Ռետտի համախտանիշ (Armenian Wikipedia)

Analysis of information sources in references of the Wikipedia article "Ռետտի համախտանիշ" in Armenian language version.

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archive.org

Neul, Jeffrey l.; Kaufmann, Walter E.; Glaze, Daniel G.; Christodoulou, John; Clarke, Angus J.; Bahi-Buisson, Nadia; Leonard, Helen; Bailey, Mark E. S.; Schanen, N. Carolyn; Zappella, Michele; Renieri, Alessandra; Huppke, Peter; Percy, Alan K.; և այլք: (Rettsearch Consortium) (2010). «Rett syndrome: Revised diagnostic criteria and nomenclature». Annals of Neurology. 68 (6): 944–50. doi:10.1002/ana.22124. PMC 3058521. PMID 21154482.
Ariani, Francesca; Hayek, Giuseppe; Rondinella, Dalila; Artuso, Rosangela; Mencarelli, Maria Antonietta; Spanhol-Rosseto, Ariele; Pollazzon, Marzia; Buoni, Sabrina; Spiga, Ottavia; Ricciardi, Sara; Meloni, Ilaria; Longo, Ilaria; Mari, Francesca; Broccoli, Vania; Zappella, Michele; Renieri, Alessandra (2008 թ․ հուլիսի 11). «FOXG1 is Responsible for the Congenital Variant of Rett Syndrome». The American Journal of Human Genetics. 83 (1): 89–93. doi:10.1016/j.ajhg.2008.05.015. PMC 2443837. PMID 18571142.
Zappella, Michele; Gillberg, Christopher; Ehlers, Stephan (1998). «The preserved speech variant: A subgroup of the Rett complex: A clinical report of 30 cases». Journal of Autism and Developmental Disorders. 28 (6): 519–26. doi:10.1023/A:1026052128305. PMID 9932238.
Trappe, R.; Laccone, F.; Cobilanschi, J.; Meins, M.; Huppke, P.; Hanefeld, F.; Engel, W. (2001). «MECP2 Mutations in Sporadic Cases of Rett Syndrome Are Almost Exclusively of Paternal Origin». The American Journal of Human Genetics. 68 (5): 1093–101. doi:10.1086/320109. PMC 1226090. PMID 11309679.
Berridge, Craig W; Waterhouse, Barry D (2003). «The locus coeruleus–noradrenergic system: Modulation of behavioral state and state-dependent cognitive processes». Brain Research Reviews. 42 (1): 33–84. doi:10.1016/S0165-0173(03)00143-7. PMID 12668290.

