Λευκοδυστροφία (Greek Wikipedia)

Analysis of information sources in references of the Wikipedia article "Λευκοδυστροφία" in Greek language version.

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Global rank Greek rank

34nih.gov

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21doi.org

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3archive.org

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1books.google.com

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1forbes.com

54^th place

103^rd place

1inserm.fr

9,568^th place

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1ulf.org

low place

1zenodo.org

621^st place

1,469^th place

1ed.ac.uk

1,871^st place

2,026^th place

1theglia.org

low place

1ela-asso.com

low place

archive.org

Bonkowsky, Joshua (Aug 24, 2010). «The burden of inherited leukodystrophies in children». Neurology 75 (8): 718–725. doi:10.1212/WNL.0b013e3181eee46b. PMID 20660364. PMC 2931652. https://archive.org/details/sim_neurology_2010-08-24_75_8/page/718.
Yang, Edward; Prabhu, Sanjay P. (March 5, 2014). «Imaging manifestations of the leukodystrophies, inherited disorders of white matter.». Radiologic Clinics of North America 52 (2): 279–319. doi:10.1016/j.rcl.2013.11.008. PMID 24582341. https://archive.org/details/sim_radiologic-clinics-of-north-america_2014-03_52_2/page/279.
Coulter-Mackie, MB; Rip, J; Ludman, MD; Beis, J; Cole, DEC (October 1995). «Metachromatic leucodystrophy (MLD) in a patient with a constitutional ring chromosome 22». Journal of Medical Genetics 32 (10): 787–91. doi:10.1136/jmg.32.10.787. PMID 8558556. PMC 1051701. https://archive.org/details/sim_journal-of-medical-genetics_1995-10_32_10/page/787.

books.google.com

Sachdev, Perminder S.· Keshavan, Matcheri S. (15 Μαρτίου 2010). Secondary Schizophrenia. Cambridge University Press. σελίδες 241–. ISBN 978-0-521-85697-3. Ανακτήθηκε στις 15 Αυγούστου 2011.

