متلازمة بارث (Arabic Wikipedia)

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

refsWebsite

Global rank Arabic rank

15nih.gov

4^th place

6^th place

11doi.org

2^nd place

5^th place

3wikidata.org

43^rd place

2^nd place

3web.archive.org

1^st place

2worldcat.org

5^th place

4^th place

2archive.org

6^th place

3^rd place

1disease-ontology.org

low place

594^th place

1obolibrary.org

2,299^th place

836^th place

1hopkinsmedicine.org

5,712^th place

1,825^th place

1barthsyndrome.org

low place

1ufhealth.org

low place

archive.org

Kelley RI، Cheatham JP، Clark BJ، وآخرون (نوفمبر 1991). "X-linked dilated cardiomyopathy with neutropenia, growth retardation, and 3-methylglutaconic aciduria". The Journal of Pediatrics. ج. 119 ع. 5: 738–47. DOI:10.1016/S0022-3476(05)80289-6. PMID:1719174.
Cantlay AM، Shokrollahi K، Allen JT، Lunt PW، Newbury-Ecob RA، Steward CG (سبتمبر 1999). "Genetic analysis of the G4.5 gene in families with suspected Barth syndrome". The Journal of Pediatrics. ج. 135 ع. 3: 311–5. DOI:10.1016/S0022-3476(99)70126-5. PMID:10484795.

barthsyndrome.org

Barth Syndrome Foundation, 28 Jun 2011. “Diagnosis of Barth Syndrome”. Available from: "Barth Syndrome Foundation : Home". مؤرشف من الأصل في 2012-04-26. اطلع عليه بتاريخ 2011-12-06.

disease-ontology.org

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

doi.org

Anders O Garlid; Calvin T Schaffer; Jaewoo Kim; Hirsh Bhatt; Vladimir Guevara-Gonzalez; Peipei Ping (21 Oct 2019). "TAZ encodes tafazzin, a transacylase essential for cardiolipin formation and central to the etiology of Barth syndrome". Gene. Gene Wiki Review Series (بالإنجليزية). 726: 144148. DOI:10.1016/J.GENE.2019.144148. ISSN:0378-1119. PMC:7646589. PMID:31647997. QID:Q81446954.
Claypool SM، Boontheung P، McCaffery JM، Loo JA، Koehler CM (ديسمبر 2008). "The cardiolipin transacylase, tafazzin, associates with two distinct respiratory components providing insight into Barth syndrome". Mol. Biol. Cell. ج. 19 ع. 12: 5143–55. DOI:10.1091/mbc.E08-09-0896. PMC:2592642. PMID:18799610.
Spencer CT، Bryant RM، Day J، وآخرون (أغسطس 2006). "Cardiac and clinical phenotype in Barth syndrome". Pediatrics. ج. 118 ع. 2: e337–46. DOI:10.1542/peds.2005-2667. PMID:16847078.
Kelley RI، Cheatham JP، Clark BJ، وآخرون (نوفمبر 1991). "X-linked dilated cardiomyopathy with neutropenia, growth retardation, and 3-methylglutaconic aciduria". The Journal of Pediatrics. ج. 119 ع. 5: 738–47. DOI:10.1016/S0022-3476(05)80289-6. PMID:1719174.
Barth PG، Scholte HR، Berden JA، وآخرون (ديسمبر 1983). "An X-linked mitochondrial disease affecting cardiac muscle, skeletal muscle and neutrophil leucocytes". Journal of the Neurological Sciences. ج. 62 ع. 1–3: 327–55. DOI:10.1016/0022-510X(83)90209-5. PMID:6142097.
Schlame M، Kelley RI، Feigenbaum A، وآخرون (ديسمبر 2003). "Phospholipid abnormalities in children with Barth syndrome". Journal of the American College of Cardiology. ج. 42 ع. 11: 1994–9. DOI:10.1016/j.jacc.2003.06.015. PMID:14662265.
Vreken P، Valianpour F، Nijtmans LG، وآخرون (ديسمبر 2000). "Defective remodeling of cardiolipin and phosphatidylglycerol in Barth syndrome". Biochemical and Biophysical Research Communications. ج. 279 ع. 2: 378–82. DOI:10.1006/bbrc.2000.3952. PMID:11118295.
Steward CG، Newbury-Ecob RA، Hastings R، وآخرون (أكتوبر 2010). "Barth syndrome: an X-linked cause of fetal cardiomyopathy and stillbirth". Prenat. Diagn. ج. 30 ع. 10: 970–6. DOI:10.1002/pd.2599. PMC:2995309. PMID:20812380.
Suzuki-Hatano, Silveli; Saha, Madhurima; Rizzo, Skylar A.; Witko, Rachael L.; Gosiker, Bennett J.; Ramanathan, Manashwi; Soustek, Meghan S.; Jones, Michael D.; Kang, Peter B. (2 Aug 2018). "AAV-Mediated TAZ Gene Replacement Restores Mitochondrial and Cardioskeletal Function in Barth Syndrome". Human Gene Therapy (بالإنجليزية). 30 (2): 139–154. DOI:10.1089/hum.2018.020. ISSN:1043-0342. PMC:6383582. PMID:30070157.
Cosson L، Toutain A، Simard G، Kulik W، Matyas G، Guichet A، Blasco H، Maakaroun-Vermesse Z، Vaillant MC، Le Caignec C، Chantepie A، Labarthe F (مايو 2012). "Barth syndrome in a female patient". Mol Genet Metab. ج. 106 ع. 1: 115–20. DOI:10.1016/j.ymgme.2012.01.015. PMID:22410210.
Cantlay AM، Shokrollahi K، Allen JT، Lunt PW، Newbury-Ecob RA، Steward CG (سبتمبر 1999). "Genetic analysis of the G4.5 gene in families with suspected Barth syndrome". The Journal of Pediatrics. ج. 135 ع. 3: 311–5. DOI:10.1016/S0022-3476(99)70126-5. PMID:10484795.