doi.org

Percy, Alan (January 2014). «The American History of Rett Syndrome». Pediatric Neurology. 50 (1): 1–3. doi:10.1016/j.pediatrneurol.2013.08.018. PMC 3874243.
Amir, Ruthie; Van den Veyver, Ignatia; Wan, Mimi; Tran, Charles; Francke, Uta; Zoghbi, Huda (1999). «Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2». Nature Genetics. 23 (2): 185–8. doi:10.1038/13810. PMID 10508514.
Neul, Jeffrey l.; Kaufmann, Walter E.; Glaze, Daniel G.; Christodoulou, John; Clarke, Angus J.; Bahi-Buisson, Nadia; Leonard, Helen; Bailey, Mark E. S.; Schanen, N. Carolyn; Zappella, Michele; Renieri, Alessandra; Huppke, Peter; Percy, Alan K.; և այլք: (Rettsearch Consortium) (2010). «Rett syndrome: Revised diagnostic criteria and nomenclature». Annals of Neurology. 68 (6): 944–50. doi:10.1002/ana.22124. PMC 3058521. PMID 21154482.
Ariani, Francesca; Hayek, Giuseppe; Rondinella, Dalila; Artuso, Rosangela; Mencarelli, Maria Antonietta; Spanhol-Rosseto, Ariele; Pollazzon, Marzia; Buoni, Sabrina; Spiga, Ottavia; Ricciardi, Sara; Meloni, Ilaria; Longo, Ilaria; Mari, Francesca; Broccoli, Vania; Zappella, Michele; Renieri, Alessandra (2008 թ․ հուլիսի 11). «FOXG1 is Responsible for the Congenital Variant of Rett Syndrome». The American Journal of Human Genetics. 83 (1): 89–93. doi:10.1016/j.ajhg.2008.05.015. PMC 2443837. PMID 18571142.
Zappella, Michele (1992). «The rett girls with preserved speech». Brain and Development. 14 (2): 98–101. doi:10.1016/S0387-7604(12)80094-5. PMID 1621933.
Skjeldal, O. H.; Von Tetzchner, S.; Jacobsen, K.; Smith, L.; Heiberg, A. (2007). «Rett Syndrome - Distribution of Phenotypes with Special Attention to the Preserved Speech Variant». Neuropediatrics. 26 (2): 87. doi:10.1055/s-2007-979732. PMID 7566462.
Renieri, A.; Mari, F.; Mencarelli, M.A.; Scala, E.; Ariani, F.; Longo, I.; Meloni, I.; Cevenini, G.; Pini, G.; Hayek, G.; Zappella, M. (March 2009). «Diagnostic criteria for the Zappella variant of Rett syndrome (the preserved speech variant)». Brain and Development. 31 (3): 208–16. doi:10.1016/j.braindev.2008.04.007. PMID 18562141.
Buoni, Sabrina; Zannolli, Raffaella; De Felice, Claudio; De Nicola, Anna; Guerri, Vanessa; Guerra, Beatrice; Casali, Stefania; Pucci, Barbara; Corbini, Letizia; Mari, Francesca; Renieri, Alessandra; Zappella, Michele; Hayek, Joseph (May 2010). «EEG features and epilepsy in MECP2-mutated patients with the Zappella variant of Rett syndrome». Clinical Neurophysiology. 121 (5): 652–7. doi:10.1016/j.clinph.2010.01.003. PMID 20153689.
Huppke, Peter; Held, Melanie; Laccone, Franco; Hanefeld, Folker (2003). «The spectrum of phenotypes in females with Rett Syndrome». Brain and Development. 25 (5): 346–51. doi:10.1016/S0387-7604(03)00018-4. PMID 12850514.
Zappella, Michele; Gillberg, Christopher; Ehlers, Stephan (1998). «The preserved speech variant: A subgroup of the Rett complex: A clinical report of 30 cases». Journal of Autism and Developmental Disorders. 28 (6): 519–26. doi:10.1023/A:1026052128305. PMID 9932238.
Guy, J.; Gan, J.; Selfridge, J.; Cobb, S.; Bird, A. (2007). «Reversal of Neurological Defects in a Mouse Model of Rett Syndrome». Science. 315 (5815): 1143–7. Bibcode:2007Sci...315.1143G. doi:10.1126/science.1138389. PMID 17289941.
Trappe, R.; Laccone, F.; Cobilanschi, J.; Meins, M.; Huppke, P.; Hanefeld, F.; Engel, W. (2001). «MECP2 Mutations in Sporadic Cases of Rett Syndrome Are Almost Exclusively of Paternal Origin». The American Journal of Human Genetics. 68 (5): 1093–101. doi:10.1086/320109. PMC 1226090. PMID 11309679.
Zoghbi, Huda Y.; Van Den Veyver, Ruthie E.; Wan, Ignatia B.; Tran, Mimi; Francke, Charles Q.; Zoghbi, Uta (1999). «Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2». Nature Genetics. 23 (2): 185–8. doi:10.1038/13810. PMID 10508514.
Zoghbi, Huda Y.; Milstien, Sheldon; Butler, Ian J.; Smith, E. O'Brian; Kaufman, Seymour; Glaze, Daniel G.; Percy, Alan K. (1989). «Cerebrospinal fluid biogenic amines and biopterin in Rett syndrome». Annals of Neurology. 25 (1): 56–60. doi:10.1002/ana.410250109. PMID 2913929.
Roux, Jean-Christophe; Villard, Laurent (2009). «Biogenic Amines in Rett Syndrome: The Usual Suspects». Behavior Genetics. 40 (1): 59–75. doi:10.1007/s10519-009-9303-y. PMID 19851857.
Berridge, Craig W; Waterhouse, Barry D (2003). «The locus coeruleus–noradrenergic system: Modulation of behavioral state and state-dependent cognitive processes». Brain Research Reviews. 42 (1): 33–84. doi:10.1016/S0165-0173(03)00143-7. PMID 12668290.
Taneja, P.; Ogier, M.; Brooks-Harris, G.; Schmid, D. A.; Katz, D. M.; Nelson, S. B. (2009). «Pathophysiology of Locus Ceruleus Neurons in a Mouse Model of Rett Syndrome». Journal of Neuroscience. 29 (39): 12187–95. doi:10.1523/JNEUROSCI.3156-09.2009. PMC 2846656. PMID 19793977.
Roux, Jean-Christophe; Panayotis, Nicolas; Dura, Emmanuelle; Villard, Laurent (2009). «Progressive noradrenergic deficits in the locus coeruleus of Mecp2 deficient mice». Journal of Neuroscience Research. 88 (7): 1500–9. doi:10.1002/jnr.22312. PMID 19998492.
Ehrhart, Friederike; Coort, Susan L. M.; Cirillo, Elisa; Smeets, Eric; Evelo, Chris T.; Curfs, Leopold M. G. (2016 թ․ նոյեմբերի 25). «Rett syndrome – biological pathways leading from MECP2 to disorder phenotypes». Orphanet Journal of Rare Diseases. 11 (1). doi:10.1186/s13023-016-0545-5.{{cite journal}}: CS1 սպաս․ չպիտակված ազատ DOI (link)