doi.org

dx.doi.org

Bonkowsky, Joshua (Aug 24, 2010). «The burden of inherited leukodystrophies in children». Neurology 75 (8): 718–725. doi:10.1212/WNL.0b013e3181eee46b. PMID 20660364. PMC 2931652. https://archive.org/details/sim_neurology_2010-08-24_75_8/page/718.
Graziano, AC; Cardile, V (26 September 2014). «History, genetic, and recent advances on Krabbe disease». Gene 555 (1): 2–13. doi:10.1016/j.gene.2014.09.046. PMID 25260228.
Turon-Vinas, E; Pineda, M; Cusi, V; Lopez-Laso, E; Del Pozo, RL; Gutierez-Solana, LG; Moreno, DC; Sierra-Corcoles, C και άλλοι. (13 July 2014). «Vanishing white matter disease in a Spanish population.». J Cent Nerv Syst Dis. 6: 59–68. doi:10.4137/JCNSD.S13540. PMID 25089094.
Biffi, A.; Aubourg, P.; Cartier, N. (2011). «Gene therapy for leukodystrophies». Human Molecular Genetics 20 (R1): R42–R53. doi:10.1093/hmg/ddr142. PMID 21459776.
Duchange, N; Darguy, S; d'Audiffret, D; Callies, I; Lapointe, AS; Loeve, B; Boespflug-Tanguy, O; Moutel, G (18 September 2014). «Ethical management in the constitution of a European database for leukodystrophies rare diseases.». Eur J Paediatr Neurol. 18 (5): 597–603. doi:10.1016/j.ejpn.2014.04.002. PMID 24786336. http://www.hal.inserm.fr/inserm-00995366/document.
Yang, Edward; Prabhu, Sanjay P. (March 5, 2014). «Imaging manifestations of the leukodystrophies, inherited disorders of white matter.». Radiologic Clinics of North America 52 (2): 279–319. doi:10.1016/j.rcl.2013.11.008. PMID 24582341. https://archive.org/details/sim_radiologic-clinics-of-north-america_2014-03_52_2/page/279.
Lin, Shu-Ting; Ptacek, Louis J.; Fu, Ying-Hui (January 26, 2011). «Adult-Onset Autosomal Dominant Leukodystrophy: Linking Nuclear Envelope to Myelin». The Journal of Neuroscience 31 (4): 1163–1166. doi:10.1523/jneurosci.5994-10.2011. PMID 21273400.
Coulter-Mackie, MB; Rip, J; Ludman, MD; Beis, J; Cole, DEC (October 1995). «Metachromatic leucodystrophy (MLD) in a patient with a constitutional ring chromosome 22». Journal of Medical Genetics 32 (10): 787–91. doi:10.1136/jmg.32.10.787. PMID 8558556. PMC 1051701. https://archive.org/details/sim_journal-of-medical-genetics_1995-10_32_10/page/787.
Sassa, Takayuki; Kihara, Akio (March 22, 2014). «Metabolism of Very Long-Chain Fatty Acids: Genes and Pathophysiology». Biomolecules & Therapeutics 22 (2): 83–92. doi:10.4062/biomolther.2014.017. PMID 24753812.
Barboura, Ilhem; Ferchichi, Salima; Dandana, Azza; Jaidane, Zaineb; Ben Khelifa, Souhaira; Chahed, Hinda; Ben Mansour, Rachida; Chebel, Saber και άλλοι. (2010). «Metachromatic leucodystrophy. Clinical, biological, and therapeutic aspects». Annales de Biologie Clinique 68 (4): 385–91. doi:10.1684/abc.2010.0448. PMID 20650733.
Gieselman, V; Krageloh-Mann, I (2010). «Metachromatic Leukodystrophy - An Update». Neuropediatrics 41 (1): 1–6. doi:10.1055/s-0030-1253412. PMID 20571983.
Szymanska, Krystyna; Lugowska, Agnieszka; Laure-Kamionowska, Milena; Gieruszczak-Bialek, Dorota; Musielak, Malgorzata; Eichler, Sabrina; Giese, Anne-Katrin; Rolfs, Arndt (2012). «Diagnostic difficulties in Krabbe disesase: a report of two cases and review of literature». Folia Neuropathol 50 (4): 346–356. doi:10.5114/fn.2012.32364. PMID 23319190.
Maghazachi, Azzam A. (February 5, 2013). «On the Role of Natural Killer Cells in Neurodegenerative Diseases». Toxins (Basel) 5 (2): 363–375. doi:10.3390/toxins5020363. PMID 23430541.
Berger, J; Forss-Petter, S; Eichler, F.S. (March 2014). «Pathophysiology of X-Linked Adrenoleukodystrophy». Biochimie 98: 135–142. doi:10.1016/j.biochi.2013.11.023. PMID 24316281.
Singh, Navneet; Bixby, Catherine; Etienne, Denzil; Tubbs, R. Shane; Loukas, Marios (December 2012). «Alexander's disease: reassessment of a neonatal form». Child's Nervous System 28 (12): 2029–2031. doi:10.1007/s00381-012-1868-8. PMID 22890470.
Hol, Elly M.; Pekny, Milos (February 2015). «Glial fibrillary acidic protein (GFAP) and the astrocyte intermediate filament system in diseases of the central nervous system». Current Opinion in Cell Biology 32 (Cell Architecture): 121–130. doi:10.1016/j.ceb.2015.02.004. PMID 25726916.
Kohlschutter, Alfried; Eichler, Florian (October 2011). «Childhood leukodystrophies: a clinical perspective». Expert Review of Neurotherapeutics 11 (10): 1485–1496. doi:10.1586/ern.11.135. PMID 21955203. https://zenodo.org/record/3440302. ^{[νεκρός σύνδεσμος]}
Pouwels, P. J. W.; Vanderver, A.; Bernard, G.; Wolf, N.; Dreha-Kulczewski, S. W.; Deoni, S. C. L.; Bertini, E.; Kohlschutter, A. και άλλοι. (2014). «Hypomyelinating Leukodystrophies: Translational Research Progress and Prospects». Ann. Neurol. 76 (1): 5–19. doi:10.1002/ana.24194. PMID 24916848. https://www.pure.ed.ac.uk/ws/files/16949724/Hypomyelinating_leukodystrophies_Translational_research_progress_and_prospects.pdf.
Rosenberg, J. B.; Kaminsky, S. M.; Aubourg, P.; Crystal, R. G.; Sondhi, D. (2016). «Gene therapy for metachromatic leukodystrophy». Journal of Neuroscience Research 94 (11): 1169–79. doi:10.1002/jnr.23792. PMID 27638601. PMC 5027970. https://pubmed.ncbi.nlm.nih.gov/27638601/.
Fiegenbaum, Annette; Moore, Robert; Clarke, Joe; Hewson, Stacy; Chityat, David; Ray, Peter N.; Stockley, Tracy L. (January 15, 2004). «Canavan disease: Carrier-frequency determination in the Ashkenazi Jewish population and development of a novel molecular diagnostic assay». American Journal of Medical Genetics 124A (2): 142–7. doi:10.1002/ajmg.a.20334. PMID 14699612.
Lesca, G; Vanier, MT; Creisson, E; Bendelac, N; Hainque, B; Ollagnon-Roman, E; Aubourg, P (August 2005). «X-linked adrenoleukodystrophy in a female proband: clinical presentation, biological diagnosis and family consequences». Archives de Pédiatrie 12 (8): 1237–40. doi:10.1016/j.arcped.2005.03.050. PMID 15878823.

