Прогресивна окоштавајућа фибродисплазија (Serbian Wikipedia)

Analysis of information sources in references of the Wikipedia article "Прогресивна окоштавајућа фибродисплазија" in Serbian language version.

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20nih.gov

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16doi.org

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3web.archive.org

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3semanticscholar.org

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2archive.org

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2harvard.edu

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1nationalgeographic.com

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1proquest.com

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1sciencedaily.com

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1rarediseases.org

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1aaos.org

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1d3n8a8pro7vhmx.cloudfront.net

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1muttermuseum.org

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1philly.com

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1ifopa.org

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1inquirer.com

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1worldcat.org

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aaos.org

orthoinfo.aaos.org

American Academy of Orthopaedic Surgeons (мај 2006). „Fibrodysplasia Ossificans Progressiva (FOP)”. orthoinfo.aaos.org. Архивирано из оригинала 21. 6. 2012. г. Приступљено 2011-10-07.

archive.org

Kierszenbaum, Abraham (2002). Histology and cell biology. New York: Mosby. ISBN 978-0-323-01639-1.
Newton, M.C.; Allen, P.W.; Ryan, D.C. (фебруар 1990). „Fibrodysplasia Ossificans Progressiva”. British Journal of Anaesthesia. 64 (2): 246—250. PMID 2317429. doi:10.1093/bja/64.2.246 .

d3n8a8pro7vhmx.cloudfront.net

„The Medical Management of Fibrodysplasia Ossificans Progressiva: Current Treatment Considerations” (PDF). International Fibrodysplasia Ossificans Progressiva Association. јануар 2020.

