متلازمة ثلاثية أ (Arabic Wikipedia)

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

refsWebsite

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16nih.gov

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12doi.org

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7semanticscholar.org

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86^th place

3web.archive.org

1^st place

2archive.org

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1karger.com

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1harvard.edu

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1orpha.net

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archive.org

M, Gazarian; Ct, Cowell; M, Bonney; Wg, Grigor (Jan 1995). "The "4A" Syndrome: Adrenocortical Insufficiency Associated With Achalasia, Alacrima, Autonomic and Other Neurological Abnormalities". European Journal of Pediatrics (بالإنجليزية). 154 (1): 18–23. DOI:10.1007/BF01972967. PMID:7895750. S2CID:8904441.
M, Krumbholz; K, Koehler; A, Huebner (Apr 2006). "Cellular Localization of 17 Natural Mutant Variants of ALADIN Protein in Triple A Syndrome - Shedding Light on an Unexpected Splice Mutation". Biochemistry and Cell Biology (بالإنجليزية). 84 (2): 243–9. DOI:10.1139/o05-198. PMID:16609705.

doi.org

Dusek, Tina؛ Korsic, Marta؛ Koehler, Katrin؛ Perkovic, Zdravko؛ Huebner, Angela؛ Korsic, Mirko (2006). "A Novel AAAS Gene Mutation (p.R194X) in a Patient with Triple A Syndrome". Hormone Research. ج. 65 ع. 4: 171–176. DOI:10.1159/000092003. PMID:16543750. S2CID:36128858.
M, Gazarian; Ct, Cowell; M, Bonney; Wg, Grigor (Jan 1995). "The "4A" Syndrome: Adrenocortical Insufficiency Associated With Achalasia, Alacrima, Autonomic and Other Neurological Abnormalities". European Journal of Pediatrics (بالإنجليزية). 154 (1): 18–23. DOI:10.1007/BF01972967. PMID:7895750. S2CID:8904441.
Prpic, I.؛ Huebner, A.؛ Persic, M.؛ Handschugg, K.؛ Pavletic, M. (2003). "Triple A syndrome: genotype-phenotype assessment". Clinical Genetics. ج. 63 ع. 5: 414–417. DOI:10.1034/j.1399-0004.2003.00070.x. PMID:12752575. S2CID:19250948.
Brooks, B.P.؛ Kleta, R.؛ Stuart, C.؛ Tuchman, M.؛ Jeong, A.؛ Stergiopoulos, S.G.؛ Bei, T.؛ Bjornson, B.؛ Russell, L.؛ Chanoine, J-P.؛ Tsagarakis, S.؛ Kalsner, LR.؛ Stratakis, CA. (2005). "Genotype heterogeneity and clinical phenotype in triple A syndrome". Clinical Genetics. ج. 68 ع. 3: 215–221. DOI:10.1111/j.1399-0004.2005.00482.x. PMID:16098009. S2CID:20404052.
Huebner, Angela؛ Kaindl, A.M.؛ Knobeloch, K.P.؛ Petzold, H.؛ Mann, P.؛ Koehler, K. (2004). "The Triple A Syndrome Is Due to Mutations in Aladin, a Novel Member of the Nuclear Pore Complex". Endocrine Research. ج. 30 ع. 4: 891–899. DOI:10.1081/ERC-200044138. PMID:15666842. S2CID:31047487.
Salmaggi A، Zirilli L، Pantaleoni C، وآخرون (2008). "Late-onset triple A syndrome: a risk of overlooked or delayed diagnosis and management". Horm. Res. ج. 70 ع. 6: 364–372. DOI:10.1159/000161867. PMID:18953174. S2CID:8097415. مؤرشف من الأصل في 2019-05-18.
Huebner A، Yoon SJ، Ozkinay F، وآخرون (نوفمبر 2000). "Triple A syndrome--clinical aspects and molecular genetics". Endocr. Res. ج. 26 ع. 4: 751–759. DOI:10.3109/07435800009048596. PMID:11196451. S2CID:42579320.
M, Krumbholz; K, Koehler; A, Huebner (Apr 2006). "Cellular Localization of 17 Natural Mutant Variants of ALADIN Protein in Triple A Syndrome - Shedding Light on an Unexpected Splice Mutation". Biochemistry and Cell Biology (بالإنجليزية). 84 (2): 243–9. DOI:10.1139/o05-198. PMID:16609705.
Hirano M، Furiya Y، Asai H، Yasui A، Ueno S (فبراير 2006). "ALADINI482S causes selective failure of nuclear protein import and hypersensitivity to oxidative stress in triple A syndrome". Proc. Natl. Acad. Sci. U.S.A. ج. 103 ع. 7: 2298–303. Bibcode:2006PNAS..103.2298H. DOI:10.1073/pnas.0505598103. PMC:1413683. PMID:16467144.
Wallace، I. R.؛ Hunter، S. J. (1 أغسطس 2012). "AAA syndrome--adrenal insufficiency, alacrima and achalasia". QJM. ج. 105 ع. 8: 803–804. DOI:10.1093/qjmed/hcr145. PMID:21865313.
Gaiani، Federica؛ Gismondi، Pierpacifico؛ Minelli، Roberta؛ Casadio، Giovanni؛ de’Angelis، Nicola؛ Fornaroli، Fabiola؛ de’Angelis، Gian Luigi؛ Manfredi، Marco (29 مايو 2020). "Case report of a familial triple: a syndrome and review of the literature". Medicine. ج. 99 ع. 22: e20474. DOI:10.1097/MD.0000000000020474. PMID:32481456.
Yadav، Prakarti؛ Kumar، Deepak؛ Bohra، Gopal K؛ Garg، Mahendra K (2020). "Triple A syndrome (Allgrove syndrome) – A journey from clinical symptoms to a syndrome". Journal of Family Medicine and Primary Care. ج. 9 ع. 5: 2531–2534. DOI:10.4103/jfmpc.jfmpc_237_20. PMC:7380807. PMID:32754538.

