophageal reflux diseaseGut, 1991, Vol.32 (7), p.819-822 [Periódico revisado por pares]London: BMJTexto completo disponível |
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13 |
Material Type: Artigo
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Assessment of the rapid pullthrough technique in oesophageal manometryGoodall, R J ; Hay, D J ; Temple, J GGut, 1980-02, Vol.21 (2), p.169-173 [Periódico revisado por pares]England: BMJ Publishing Group Ltd and British Society of GastroenterologyTexto completo disponível |
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14 |
Material Type: Artigo
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Temple syndrome: improving the recognition of an underdiagnosed chromosome 14 imprinting disorder: an analysis of 51 published casesIoannides, Yiannis ; Lokulo-Sodipe, Kemi ; Mackay, Deborah J G ; Davies, Justin H ; Temple, I KarenJournal of Medical Genetics, 2014-08, Vol.51 (8), p.495-501 [Periódico revisado por pares]England: BMJ Publishing Group LTDTexto completo disponível |
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15 |
Material Type: Artigo
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Effective of highly selective vagotomy upon the lower oesophageal sphincterTemple, J G ; Goodall, R J ; Hay, D J ; Miller, DGut, 1981-05, Vol.22 (5), p.368-370 [Periódico revisado por pares]England: BMJ Publishing Group Ltd and British Society of GastroenterologyTexto completo disponível |
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16 |
Material Type: Artigo
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Whole-genome analysis as a diagnostic tool for patients referred for diagnosis of Silver-Russell syndrome: a real-world studyAlhendi, Ahmed S N ; Lim, Derek ; McKee, Shane ; McEntagart, Meriel ; Tatton-Brown, Katriona ; Temple, I Karen ; Davies, Justin H ; Mackay, Deborah J GJournal of medical genetics, 2022-06, Vol.59 (6), p.613-622 [Periódico revisado por pares]England: BMJ Publishing Group LtdTexto completo disponível |
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17 |
Material Type: Artigo
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Phenotype of genetically confirmed Silver-Russell syndrome beyond childhoodLokulo-Sodipe, Oluwakemi ; Ballard, Lisa ; Child, Jenny ; Inskip, Hazel M ; Byrne, Christopher D ; Ishida, Miho ; Moore, Gudrun E ; Wakeling, Emma L ; Fenwick, Angela ; Mackay, Deborah J G ; Davies, Justin Huw ; Temple, I KarenJournal of medical genetics, 2020-10, Vol.57 (10), p.683-691 [Periódico revisado por pares]England: BMJ Publishing Group LTDTexto completo disponível |
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18 |
Material Type: Artigo
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Epigenotype–phenotype correlations in Silver–Russell syndromeWakeling, E L ; Amero, S Abu ; Alders, M ; Bliek, J ; Forsythe, E ; Kumar, S ; Lim, D H ; MacDonald, F ; Mackay, D J ; Maher, E R ; Moore, G E ; Poole, R L ; Price, S M ; Tangeraas, T ; Turner, C L S ; Van Haelst, M M ; Willoughby, C ; Temple, I K ; Cobben, J MJournal of medical genetics, 2010-11, Vol.47 (11), p.760-768 [Periódico revisado por pares]London: BMJ Publishing Group LtdTexto completo disponível |
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19 |
Material Type: Artigo
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Effectiveness of continuous glucose monitoring in pregnant women with diabetes: randomised clinical trialMurphy, Helen R ; Rayman, Gerry ; Lewis, Karen ; Kelly, Susan ; Johal, Balroop ; Duffield, Katherine ; Fowler, Duncan ; Campbell, Peter J ; Temple, Rosemary CBMJ, 2008-10, Vol.337 (7675), p.907-910 [Periódico revisado por pares]England: British Medical Journal Publishing GroupTexto completo disponível |
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20 |
Material Type: Artigo
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Maternal variants in NLRP and other maternal effect proteins are associated with multilocus imprinting disturbance in offspringBegemann, Matthias ; Rezwan, Faisal I ; Beygo, Jasmin ; Docherty, Louise E ; Kolarova, Julia ; Schroeder, Christopher ; Buiting, Karin ; Chokkalingam, Kamal ; Degenhardt, Franziska ; Wakeling, Emma L ; Kleinle, Stephanie ; González Fassrainer, Daniela ; Oehl-Jaschkowitz, Barbara ; Turner, Claire L S ; Patalan, Michal ; Gizewska, Maria ; Binder, Gerhard ; Bich Ngoc, Can Thi ; Chi Dung, Vu ; Mehta, Sarju G ; Baynam, Gareth ; Hamilton-Shield, Julian P ; Aljareh, Sara ; Lokulo-Sodipe, Oluwakemi ; Horton, Rachel ; Siebert, Reiner ; Elbracht, Miriam ; Temple, Isabel Karen ; Eggermann, Thomas ; Mackay, Deborah J GJournal of medical genetics, 2018-07, Vol.55 (7), p.497-504 [Periódico revisado por pares]England: BMJ Publishing Group LTDTexto completo disponível |