doi.org

Kaplan, Frederick S.; Shen, Qi; Lounev, Vitali; Seemann, Petra; Groppe, Jay; Katagiri, Takenobu; Pignolo, Robert J.; Shore, Eileen M. (2008). „Skeletal metamorphosis in fibrodysplasia ossificans progressiva (FOP)”. Journal of Bone and Mineral Metabolism. 26 (6): 521—530. PMC 3620015 . PMID 18979151. doi:10.1007/s00774-008-0879-8.
Kaplan, Frederick S.; Le Merrer, Martine; Glaser, David L.; Pignolo, Robert J.; Goldsby, Robert E.; Kitterman, Joseph A.; Groppe, Jay; Shore, Eileen M. (март 2008). „Fibrodysplasia ossificans progressiva”. Best Practice & Research Clinical Rheumatology. 22 (1): 191—205. PMC 2424023 . PMID 18328989. doi:10.1016/j.berh.2007.11.007.
Saleh, Mohammed; Commandeur, Joost; Bocciardi, Renata; Kinabo, Grace; Hamel, Ben (2015). „Fibrodysplasia ossificans progressiva with minor unilateral hallux anomaly in a sporadic case from Northern Tanzania with the common ACVR1c.617G>A mutation”. Pan African Medical Journal. 22: 299. PMC 4769042 . PMID 26966495. doi:10.11604/pamj.2015.22.299.8032.
Shore, Eileen M; Xu, Meiqi; Feldman, George J; Fenstermacher, David A; Cho, Tae-Joon; Choi, In Ho; Connor, J Michael; Delai, Patricia; Glaser, David L; LeMerrer, Martine; Morhart, Rolf; Rogers, John G; Smith, Roger; Triffitt, James T; Urtizberea, J Andoni; Zasloff, Michael; Brown, Matthew A; Kaplan, Frederick S (мај 2006). „A recurrent mutation in the BMP type I receptor ACVR1 causes inherited and sporadic fibrodysplasia ossificans progressiva”. Nature Genetics. 38 (5): 525—527. PMID 16642017. S2CID 41579747. doi:10.1038/ng1783.
Hatsell, Sarah J.; Idone, Vincent; Wolken, Dana M. Alessi; Huang, Lily; Kim, Hyon J.; Wang, Lili; Wen, Xialing; Nannuru, Kalyan C.; Jimenez, Johanna; Xie, Liqin; Das, Nanditha; Makhoul, Genevieve; Chernomorsky, Rostislav; D’Ambrosio, David; Corpina, Richard A.; Schoenherr, Christopher J.; Feeley, Kieran; Yu, Paul B.; Yancopoulos, George D.; Murphy, Andrew J.; Economides, Aris N. (2. 9. 2015). „ACVR1 R206H receptor mutation causes fibrodysplasia ossificans progressiva by imparting responsiveness to activin A”. Science Translational Medicine. 7 (303): 303ra137. PMC 6164166 . PMID 26333933. doi:10.1126/scitranslmed.aac4358.
van Dinther, Maarten; Visser, Nils; de Gorter, David JJ; Doorn, Joyce; Goumans, Marie-José; de Boer, Jan; ten Dijke, Peter (23. 11. 2009). „ALK2 R206H Mutation Linked to Fibrodysplasia Ossificans Progressiva Confers Constitutive Activity to the BMP Type I Receptor and Sensitizes Mesenchymal Cells to BMP-Induced Osteoblast Differentiation and Bone Formation”. Journal of Bone and Mineral Research. 25 (6): 091211115834058—35. PMID 19929436. S2CID 207269687. doi:10.1359/jbmr.091110 .
Shore, Eileen M.; Kaplan, Frederick S. (2008). „Insights from a Rare Genetic Disorder of Extra-Skeletal Bone Formation, Fibrodysplasia Ossificans Progressiva (FOP)”. Bone. 43 (3): 427—443. PMC 2601573 . PMID 18590993. doi:10.1016/j.bone.2008.05.013.
Petrie, KA; Lee, WH; Bullock, AN; Pointon, JJ; Smith, R; Russell, RG; Brown, MA; Wordsworth, BP; Triffitt, JT (2009). „Novel mutations in ACVR1 result in atypical features in two fibrodysplasia ossificans progressiva patients.”. PLOS ONE. 4 (3): e5005. Bibcode:2009PLoSO...4.5005P. PMC 2658887 . PMID 19330033. doi:10.1371/journal.pone.0005005 .
Kitoh, Hiroshi; Achiwa, Masataka; Kaneko, Hiroshi; Mishima, Kenichi; Matsushita, Masaki; Kadono, Izumi; Horowitz, John D; Sallustio, Benedetta C; Ohno, Kinji; Ishiguro, Naoki (2013). „Perhexiline maleate in the treatment of fibrodysplasia ossificans progressiva: an open-labeled clinical trial”. Orphanet Journal of Rare Diseases. 8 (1): 163. PMC 4015865 . PMID 24131551. doi:10.1186/1750-1172-8-163.
Martelli, Anderson; Santos, Arnaldo Rodrigues (3. 7. 2014). „Cellular and morphological aspects of fibrodysplasia ossificans progressiva: Lessons of formation, repair, and bone bioengineering”. Organogenesis. 10 (3): 303—311. PMC 4750545 . PMID 25482313. doi:10.4161/org.29206.
Newton, M.C.; Allen, P.W.; Ryan, D.C. (фебруар 1990). „Fibrodysplasia Ossificans Progressiva”. British Journal of Anaesthesia. 64 (2): 246—250. PMID 2317429. doi:10.1093/bja/64.2.246 .
Kaplan, F. S. (2013). The skeleton in the closet. Gene, 528(1), 7–11. https://doi.org/10.1016/j.gene.2013.06.022
Kitoh, Hiroshi; Achiwa, Masataka; Kaneko, Hiroshi; Mishima, Kenichi; Matsushita, Masaki; Kadono, Izumi; Horowitz, John D; Sallustio, Benedetta C; Ohno, Kinji; Ishiguro, Naoki (2013). „Perhexiline maleate in the treatment of fibrodysplasia ossificans progressiva: an open-labeled clinical trial”. Orphanet Journal of Rare Diseases. 8 (1): 163. PMC 4015865 . PMID 24131551. doi:10.1186/1750-1172-8-163.
J. W. Lowery; V. Rosen (2012). „Allele-Specific RNA Interference in FOP Silencing the FOP gene”. Gene Therapy. 19 (7): 701—702. PMID 22130446. S2CID 24990800. doi:10.1038/gt.2011.190 .
Lees-Shepard, John B.; Yamamoto, Masakazu; Biswas, Arpita A.; Stoessel, Sean J.; Nicholas, Sarah-Anne E.; Cogswell, Cathy A.; Devarakonda, Parvathi M.; Schneider, Michael J.; Cummins, Samantha M.; Legendre, Nicholas P.; Yamamoto, Shoko; Kaartinen, Vesa; Hunter, Jeffrey W.; Goldhamer, David J. (децембар 2018). „Activin-dependent signaling in fibro/adipogenic progenitors causes fibrodysplasia ossificans progressiva”. Nature Communications. 9 (1): 471. Bibcode:2018NatCo...9..471L. PMC 5797136 . PMID 29396429. doi:10.1038/s41467-018-02872-2.
Williams, Eleanor; Bagarova, Jana; Kerr, Georgina; Xia, Dong-Dong; Place, Elsie S.; Dey, Devaveena; Shen, Yue; Bocobo, Geoffrey A.; Mohedas, Agustin H.; Huang, Xiuli; Sanderson, Philip E. (2021). „Saracatinib is an efficacious clinical candidate for fibrodysplasia ossificans progressiva”. JCI Insight. 6 (8): e95042. ISSN 2379-3708. PMC 8119212 . PMID 33705358. doi:10.1172/jci.insight.95042.