dx.doi.org

Neul J. L., Kaufmann W. E., Glaze D. G., Renieri A., Percy A. K., Christodoulou J., Bahi-Buisson N. Rett syndrome: revised diagnostic criteria and nomenclature // Ann. Neurol. / C. B. Saper — Wiley, 2010. — Vol. 68, Iss. 6. — P. 944—50. — ISSN 0364-5134; 1531-8249 — doi:10.1002/ANA.22124 — PMID:21154482

elsevier.com

linkinghub.elsevier.com

Percy, Alan (January 2014). «The American History of Rett Syndrome». Pediatric Neurology. 50 (1): 1–3. doi:10.1016/j.pediatrneurol.2013.08.018. PMC 3874243.

google.am

books.google.am

Davis, Andrew S. (2010 թ․ հոկտեմբերի 25). Handbook of Pediatric Neuropsychology. Springer Publishing Company. ISBN 082615736X. Արխիվացված օրիգինալից 2017 թ․ նոյեմբերի 5-ին. «Rett initially called this syndrome cerebroaatrophic hyperammonemia, but the elevated ammonia levels in the bloodstream were later found to be only rarely associated with this condition (can Acker, Loncola, & Can Acker, 2005).»

harvard.edu

ui.adsabs.harvard.edu

Guy, J.; Gan, J.; Selfridge, J.; Cobb, S.; Bird, A. (2007). «Reversal of Neurological Defects in a Mouse Model of Rett Syndrome». Science. 315 (5815): 1143–7. Bibcode:2007Sci...315.1143G. doi:10.1126/science.1138389. PMID 17289941.