hopkinsmedicine.org

Kelley RI, [cited 6 Dec 2011]. “Barth Syndrome - X-linked Cardiomyopathy and Neutropenia”. Department of Pediatrics, Johns Hopkins Medical Institutions. Available from: "Archived copy". مؤرشف من الأصل في 2004-12-14. اطلع عليه بتاريخ 2004-12-19.{{استشهاد ويب}}: صيانة الاستشهاد: الأرشيف كعنوان (link)

nih.gov

pubmed.ncbi.nlm.nih.gov

Anders O Garlid; Calvin T Schaffer; Jaewoo Kim; Hirsh Bhatt; Vladimir Guevara-Gonzalez; Peipei Ping (21 Oct 2019). "TAZ encodes tafazzin, a transacylase essential for cardiolipin formation and central to the etiology of Barth syndrome". Gene. Gene Wiki Review Series (بالإنجليزية). 726: 144148. DOI:10.1016/J.GENE.2019.144148. ISSN:0378-1119. PMC:7646589. PMID:31647997. QID:Q81446954.
Claypool SM، Boontheung P، McCaffery JM، Loo JA، Koehler CM (ديسمبر 2008). "The cardiolipin transacylase, tafazzin, associates with two distinct respiratory components providing insight into Barth syndrome". Mol. Biol. Cell. ج. 19 ع. 12: 5143–55. DOI:10.1091/mbc.E08-09-0896. PMC:2592642. PMID:18799610.
Spencer CT، Bryant RM، Day J، وآخرون (أغسطس 2006). "Cardiac and clinical phenotype in Barth syndrome". Pediatrics. ج. 118 ع. 2: e337–46. DOI:10.1542/peds.2005-2667. PMID:16847078.
Kelley RI، Cheatham JP، Clark BJ، وآخرون (نوفمبر 1991). "X-linked dilated cardiomyopathy with neutropenia, growth retardation, and 3-methylglutaconic aciduria". The Journal of Pediatrics. ج. 119 ع. 5: 738–47. DOI:10.1016/S0022-3476(05)80289-6. PMID:1719174.
Barth PG، Scholte HR، Berden JA، وآخرون (ديسمبر 1983). "An X-linked mitochondrial disease affecting cardiac muscle, skeletal muscle and neutrophil leucocytes". Journal of the Neurological Sciences. ج. 62 ع. 1–3: 327–55. DOI:10.1016/0022-510X(83)90209-5. PMID:6142097.
Schlame M، Kelley RI، Feigenbaum A، وآخرون (ديسمبر 2003). "Phospholipid abnormalities in children with Barth syndrome". Journal of the American College of Cardiology. ج. 42 ع. 11: 1994–9. DOI:10.1016/j.jacc.2003.06.015. PMID:14662265.
Vreken P، Valianpour F، Nijtmans LG، وآخرون (ديسمبر 2000). "Defective remodeling of cardiolipin and phosphatidylglycerol in Barth syndrome". Biochemical and Biophysical Research Communications. ج. 279 ع. 2: 378–82. DOI:10.1006/bbrc.2000.3952. PMID:11118295.
Steward CG، Newbury-Ecob RA، Hastings R، وآخرون (أكتوبر 2010). "Barth syndrome: an X-linked cause of fetal cardiomyopathy and stillbirth". Prenat. Diagn. ج. 30 ع. 10: 970–6. DOI:10.1002/pd.2599. PMC:2995309. PMID:20812380.
