Caffey disease: an unlikely collagenopathy

Por Glorieux, Francis H.
Publicado em 2005

Vitamin D/dietary calcium deficiency rickets and pseudo-vitamin D deficiency rickets

Por Glorieux, Francis H, Pettifor, John M
Publicado em 2014

The effects of intravenous pamidronate on the bone tissue of children and adolescents with osteogenesis imperfecta

Por Rauch, Frank, Travers, Rose, Plotkin, Horacio, Glorieux, Francis H.
Publicado em 2002

Genotype–phenotype correlations in nonlethal osteogenesis imperfecta caused by mutations in the helical domain of collagen type I

Por Rauch, Frank, Lalic, Liljana, Roughley, Peter, Glorieux, Francis H
Publicado em 2010

Genotype-Phenotype Correlations in Autosomal Dominant Osteogenesis Imperfecta

Por Ben Amor, I. Mouna, Glorieux, Francis H., Rauch, Frank
Publicado em 2011

Transport and metabolism of sarcosine in hypersarcosinemic and normal phenotypes

Por Glorieux, Francis H., Scriver, Charles R., Delvin, Edgard, Mohyuddin, Fazl
Publicado em 1971

Early diagnosis in Niemann-Pick disease

Por Toussi, Tahmouresse, Delvin, Edgar E., Glorieux, Francis H., Goldman, Hy
Publicado em 1974

Bone-Specific Expression of the Alpha Chain of the Nascent Polypeptide-Associated Complex, a Coactivator Potentiating c-Jun-Mediated Transcription

Por Moreau, Alain, Yotov, Wagner V., Glorieux, Francis H., St-Arnaud, René
Publicado em 1998

From pediatric to adult care: strategic evaluation of a transition program for patients with osteogenesis imperfecta

Por Dogba, Maman Joyce, Rauch, Frank, Wong, Trudy, Ruck, Joanne, Glorieux, Francis H, Bedos, Christophe
Publicado no BMC Health Serv Res (2014)

Spondyloepimetaphysial Dysplasia with Joint Laxity in Three Siblings with B3GALT6 Mutations

Por Trejo, Pamela, Rauch, Frank, Glorieux, Francis H., Ouellet, Jean, Benaroch, Thierry, Campeau, Philippe M.
Publicado no Mol Syndromol (2017)

The impact of severe osteogenesis imperfecta on the lives of young patients and their parents – a qualitative analysis

Por Dogba, Maman Joyce, Bedos, Christophe, Durigova, Michaela, Montpetit, Kathleen, Wong, Trudy, Glorieux, Francis H, Rauch, Frank
Publicado em 2013

Hypermineralization and high osteocyte lacunar density in osteogenesis imperfecta type V bone indicate exuberant primary bone formation

Por Blouin, Stéphane, Fratzl-Zelman, Nadja, Glorieux, Francis H, Roschger, Paul, Klaushofer, Klaus, Marini, Joan C., Rauch, Frank
Publicado no J Bone Miner Res (2017)

Cole-Carpenter Syndrome Is Caused by a Heterozygous Missense Mutation in P4HB

Por Rauch, Frank, Fahiminiya, Somayyeh, Majewski, Jacek, Carrot-Zhang, Jian, Boudko, Sergei, Glorieux, Francis, Mort, John S., Bächinger, Hans-Peter, Moffatt, Pierre
Publicado no Am J Hum Genet (2015)

Involving Families with Osteogenesis Imperfecta in Health Service Research: Joint Development of the OI/ECE Questionnaire

Por Dogba, Maman Joyce, Dahan-Oliel, Noémi, Snider, Laurie, Glorieux, Francis H., Durigova, Michaela, Palomo, Telma, Cordey, Michel, Bédard, Marie-Hélène, Bedos, Christophe, Rauch, Frank
Publicado no PLoS One (2016)

A Novel IFITM5 Mutation in Severe Atypical Osteogenesis Imperfecta Type VI Impairs Osteoblast Production of Pigment Epithelium-Derived Factor

Por Farber, Charles R, Reich, Adi, Barnes, Aileen M, Becerra, Patricia, Rauch, Frank, Cabral, Wayne A, Bae, Alison, Quinlan, Aaron, Glorieux, Francis H, Clemens, Thomas L, Marini, Joan C
Publicado no J Bone Miner Res (2014)

Standardized Nomenclature, Symbols, and Units for Bone Histomorphometry: A 2012 Update of the Report of the ASBMR Histomorphometry Nomenclature Committee

Por Dempster, David W, Compston, Juliet E, Drezner, Marc K, Glorieux, Francis H, Kanis, John A, Malluche, Hartmut, Meunier, Pierre J, Ott, Susan M, Recker, Robert R, Parfitt, A Michael
Publicado em 2013

Homozygosity for Frameshift Mutations in XYLT2 Result in a Spondylo-Ocular Syndrome with Bone Fragility, Cataracts, and Hearing Defects

Por Munns, Craig F., Fahiminiya, Somayyeh, Poudel, Nabin, Munteanu, Maria Cristina, Majewski, Jacek, Sillence, David O., Metcalf, Jordan P., Biggin, Andrew, Glorieux, Francis, Fassier, François, Rauch, Frank, Hinsdale, Myron E.
Publicado no Am J Hum Genet (2015)

Prolonged Correction of Serum Phosphorus in Adults With X-Linked Hypophosphatemia Using Monthly Doses of KRN23

Por Imel, Erik A., Zhang, Xiaoping, Ruppe, Mary D., Weber, Thomas J., Klausner, Mark A., Ito, Takahiro, Vergeire, Maria, Humphrey, Jeffrey S., Glorieux, Francis H., Portale, Anthony A., Insogna, Karl, Peacock, Munro, Carpenter, Thomas O.
Publicado no J Clin Endocrinol Metab (2015)

Effect of four monthly doses of a human monoclonal anti-FGF23 antibody (KRN23) on quality of life in X-linked hypophosphatemia

Por Ruppe, Mary D., Zhang, Xiaoping, Imel, Erik A., Weber, Thomas J., Klausner, Mark A., Ito, Takahiro, Vergeire, Maria, Humphrey, Jeffrey S., Glorieux, Francis H., Portale, Anthony A., Insogna, Karl, Peacock, Munro, Carpenter, Thomas O.
Publicado no Bone Rep (2016)

Pharmacokinetics and pharmacodynamics of a human monoclonal anti‐FGF23 antibody (KRN23) in the first multiple ascending‐dose trial treating adults with X‐linked hypophosphatemia...

Por Zhang, Xiaoping, Imel, Erik A., Ruppe, Mary D., Weber, Thomas J., Klausner, Mark A., Ito, Takahiro, Vergeire, Maria, Humphrey, Jeffrey, Glorieux, Francis H., Portale, Anthony A., Insogna, Karl, Carpenter, Thomas O., Peacock, Munro
Publicado no J Clin Pharmacol (2015)