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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
4th place
6th place
6doi.org
2nd place
5th place
2worldcat.org
5th place
4th place
2wikidata.org
43rd place
2nd place
1europepmc.org
8,929th place
5,455th place
1rettsyndrome.org
low place
low place
1web.archive.org
1st place
1st place

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

web.archive.org

wikidata.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.

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.