Suzuki-Hatano, Silveli; Saha, Madhurima; Rizzo, Skylar A.; Witko, Rachael L.; Gosiker, Bennett J.; Ramanathan, Manashwi; Soustek, Meghan S.; Jones, Michael D.; Kang, Peter B. (2 Aug 2018). "AAV-Mediated TAZ Gene Replacement Restores Mitochondrial and Cardioskeletal Function in Barth Syndrome". Human Gene Therapy (بالإنجليزية). 30 (2): 139–154. DOI:10.1089/hum.2018.020. ISSN:1043-0342. PMC:6383582. PMID:30070157.
Cosson L، Toutain A، Simard G، Kulik W، Matyas G، Guichet A، Blasco H، Maakaroun-Vermesse Z، Vaillant MC، Le Caignec C، Chantepie A، Labarthe F (مايو 2012). "Barth syndrome in a female patient". Mol Genet Metab. ج. 106 ع. 1: 115–20. DOI:10.1016/j.ymgme.2012.01.015. PMID:22410210.
Cantlay AM، Shokrollahi K، Allen JT، Lunt PW، Newbury-Ecob RA، Steward CG (سبتمبر 1999). "Genetic analysis of the G4.5 gene in families with suspected Barth syndrome". The Journal of Pediatrics. ج. 135 ع. 3: 311–5. DOI:10.1016/S0022-3476(99)70126-5. PMID:10484795.

ncbi.nlm.nih.gov

Anders O Garlid; Calvin T Schaffer; Jaewoo Kim; Hirsh Bhatt; Vladimir Guevara-Gonzalez; Peipei Ping (21 Oct 2019). "TAZ encodes tafazzin, a transacylase essential for cardiolipin formation and central to the etiology of Barth syndrome". Gene. Gene Wiki Review Series (بالإنجليزية). 726: 144148. DOI:10.1016/J.GENE.2019.144148. ISSN:0378-1119. PMC:7646589. PMID:31647997. QID:Q81446954.
Claypool SM، Boontheung P، McCaffery JM، Loo JA، Koehler CM (ديسمبر 2008). "The cardiolipin transacylase, tafazzin, associates with two distinct respiratory components providing insight into Barth syndrome". Mol. Biol. Cell. ج. 19 ع. 12: 5143–55. DOI:10.1091/mbc.E08-09-0896. PMC:2592642. PMID:18799610.
Steward CG، Newbury-Ecob RA، Hastings R، وآخرون (أكتوبر 2010). "Barth syndrome: an X-linked cause of fetal cardiomyopathy and stillbirth". Prenat. Diagn. ج. 30 ع. 10: 970–6. DOI:10.1002/pd.2599. PMC:2995309. PMID:20812380.
Suzuki-Hatano, Silveli; Saha, Madhurima; Rizzo, Skylar A.; Witko, Rachael L.; Gosiker, Bennett J.; Ramanathan, Manashwi; Soustek, Meghan S.; Jones, Michael D.; Kang, Peter B. (2 Aug 2018). "AAV-Mediated TAZ Gene Replacement Restores Mitochondrial and Cardioskeletal Function in Barth Syndrome". Human Gene Therapy (بالإنجليزية). 30 (2): 139–154. DOI:10.1089/hum.2018.020. ISSN:1043-0342. PMC:6383582. PMID:30070157.