harvard.edu

adsabs.harvard.edu

Petrie, KA; Lee, WH; Bullock, AN; Pointon, JJ; Smith, R; Russell, RG; Brown, MA; Wordsworth, BP; Triffitt, JT (2009). „Novel mutations in ACVR1 result in atypical features in two fibrodysplasia ossificans progressiva patients.”. PLOS ONE. 4 (3): e5005. Bibcode:2009PLoSO...4.5005P. PMC 2658887 . PMID 19330033. doi:10.1371/journal.pone.0005005 .
Lees-Shepard, John B.; Yamamoto, Masakazu; Biswas, Arpita A.; Stoessel, Sean J.; Nicholas, Sarah-Anne E.; Cogswell, Cathy A.; Devarakonda, Parvathi M.; Schneider, Michael J.; Cummins, Samantha M.; Legendre, Nicholas P.; Yamamoto, Shoko; Kaartinen, Vesa; Hunter, Jeffrey W.; Goldhamer, David J. (децембар 2018). „Activin-dependent signaling in fibro/adipogenic progenitors causes fibrodysplasia ossificans progressiva”. Nature Communications. 9 (1): 471. Bibcode:2018NatCo...9..471L. PMC 5797136 . PMID 29396429. doi:10.1038/s41467-018-02872-2.

ifopa.org

„Regeneron Shares Updates on its Ongoing FOP Research Program”. International Fibrodysplasia Ossificans Progressiva Association. 9. 3. 2017.

inquirer.com

McCullough, Marie (28. 2. 2019). „Therapies in sight for FOP, a disease that turns muscle to bone”. The Philadelphia Inquirer.

muttermuseum.org

„Mütter Museum Reveals New Exhibit: Philadelphia Woman's Skeleton With Rare Bone Disease”. Mütter Museum. 5. 3. 2019. Архивирано из оригинала 28. 8. 2021. г. Приступљено 7. 3. 2020.

nationalgeographic.com

Pinkowski, Jen (1. 3. 2019). „Here's what happens when your body tissues turn to bone”. National Geographic. Архивирано из оригинала 3. 3. 2019. г.