ed.ac.uk

pure.ed.ac.uk

Pouwels, P. J. W.; Vanderver, A.; Bernard, G.; Wolf, N.; Dreha-Kulczewski, S. W.; Deoni, S. C. L.; Bertini, E.; Kohlschutter, A. και άλλοι. (2014). «Hypomyelinating Leukodystrophies: Translational Research Progress and Prospects». Ann. Neurol. 76 (1): 5–19. doi:10.1002/ana.24194. PMID 24916848. https://www.pure.ed.ac.uk/ws/files/16949724/Hypomyelinating_leukodystrophies_Translational_research_progress_and_prospects.pdf.

ela-asso.com

«Accueil -». ela-asso.com.

forbes.com

Rubin, Rita (13 Μαρτίου 2016). «Forbes.com: Lorenzo's Oil Could Not Cure Lorenzo, But Newborn Screening Is Expected To Save Others From His Fate». Forbes.com. Ανακτήθηκε στις 31 Ιουλίου 2018. .

inserm.fr

hal.inserm.fr

Duchange, N; Darguy, S; d'Audiffret, D; Callies, I; Lapointe, AS; Loeve, B; Boespflug-Tanguy, O; Moutel, G (18 September 2014). «Ethical management in the constitution of a European database for leukodystrophies rare diseases.». Eur J Paediatr Neurol. 18 (5): 597–603. doi:10.1016/j.ejpn.2014.04.002. PMID 24786336. http://www.hal.inserm.fr/inserm-00995366/document.

