متلازمة ريت (Arabic Wikipedia)

Analysis of information sources in references of the Wikipedia article "متلازمة ريت" in Arabic language version.

refsWebsite

Global rank Arabic rank

10nih.gov

4^th place

6^th place

6doi.org

2^nd place

5^th place

3wikidata.org

43^rd place

2^nd place

2worldcat.org

5^th place

4^th place

1disease-ontology.org

low place

594^th place

1europepmc.org

8,929^th place

5,455^th place

1rettsyndrome.org

low place

1web.archive.org

1^st place

disease-ontology.org

Disease Ontology (بالإنجليزية), 27 May 2016, QID:Q5282129

doi.org

Jeffrey L Neul; Walter E Kaufmann; Daniel G Glaze; John Christodoulou; Nadia Bahi-Buisson; Alessandra Renieri; Alan K Percy (Dec 2010). "Rett syndrome: revised diagnostic criteria and nomenclature". Annals of Neurology (بالإنجليزية). 68 (6): 944–50. DOI:10.1002/ANA.22124. ISSN:0364-5134. PMC:3058521. PMID:21154482. QID:Q24596295.
Hong Xue (30 Jan 2022). "GABRB2, a key player in neuropsychiatric disorders and beyond". Gene. Gene Wiki Review Series (بالإنجليزية). 809. DOI:10.1016/J.GENE.2021.146021. ISSN:0378-1119. PMID:34673206. QID:Q109615004.
McCauley MD، Wang T، Mike E، وآخرون (ديسمبر 2011). "Pathogenesis of lethal cardiac arrhythmias in Mecp2 mutant mice: implication for therapy in Rett syndrome". Science Translational Medicine. ج. 3 ع. 113: 113ra125. DOI:10.1126/scitranslmed.3002982. PMC:3633081. PMID:22174313.
Zappella، Michele (1992). "The rett girls with preserved speech". Brain and Development. ج. 14 ع. 2: 98–101. DOI:10.1016/S0387-7604(12)80094-5. PMID:1621933.
Chen، Richard Z.؛ Akbarian، Schahram؛ Tudor، Matthew؛ Jaenisch، Rudolf (2001). "Deficiency of methyl-CpG binding protein-2 in CNS neurons results in a Rett-like phenotype in mice". Nature Genetics. ج. 27 ع. 3: 327–31. DOI:10.1038/85906. PMID:11242118.
Ehrhart، Friederike؛ Coort، Susan L. M.؛ Cirillo، Elisa؛ Smeets، Eric؛ Evelo، Chris T.؛ Curfs، Leopold M. G. (25 نوفمبر 2016). "Rett syndrome – biological pathways leading from MECP2 to disorder phenotypes". Orphanet Journal of Rare Diseases. ج. 11 ع. 1: 158. DOI:10.1186/s13023-016-0545-5. PMC:5123333. PMID:27884167.{{استشهاد بدورية محكمة}}: صيانة الاستشهاد: دوي مجاني غير معلم (link)

europepmc.org

Jeffrey L Neul; Walter E Kaufmann; Daniel G Glaze; John Christodoulou; Nadia Bahi-Buisson; Alessandra Renieri; Alan K Percy (Dec 2010). "Rett syndrome: revised diagnostic criteria and nomenclature". Annals of Neurology (بالإنجليزية). 68 (6): 944–50. DOI:10.1002/ANA.22124. ISSN:0364-5134. PMC:3058521. PMID:21154482. QID:Q24596295.

nih.gov

pubmed.ncbi.nlm.nih.gov

Jeffrey L Neul; Walter E Kaufmann; Daniel G Glaze; John Christodoulou; Nadia Bahi-Buisson; Alessandra Renieri; Alan K Percy (Dec 2010). "Rett syndrome: revised diagnostic criteria and nomenclature". Annals of Neurology (بالإنجليزية). 68 (6): 944–50. DOI:10.1002/ANA.22124. ISSN:0364-5134. PMC:3058521. PMID:21154482. QID:Q24596295.
Hong Xue (30 Jan 2022). "GABRB2, a key player in neuropsychiatric disorders and beyond". Gene. Gene Wiki Review Series (بالإنجليزية). 809. DOI:10.1016/J.GENE.2021.146021. ISSN:0378-1119. PMID:34673206. QID:Q109615004.
McCauley MD، Wang T، Mike E، وآخرون (ديسمبر 2011). "Pathogenesis of lethal cardiac arrhythmias in Mecp2 mutant mice: implication for therapy in Rett syndrome". Science Translational Medicine. ج. 3 ع. 113: 113ra125. DOI:10.1126/scitranslmed.3002982. PMC:3633081. PMID:22174313.
Zappella، Michele (1992). "The rett girls with preserved speech". Brain and Development. ج. 14 ع. 2: 98–101. DOI:10.1016/S0387-7604(12)80094-5. PMID:1621933.
Chen، Richard Z.؛ Akbarian، Schahram؛ Tudor، Matthew؛ Jaenisch، Rudolf (2001). "Deficiency of methyl-CpG binding protein-2 in CNS neurons results in a Rett-like phenotype in mice". Nature Genetics. ج. 27 ع. 3: 327–31. DOI:10.1038/85906. PMID:11242118.
Ehrhart، Friederike؛ Coort، Susan L. M.؛ Cirillo، Elisa؛ Smeets، Eric؛ Evelo، Chris T.؛ Curfs، Leopold M. G. (25 نوفمبر 2016). "Rett syndrome – biological pathways leading from MECP2 to disorder phenotypes". Orphanet Journal of Rare Diseases. ج. 11 ع. 1: 158. DOI:10.1186/s13023-016-0545-5. PMC:5123333. PMID:27884167.{{استشهاد بدورية محكمة}}: صيانة الاستشهاد: دوي مجاني غير معلم (link)

