Syndromes with congenital brittle bones von Plotkin, Horacio

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Dual inhibition of renin-angiotensin-aldosterone system and endothelin-1 in treatment of chronic kidney disease von Komers, Radko, Plotkin, Horacio

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Type V Osteogenesis Imperfecta: A New Form of Brittle Bone Disease von Glorieux, Francis H., Rauch, Frank, Plotkin, Horacio, Ward, Leanne, Travers, Rose, Roughley, Peter, Lalic, Ljiljana, Glorieux, Delphine F., Fassier, François, Bishop, Nicholas J.

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Osteogenesis Imperfecta Types I, III, and IV: Effect of Pamidronate Therapy on Bone and Mineral Metabolism von Rauch, Frank, Plotkin, Horacio, Travers, Rose, Zeitlin, Leonid, Glorieux, Francis H.

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Open-Label Fosmetpantotenate, a Phosphopantothenate Replacement Therapy in a Single Patient with Atypical PKAN von Kleopa, Kleopas A., Plotkin, Horacio, Beconi, Maria, Konstantopoulos, Kostas, Ormiston, Annita, Kkolou, Elena, Tanteles, George A., Christou, Yiolanda, Marshall, Randall D.

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Surgical treatment of osteogenesis imperfecta: current concepts von Esposito, Paul, Plotkin, Horacio

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Nedosiran population pharmacokinetic and pharmacodynamic modelling and simulation to guide clinical development and dose selection in patients with primary hyperoxaluria type 1 von Zhang, Steven, Amrite, Aniruddha, Tan, Beesan, Jamsen, Kris, Pradhan, Sudeep, Choy, Steve, Plotkin, Horacio

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Genotype/Phenotype Relationship: Lessons From 137 Patients With PMM2-CDG von Pajusalu, Sander, Vals, Mari-Anne, Serrano, Mercedes, Witters, Peter, Cechova, Anna, Honzik, Tomas, Edmondson, Andrew C, Ficicioglu, Can, Barone, Rita, De Lonlay, Pascale, Berat, Claire-Marine, Vuillaumier-Barrot, Sandrine, Lam, Christina, Patterson, Marc C, Janssen, Mirian C.H, Martins, Esmeralda, Quelhas, Dulce, Sykut-Cegielska, Jolanta, Mousa, Jehan, Urreizti, Roser, Mcwilliams, Peter, Vernhes, Frederique, Plotkin, Horacio, Morava, Eva, Ounap, Katrin

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Risedronate in children with osteogenesis imperfecta: a randomised, double-blind, placebo-controlled trial von 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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The effects of intravenous pamidronate on the bone tissue of children and adolescents with osteogenesis imperfecta von Rauch, Frank, Travers, Rose, Plotkin, Horacio, Glorieux, Francis H

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Coalescing expansile skeletal disease: Delineation of an extraordinary osteopathy involving the IFITM5 mutation of osteogenesis imperfecta type V von Whyte, Michael P., Aronson, James, McAlister, William H., Weinstein, Robert S., Wenkert, Deborah, Clements, Karen L., Gottesman, Gary S., Madson, Katherine L., Stolina, Marina, Bijanki, Vinieth N., Plotkin, Horacio, Huskey, Margaret, Duan, Shenghui, Mumm, Steven

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The relationship between fractures and DXA measures of BMD in the distal femur of children and adolescents with cerebral palsy or muscular dystrophy von Henderson, Richard C, Berglund, Lisa M, May, Ryan, Zemel, Babette S, Grossberg, Richard I, Johnson, Julie, Plotkin, Horacio, Stevenson, Richard D, Szalay, Elizabeth, Wong, Brenda, Kecskemethy, Heidi H, Harcke, H Theodore

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Genotype/Phenotype Relationship: Lessons From 137 Patients With PMM2‐CDG von Pajusalu, Sander, Vals, Mari-Anne, Serrano, Mercedes, Witters, Peter, Cechova, Anna, Honzik, Tomáš, Edmondson, Andrew C., Ficicioglu, Can, Barone, Rita, De Lonlay, Pascale, Bérat, Claire-Marine, Vuillaumier-Barrot, Sandrine, Lam, Christina, Patterson, Marc C., Janssen, Mirian C. H., Martins, Esmeralda, Quelhas, Dulce, Sykut-Cegielska, Jolanta, Mousa, Jehan, Urreizti, Roser, McWilliams, Peter, Vernhes, Frederique, Plotkin, Horacio, Morava, Eva, Õunap, Katrin

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Should patients with Phosphomannomutase 2-CDG (PMM2-CDG) be screened for adrenal insufficiency? von Cechova, Anna, Honzik, Tomas, Edmondson, Andrew C, Ficicioglu, Can, Serrano, Mercedes, Barone, Rita, De Lonlay, Pascale, Schiff, Manuel, Witters, Peter, Lam, Christina, Patterson, Marc, Janssen, Mirian C.H, Correia, Joana, Quelhas, Dulce, Sykut-Cegielska, Jolanta, Plotkin, Horacio, Morava, Eva, Sarafoglou, Kyriakie

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Open-label extension study following the Late-Onset Treatment Study (LOTS) of alglucosidase alfa von van der Ploeg, Ans T., Barohn, Richard, Carlson, Lisa, Charrow, Joel, Clemens, Paula R., Hopkin, Robert J., Kishnani, Priya S., Laforêt, Pascal, Morgan, Claire, Nations, Sharon, Pestronk, Alan, Plotkin, Horacio, Rosenbloom, Barry E., Sims, Katherine B., Tsao, Elisa

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Should patients with Phosphomannomutase 2-CDG (PMM2-CDG) be screened for adrenal insufficiency? von Čechová, Anna, Honzík, Tomáš, Edmondson, Andrew C., Ficicioglu, Can, Serrano, Mercedes, Barone, Rita, De Lonlay, Pascale, Schiff, Manuel, Witters, Peter, Lam, Christina, Patterson, Marc, Janssen, Mirian C.H., Correia, Joana, Quelhas, Dulce, Sykut-Cegielska, Jolanta, Plotkin, Horacio, Morava, Eva, Sarafoglou, Kyriakie

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Effect of Pamidronate Treatment in Children with Polyostotic Fibrous Dysplasia of Bone von Plotkin, Horacio, Rauch, Frank, Zeitlin, Leonid, Munns, Craig, Travers, Rose, Glorieux, Francis H.

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Bone Mass, Size, and Density in Children and Adolescents With Osteogenesis Imperfecta: Effect of Intravenous Pamidronate Therapy von Rauch, Frank, Plotkin, Horacio, Zeitlin, Leonid, Glorieux, Francis H

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Cyclic Administration of Pamidronate in Children with Severe Osteogenesis Imperfecta von Glorieux, Francis H, Bishop, Nicholas J, Plotkin, Horacio, Chabot, Gilles, Lanoue, Ginette, Travers, Rose

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Height and Weight Development During Four Years of Therapy With Cyclical Intravenous Pamidronate in Children and Adolescents With Osteogenesis Imperfecta Types I, III, and IV von Zeitlin, Leonid, Rauch, Frank, Plotkin, Horacio, Glorieux, Francis H

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