nih.gov

ncbi.nlm.nih.gov

Vanderver, Adeline; Tonduti, Davide; Schiffmann, Raphael; Schmidt, Johanna; van der Knaap, Marjo S. (1993), Adam, Margaret P.; Ardinger, Holly H.; Pagon, Roberta A. και άλλοι, επιμ., «Leukodystrophy Overview», GeneReviews® (University of Washington, Seattle), PMID 24501781, http://www.ncbi.nlm.nih.gov/books/NBK184570/, ανακτήθηκε στις 2020-01-23
Bonkowsky, Joshua (Aug 24, 2010). «The burden of inherited leukodystrophies in children». Neurology 75 (8): 718–725. doi:10.1212/WNL.0b013e3181eee46b. PMID 20660364. PMC 2931652. https://archive.org/details/sim_neurology_2010-08-24_75_8/page/718.
Graziano, AC; Cardile, V (26 September 2014). «History, genetic, and recent advances on Krabbe disease». Gene 555 (1): 2–13. doi:10.1016/j.gene.2014.09.046. PMID 25260228.
Liu, Y; Zou, L; Meng, Y; Zhang, Y; Shi, X; Ju, J; Yang, G; Hu, L και άλλοι. (June 2014). «[A family with two children diagnosed with aspartylglucosaminuria-case report and literature review].». Zhonghua Er Za Zhi 52 (6): 455–9. PMID 25190167.
Turon-Vinas, E; Pineda, M; Cusi, V; Lopez-Laso, E; Del Pozo, RL; Gutierez-Solana, LG; Moreno, DC; Sierra-Corcoles, C και άλλοι. (13 July 2014). «Vanishing white matter disease in a Spanish population.». J Cent Nerv Syst Dis. 6: 59–68. doi:10.4137/JCNSD.S13540. PMID 25089094.
Biffi, A.; Aubourg, P.; Cartier, N. (2011). «Gene therapy for leukodystrophies». Human Molecular Genetics 20 (R1): R42–R53. doi:10.1093/hmg/ddr142. PMID 21459776.
Duchange, N; Darguy, S; d'Audiffret, D; Callies, I; Lapointe, AS; Loeve, B; Boespflug-Tanguy, O; Moutel, G (18 September 2014). «Ethical management in the constitution of a European database for leukodystrophies rare diseases.». Eur J Paediatr Neurol. 18 (5): 597–603. doi:10.1016/j.ejpn.2014.04.002. PMID 24786336. http://www.hal.inserm.fr/inserm-00995366/document.
Yang, Edward; Prabhu, Sanjay P. (March 5, 2014). «Imaging manifestations of the leukodystrophies, inherited disorders of white matter.». Radiologic Clinics of North America 52 (2): 279–319. doi:10.1016/j.rcl.2013.11.008. PMID 24582341. https://archive.org/details/sim_radiologic-clinics-of-north-america_2014-03_52_2/page/279.
Lin, Shu-Ting; Ptacek, Louis J.; Fu, Ying-Hui (January 26, 2011). «Adult-Onset Autosomal Dominant Leukodystrophy: Linking Nuclear Envelope to Myelin». The Journal of Neuroscience 31 (4): 1163–1166. doi:10.1523/jneurosci.5994-10.2011. PMID 21273400.
Coulter-Mackie, MB; Rip, J; Ludman, MD; Beis, J; Cole, DEC (October 1995). «Metachromatic leucodystrophy (MLD) in a patient with a constitutional ring chromosome 22». Journal of Medical Genetics 32 (10): 787–91. doi:10.1136/jmg.32.10.787. PMID 8558556. PMC 1051701. https://archive.org/details/sim_journal-of-medical-genetics_1995-10_32_10/page/787.
Sassa, Takayuki; Kihara, Akio (March 22, 2014). «Metabolism of Very Long-Chain Fatty Acids: Genes and Pathophysiology». Biomolecules & Therapeutics 22 (2): 83–92. doi:10.4062/biomolther.2014.017. PMID 24753812.
Barboura, Ilhem; Ferchichi, Salima; Dandana, Azza; Jaidane, Zaineb; Ben Khelifa, Souhaira; Chahed, Hinda; Ben Mansour, Rachida; Chebel, Saber και άλλοι. (2010). «Metachromatic leucodystrophy. Clinical, biological, and therapeutic aspects». Annales de Biologie Clinique 68 (4): 385–91. doi:10.1684/abc.2010.0448. PMID 20650733.
