Bisphosphonate treatment for skeletal complications in paediatric cancer—Experience from a single tertiary centre von Utriainen, Pauliina, Stenberg, Jalmari E. E., Vettenranta, Kim K., Mäkitie, Outi M.

Volltext

Impaired WNT signaling and the spine—Heterozygous WNT1 mutation causes severe age-related spinal pathology von Mäkitie, Riikka E, Niinimäki, Tuukka, Nieminen, Miika T, Schalin-Jäntti, Camilla, Niinimäki, Jaakko, Mäkitie, Outi

Volltext

Oral findings in patients with cartilage-hair hypoplasia - cross-sectional observational study von Arponen, Heidi, Vakkilainen, Svetlana, Rautava, Jaana, Mäkitie, Outi

Volltext

Early‐Onset Osteoporosis: Rare Monogenic Forms Elucidate the Complexity of Disease Pathogenesis Beyond Type I Collagen von Costantini, Alice, Mäkitie, Riikka E., Hartmann, Markus A., Fratzl‐Zelman, Nadja, Zillikens, M. Carola, Kornak, Uwe, Søe, Kent, Mäkitie, Outi

Volltext

Caffey disease: New perspectives on old questions von Nistala, Harikiran, Mäkitie, Outi, Jüppner, Harald

Volltext

Diagnosis and management of pseudohypoparathyroidism and related disorders: first international Consensus Statement von Mantovani, Giovanna, Bastepe, Murat, Monk, David, de Sanctis, Luisa, Thiele, Susanne, Usardi, Alessia, Ahmed, S. Faisal, Bufo, Roberto, Choplin, Timothée, De Filippo, Gianpaolo, Devernois, Guillemette, Eggermann, Thomas, Elli, Francesca M., Freson, Kathleen, García Ramirez, Aurora, Germain-Lee, Emily L., Groussin, Lionel, Hamdy, Neveen, Hanna, Patrick, Hiort, Olaf, Jüppner, Harald, Kamenický, Peter, Knight, Nina, Kottler, Marie-Laure, Le Norcy, Elvire, Lecumberri, Beatriz, Levine, Michael A., Mäkitie, Outi, Martin, Regina, Martos-Moreno, Gabriel Ángel, Minagawa, Masanori, Murray, Philip, Pereda, Arrate, Pignolo, Robert, Rejnmark, Lars, Rodado, Rebecca, Rothenbuhler, Anya, Saraff, Vrinda, Shoemaker, Ashley H., Shore, Eileen M., Silve, Caroline, Turan, Serap, Woods, Philip, Zillikens, M. Carola, Perez de Nanclares, Guiomar, Linglart, Agnès

Volltext

Mesenchymal Cell‐Derived Juxtacrine Wnt1 Signaling Regulates Osteoblast Activity and Osteoclast Differentiation von Wang, Fan, Tarkkonen, Kati, Nieminen‐Pihala, Vappu, Nagano, Kenichi, Majidi, Rana Al, Puolakkainen, Tero, Rummukainen, Petri, Lehto, Jemina, Roivainen, Anne, Zhang, Fu‐Ping, Mäkitie, Outi, Baron, Roland, Kiviranta, Riku

Volltext

Growth in achondroplasia: Development of height, weight, head circumference, and body mass index in a European cohort von Merker, Andrea, Neumeyer, Luitgard, Hertel, Niels Thomas, Grigelioniene, Giedre, Mäkitie, Outi, Mohnike, Klaus, Hagenäs, Lars

Volltext

Genetic variation in GC and CYP2R1 affects 25-hydroxyvitamin D concentration and skeletal parameters: A genome-wide association study in 24-month-old Finnish children von Kämpe, Anders, Enlund-Cerullo, Maria, Valkama, Saara, Holmlund-Suila, Elisa, Rosendahl, Jenni, Hauta-Alus, Helena, Pekkinen, Minna, Andersson, Sture, Mäkitie, Outi

Volltext

SGMS2 in primary osteoporosis with facial nerve palsy von Pihlström, Sandra, Richardt, Sampo, Määttä, Kirsi, Pekkinen, Minna, Olkkonen, Vesa M., Mäkitie, Outi, Mäkitie, Riikka E.

Volltext

Lipocalin-2 is associated with FGF23 in WNT1 and PLS3 osteoporosis von Loid, Petra, Hauta-alus, Helena, Mäkitie, Outi, Magnusson, Per, Mäkitie, Riikka E.

Volltext

Low Copy Number of the AMY1 Locus Is Associated with Early-Onset Female Obesity in Finland von Viljakainen, Heli, Andersson-Assarsson, Johanna C, Armenio, Miriam, Pekkinen, Minna, Pettersson, Maria, Valta, Helena, Lipsanen-Nyman, Marita, Mäkitie, Outi, Lindstrand, Anna

Volltext

A 30-Year Prospective Follow-Up Study Reveals Risk Factors for Early Death in Cartilage-Hair Hypoplasia von Vakkilainen, Svetlana, Taskinen, Mervi, Klemetti, Paula, Pukkala, Eero, Mäkitie, Outi

Volltext

A novel link between chronic inflammation and humanin regulation in children von Zhao, Yunhan, Mäkitie, Outi, Laakso, Saila, Fedosova, Vera, Sävendahl, Lars, Zaman, Farasat

Volltext

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

Volltext

Rare Variants in Genes Linked to Appetite Control and Hypothalamic Development in Early-Onset Severe Obesity von Loid, Petra, Mustila, Taina, Makitie, Riikka E., Viljakainen, Heli, Kampe, Anders, Tossavainen, Paivi, Lipsanen-Nyman, Marita, Pekkinen, Minna, Makitie, Outi

Volltext

Positive airway pressure therapy for obstructive sleep apnea in patients with Osteogenesis imperfecta: a prospective pilot study von Arponen, Heidi, Bachour, Adel, Back, Leif, Valta, Helena, Makitie, Antti, Makitie, Outi, Waltimo-Siren, Janna

Volltext

Skeletal Characteristics of WNT1 Osteoporosis in Children and Young Adults von Mäkitie, Riikka E, Haanpää, Maria, Valta, Helena, Pekkinen, Minna, Laine, Christine M, Lehesjoki, Anna‐Elina, Schalin‐Jäntti, Camilla, Mäkitie, Outi

Volltext

Spondyloocular Syndrome: Novel Mutations in XYLT2 Gene and Expansion of the Phenotypic Spectrum von Taylan, Fulya, Costantini, Alice, Coles, Nicole, Pekkinen, Minna, Héon, Elise, Şıklar, Zeynep, Berberoğlu, Merih, Kämpe, Anders, Kıykım, Ertuğrul, Grigelioniene, Giedre, Tüysüz, Beyhan, Mäkitie, Outi

Volltext

Osteoporosis and Bone Mass Disorders: From Gene Pathways to Treatments von Rivadeneira, Fernando, Mäkitie, Outi

Volltext