nih.gov

pubmed.ncbi.nlm.nih.gov

Rett, A. (1966 թ․ սեպտեմբերի 10). «[On a unusual brain atrophy syndrome in hyperammonemia in childhood]». Wiener Medizinische Wochenschrift (գերմաներեն). 116 (37): 723–726. ISSN 0043-5341. PMID 5300597.
Amir, Ruthie; Van den Veyver, Ignatia; Wan, Mimi; Tran, Charles; Francke, Uta; Zoghbi, Huda (1999). «Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2». Nature Genetics. 23 (2): 185–8. doi:10.1038/13810. PMID 10508514.
Neul, Jeffrey l.; Kaufmann, Walter E.; Glaze, Daniel G.; Christodoulou, John; Clarke, Angus J.; Bahi-Buisson, Nadia; Leonard, Helen; Bailey, Mark E. S.; Schanen, N. Carolyn; Zappella, Michele; Renieri, Alessandra; Huppke, Peter; Percy, Alan K.; և այլք: (Rettsearch Consortium) (2010). «Rett syndrome: Revised diagnostic criteria and nomenclature». Annals of Neurology. 68 (6): 944–50. doi:10.1002/ana.22124. PMC 3058521. PMID 21154482.
Ariani, Francesca; Hayek, Giuseppe; Rondinella, Dalila; Artuso, Rosangela; Mencarelli, Maria Antonietta; Spanhol-Rosseto, Ariele; Pollazzon, Marzia; Buoni, Sabrina; Spiga, Ottavia; Ricciardi, Sara; Meloni, Ilaria; Longo, Ilaria; Mari, Francesca; Broccoli, Vania; Zappella, Michele; Renieri, Alessandra (2008 թ․ հուլիսի 11). «FOXG1 is Responsible for the Congenital Variant of Rett Syndrome». The American Journal of Human Genetics. 83 (1): 89–93. doi:10.1016/j.ajhg.2008.05.015. PMC 2443837. PMID 18571142.
Zappella, Michele (1992). «The rett girls with preserved speech». Brain and Development. 14 (2): 98–101. doi:10.1016/S0387-7604(12)80094-5. PMID 1621933.
Skjeldal, O. H.; Von Tetzchner, S.; Jacobsen, K.; Smith, L.; Heiberg, A. (2007). «Rett Syndrome - Distribution of Phenotypes with Special Attention to the Preserved Speech Variant». Neuropediatrics. 26 (2): 87. doi:10.1055/s-2007-979732. PMID 7566462.
Sørensen, E.; Viken, B. (1995 թ․ փետրվարի 20). «[Rett syndrome a developmental disorder. Presentation of a variant with preserved speech]». Tidsskrift for Den Norske Laegeforening: Tidsskrift for Praktisk Medicin, Ny Raekke (նորվեգերեն). 115 (5): 588–590. ISSN 0029-2001. PMID 7900110.
Zappella, M (1997). «The preserved speech variant of the Rett complex: A report of 8 cases». European Child & Adolescent Psychiatry. 6 Suppl 1: 23–5. PMID 9452915.
Renieri, A.; Mari, F.; Mencarelli, M.A.; Scala, E.; Ariani, F.; Longo, I.; Meloni, I.; Cevenini, G.; Pini, G.; Hayek, G.; Zappella, M. (March 2009). «Diagnostic criteria for the Zappella variant of Rett syndrome (the preserved speech variant)». Brain and Development. 31 (3): 208–16. doi:10.1016/j.braindev.2008.04.007. PMID 18562141.
Buoni, Sabrina; Zannolli, Raffaella; De Felice, Claudio; De Nicola, Anna; Guerri, Vanessa; Guerra, Beatrice; Casali, Stefania; Pucci, Barbara; Corbini, Letizia; Mari, Francesca; Renieri, Alessandra; Zappella, Michele; Hayek, Joseph (May 2010). «EEG features and epilepsy in MECP2-mutated patients with the Zappella variant of Rett syndrome». Clinical Neurophysiology. 121 (5): 652–7. doi:10.1016/j.clinph.2010.01.003. PMID 20153689.
Huppke, Peter; Held, Melanie; Laccone, Franco; Hanefeld, Folker (2003). «The spectrum of phenotypes in females with Rett Syndrome». Brain and Development. 25 (5): 346–51. doi:10.1016/S0387-7604(03)00018-4. PMID 12850514.
Gillberg, C. (1997). «Communication in Rett syndrome complex». European Child & Adolescent Psychiatry. 6 Suppl 1: 21–2. PMID 9452914.
Zappella, Michele; Gillberg, Christopher; Ehlers, Stephan (1998). «The preserved speech variant: A subgroup of the Rett complex: A clinical report of 30 cases». Journal of Autism and Developmental Disorders. 28 (6): 519–26. doi:10.1023/A:1026052128305. PMID 9932238.
Guy, J.; Gan, J.; Selfridge, J.; Cobb, S.; Bird, A. (2007). «Reversal of Neurological Defects in a Mouse Model of Rett Syndrome». Science. 315 (5815): 1143–7. Bibcode:2007Sci...315.1143G. doi:10.1126/science.1138389. PMID 17289941.
Trappe, R.; Laccone, F.; Cobilanschi, J.; Meins, M.; Huppke, P.; Hanefeld, F.; Engel, W. (2001). «MECP2 Mutations in Sporadic Cases of Rett Syndrome Are Almost Exclusively of Paternal Origin». The American Journal of Human Genetics. 68 (5): 1093–101. doi:10.1086/320109. PMC 1226090. PMID 11309679.
Zoghbi, Huda Y.; Van Den Veyver, Ruthie E.; Wan, Ignatia B.; Tran, Mimi; Francke, Charles Q.; Zoghbi, Uta (1999). «Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2». Nature Genetics. 23 (2): 185–8. doi:10.1038/13810. PMID 10508514.
Zoghbi, Huda Y.; Milstien, Sheldon; Butler, Ian J.; Smith, E. O'Brian; Kaufman, Seymour; Glaze, Daniel G.; Percy, Alan K. (1989). «Cerebrospinal fluid biogenic amines and biopterin in Rett syndrome». Annals of Neurology. 25 (1): 56–60. doi:10.1002/ana.410250109. PMID 2913929.
Roux, Jean-Christophe; Villard, Laurent (2009). «Biogenic Amines in Rett Syndrome: The Usual Suspects». Behavior Genetics. 40 (1): 59–75. doi:10.1007/s10519-009-9303-y. PMID 19851857.
Berridge, Craig W; Waterhouse, Barry D (2003). «The locus coeruleus–noradrenergic system: Modulation of behavioral state and state-dependent cognitive processes». Brain Research Reviews. 42 (1): 33–84. doi:10.1016/S0165-0173(03)00143-7. PMID 12668290.
Taneja, P.; Ogier, M.; Brooks-Harris, G.; Schmid, D. A.; Katz, D. M.; Nelson, S. B. (2009). «Pathophysiology of Locus Ceruleus Neurons in a Mouse Model of Rett Syndrome». Journal of Neuroscience. 29 (39): 12187–95. doi:10.1523/JNEUROSCI.3156-09.2009. PMC 2846656. PMID 19793977.
Roux, Jean-Christophe; Panayotis, Nicolas; Dura, Emmanuelle; Villard, Laurent (2009). «Progressive noradrenergic deficits in the locus coeruleus of Mecp2 deficient mice». Journal of Neuroscience Research. 88 (7): 1500–9. doi:10.1002/jnr.22312. PMID 19998492.