harvard.edu

ui.adsabs.harvard.edu

Hirano M، Furiya Y، Asai H، Yasui A، Ueno S (فبراير 2006). "ALADINI482S causes selective failure of nuclear protein import and hypersensitivity to oxidative stress in triple A syndrome". Proc. Natl. Acad. Sci. U.S.A. ج. 103 ع. 7: 2298–303. Bibcode:2006PNAS..103.2298H. DOI:10.1073/pnas.0505598103. PMC:1413683. PMID:16467144.

karger.com

Salmaggi A، Zirilli L، Pantaleoni C، وآخرون (2008). "Late-onset triple A syndrome: a risk of overlooked or delayed diagnosis and management". Horm. Res. ج. 70 ع. 6: 364–372. DOI:10.1159/000161867. PMID:18953174. S2CID:8097415. مؤرشف من الأصل في 2019-05-18.

nih.gov

pubmed.ncbi.nlm.nih.gov

Dusek, Tina؛ Korsic, Marta؛ Koehler, Katrin؛ Perkovic, Zdravko؛ Huebner, Angela؛ Korsic, Mirko (2006). "A Novel AAAS Gene Mutation (p.R194X) in a Patient with Triple A Syndrome". Hormone Research. ج. 65 ع. 4: 171–176. DOI:10.1159/000092003. PMID:16543750. S2CID:36128858.
M, Gazarian; Ct, Cowell; M, Bonney; Wg, Grigor (Jan 1995). "The "4A" Syndrome: Adrenocortical Insufficiency Associated With Achalasia, Alacrima, Autonomic and Other Neurological Abnormalities". European Journal of Pediatrics (بالإنجليزية). 154 (1): 18–23. DOI:10.1007/BF01972967. PMID:7895750. S2CID:8904441.
Bharadia, Lalit؛ Kalla, Mukesh؛ Sharma, S K؛ Charan, Rohit؛ Gupta, J B؛ Khan, Firoz (2005). "Triple A Syndrome". Indian Journal of Gastroenterology. ج. 24 ع. 5: 217–8. PMID:16361769.
Prpic, I.؛ Huebner, A.؛ Persic, M.؛ Handschugg, K.؛ Pavletic, M. (2003). "Triple A syndrome: genotype-phenotype assessment". Clinical Genetics. ج. 63 ع. 5: 414–417. DOI:10.1034/j.1399-0004.2003.00070.x. PMID:12752575. S2CID:19250948.
Brooks, B.P.؛ Kleta, R.؛ Stuart, C.؛ Tuchman, M.؛ Jeong, A.؛ Stergiopoulos, S.G.؛ Bei, T.؛ Bjornson, B.؛ Russell, L.؛ Chanoine, J-P.؛ Tsagarakis, S.؛ Kalsner, LR.؛ Stratakis, CA. (2005). "Genotype heterogeneity and clinical phenotype in triple A syndrome". Clinical Genetics. ج. 68 ع. 3: 215–221. DOI:10.1111/j.1399-0004.2005.00482.x. PMID:16098009. S2CID:20404052.
Huebner, Angela؛ Kaindl, A.M.؛ Knobeloch, K.P.؛ Petzold, H.؛ Mann, P.؛ Koehler, K. (2004). "The Triple A Syndrome Is Due to Mutations in Aladin, a Novel Member of the Nuclear Pore Complex". Endocrine Research. ج. 30 ع. 4: 891–899. DOI:10.1081/ERC-200044138. PMID:15666842. S2CID:31047487.
