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C Marini

Showing results (541-550 of 852) with videos related to

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The Journal of Clinical Endocrinology and Metabolism|March 22, 2017
Phenotypic Spectrum in Osteogenesis Imperfecta Due to Mutations in TMEM38B: Unraveling a Complex Cellular DefectEmma A Webb, Meena Balasubramanian, Nadja Fratzl-Zelman, et al.
Biomaterials|May 18, 2013
Discarded human kidneys as a source of ECM scaffold for kidney regeneration technologiesGiuseppe Orlando, Christopher Booth, Zhan Wang, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|August 24, 2018
Distinct Clinical and Pathological Features of Melorheostosis Associated With Somatic MAP2K1 MutationsSmita Jha, Nadja Fratzl-Zelman, Paul Roschger, et al.
Pediatric Rheumatology Online Journal|September 9, 2010
The effect of infliximab plus methotrexate on the modulation of inflammatory disease markers in juvenile idiopathic arthritis: analyses from a randomized, placebo-controlled trialSudha Visvanathan, Carrie Wagner, Joseph C Marini, et al.
Nature Communications|July 7, 2016
MBTPS2 mutations cause defective regulated intramembrane proteolysis in X-linked osteogenesis imperfectaUschi Lindert, Wayne A Cabral, Surasawadee Ausavarat, et al.
European Journal of Neurology|July 23, 2020
Deep phenotyping of facioscapulohumeral muscular dystrophy type 2 by magnetic resonance imagingG Giacomucci, M Monforte, J Diaz-Manera, et al.
American Journal of Human Genetics|May 1, 2012
Nitric-oxide supplementation for treatment of long-term complications in argininosuccinic aciduriaSandesh C S Nagamani, Philippe M Campeau, Oleg A Shchelochkov, et al.
Bioanalysis|November 30, 2010
2010 white paper on recent issues in regulated bioanalysis & global harmonization of bioanalytical guidanceNatasha Savoie, Fabio Garofolo, Peter van Amsterdam, et al.
Brain : a Journal of Neurology|May 11, 2006
Periventricular heterotopia: phenotypic heterogeneity and correlation with Filamin A mutationsE Parrini, A Ramazzotti, W B Dobyns, et al.
Neuromuscular Disorders : NMD|February 4, 2026
Refining functional phenotypes in an international cohort of untreated paediatric type 2 and 3 SMA patients using the Revised Hammersmith ScaleE Milev, G Stimpson, D Ramsey, et al.
Pageof 86

Showing results (541-550 of 852) with videos related to

Sort By:
Pageof 86
The Journal of Clinical Endocrinology and Metabolism|March 22, 2017
Phenotypic Spectrum in Osteogenesis Imperfecta Due to Mutations in TMEM38B: Unraveling a Complex Cellular DefectEmma A Webb, Meena Balasubramanian, Nadja Fratzl-Zelman, et al.
Biomaterials|May 18, 2013
Discarded human kidneys as a source of ECM scaffold for kidney regeneration technologiesGiuseppe Orlando, Christopher Booth, Zhan Wang, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|August 24, 2018
Distinct Clinical and Pathological Features of Melorheostosis Associated With Somatic MAP2K1 MutationsSmita Jha, Nadja Fratzl-Zelman, Paul Roschger, et al.
Pediatric Rheumatology Online Journal|September 9, 2010
The effect of infliximab plus methotrexate on the modulation of inflammatory disease markers in juvenile idiopathic arthritis: analyses from a randomized, placebo-controlled trialSudha Visvanathan, Carrie Wagner, Joseph C Marini, et al.
Nature Communications|July 7, 2016
MBTPS2 mutations cause defective regulated intramembrane proteolysis in X-linked osteogenesis imperfectaUschi Lindert, Wayne A Cabral, Surasawadee Ausavarat, et al.
European Journal of Neurology|July 23, 2020
Deep phenotyping of facioscapulohumeral muscular dystrophy type 2 by magnetic resonance imagingG Giacomucci, M Monforte, J Diaz-Manera, et al.
American Journal of Human Genetics|May 1, 2012
Nitric-oxide supplementation for treatment of long-term complications in argininosuccinic aciduriaSandesh C S Nagamani, Philippe M Campeau, Oleg A Shchelochkov, et al.
Bioanalysis|November 30, 2010
2010 white paper on recent issues in regulated bioanalysis & global harmonization of bioanalytical guidanceNatasha Savoie, Fabio Garofolo, Peter van Amsterdam, et al.
Brain : a Journal of Neurology|May 11, 2006
Periventricular heterotopia: phenotypic heterogeneity and correlation with Filamin A mutationsE Parrini, A Ramazzotti, W B Dobyns, et al.
Neuromuscular Disorders : NMD|February 4, 2026
Refining functional phenotypes in an international cohort of untreated paediatric type 2 and 3 SMA patients using the Revised Hammersmith ScaleE Milev, G Stimpson, D Ramsey, et al.
Pageof 86