nih.gov

ncbi.nlm.nih.gov

Kaplan, Frederick S.; Shen, Qi; Lounev, Vitali; Seemann, Petra; Groppe, Jay; Katagiri, Takenobu; Pignolo, Robert J.; Shore, Eileen M. (2008). „Skeletal metamorphosis in fibrodysplasia ossificans progressiva (FOP)”. Journal of Bone and Mineral Metabolism. 26 (6): 521—530. PMC 3620015 . PMID 18979151. doi:10.1007/s00774-008-0879-8.
Kaplan, Frederick S.; Le Merrer, Martine; Glaser, David L.; Pignolo, Robert J.; Goldsby, Robert E.; Kitterman, Joseph A.; Groppe, Jay; Shore, Eileen M. (март 2008). „Fibrodysplasia ossificans progressiva”. Best Practice & Research Clinical Rheumatology. 22 (1): 191—205. PMC 2424023 . PMID 18328989. doi:10.1016/j.berh.2007.11.007.
Obamuyide, HA; Ogunlade, SO (март 2015). „A Tumour for which Surgery will do more harm than good: A Case Report of Fibrodysplasia Ossificans Progressiva.”. The Nigerian Postgraduate Medical Journal. 22 (1): 83—8. PMID 25875418. ProQuest 1850178336.
Saleh, Mohammed; Commandeur, Joost; Bocciardi, Renata; Kinabo, Grace; Hamel, Ben (2015). „Fibrodysplasia ossificans progressiva with minor unilateral hallux anomaly in a sporadic case from Northern Tanzania with the common ACVR1c.617G>A mutation”. Pan African Medical Journal. 22: 299. PMC 4769042 . PMID 26966495. doi:10.11604/pamj.2015.22.299.8032.
Shore, Eileen M; Xu, Meiqi; Feldman, George J; Fenstermacher, David A; Cho, Tae-Joon; Choi, In Ho; Connor, J Michael; Delai, Patricia; Glaser, David L; LeMerrer, Martine; Morhart, Rolf; Rogers, John G; Smith, Roger; Triffitt, James T; Urtizberea, J Andoni; Zasloff, Michael; Brown, Matthew A; Kaplan, Frederick S (мај 2006). „A recurrent mutation in the BMP type I receptor ACVR1 causes inherited and sporadic fibrodysplasia ossificans progressiva”. Nature Genetics. 38 (5): 525—527. PMID 16642017. S2CID 41579747. doi:10.1038/ng1783.
Hatsell, Sarah J.; Idone, Vincent; Wolken, Dana M. Alessi; Huang, Lily; Kim, Hyon J.; Wang, Lili; Wen, Xialing; Nannuru, Kalyan C.; Jimenez, Johanna; Xie, Liqin; Das, Nanditha; Makhoul, Genevieve; Chernomorsky, Rostislav; D’Ambrosio, David; Corpina, Richard A.; Schoenherr, Christopher J.; Feeley, Kieran; Yu, Paul B.; Yancopoulos, George D.; Murphy, Andrew J.; Economides, Aris N. (2. 9. 2015). „ACVR1 R206H receptor mutation causes fibrodysplasia ossificans progressiva by imparting responsiveness to activin A”. Science Translational Medicine. 7 (303): 303ra137. PMC 6164166 . PMID 26333933. doi:10.1126/scitranslmed.aac4358.
van Dinther, Maarten; Visser, Nils; de Gorter, David JJ; Doorn, Joyce; Goumans, Marie-José; de Boer, Jan; ten Dijke, Peter (23. 11. 2009). „ALK2 R206H Mutation Linked to Fibrodysplasia Ossificans Progressiva Confers Constitutive Activity to the BMP Type I Receptor and Sensitizes Mesenchymal Cells to BMP-Induced Osteoblast Differentiation and Bone Formation”. Journal of Bone and Mineral Research. 25 (6): 091211115834058—35. PMID 19929436. S2CID 207269687. doi:10.1359/jbmr.091110 .