Salmaggi A، Zirilli L، Pantaleoni C، وآخرون (2008). "Late-onset triple A syndrome: a risk of overlooked or delayed diagnosis and management". Horm. Res. ج. 70 ع. 6: 364–372. DOI:10.1159/000161867. PMID:18953174. S2CID:8097415. مؤرشف من الأصل في 2019-05-18.
Huebner A، Yoon SJ، Ozkinay F، وآخرون (نوفمبر 2000). "Triple A syndrome--clinical aspects and molecular genetics". Endocr. Res. ج. 26 ع. 4: 751–759. DOI:10.3109/07435800009048596. PMID:11196451. S2CID:42579320.
M, Krumbholz; K, Koehler; A, Huebner (Apr 2006). "Cellular Localization of 17 Natural Mutant Variants of ALADIN Protein in Triple A Syndrome - Shedding Light on an Unexpected Splice Mutation". Biochemistry and Cell Biology (بالإنجليزية). 84 (2): 243–9. DOI:10.1139/o05-198. PMID:16609705.
Hirano M، Furiya Y، Asai H، Yasui A، Ueno S (فبراير 2006). "ALADINI482S causes selective failure of nuclear protein import and hypersensitivity to oxidative stress in triple A syndrome". Proc. Natl. Acad. Sci. U.S.A. ج. 103 ع. 7: 2298–303. Bibcode:2006PNAS..103.2298H. DOI:10.1073/pnas.0505598103. PMC:1413683. PMID:16467144.
Wallace، I. R.؛ Hunter، S. J. (1 أغسطس 2012). "AAA syndrome--adrenal insufficiency, alacrima and achalasia". QJM. ج. 105 ع. 8: 803–804. DOI:10.1093/qjmed/hcr145. PMID:21865313.
Gaiani، Federica؛ Gismondi، Pierpacifico؛ Minelli، Roberta؛ Casadio، Giovanni؛ de’Angelis، Nicola؛ Fornaroli، Fabiola؛ de’Angelis، Gian Luigi؛ Manfredi، Marco (29 مايو 2020). "Case report of a familial triple: a syndrome and review of the literature". Medicine. ج. 99 ع. 22: e20474. DOI:10.1097/MD.0000000000020474. PMID:32481456.
Yadav، Prakarti؛ Kumar، Deepak؛ Bohra، Gopal K؛ Garg، Mahendra K (2020). "Triple A syndrome (Allgrove syndrome) – A journey from clinical symptoms to a syndrome". Journal of Family Medicine and Primary Care. ج. 9 ع. 5: 2531–2534. DOI:10.4103/jfmpc.jfmpc_237_20. PMC:7380807. PMID:32754538.

ncbi.nlm.nih.gov

Hirano M، Furiya Y، Asai H، Yasui A، Ueno S (فبراير 2006). "ALADINI482S causes selective failure of nuclear protein import and hypersensitivity to oxidative stress in triple A syndrome". Proc. Natl. Acad. Sci. U.S.A. ج. 103 ع. 7: 2298–303. Bibcode:2006PNAS..103.2298H. DOI:10.1073/pnas.0505598103. PMC:1413683. PMID:16467144.
Yadav، Prakarti؛ Kumar، Deepak؛ Bohra، Gopal K؛ Garg، Mahendra K (2020). "Triple A syndrome (Allgrove syndrome) – A journey from clinical symptoms to a syndrome". Journal of Family Medicine and Primary Care. ج. 9 ع. 5: 2531–2534. DOI:10.4103/jfmpc.jfmpc_237_20. PMC:7380807. PMID:32754538.

