Risedronate in children with osteogenesis imperfecta: a randomised, double-blind, placebo-controlled trial by Bishop, Nick, Prof, Adami, Silvano, MD, Ahmed, S Faisal, MD, Antón, Jordi, MD, Arundel, Paul, MD, Burren, Christine P, MD, Devogelaer, Jean-Pierre, MD, Hangartner, Thomas, PhD, Hosszú, Eva, MD, Lane, Joseph M, MD, Lorenc, Roman, MD, Mäkitie, Outi, MD, Munns, Craig F, MD, Paredes, Ana, MD, Pavlov, Helene, MD, Plotkin, Horacio, MD, Raggio, Cathleen L, MD, Reyes, Maria Loreto, MD, Schoenau, Eckhard, MD, Semler, Oliver, MD, Sillence, David O, MD, Steiner, Robert D, MD

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Compromised Peak Bone Mass in Patients with Inflammatory Bowel Disease–A Prospective Study by Laakso, Saila, MD, PhD, Valta, Helena, MD, PhD, Verkasalo, Matti, MD, PhD, Toiviainen-Salo, Sanna, MD, PhD, Mäkitie, Outi, MD, PhD

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Analysis of Clinical and Immunologic Phenotype in a Large Cohort of Children and Adults with Cartilage-hair Hypoplasia by Kostjukovits, Svetlana, MD, Klemetti, Paula, MD, PhD, Valta, Helena, MD, PhD, Martelius, Timi, MD, PhD, Notarangelo, Luigi D., MD, Seppänen, Mikko, MD, PhD, Taskinen, Mervi, MD, PhD, Mäkitie, Outi, MD, PhD

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Shorter birth length and decreased T-cell production and function predict severe infections in children with non–severe combined immunodeficiency cartilage–hair hypoplasia by Pello, Eetu, Kainulainen, Leena, Vakkilainen, Mikko, Klemetti, Paula, Taskinen, Mervi, Mäkitie, Outi, Vakkilainen, Svetlana

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High prevalence of bronchiectasis in patients with cartilage-hair hypoplasia by Kostjukovits, Svetlana, MD, Klemetti, Paula, MD, PhD, Föhr, Anna, MD, Kajosaari, Merja, MD, PhD, Valta, Helena, MD, PhD, Taskinen, Mervi, MD, PhD, Toiviainen-Salo, Sanna, MD, PhD, Mäkitie, Outi, MD, PhD

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Maternal preeclampsia and bone mineral density of the adult offspring by Miettola, Satu, MD, Hovi, Petteri, MD, PhD, Andersson, Sture, MD, PhD, Strang-Karlsson, Sonja, MD, PhD, Pouta, Anneli, MD, PhD, Laivuori, Hannele, MD, PhD, Järvenpää, Anna-Liisa, MD, PhD, Eriksson, Johan G., MD, DMSC, Mäkitie, Outi, MD, PhD, Kajantie, Eero, MD, PhD

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The Natural History of Shwachman-Diamond Syndrome–Associated Liver Disease from Childhood to Adulthood by Toiviainen-Salo, Sanna, MD, PhD, Durie, Peter R., MD, FRCPC, Numminen, Kirsti, MD, PhD, Heikkilä, Päivi, MD, PhD, Marttinen, Eino, MD, PhD, Savilahti, Erkki, MD, PhD, Mäkitie, Outi, MD, PhD

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Hypoplastic Anemia in Cartilage-Hair Hypoplasia—Balancing between Iron Overload and Chelation by Taskinen, Mervi, MD, PhD, Toiviainen-Salo, Sanna, MD, PhD, Lohi, Jouko, MD, PhD, Vuolukka, Pentti, MD, Gräsbeck, Michaela, MD, Mäkitie, Outi, MD, PhD

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The Thoracic and Lumbar Spine in Severe Juvenile Idiopathic Arthritis: Magnetic Resonance Imaging Analysis in 50 Children by Toiviainen-Salo, Sanna, MD, PhD, Markula-Patjas, Kati, MD, Kerttula, Liisa, MD, PhD, Soini, Irma, MD, PhD, Valta, Helena, MD, PhD, Mäkitie, Outi, MD, PhD

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Reduced Body Size and Shape-Related Symptoms in Young Adults Born Preterm with Very Low Birth Weight: Helsinki Study of Very Low Birth Weight Adults by Wehkalampi, Karoliina, MD, PhD, Hovi, Petteri, MD, Strang-Karlsson, Sonja, MD, Räikkönen, Katri, PhD, Pesonen, Anu-Katriina, PhD, Heinonen, Kati, PhD, Mäkitie, Outi, MD, PhD, Järvenpää, Anna-Liisa, MD, PhD, Eriksson, Johan G., MD, PhD, Andersson, Sture, MD, PhD, Kajantie, Eero, MD, PhD

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Magnetic Resonance Imaging Findings of the Pancreas in Patients with Shwachman-Diamond Syndrome and Mutations in the SBDS Gene by Toiviainen-Salo, Sanna, MD, Raade, Merja, MD, Durie, Peter R., MD, FRCPC, Ip, Wan, MSc, Marttinen, Eino, MD, PhD, Savilahti, Erkki, MD, PhD, Mäkitie, Outi, MD, PhD

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Patients with Cartilage-Hair Hypoplasia Have an Increased Risk for Bronchiectasis by Toiviainen-Salo, Sanna, MD, Kajosaari, Merja, MD, PhD, Piilonen, Anneli, MD, Mäkitie, Outi, MD, PhD

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Multiple epiphyseal dysplasia mutations in MATN3 cause misfolding of the A-domain and prevent secretion of mutant matrilin-3 by Cotterill, Sally L., Jackson, Gail C., Leighton, Matthew P., Wagener, Raimund, Mäkitie, Outi, Cole, William G., Briggs, Michael D.

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Clinical and radiographic findings in multiple epiphyseal dysplasia caused by MATN3 mutations: Description of 12 patients by Mäkitie, Outi, Mortier, Geert R., Czarny-Ratajczak, Malwina, Wright, Michael J., Suri, Mohnish, Rogala, Piotr, Freund, Margarida, Jackson, Gail C., Jakkula, Eveliina, Ala-Kokko, Leena, Briggs, Michael D., Cole, William G.

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