ncbi.nlm.nih.gov

Jeffrey L Neul; Walter E Kaufmann; Daniel G Glaze; John Christodoulou; Nadia Bahi-Buisson; Alessandra Renieri; Alan K Percy (Dec 2010). "Rett syndrome: revised diagnostic criteria and nomenclature". Annals of Neurology (بالإنجليزية). 68 (6): 944–50. DOI:10.1002/ANA.22124. ISSN:0364-5134. PMC:3058521. PMID:21154482. QID:Q24596295.
McCauley MD، Wang T، Mike E، وآخرون (ديسمبر 2011). "Pathogenesis of lethal cardiac arrhythmias in Mecp2 mutant mice: implication for therapy in Rett syndrome". Science Translational Medicine. ج. 3 ع. 113: 113ra125. DOI:10.1126/scitranslmed.3002982. PMC:3633081. PMID:22174313.
Sharifi O, Yasui DH. The Molecular Functions of MeCP2 in Rett Syndrome Pathology. Front Genet. 2021 Apr 23;12:624290. doi: 10.3389/fgene.2021.624290. PMID 33968128; PMCID: PMC8102816
Ehrhart، Friederike؛ Coort، Susan L. M.؛ Cirillo، Elisa؛ Smeets، Eric؛ Evelo، Chris T.؛ Curfs، Leopold M. G. (25 نوفمبر 2016). "Rett syndrome – biological pathways leading from MECP2 to disorder phenotypes". Orphanet Journal of Rare Diseases. ج. 11 ع. 1: 158. DOI:10.1186/s13023-016-0545-5. PMC:5123333. PMID:27884167.{{استشهاد بدورية محكمة}}: صيانة الاستشهاد: دوي مجاني غير معلم (link)

rettsyndrome.org

"About Rett syndrome - Rett Syndrome Diagnosis". www.rettsyndrome.org (بالإنجليزية الأمريكية). International Rett Syndrome Foundation. Archived from the original on 2017-10-29. Retrieved 2020-05-10.

web.archive.org

"About Rett syndrome - Rett Syndrome Diagnosis". www.rettsyndrome.org (بالإنجليزية الأمريكية). International Rett Syndrome Foundation. Archived from the original on 2017-10-29. Retrieved 2020-05-10.

wikidata.org

Disease Ontology (بالإنجليزية), 27 May 2016, QID:Q5282129
Jeffrey L Neul; Walter E Kaufmann; Daniel G Glaze; John Christodoulou; Nadia Bahi-Buisson; Alessandra Renieri; Alan K Percy (Dec 2010). "Rett syndrome: revised diagnostic criteria and nomenclature". Annals of Neurology (بالإنجليزية). 68 (6): 944–50. DOI:10.1002/ANA.22124. ISSN:0364-5134. PMC:3058521. PMID:21154482. QID:Q24596295.
Hong Xue (30 Jan 2022). "GABRB2, a key player in neuropsychiatric disorders and beyond". Gene. Gene Wiki Review Series (بالإنجليزية). 809. DOI:10.1016/J.GENE.2021.146021. ISSN:0378-1119. PMID:34673206. QID:Q109615004.

worldcat.org

Jeffrey L Neul; Walter E Kaufmann; Daniel G Glaze; John Christodoulou; Nadia Bahi-Buisson; Alessandra Renieri; Alan K Percy (Dec 2010). "Rett syndrome: revised diagnostic criteria and nomenclature". Annals of Neurology (بالإنجليزية). 68 (6): 944–50. DOI:10.1002/ANA.22124. ISSN:0364-5134. PMC:3058521. PMID:21154482. QID:Q24596295.
Hong Xue (30 Jan 2022). "GABRB2, a key player in neuropsychiatric disorders and beyond". Gene. Gene Wiki Review Series (بالإنجليزية). 809. DOI:10.1016/J.GENE.2021.146021. ISSN:0378-1119. PMID:34673206. QID:Q109615004.