ghr.nlm.nih.gov

"Triple A Syndrome". Genetics Home Reference. فبراير 2010. مؤرشف من الأصل في 2020-09-18. اطلع عليه بتاريخ 2020-05-10.

orpha.net

Nicolino، Marc (أبريل 2013). "Triple A syndrome". Orphanet. مؤرشف من الأصل في 2021-06-13. اطلع عليه بتاريخ 2020-08-31.

semanticscholar.org

api.semanticscholar.org

Dusek, Tina؛ Korsic, Marta؛ Koehler, Katrin؛ Perkovic, Zdravko؛ Huebner, Angela؛ Korsic, Mirko (2006). "A Novel AAAS Gene Mutation (p.R194X) in a Patient with Triple A Syndrome". Hormone Research. ج. 65 ع. 4: 171–176. DOI:10.1159/000092003. PMID:16543750. S2CID:36128858.
M, Gazarian; Ct, Cowell; M, Bonney; Wg, Grigor (Jan 1995). "The "4A" Syndrome: Adrenocortical Insufficiency Associated With Achalasia, Alacrima, Autonomic and Other Neurological Abnormalities". European Journal of Pediatrics (بالإنجليزية). 154 (1): 18–23. DOI:10.1007/BF01972967. PMID:7895750. S2CID:8904441.
Prpic, I.؛ Huebner, A.؛ Persic, M.؛ Handschugg, K.؛ Pavletic, M. (2003). "Triple A syndrome: genotype-phenotype assessment". Clinical Genetics. ج. 63 ع. 5: 414–417. DOI:10.1034/j.1399-0004.2003.00070.x. PMID:12752575. S2CID:19250948.
Brooks, B.P.؛ Kleta, R.؛ Stuart, C.؛ Tuchman, M.؛ Jeong, A.؛ Stergiopoulos, S.G.؛ Bei, T.؛ Bjornson, B.؛ Russell, L.؛ Chanoine, J-P.؛ Tsagarakis, S.؛ Kalsner, LR.؛ Stratakis, CA. (2005). "Genotype heterogeneity and clinical phenotype in triple A syndrome". Clinical Genetics. ج. 68 ع. 3: 215–221. DOI:10.1111/j.1399-0004.2005.00482.x. PMID:16098009. S2CID:20404052.
Huebner, Angela؛ Kaindl, A.M.؛ Knobeloch, K.P.؛ Petzold, H.؛ Mann, P.؛ Koehler, K. (2004). "The Triple A Syndrome Is Due to Mutations in Aladin, a Novel Member of the Nuclear Pore Complex". Endocrine Research. ج. 30 ع. 4: 891–899. DOI:10.1081/ERC-200044138. PMID:15666842. S2CID:31047487.
Salmaggi A، Zirilli L، Pantaleoni C، وآخرون (2008). "Late-onset triple A syndrome: a risk of overlooked or delayed diagnosis and management". Horm. Res. ج. 70 ع. 6: 364–372. DOI:10.1159/000161867. PMID:18953174. S2CID:8097415. مؤرشف من الأصل في 2019-05-18.
Huebner A، Yoon SJ، Ozkinay F، وآخرون (نوفمبر 2000). "Triple A syndrome--clinical aspects and molecular genetics". Endocr. Res. ج. 26 ع. 4: 751–759. DOI:10.3109/07435800009048596. PMID:11196451. S2CID:42579320.

web.archive.org

Salmaggi A، Zirilli L، Pantaleoni C، وآخرون (2008). "Late-onset triple A syndrome: a risk of overlooked or delayed diagnosis and management". Horm. Res. ج. 70 ع. 6: 364–372. DOI:10.1159/000161867. PMID:18953174. S2CID:8097415. مؤرشف من الأصل في 2019-05-18.
"Triple A Syndrome". Genetics Home Reference. فبراير 2010. مؤرشف من الأصل في 2020-09-18. اطلع عليه بتاريخ 2020-05-10.
Nicolino، Marc (أبريل 2013). "Triple A syndrome". Orphanet. مؤرشف من الأصل في 2021-06-13. اطلع عليه بتاريخ 2020-08-31.