Search Results - "Curro‐ Tafili, Katie R."

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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Longitudinal retinal microvascular changes in preclinical Alzheimer’s disease by Curro‐Tafili, Katie R., Bouwman, Femke H., den Braber, Anouk, Verbraak, Frank D., van Nispen, Ruth, van de Kreeke, Aleid, van de Giessen, Elsmarieke, Tan, H. Stevie

“…Background The retina has become an area of increasing interest as a potential biomarker for neurodegeneration, as it is easily accessible and patient…”
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Hyperspectral retinal imaging as a biomarker for Alzheimer’s disease by Thach, Michelle, de Ruyter, Frederique J. Hart, Curro‐Tafili, Katie R., van de Giessen, Elsmarieke, Collij, Lyduine E., den Braber, Anouk, Tan, H. Stevie, Visser, Pieter Jelle, Verbraak, Frank D., Osseiran, Sam, Grondin, Jean‐Sébastien, Orellina, Julie Antonelle, Campbell, Shannon, Chevrefils, Claudia, Sylvestre, Jean‐Philippe, Bouwman, Femke H.

“…Background Currently, Alzheimer’s disease (AD) diagnosis relies on biomarkers that are either expensive, invasive or time‐consuming. The retina is easily…”
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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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