Torthaí cuardaigh - Nadja Fratzl‐Zelman
- 1 - 13 toradh as 13 á dtaispeáint
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Mineralization density distribution of postmenopausal osteoporotic bone is restored to normal after long-term alendronate treatment: qBEI and sSAXS data from the fracture intervent... de réir Paul Roschger, Assunta Lombardi, Barbara M. Misof, G. Maier, Nadja Fratzl‐Zelman, Peter Fratzl, K. Klaushofer
Foilsithe / Cruthaithe 2009Artigo -
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Hypermineralization and High Osteocyte Lacunar Density in Osteogenesis Imperfecta Type V Bone Indicate Exuberant Primary Bone Formation de réir Stéphane Blouin, Nadja Fratzl‐Zelman, Francis H. Glorieux, Paul Roschger, Klaus Klaushofer, Joan C. Marini, Frank Rauch
Foilsithe / Cruthaithe 2017Artigo -
3
The Regulatory Role of Thyroid Hormones in Bone Cell Growth and Differentiation de réir K. Klaushofer, Franz Varga, Helmut Glantschnig, Nadja Fratzl‐Zelman, Erwin Czerwenka, Hans Jörg Leis, K. Koller, Meinrad Peterlik
Foilsithe / Cruthaithe 1995Revisão -
4
CRTAP deficiency leads to abnormally high bone matrix mineralization in a murine model and in children with osteogenesis imperfecta type VII de réir Nadja Fratzl‐Zelman, Roy Morello, B. Lee, Frank Rauch, Francis H. Glorieux, Barbara M. Misof, K. Klaushofer, Paul Roschger
Foilsithe / Cruthaithe 2009Artigo -
5
Combination of Nanoindentation and Quantitative Backscattered Electron Imaging Revealed Altered Bone Material Properties Associated with Femoral Neck Fragility de réir Nadja Fratzl‐Zelman, Paul Roschger, Aurélien Gourrier, Markus Weber, Barbara M. Misof, N. Loveridge, J. Reeve, K. Klaushofer, Peter Fratzl
Foilsithe / Cruthaithe 2009Artigo -
6
Cardiac, bone and growth plate manifestations in hypocalcemic infants: revealing the hidden body of the vitamin D deficiency iceberg de réir Suma Uday, Nadja Fratzl‐Zelman, Paul Roschger, Klaus Klaushofer, Ashish Chikermane, Vrinda Saraff, T H Tulchinsky, Tom D. Thacher, Tamás Marton, Wolfgang Högler
Foilsithe / Cruthaithe 2018Artigo -
7
Reversible Deterioration in Hypophosphatasia Caused by Renal Failure With Bisphosphonate Treatment de réir Tim Cundy, Toshimi Michigami, Kanako Tachikawa, Michael Dray, John Collins, Eleftherios P. Paschalis, Sonja Gamsjaeger, Andreas Roschger, Nadja Fratzl‐Zelman, Paul Roschger, Klaus Klaushofer
Foilsithe / Cruthaithe 2015Artigo -
8
Evidence for a Role for Nanoporosity and Pyridinoline Content in Human Mild Osteogenesis Imperfecta de réir Eleftherios P. Paschalis, Sonja Gamsjaeger, Nadja Fratzl‐Zelman, Paul Roschger, Admir Mašić, Wolfgang Brozek, N. Hassler, Francis H. Glorieux, Frank Rauch, Klaus Klaushofer, Peter Fratzl
Foilsithe / Cruthaithe 2016Artigo -
9
A neomorphic variant in SP7 alters sequence specificity and causes a high-turnover bone disorder de réir Julian C. Lui, Adalbert Raimann, Hironori Hojo, Lijin Dong, Paul Roschger, Bijal Kikani, Uwe Wintergerst, Nadja Fratzl‐Zelman, Youn Hee Jee, G. Haeusler, Jeffrey Baron
Foilsithe / Cruthaithe 2022Artigo -
10
Bone material quality in transiliac bone biopsies of postmenopausal osteoporotic women after 3 years of strontium ranelate treatment de réir Paul Roschger, I. Manjubala, N. Zoeger, Florian Meirer, Rolf Simon, Chenghao Li, Nadja Fratzl‐Zelman, Barbara M. Misof, Eleftherios P. Paschalis, Christina Streli, Peter Fratzl, Klaus Klaushofer
Foilsithe / Cruthaithe 2009Artigo -
11
Somatic activating mutations in MAP2K1 cause melorheostosis de réir Heeseog Kang, Smita Jha, Zuoming Deng, Nadja Fratzl‐Zelman, Wayne A. Cabral, Aleksandra Ivovic, Françoise Meylan, Eric P. Hanson, Eileen Lange, James D. Katz, Paul Roschger, Klaus Klaushofer, Edward W. Cowen, Richard M. Siegel, Joan C. Marini, Timothy Bhattacharyya
Foilsithe / Cruthaithe 2018Artigo -
12
Somatic <i>SMAD3</i>-activating mutations cause melorheostosis by up-regulating the TGF-β/SMAD pathway de réir Heeseog Kang, Smita Jha, Aleksandra Ivovic, Nadja Fratzl‐Zelman, Zuoming Deng, Apratim Mitra, Wayne A. Cabral, Eric P. Hanson, Eileen Lange, Edward W. Cowen, James D. Katz, Paul Roschger, Klaus Klaushofer, Ryan Dale, Richard M. Siegel, Timothy Bhattacharyya, Joan C. Marini
Foilsithe / Cruthaithe 2020Artigo -
13
COL1 C-propeptide cleavage site mutations cause high bone mass osteogenesis imperfecta de réir Katarina Lindahl, Aileen M. Barnes, Nadja Fratzl‐Zelman, Michael P. Whyte, Theresa E. Hefferan, Elena Makareeva, Marina Brusel, Michael J. Yaszemski, Carl‐Johan Rubin, Andreas Kindmark, Paul Roschger, Klaus Klaushofer, William H. McAlister, Steven Mumm, Sergey Leikin, Efrat Kessler, Adele L. Boskey, Östen Ljunggren, Joan C. Marini
Foilsithe / Cruthaithe 2011Artigo
Uirlisí cuardaigh:
Ábhair a bhaineann le hábhar
Medicine
Internal medicine
Chemistry
Osteoporosis
Endocrinology
Anatomy
Biology
Gene
Genetics
In vitro
Osteoblast
Osteogenesis imperfecta
Type I collagen
Biochemistry
Bone mineral
Bone remodeling
Dentistry
Mineralization (soil science)
Mutation
Pathology
Alkaline phosphatase
Bone density
Cancellous bone
Cancer research
Cell biology
Composite material
Dentinogenesis imperfecta
Enzyme
Materials science
Mathematics