خلل الأداء اللفظي التطوري (Arabic Wikipedia)

Analysis of information sources in references of the Wikipedia article "خلل الأداء اللفظي التطوري" in Arabic language version.

refsWebsite

Global rank Arabic rank

19nih.gov

4^th place

6^th place

10doi.org

2^nd place

5^th place

4web.archive.org

1^st place

2asha.org

low place

7,446^th place

1minervamedica.it

low place

1harvard.edu

18^th place

33^rd place

1zenodo.org

621^st place

1,331^st place

asha.org

"Childhood Apraxia of Speech". American Speech-Language-Hearing Association (ASHA) (2014). مؤرشف من الأصل (web page) في 2021-01-25.
"Childhood Apraxia of Speech". American Speech-Language-Hearing Association (ASHA). مؤرشف من الأصل في 2021-05-27. اطلع عليه بتاريخ 2013-10-07.

doi.org

Vargha-Khadem F، Watkins K، Alcock K، Fletcher P، Passingham R (يناير 1995). "Praxic and nonverbal cognitive deficits in a large family with a genetically transmitted speech and language disorder". Proceedings of the National Academy of Sciences of the United States of America. ج. 92 ع. 3: 930–3. Bibcode:1995PNAS...92..930V. DOI:10.1073/pnas.92.3.930. PMC:42734. PMID:7846081.
Watkins KE، Gadian DG، Vargha-Khadem F (نوفمبر 1999). "Functional and structural brain abnormalities associated with a genetic disorder of speech and language". American Journal of Human Genetics. ج. 65 ع. 5: 1215–21. DOI:10.1086/302631. PMC:1288272. PMID:10521285.
Newbury DF، Monaco AP (أكتوبر 2010). "Genetic advances in the study of speech and language disorders". Neuron. ج. 68 ع. 2: 309–20. DOI:10.1016/j.neuron.2010.10.001. PMC:2977079. PMID:20955937.
Vernes SC، MacDermot KD، Monaco AP، Fisher SE (أكتوبر 2009). "Assessing the impact of FOXP1 mutations on developmental verbal dyspraxia". European Journal of Human Genetics. ج. 17 ع. 10: 1354–8. DOI:10.1038/ejhg.2009.43. PMC:2784575. PMID:19352412.
Kang C، Drayna D (2011). "Genetics of speech and language disorders" (PDF). Annual Review of Genomics and Human Genetics. ج. 12: 145–64. DOI:10.1146/annurev-genom-090810-183119. PMID:21663442. مؤرشف من الأصل (PDF) في 2018-07-22.
MacDermot KD، Bonora E، Sykes N، Coupe AM، Lai CS، Vernes SC، Vargha-Khadem F، McKenzie F، Smith RL، Monaco AP، Fisher SE (يونيو 2005). "Identification of FOXP2 truncation as a novel cause of developmental speech and language deficits". American Journal of Human Genetics. ج. 76 ع. 6: 1074–80. DOI:10.1086/430841. PMC:1196445. PMID:15877281.
Preuss TM (يونيو 2012). "Human brain evolution: from gene discovery to phenotype discovery". Proceedings of the National Academy of Sciences of the United States of America. 109 Suppl 1: 10709–16. DOI:10.1073/pnas.1201894109. PMC:3386880. PMID:22723367.
Smith RS، Kenny CJ، Ganesh V، Jang A، Borges-Monroy R، Partlow JN، وآخرون (سبتمبر 2018). "V1.3) Regulation of Human Cerebral Cortical Folding and Oral Motor Development". Neuron. ج. 99 ع. 5: 905–913.e7. DOI:10.1016/j.neuron.2018.07.052. PMC:6226006. PMID:30146301.
Newbury DF، Mari F، Sadighi Akha E، Macdermot KD، Canitano R، Monaco AP، Taylor JC، Renieri A، Fisher SE، Knight SJ (أبريل 2013). "Dual copy number variants involving 16p11 and 6q22 in a case of childhood apraxia of speech and pervasive developmental disorder". European Journal of Human Genetics. ج. 21 ع. 4: 361–5. DOI:10.1038/ejhg.2012.166. PMC:3598310. PMID:22909776.
Lennon PA، Cooper ML، Peiffer DA، Gunderson KL، Patel A، Peters S، Cheung SW، Bacino CA (أبريل 2007). "Deletion of 7q31.1 supports involvement of FOXP2 in language impairment: clinical report and review". American Journal of Medical Genetics. Part A. ج. 143A ع. 8: 791–8. DOI:10.1002/ajmg.a.31632. PMID:17330859.

