Search Results - "Eekhoff, Elisabeth Marelise W."

Ocular characteristics and complications in patients with osteogenesis imperfecta: a systematic review by Treurniet, Sanne, Burger, Pia, Ghyczy, Ebba A.E., Verbraak, Frank D., Curro‐ Tafili, Katie R., Micha, Dimitra, Bravenboer, Nathalie, Ralston, Stuart H., Vries, Ralph, Moll, Annette C., Eekhoff, Elisabeth Marelise W.

“…Purpose Osteogenesis imperfecta (OI) is a rare inherited heterogeneous connective tissue disorder characterized by bone fragility, low bone mineral density,…”
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Prevalence and Hospital Admissions in Patients With Osteogenesis Imperfecta in The Netherlands: A Nationwide Registry Study by Storoni, Silvia, Treurniet, Sanne, Maugeri, Alessandra, Pals, Gerard, van den Aardweg, Joost G, van der Pas, Stéphanie L, Elting, Mariet W, Kloen, Peter, Micha, Dimitra, Eekhoff, Elisabeth Marelise W

“…Osteogenesis Imperfecta (OI) is a complex disease caused by genetic alterations in production of collagen type I, and collagen-related proteins. Bone fragility…”
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Performance of simplified methods for quantification of [ 18 F]NaF uptake in fibrodysplasia ossificans progressiva by de Ruiter, Ruben Daniel, Botman, Esmée, Teunissen, Bernd P, Lammertsma, Adriaan Anthonius, Boellaard, Ronald, Raijmakers, Pieter G, Schwarte, Lothar A, Nieuwenhuijzen, Jakko A, Gonzalez Trotter, Dinko, Eekhoff, Elisabeth Marelise W, Yaqub, Maqsood

“…Fibrodysplasia Ossificans Progressiva (FOP) is a rare, genetic disease in which heterotopic bone is formed in muscles, tendons and ligaments throughout the…”
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Limitations of Jaw Movement in Fibrodysplasia Ossificans Progressiva: A Review by Schoenmaker, Ton, Dahou Bouchankouk, Amine, Özkan, Semih, Gilijamse, Marjolijn, Bouvy-Berends, Elinor, Netelenbos, Coen, Lobbezoo, Frank, Eekhoff, Elisabeth Marelise W, de Vries, Teun J

“…Fibrodysplasia ossificans progressiva (FOP) is a rare genetic disorder characterized by heterotopic ossification (HO) of the skeletal muscles, fascia, tendons…”
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Adapting to Adulthood: A Review of Transition Strategies for Osteogenesis Imperfecta by 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.

“…Abstract Osteogenesis Imperfecta (OI), known as “brittle bone disease,” presents a rare genetic disorder characterized by bone fragility, often accompanied by…”
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Performance of simplified methods for quantification of 18FNaF uptake in fibrodysplasia ossificans progressiva by de Ruiter, Ruben Daniel, Botman, Esmée, Teunissen, Bernd P, Lammertsma, Adriaan Anthonius, Boellaard, Ronald, Raijmakers, Pieter G, Schwarte, Lothar A, Nieuwenhuijzen, Jakko A, Gonzalez Trotter, Dinko, Eekhoff, Elisabeth Marelise W, Yaqub, Maqsood

“…Fibrodysplasia Ossificans Progressiva (FOP) is a rare, genetic disease in which heterotopic bone is formed in muscles, tendons and ligaments throughout the…”
Get full text