Shore, Eileen M.; Kaplan, Frederick S. (2008). „Insights from a Rare Genetic Disorder of Extra-Skeletal Bone Formation, Fibrodysplasia Ossificans Progressiva (FOP)”. Bone. 43 (3): 427—443. PMC 2601573 . PMID 18590993. doi:10.1016/j.bone.2008.05.013.
Petrie, KA; Lee, WH; Bullock, AN; Pointon, JJ; Smith, R; Russell, RG; Brown, MA; Wordsworth, BP; Triffitt, JT (2009). „Novel mutations in ACVR1 result in atypical features in two fibrodysplasia ossificans progressiva patients.”. PLOS ONE. 4 (3): e5005. Bibcode:2009PLoSO...4.5005P. PMC 2658887 . PMID 19330033. doi:10.1371/journal.pone.0005005 .
Kitoh, Hiroshi; Achiwa, Masataka; Kaneko, Hiroshi; Mishima, Kenichi; Matsushita, Masaki; Kadono, Izumi; Horowitz, John D; Sallustio, Benedetta C; Ohno, Kinji; Ishiguro, Naoki (2013). „Perhexiline maleate in the treatment of fibrodysplasia ossificans progressiva: an open-labeled clinical trial”. Orphanet Journal of Rare Diseases. 8 (1): 163. PMC 4015865 . PMID 24131551. doi:10.1186/1750-1172-8-163.
Martelli, Anderson; Santos, Arnaldo Rodrigues (3. 7. 2014). „Cellular and morphological aspects of fibrodysplasia ossificans progressiva: Lessons of formation, repair, and bone bioengineering”. Organogenesis. 10 (3): 303—311. PMC 4750545 . PMID 25482313. doi:10.4161/org.29206.
Newton, M.C.; Allen, P.W.; Ryan, D.C. (фебруар 1990). „Fibrodysplasia Ossificans Progressiva”. British Journal of Anaesthesia. 64 (2): 246—250. PMID 2317429. doi:10.1093/bja/64.2.246 .
Kitoh, Hiroshi; Achiwa, Masataka; Kaneko, Hiroshi; Mishima, Kenichi; Matsushita, Masaki; Kadono, Izumi; Horowitz, John D; Sallustio, Benedetta C; Ohno, Kinji; Ishiguro, Naoki (2013). „Perhexiline maleate in the treatment of fibrodysplasia ossificans progressiva: an open-labeled clinical trial”. Orphanet Journal of Rare Diseases. 8 (1): 163. PMC 4015865 . PMID 24131551. doi:10.1186/1750-1172-8-163.
J. W. Lowery; V. Rosen (2012). „Allele-Specific RNA Interference in FOP Silencing the FOP gene”. Gene Therapy. 19 (7): 701—702. PMID 22130446. S2CID 24990800. doi:10.1038/gt.2011.190 .
Lees-Shepard, John B.; Yamamoto, Masakazu; Biswas, Arpita A.; Stoessel, Sean J.; Nicholas, Sarah-Anne E.; Cogswell, Cathy A.; Devarakonda, Parvathi M.; Schneider, Michael J.; Cummins, Samantha M.; Legendre, Nicholas P.; Yamamoto, Shoko; Kaartinen, Vesa; Hunter, Jeffrey W.; Goldhamer, David J. (децембар 2018). „Activin-dependent signaling in fibro/adipogenic progenitors causes fibrodysplasia ossificans progressiva”. Nature Communications. 9 (1): 471. Bibcode:2018NatCo...9..471L. PMC 5797136 . PMID 29396429. doi:10.1038/s41467-018-02872-2.
Williams, Eleanor; Bagarova, Jana; Kerr, Georgina; Xia, Dong-Dong; Place, Elsie S.; Dey, Devaveena; Shen, Yue; Bocobo, Geoffrey A.; Mohedas, Agustin H.; Huang, Xiuli; Sanderson, Philip E. (2021). „Saracatinib is an efficacious clinical candidate for fibrodysplasia ossificans progressiva”. JCI Insight. 6 (8): e95042. ISSN 2379-3708. PMC 8119212 . PMID 33705358. doi:10.1172/jci.insight.95042.