harvard.edu

ui.adsabs.harvard.edu

Vargha-Khadem F، Watkins K، Alcock K، Fletcher P، Passingham R (يناير 1995). "Praxic and nonverbal cognitive deficits in a large family with a genetically transmitted speech and language disorder". Proceedings of the National Academy of Sciences of the United States of America. ج. 92 ع. 3: 930–3. Bibcode:1995PNAS...92..930V. DOI:10.1073/pnas.92.3.930. PMC:42734. PMID:7846081.

minervamedica.it

Morgan AT، Vogel AP (مارس 2009). "A Cochrane review of treatment for childhood apraxia of speech". European Journal of Physical and Rehabilitation Medicine. ج. 45 ع. 1: 103–10. PMID:19156019. مؤرشف من الأصل في 2020-10-22.

nih.gov

pubmed.ncbi.nlm.nih.gov

Morgan AT، Vogel AP (مارس 2009). "A Cochrane review of treatment for childhood apraxia of speech". European Journal of Physical and Rehabilitation Medicine. ج. 45 ع. 1: 103–10. PMID:19156019. مؤرشف من الأصل في 2020-10-22.
Vargha-Khadem F، Watkins K، Alcock K، Fletcher P، Passingham R (يناير 1995). "Praxic and nonverbal cognitive deficits in a large family with a genetically transmitted speech and language disorder". Proceedings of the National Academy of Sciences of the United States of America. ج. 92 ع. 3: 930–3. Bibcode:1995PNAS...92..930V. DOI:10.1073/pnas.92.3.930. PMC:42734. PMID:7846081.
Watkins KE، Gadian DG، Vargha-Khadem F (نوفمبر 1999). "Functional and structural brain abnormalities associated with a genetic disorder of speech and language". American Journal of Human Genetics. ج. 65 ع. 5: 1215–21. DOI:10.1086/302631. PMC:1288272. PMID:10521285.
Newbury DF، Monaco AP (أكتوبر 2010). "Genetic advances in the study of speech and language disorders". Neuron. ج. 68 ع. 2: 309–20. DOI:10.1016/j.neuron.2010.10.001. PMC:2977079. PMID:20955937.
Vernes SC، MacDermot KD، Monaco AP، Fisher SE (أكتوبر 2009). "Assessing the impact of FOXP1 mutations on developmental verbal dyspraxia". European Journal of Human Genetics. ج. 17 ع. 10: 1354–8. DOI:10.1038/ejhg.2009.43. PMC:2784575. PMID:19352412.
Kang C، Drayna D (2011). "Genetics of speech and language disorders" (PDF). Annual Review of Genomics and Human Genetics. ج. 12: 145–64. DOI:10.1146/annurev-genom-090810-183119. PMID:21663442. مؤرشف من الأصل (PDF) في 2018-07-22.
MacDermot KD، Bonora E، Sykes N، Coupe AM، Lai CS، Vernes SC، Vargha-Khadem F، McKenzie F، Smith RL، Monaco AP، Fisher SE (يونيو 2005). "Identification of FOXP2 truncation as a novel cause of developmental speech and language deficits". American Journal of Human Genetics. ج. 76 ع. 6: 1074–80. DOI:10.1086/430841. PMC:1196445. PMID:15877281.
Preuss TM (يونيو 2012). "Human brain evolution: from gene discovery to phenotype discovery". Proceedings of the National Academy of Sciences of the United States of America. 109 Suppl 1: 10709–16. DOI:10.1073/pnas.1201894109. PMC:3386880. PMID:22723367.
Smith RS، Kenny CJ، Ganesh V، Jang A، Borges-Monroy R، Partlow JN، وآخرون (سبتمبر 2018). "V1.3) Regulation of Human Cerebral Cortical Folding and Oral Motor Development". Neuron. ج. 99 ع. 5: 905–913.e7. DOI:10.1016/j.neuron.2018.07.052. PMC:6226006. PMID:30146301.
Newbury DF، Mari F، Sadighi Akha E، Macdermot KD، Canitano R، Monaco AP، Taylor JC، Renieri A، Fisher SE، Knight SJ (أبريل 2013). "Dual copy number variants involving 16p11 and 6q22 in a case of childhood apraxia of speech and pervasive developmental disorder". European Journal of Human Genetics. ج. 21 ع. 4: 361–5. DOI:10.1038/ejhg.2012.166. PMC:3598310. PMID:22909776.
Lennon PA، Cooper ML، Peiffer DA، Gunderson KL، Patel A، Peters S، Cheung SW، Bacino CA (أبريل 2007). "Deletion of 7q31.1 supports involvement of FOXP2 in language impairment: clinical report and review". American Journal of Medical Genetics. Part A. ج. 143A ع. 8: 791–8. DOI:10.1002/ajmg.a.31632. PMID:17330859.