Gieselman, V; Krageloh-Mann, I (2010). «Metachromatic Leukodystrophy - An Update». Neuropediatrics 41 (1): 1–6. doi:10.1055/s-0030-1253412. PMID 20571983.
Szymanska, Krystyna; Lugowska, Agnieszka; Laure-Kamionowska, Milena; Gieruszczak-Bialek, Dorota; Musielak, Malgorzata; Eichler, Sabrina; Giese, Anne-Katrin; Rolfs, Arndt (2012). «Diagnostic difficulties in Krabbe disesase: a report of two cases and review of literature». Folia Neuropathol 50 (4): 346–356. doi:10.5114/fn.2012.32364. PMID 23319190.
Maghazachi, Azzam A. (February 5, 2013). «On the Role of Natural Killer Cells in Neurodegenerative Diseases». Toxins (Basel) 5 (2): 363–375. doi:10.3390/toxins5020363. PMID 23430541.
Berger, J; Forss-Petter, S; Eichler, F.S. (March 2014). «Pathophysiology of X-Linked Adrenoleukodystrophy». Biochimie 98: 135–142. doi:10.1016/j.biochi.2013.11.023. PMID 24316281.
Singh, Navneet; Bixby, Catherine; Etienne, Denzil; Tubbs, R. Shane; Loukas, Marios (December 2012). «Alexander's disease: reassessment of a neonatal form». Child's Nervous System 28 (12): 2029–2031. doi:10.1007/s00381-012-1868-8. PMID 22890470.
Hol, Elly M.; Pekny, Milos (February 2015). «Glial fibrillary acidic protein (GFAP) and the astrocyte intermediate filament system in diseases of the central nervous system». Current Opinion in Cell Biology 32 (Cell Architecture): 121–130. doi:10.1016/j.ceb.2015.02.004. PMID 25726916.
Kohlschutter, Alfried; Eichler, Florian (October 2011). «Childhood leukodystrophies: a clinical perspective». Expert Review of Neurotherapeutics 11 (10): 1485–1496. doi:10.1586/ern.11.135. PMID 21955203. https://zenodo.org/record/3440302. ^{[νεκρός σύνδεσμος]}
Pouwels, P. J. W.; Vanderver, A.; Bernard, G.; Wolf, N.; Dreha-Kulczewski, S. W.; Deoni, S. C. L.; Bertini, E.; Kohlschutter, A. και άλλοι. (2014). «Hypomyelinating Leukodystrophies: Translational Research Progress and Prospects». Ann. Neurol. 76 (1): 5–19. doi:10.1002/ana.24194. PMID 24916848. https://www.pure.ed.ac.uk/ws/files/16949724/Hypomyelinating_leukodystrophies_Translational_research_progress_and_prospects.pdf.
Rosenberg, J. B.; Kaminsky, S. M.; Aubourg, P.; Crystal, R. G.; Sondhi, D. (2016). «Gene therapy for metachromatic leukodystrophy». Journal of Neuroscience Research 94 (11): 1169–79. doi:10.1002/jnr.23792. PMID 27638601. PMC 5027970. https://pubmed.ncbi.nlm.nih.gov/27638601/.
Fiegenbaum, Annette; Moore, Robert; Clarke, Joe; Hewson, Stacy; Chityat, David; Ray, Peter N.; Stockley, Tracy L. (January 15, 2004). «Canavan disease: Carrier-frequency determination in the Ashkenazi Jewish population and development of a novel molecular diagnostic assay». American Journal of Medical Genetics 124A (2): 142–7. doi:10.1002/ajmg.a.20334. PMID 14699612.
Lesca, G; Vanier, MT; Creisson, E; Bendelac, N; Hainque, B; Ollagnon-Roman, E; Aubourg, P (August 2005). «X-linked adrenoleukodystrophy in a female proband: clinical presentation, biological diagnosis and family consequences». Archives de Pédiatrie 12 (8): 1237–40. doi:10.1016/j.arcped.2005.03.050. PMID 15878823.