ghr.nlm.nih.gov

„Fibrodysplasia ossificans progressiva”. Lister Hill National Center for Biomedical Communications. Приступљено 2013-12-12.
"AVCR1", Genetics Home Reference, U.S. National Library of Medicine, August 2007. Accessed February 18, 2014.
"Fibrodysplasia ossificans progressiva", Genetics Home Reference, U.S. National Library of Medicine, August 2007. Accessed February 18, 2014.
"Fibrodysplasia ossificans progressiva", Genetics Home Reference, U.S. National Library of Medicine, August 2007. Accessed February 18, 2014.

philly.com

McCullough, Marie (28. 2. 2019). „New Mutter Museum exhibit grants final wish for woman who turned to bone”. The Philadelphia Inquirer. Приступљено 28. 2. 2019.

proquest.com

search.proquest.com

Obamuyide, HA; Ogunlade, SO (март 2015). „A Tumour for which Surgery will do more harm than good: A Case Report of Fibrodysplasia Ossificans Progressiva.”. The Nigerian Postgraduate Medical Journal. 22 (1): 83—8. PMID 25875418. ProQuest 1850178336.

rarediseases.org

„Fibrodysplasia Ossificans Progressiva”. август 2020.

sciencedaily.com

„Penn Researchers Discover Gene That Creates Second Skeleton” (Саопштење). University of Pennsylvania School of Medicine. 23. 4. 2006.

semanticscholar.org

api.semanticscholar.org

Shore, Eileen M; Xu, Meiqi; Feldman, George J; Fenstermacher, David A; Cho, Tae-Joon; Choi, In Ho; Connor, J Michael; Delai, Patricia; Glaser, David L; LeMerrer, Martine; Morhart, Rolf; Rogers, John G; Smith, Roger; Triffitt, James T; Urtizberea, J Andoni; Zasloff, Michael; Brown, Matthew A; Kaplan, Frederick S (мај 2006). „A recurrent mutation in the BMP type I receptor ACVR1 causes inherited and sporadic fibrodysplasia ossificans progressiva”. Nature Genetics. 38 (5): 525—527. PMID 16642017. S2CID 41579747. doi:10.1038/ng1783.
van Dinther, Maarten; Visser, Nils; de Gorter, David JJ; Doorn, Joyce; Goumans, Marie-José; de Boer, Jan; ten Dijke, Peter (23. 11. 2009). „ALK2 R206H Mutation Linked to Fibrodysplasia Ossificans Progressiva Confers Constitutive Activity to the BMP Type I Receptor and Sensitizes Mesenchymal Cells to BMP-Induced Osteoblast Differentiation and Bone Formation”. Journal of Bone and Mineral Research. 25 (6): 091211115834058—35. PMID 19929436. S2CID 207269687. doi:10.1359/jbmr.091110 .
J. W. Lowery; V. Rosen (2012). „Allele-Specific RNA Interference in FOP Silencing the FOP gene”. Gene Therapy. 19 (7): 701—702. PMID 22130446. S2CID 24990800. doi:10.1038/gt.2011.190 .

web.archive.org

Pinkowski, Jen (1. 3. 2019). „Here's what happens when your body tissues turn to bone”. National Geographic. Архивирано из оригинала 3. 3. 2019. г.
American Academy of Orthopaedic Surgeons (мај 2006). „Fibrodysplasia Ossificans Progressiva (FOP)”. orthoinfo.aaos.org. Архивирано из оригинала 21. 6. 2012. г. Приступљено 2011-10-07.
„Mütter Museum Reveals New Exhibit: Philadelphia Woman's Skeleton With Rare Bone Disease”. Mütter Museum. 5. 3. 2019. Архивирано из оригинала 28. 8. 2021. г. Приступљено 7. 3. 2020.

worldcat.org

Williams, Eleanor; Bagarova, Jana; Kerr, Georgina; Xia, Dong-Dong; Place, Elsie S.; Dey, Devaveena; Shen, Yue; Bocobo, Geoffrey A.; Mohedas, Agustin H.; Huang, Xiuli; Sanderson, Philip E. (2021). „Saracatinib is an efficacious clinical candidate for fibrodysplasia ossificans progressiva”. JCI Insight. 6 (8): e95042. ISSN 2379-3708. PMC 8119212 . PMID 33705358. doi:10.1172/jci.insight.95042.