ncbi.nlm.nih.gov

Vargha-Khadem F، Watkins K، Alcock K، Fletcher P، Passingham R (يناير 1995). "Praxic and nonverbal cognitive deficits in a large family with a genetically transmitted speech and language disorder". Proceedings of the National Academy of Sciences of the United States of America. ج. 92 ع. 3: 930–3. Bibcode:1995PNAS...92..930V. DOI:10.1073/pnas.92.3.930. PMC:42734. PMID:7846081.
Watkins KE، Gadian DG، Vargha-Khadem F (نوفمبر 1999). "Functional and structural brain abnormalities associated with a genetic disorder of speech and language". American Journal of Human Genetics. ج. 65 ع. 5: 1215–21. DOI:10.1086/302631. PMC:1288272. PMID:10521285.
Newbury DF، Monaco AP (أكتوبر 2010). "Genetic advances in the study of speech and language disorders". Neuron. ج. 68 ع. 2: 309–20. DOI:10.1016/j.neuron.2010.10.001. PMC:2977079. PMID:20955937.
Vernes SC، MacDermot KD، Monaco AP، Fisher SE (أكتوبر 2009). "Assessing the impact of FOXP1 mutations on developmental verbal dyspraxia". European Journal of Human Genetics. ج. 17 ع. 10: 1354–8. DOI:10.1038/ejhg.2009.43. PMC:2784575. PMID:19352412.
MacDermot KD، Bonora E، Sykes N، Coupe AM، Lai CS، Vernes SC، Vargha-Khadem F، McKenzie F، Smith RL، Monaco AP، Fisher SE (يونيو 2005). "Identification of FOXP2 truncation as a novel cause of developmental speech and language deficits". American Journal of Human Genetics. ج. 76 ع. 6: 1074–80. DOI:10.1086/430841. PMC:1196445. PMID:15877281.
Preuss TM (يونيو 2012). "Human brain evolution: from gene discovery to phenotype discovery". Proceedings of the National Academy of Sciences of the United States of America. 109 Suppl 1: 10709–16. DOI:10.1073/pnas.1201894109. PMC:3386880. PMID:22723367.
Smith RS، Kenny CJ، Ganesh V، Jang A، Borges-Monroy R، Partlow JN، وآخرون (سبتمبر 2018). "V1.3) Regulation of Human Cerebral Cortical Folding and Oral Motor Development". Neuron. ج. 99 ع. 5: 905–913.e7. DOI:10.1016/j.neuron.2018.07.052. PMC:6226006. PMID:30146301.
Newbury DF، Mari F، Sadighi Akha E، Macdermot KD، Canitano R، Monaco AP، Taylor JC، Renieri A، Fisher SE، Knight SJ (أبريل 2013). "Dual copy number variants involving 16p11 and 6q22 in a case of childhood apraxia of speech and pervasive developmental disorder". European Journal of Human Genetics. ج. 21 ع. 4: 361–5. DOI:10.1038/ejhg.2012.166. PMC:3598310. PMID:22909776.

web.archive.org

"Childhood Apraxia of Speech". American Speech-Language-Hearing Association (ASHA) (2014). مؤرشف من الأصل (web page) في 2021-01-25.
Morgan AT، Vogel AP (مارس 2009). "A Cochrane review of treatment for childhood apraxia of speech". European Journal of Physical and Rehabilitation Medicine. ج. 45 ع. 1: 103–10. PMID:19156019. مؤرشف من الأصل في 2020-10-22.
"Childhood Apraxia of Speech". American Speech-Language-Hearing Association (ASHA). مؤرشف من الأصل في 2021-05-27. اطلع عليه بتاريخ 2013-10-07.
Kang C، Drayna D (2011). "Genetics of speech and language disorders" (PDF). Annual Review of Genomics and Human Genetics. ج. 12: 145–64. DOI:10.1146/annurev-genom-090810-183119. PMID:21663442. مؤرشف من الأصل (PDF) في 2018-07-22.

zenodo.org

Kang C، Drayna D (2011). "Genetics of speech and language disorders" (PDF). Annual Review of Genomics and Human Genetics. ج. 12: 145–64. DOI:10.1146/annurev-genom-090810-183119. PMID:21663442. مؤرشف من الأصل (PDF) في 2018-07-22.