Celli, Luca; Garrelfs, Mark R.; Sakkers, Ralph J.B.; Elting, Mariet W.; Celli, Mauro; Bökenkamp, Arend; Smits, Cas; Goderie, Thadé; Smit, Jan Maerten; Schwarte, Lothar A.; Schober, Patrick R.; Lubbers, Wouter D.; Visser, Marieke C.; Kievit, Arthur J.; van Royen, Barend J.; Gilijamse, Marjolijn; Schreuder, Willem H.; Rustemeyer, Thomas; Pramana, Angela; Hendrickx, Jan Jaap; Dahele, Max R.; Saeed, Peerooz; Moll, Annette C.; Curro–Tafili, Katie R.; Ghyczy, Ebba A.E.; Dickhoff, Chris; de Leeuw, Robert A.; Bonjer, Jaap H.; Nieuwenhuijzen, Jakko A.; Konings, Thelma C.; Engelsman, Anton F.; Eeckhout, Augustinus M.; van den Aardweg, Joost G.; Thoral, Patrick J.; Noske, David P.; Dubois, Leander; Teunissen, Berend P.; Semler, Oliver; Wekre, Lena Lande; Maasalu, Katre; Märtson, Aare; Sangiorgi, Luca; Versacci, Paolo; Riminucci, Mara; Grammatico, Paola; Zambrano, Anna; Martini, Lorena; Castori, Marco; Botman, Esmee; Westerheim, Ingunn; Zhytnik, Lidiia; Micha, Dimitra; Eekhoff, Elisabeth Marelise W.
(Springer New York, 2024-12)
Osteogenesis Imperfecta (OI), known as “brittle bone disease,” presents a rare genetic disorder characterized by bone fragility, often accompanied by skeletal deformities and extraskeletal complications. OI is primarily ...