An 18-Year Follow-up Study of Chronic Gastritis and Helicobacter pylori: Association of CagA Positivity with Development of Atrophy and Activity of Gastritis by MAAROOS, H.-I, VOROBJOVA, T, SIPPONEN, P, TAMMUR, R, UIBO, R, WADSTRÖM, T, KEEVALLIK, R, VILLAKO, K

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Relation of parietal cell and thyroid antibodies to the state of gastric mucosa and basal serum gastrin levels during a 6-year follow-up by UIBO, R, KROHN, K, VILLAKO, K, TAMMUR, R, TAMM, A

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Long-term Endoscopic Follow-up of Peptic Ulcer : Clinical Course, Endoscopic Finding, State of Antral and Corpus Mucosa and C13 Breath Test after H. pylori Eradication by Maaroos, H, Keevallik, R, Kolk, H, Kull, I, Labotkin, K, Tammur, R

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Genetic Subtypes and Outcome of Patients Aged 1 to 45 Years Old With Acute Lymphoblastic Leukemia in the NOPHO ALL2008 Trial by Norén‐Nyström, Ulrika, Andersen, Mette K., Barbany, Gisela, Dirse, Vaidas, Eilert‐Olsen, Martine, Engvall, Marie, Harila‐Saari, Arja, Heyman, Mats, Hovland, Randi, Häikiö, Satu, Jónsson, Jón J., Karhu, Ritva, Kjeldsen, Eigil, Norberg, Anna, Preiss, Birgitte S., Pulkkinen, Kati, Quist‐Paulsen, Petter, Räsänen, Hannele, Schmiegelow, Kjeld, Seitsonen, Anne, Sjögren, Helene, Tammur, Pille, Johansson, Bertil

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Two new genes from the human ATP-binding cassette transporter superfamily, ABCC11 and ABCC12, tandemly duplicated on chromosome 16q12 by Tammur, Jaana, Prades, Catherine, Arnould, Isabelle, Rzhetsky, Andrey, Hutchinson, Amy, Adachi, Masashi, Schuetz, John D., Swoboda, Kathryn J., Ptácek, Louis J., Rosier, Marie, Dean, Michael, Allikmets, Rando

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Distinct Nuclear Organization of Telomeres and Centromeres in Monoclonal Gammopathy of Undetermined Significance and Multiple Myeloma by Yu, Pak Lok Ivan, Wang, Rachel R., Johnston, Grace, Wang, Yaqiong, Tammur, Pille, Tamm, Anu, Punab, Mari, Rangel-Pozzo, Aline, Mai, Sabine

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Further Evidence for an Association of ABCR Alleles with Age-Related Macular Degeneration by Allikmets, Rando

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Nonsense mediated decay downregulates conserved alternatively spliced ABCC4 transcripts bearing nonsense codons by Lamba, Jatinder Kaur, Adachi, Masashi, Sun, Daxi, Tammur, Jaana, Schuetz, Erin G., Allikmets, Rando, Schuetz, John D.

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Whole Xp Deletion in a Girl with Mental Retardation, Epilepsy, and Biochemical Features of OTC Deficiency by Joost, K., Tammur, P., Teek, R., Žilina, O., Peters, M., Kreile, M., Lace, B., Žordania, R., Talvik, I., Õunap, K.

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Characterization of two supernumerary marker chromosomes in a patient with signs of Klinefelter syndrome, mild facial anomalies, and severe speech delay by Weimer, Jörg, Metzke‐Heidemann, Simone, Plendl, Hansjörg, Caliebe, Almuth, Grunewald, Regina, Õunap, Katrin, Tammur, Pille, Jonat, Walter, Bartsch, Oliver, Siebert, Reiner, Arnold, Norbert

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Macular pigment and visual acuity in Stargardt macular dystrophy by XINYUAN ZHANG, HARGITAI, Janos, TAMMUR, Jaana, HUTCHINSON, Amy, ALLIKMETS, Rando, CHANG, Stanley, GOURAS, Peter

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Evaluation of the ELOVL4 gene in patients with age-related macular degeneration by Ayyagari, Radha, Zhang, Kang, Hutchinson, Amy, Yu, Zhengya, Swaroop, Anand, Kakuk, Laura E., Seddon, Johanna M., Bernstein, Paul S., Lewis, Richard A., Tammur, Jaana, Yang, Z., Li, Y., Zhang, Heidi, Yashar, Beverly M., Liu, Jiafan, Petrukhin, Konstantin, Sieving, Paul A., Allikmets, Rando

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