pubmedcentral.nih.gov

Bonkowsky, Joshua (Aug 24, 2010). «The burden of inherited leukodystrophies in children». Neurology 75 (8): 718–725. doi:10.1212/WNL.0b013e3181eee46b. PMID 20660364. PMC 2931652. https://archive.org/details/sim_neurology_2010-08-24_75_8/page/718.
Rosebush, P. I. (2003). «Tardive dystonia and its treatment». Journal of Psychiatry and Neuroscience 28 (3): 240.
Turon-Vinas, E; Pineda, M; Cusi, V; Lopez-Laso, E; Del Pozo, RL; Gutierez-Solana, LG; Moreno, DC; Sierra-Corcoles, C και άλλοι. (13 July 2014). «Vanishing white matter disease in a Spanish population.». J Cent Nerv Syst Dis. 6: 59–68. doi:10.4137/JCNSD.S13540. PMID 25089094.
Lin, Shu-Ting; Ptacek, Louis J.; Fu, Ying-Hui (January 26, 2011). «Adult-Onset Autosomal Dominant Leukodystrophy: Linking Nuclear Envelope to Myelin». The Journal of Neuroscience 31 (4): 1163–1166. doi:10.1523/jneurosci.5994-10.2011. PMID 21273400.
Coulter-Mackie, MB; Rip, J; Ludman, MD; Beis, J; Cole, DEC (October 1995). «Metachromatic leucodystrophy (MLD) in a patient with a constitutional ring chromosome 22». Journal of Medical Genetics 32 (10): 787–91. doi:10.1136/jmg.32.10.787. PMID 8558556. PMC 1051701. https://archive.org/details/sim_journal-of-medical-genetics_1995-10_32_10/page/787.
Sassa, Takayuki; Kihara, Akio (March 22, 2014). «Metabolism of Very Long-Chain Fatty Acids: Genes and Pathophysiology». Biomolecules & Therapeutics 22 (2): 83–92. doi:10.4062/biomolther.2014.017. PMID 24753812.
Maghazachi, Azzam A. (February 5, 2013). «On the Role of Natural Killer Cells in Neurodegenerative Diseases». Toxins (Basel) 5 (2): 363–375. doi:10.3390/toxins5020363. PMID 23430541.
Berger, J; Forss-Petter, S; Eichler, F.S. (March 2014). «Pathophysiology of X-Linked Adrenoleukodystrophy». Biochimie 98: 135–142. doi:10.1016/j.biochi.2013.11.023. PMID 24316281.
Rosenberg, J. B.; Kaminsky, S. M.; Aubourg, P.; Crystal, R. G.; Sondhi, D. (2016). «Gene therapy for metachromatic leukodystrophy». Journal of Neuroscience Research 94 (11): 1169–79. doi:10.1002/jnr.23792. PMID 27638601. PMC 5027970. https://pubmed.ncbi.nlm.nih.gov/27638601/.

pubmed.ncbi.nlm.nih.gov

Rosenberg, J. B.; Kaminsky, S. M.; Aubourg, P.; Crystal, R. G.; Sondhi, D. (2016). «Gene therapy for metachromatic leukodystrophy». Journal of Neuroscience Research 94 (11): 1169–79. doi:10.1002/jnr.23792. PMID 27638601. PMC 5027970. https://pubmed.ncbi.nlm.nih.gov/27638601/.

ninds.nih.gov

«Leukodystrophy Information Page | National Institute of Neurological Disorders and Stroke». www.ninds.nih.gov.

theglia.org

«The Global Leukodystrophy Initiative». The Global Leukodystrophy Initiative.

ulf.org

United Leukodystrophy Foundation. «Canavan Disease». United Leukodystrophy Foundation. United Leukodystrophy Foundation, Inc. Ανακτήθηκε στις 30 Μαρτίου 2015.

zenodo.org

Kohlschutter, Alfried; Eichler, Florian (October 2011). «Childhood leukodystrophies: a clinical perspective». Expert Review of Neurotherapeutics 11 (10): 1485–1496. doi:10.1586/ern.11.135. PMID 21955203. https://zenodo.org/record/3440302. ^{[νεκρός σύνδεσμος]}