obolibrary.org

purl.obolibrary.org

Monarch Disease Ontology release 2018-06-29 (ط. 2018-06-29)، 29 يونيو 2018، QID:Q55345445

ufhealth.org

"Gene therapy for heart, skeletal muscle disorder shows promise in preclinical model | UF Health, University of Florida Health". مؤرشف من الأصل في 2019-04-13.

web.archive.org

Kelley RI, [cited 6 Dec 2011]. “Barth Syndrome - X-linked Cardiomyopathy and Neutropenia”. Department of Pediatrics, Johns Hopkins Medical Institutions. Available from: "Archived copy". مؤرشف من الأصل في 2004-12-14. اطلع عليه بتاريخ 2004-12-19.{{استشهاد ويب}}: صيانة الاستشهاد: الأرشيف كعنوان (link)
Barth Syndrome Foundation, 28 Jun 2011. “Diagnosis of Barth Syndrome”. Available from: "Barth Syndrome Foundation : Home". مؤرشف من الأصل في 2012-04-26. اطلع عليه بتاريخ 2011-12-06.
"Gene therapy for heart, skeletal muscle disorder shows promise in preclinical model | UF Health, University of Florida Health". مؤرشف من الأصل في 2019-04-13.

wikidata.org

Disease Ontology (بالإنجليزية), 27 May 2016, QID:Q5282129
Monarch Disease Ontology release 2018-06-29 (ط. 2018-06-29)، 29 يونيو 2018، QID:Q55345445
Anders O Garlid; Calvin T Schaffer; Jaewoo Kim; Hirsh Bhatt; Vladimir Guevara-Gonzalez; Peipei Ping (21 Oct 2019). "TAZ encodes tafazzin, a transacylase essential for cardiolipin formation and central to the etiology of Barth syndrome". Gene. Gene Wiki Review Series (بالإنجليزية). 726: 144148. DOI:10.1016/J.GENE.2019.144148. ISSN:0378-1119. PMC:7646589. PMID:31647997. QID:Q81446954.

worldcat.org

Anders O Garlid; Calvin T Schaffer; Jaewoo Kim; Hirsh Bhatt; Vladimir Guevara-Gonzalez; Peipei Ping (21 Oct 2019). "TAZ encodes tafazzin, a transacylase essential for cardiolipin formation and central to the etiology of Barth syndrome". Gene. Gene Wiki Review Series (بالإنجليزية). 726: 144148. DOI:10.1016/J.GENE.2019.144148. ISSN:0378-1119. PMC:7646589. PMID:31647997. QID:Q81446954.
Suzuki-Hatano, Silveli; Saha, Madhurima; Rizzo, Skylar A.; Witko, Rachael L.; Gosiker, Bennett J.; Ramanathan, Manashwi; Soustek, Meghan S.; Jones, Michael D.; Kang, Peter B. (2 Aug 2018). "AAV-Mediated TAZ Gene Replacement Restores Mitochondrial and Cardioskeletal Function in Barth Syndrome". Human Gene Therapy (بالإنجليزية). 30 (2): 139–154. DOI:10.1089/hum.2018.020. ISSN:1043-0342. PMC:6383582. PMID:30070157.