1. An unexpected cause of bilateral periorbital oedema. (1st October 2019) Authors: Boger, L.; Fowler, B.; West, D.; Patel, T. Journal: Clinical and experimental dermatology Issue: Volume 44:Number 7(2019) Page Start: 781 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. An unexpected cause of bilateral periorbital oedema. (28th November 2018) Authors: Boger, L.; Fowler, B.; West, D.; Patel, T. Journal: Clinical and experimental dermatology Issue: Volume 44:Number 7(2019) Page Start: 781 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Characterization and review of MTHFD1 deficiency: four new patients, cellular delineation and response to folic and folinic acid treatment. Issue 5 (30th January 2015) Authors: Burda, P.; Kuster, A.; Hjalmarson, O.; Suormala, T.; Bürer, C.; Lutz, S.; Roussey, G.; Christa, L.; Asin‐Cayuela, J.; Kollberg, G.; Andersson, B. A.; Watkins, D.; Rosenblatt, D. S.; Fowler, B.; Holme, E.; Froese, D. S.; Baumgartner, M. R. Journal: Journal of inherited metabolic disease Issue: Volume 38:Issue 5(2015) Page Start: 863 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Clinical onset and course, response to treatment and outcome in 24 patients with the cblE or cblG remethylation defect complemented by genetic and in vitro enzyme study data. Issue 5 (20th December 2014) Authors: Huemer, M.; Bürer, C.; Ješina, P.; Kožich, V.; Landolt, M. A.; Suormala, T.; Fowler, B.; Augoustides‐ Savvopoulou, P.; Blair, E.; Brennerova, K.; Broomfield, A.; De Meirleir, L.; Gökcay, G.; Hennermann, J.; Jardine, P.; Koch, J.; Lorenzl, S.; Lotz‐Havla, A. S.; Noss, J.; Parini, R. Journal: Journal of inherited metabolic disease Issue: Volume 38:Issue 5(2015) Page Start: 957 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Detection of heterozygotes for homocystinuria by oral loading with L-methionine. Issue 249 (October 1971) Authors: Sardharwalla, I. B.; Fowler, B.; Robins, A. J. Journal: Archives of disease in childhood Issue: Volume 46:Issue 249(1971) Page Start: 738 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Detection of heterozygotes for homocystinuria: Study of sulphur-containing amino acids in plasma and urine after L-methionine loading. Issue 7 (July 1974) Authors: Sardharwalla, I. B.; Fowler, B.; Robins, A. J.; Komrower, G. M. Journal: Archives of disease in childhood Issue: Volume 49:Issue 7(1974) Page Start: 553 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Development and pilot testing of an integrated, web‐based self‐management program for irritable bowel syndrome (IBS). Issue 1 (6th December 2014) Authors: Dorn, S. D.; Palsson, O. S.; Woldeghebriel, M.; Fowler, B.; McCoy, R.; Weinberger, M.; Drossman, D. A. Journal: Neurogastroenterology & motility Issue: Volume 27:Issue 1(2015:Jan.) Page Start: 128 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