ncbi.nlm.nih.gov

Neul J. L., Kaufmann W. E., Glaze D. G., Renieri A., Percy A. K., Christodoulou J., Bahi-Buisson N. Rett syndrome: revised diagnostic criteria and nomenclature // Ann. Neurol. / C. B. Saper — Wiley, 2010. — Vol. 68, Iss. 6. — P. 944—50. — ISSN 0364-5134; 1531-8249 — doi:10.1002/ANA.22124 — PMID:21154482
Rett A. On a unusual brain atrophy syndrome in hyperammonemia in childhood (գերմ.) // Wiener Medizinische Wochenschrift — Springer Medizin, Springer Science+Business Media, 1966. — Vol. 116, Iss. 37. — S. 723—726. — ISSN 0043-5341; 1563-258X — PMID:5300597
Percy, Alan (January 2014). «The American History of Rett Syndrome». Pediatric Neurology. 50 (1): 1–3. doi:10.1016/j.pediatrneurol.2013.08.018. PMC 3874243.
Neul, Jeffrey l.; Kaufmann, Walter E.; Glaze, Daniel G.; Christodoulou, John; Clarke, Angus J.; Bahi-Buisson, Nadia; Leonard, Helen; Bailey, Mark E. S.; Schanen, N. Carolyn; Zappella, Michele; Renieri, Alessandra; Huppke, Peter; Percy, Alan K.; և այլք: (Rettsearch Consortium) (2010). «Rett syndrome: Revised diagnostic criteria and nomenclature». Annals of Neurology. 68 (6): 944–50. doi:10.1002/ana.22124. PMC 3058521. PMID 21154482.
Ariani, Francesca; Hayek, Giuseppe; Rondinella, Dalila; Artuso, Rosangela; Mencarelli, Maria Antonietta; Spanhol-Rosseto, Ariele; Pollazzon, Marzia; Buoni, Sabrina; Spiga, Ottavia; Ricciardi, Sara; Meloni, Ilaria; Longo, Ilaria; Mari, Francesca; Broccoli, Vania; Zappella, Michele; Renieri, Alessandra (2008 թ․ հուլիսի 11). «FOXG1 is Responsible for the Congenital Variant of Rett Syndrome». The American Journal of Human Genetics. 83 (1): 89–93. doi:10.1016/j.ajhg.2008.05.015. PMC 2443837. PMID 18571142.
Trappe, R.; Laccone, F.; Cobilanschi, J.; Meins, M.; Huppke, P.; Hanefeld, F.; Engel, W. (2001). «MECP2 Mutations in Sporadic Cases of Rett Syndrome Are Almost Exclusively of Paternal Origin». The American Journal of Human Genetics. 68 (5): 1093–101. doi:10.1086/320109. PMC 1226090. PMID 11309679.
Taneja, P.; Ogier, M.; Brooks-Harris, G.; Schmid, D. A.; Katz, D. M.; Nelson, S. B. (2009). «Pathophysiology of Locus Ceruleus Neurons in a Mouse Model of Rett Syndrome». Journal of Neuroscience. 29 (39): 12187–95. doi:10.1523/JNEUROSCI.3156-09.2009. PMC 2846656. PMID 19793977.

ghr.nlm.nih.gov

«Rett syndrome». Genetics Home Reference (անգլերեն). December 2013. Արխիվացված օրիգինալից 2017 թ․ հոկտեմբերի 14-ին. Վերցված է 2017 թ․ հոկտեմբերի 14-ին.

ninds.nih.gov

«Rett Syndrome Fact Sheet». National Institute of Neurological Disorders and Stroke. Արխիվացված օրիգինալից 2017 թ․ հոկտեմբերի 14-ին. Վերցված է 2017 թ․ հոկտեմբերի 14-ին.

rarediseases.org

«Rett Syndrome». NORD (National Organization for Rare Disorders). 2015. Արխիվացված օրիգինալից 2017 թ․ փետրվարի 19-ին. Վերցված է 2017 թ․ հոկտեմբերի 14-ին.

web.archive.org

«Rett syndrome». Genetics Home Reference (անգլերեն). December 2013. Արխիվացված օրիգինալից 2017 թ․ հոկտեմբերի 14-ին. Վերցված է 2017 թ․ հոկտեմբերի 14-ին.
Davis, Andrew S. (2010 թ․ հոկտեմբերի 25). Handbook of Pediatric Neuropsychology. Springer Publishing Company. ISBN 082615736X. Արխիվացված օրիգինալից 2017 թ․ նոյեմբերի 5-ին. «Rett initially called this syndrome cerebroaatrophic hyperammonemia, but the elevated ammonia levels in the bloodstream were later found to be only rarely associated with this condition (can Acker, Loncola, & Can Acker, 2005).»
«Rett Syndrome Fact Sheet». National Institute of Neurological Disorders and Stroke. Արխիվացված օրիգինալից 2017 թ․ հոկտեմբերի 14-ին. Վերցված է 2017 թ․ հոկտեմբերի 14-ին.
«Rett Syndrome». NORD (National Organization for Rare Disorders). 2015. Արխիվացված օրիգինալից 2017 թ․ փետրվարի 19-ին. Վերցված է 2017 թ․ հոկտեմբերի 14-ին.

wikidata.org

Neul J. L., Kaufmann W. E., Glaze D. G., Renieri A., Percy A. K., Christodoulou J., Bahi-Buisson N. Rett syndrome: revised diagnostic criteria and nomenclature // Ann. Neurol. / C. B. Saper — Wiley, 2010. — Vol. 68, Iss. 6. — P. 944—50. — ISSN 0364-5134; 1531-8249 — doi:10.1002/ANA.22124 — PMID:21154482
Rett A. On a unusual brain atrophy syndrome in hyperammonemia in childhood (գերմ.) // Wiener Medizinische Wochenschrift — Springer Medizin, Springer Science+Business Media, 1966. — Vol. 116, Iss. 37. — S. 723—726. — ISSN 0043-5341; 1563-258X — PMID:5300597

wikipedia.org

en.wikipedia.org

Neul J. L., Kaufmann W. E., Glaze D. G., Renieri A., Percy A. K., Christodoulou J., Bahi-Buisson N. Rett syndrome: revised diagnostic criteria and nomenclature // Ann. Neurol. / C. B. Saper — Wiley, 2010. — Vol. 68, Iss. 6. — P. 944—50. — ISSN 0364-5134; 1531-8249 — doi:10.1002/ANA.22124 — PMID:21154482

de.wikipedia.org

Rett A. On a unusual brain atrophy syndrome in hyperammonemia in childhood (գերմ.) // Wiener Medizinische Wochenschrift — Springer Medizin, Springer Science+Business Media, 1966. — Vol. 116, Iss. 37. — S. 723—726. — ISSN 0043-5341; 1563-258X — PMID:5300597

worldcat.org

Neul J. L., Kaufmann W. E., Glaze D. G., Renieri A., Percy A. K., Christodoulou J., Bahi-Buisson N. Rett syndrome: revised diagnostic criteria and nomenclature // Ann. Neurol. / C. B. Saper — Wiley, 2010. — Vol. 68, Iss. 6. — P. 944—50. — ISSN 0364-5134; 1531-8249 — doi:10.1002/ANA.22124 — PMID:21154482
Rett A. On a unusual brain atrophy syndrome in hyperammonemia in childhood (գերմ.) // Wiener Medizinische Wochenschrift — Springer Medizin, Springer Science+Business Media, 1966. — Vol. 116, Iss. 37. — S. 723—726. — ISSN 0043-5341; 1563-258X — PMID:5300597
Rett, A. (1966 թ․ սեպտեմբերի 10). «[On a unusual brain atrophy syndrome in hyperammonemia in childhood]». Wiener Medizinische Wochenschrift (գերմաներեն). 116 (37): 723–726. ISSN 0043-5341. PMID 5300597.
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