Bệnh lý nhiễm kết hợp axit malonic và methylmalonic trong nước tiểu (Vietnamese Wikipedia)

Analysis of information sources in references of the Wikipedia article "Bệnh lý nhiễm kết hợp axit malonic và methylmalonic trong nước tiểu" in Vietnamese language version.

refsWebsite

Global rank Vietnamese rank

10doi.org

2^nd place

10nih.gov

4^th place

7^th place

5worldcat.org

5^th place

13^th place

3elsevier.com

610^th place

1,100^th place

3wiley.com

222^nd place

1springer.com

274^th place

484^th place

1nature.com

234^th place

153^rd place

1frontiersin.org

4,679^th place

3,109^th place

1bmj.com

1,226^th place

1,573^rd place

bmj.com

jmg.bmj.com

Alfares, A.; Nunez, L. D.; Al-Thihli, K.; Mitchell, J.; Melancon, S.; Anastasio, N.; Ha, K. C. H.; Majewski, J.; Rosenblatt, D. S. (ngày 1 tháng 9 năm 2011). “Combined malonic and methylmalonic aciduria: exome sequencing reveals mutations in the ACSF3 gene in patients with a non-classic phenotype”. Journal of Medical Genetics (bằng tiếng Anh). 48 (9): 602–605. doi:10.1136/jmedgenet-2011-100230. ISSN 0022-2593.

doi.org

de Sain-van der Velden, Monique G. M.; van der Ham, Maria; Jans, Judith J.; Visser, Gepke; Prinsen, Hubertus C. M. T.; Verhoeven-Duif, Nanda M.; van Gassen, Koen L. I.; van Hasselt, Peter M. (2016), Morava, Eva; Baumgartner, Matthias; Patterson, Marc; Rahman, Shamima (biên tập), “A New Approach for Fast Metabolic Diagnostics in CMAMMA”, JIMD Reports, Volume 30, Berlin, Heidelberg: Springer Berlin Heidelberg, 30, tr. 15–22, doi:10.1007/8904_2016_531, ISBN 978-3-662-53680-3, PMC 5110436, PMID 26915364
NIH Intramural Sequencing Center Group; Sloan, Jennifer L; Johnston, Jennifer J; Manoli, Irini; Chandler, Randy J; Krause, Caitlin; Carrillo-Carrasco, Nuria; Chandrasekaran, Suma D; Sysol, Justin R (tháng 9 năm 2011). “Exome sequencing identifies ACSF3 as a cause of combined malonic and methylmalonic aciduria”. Nature Genetics (bằng tiếng Anh). 43 (9): 883–886. doi:10.1038/ng.908. ISSN 1061-4036. PMC 3163731. PMID 21841779.
Sniderman, Lisa C.; Lambert, Marie; Giguère, Robert; Auray-Blais, Christiane; Lemieux, Bernard; Laframboise, Rachel; Rosenblatt, David S.; Treacy, Eileen P. (tháng 6 năm 1999). “Outcome of individuals with low-moderate methylmalonic aciduria detected through a neonatal screening program”. The Journal of Pediatrics (bằng tiếng Anh). 134 (6): 675–680. doi:10.1016/S0022-3476(99)70280-5.
Wang, Ping; Shu, Jianbo; Gu, Chunyu; Yu, Xiaoli; Zheng, Jie; Zhang, Chunhua; Cai, Chunquan (ngày 25 tháng 11 năm 2021). “Combined Malonic and Methylmalonic Aciduria Due to ACSF3 Variants Results in Benign Clinical Course in Three Chinese Patients”. Frontiers in Pediatrics. 9: 751895. doi:10.3389/fped.2021.751895. ISSN 2296-2360. PMC 8658908. PMID 34900860.
Alfares, A.; Nunez, L. D.; Al-Thihli, K.; Mitchell, J.; Melancon, S.; Anastasio, N.; Ha, K. C. H.; Majewski, J.; Rosenblatt, D. S. (ngày 1 tháng 9 năm 2011). “Combined malonic and methylmalonic aciduria: exome sequencing reveals mutations in the ACSF3 gene in patients with a non-classic phenotype”. Journal of Medical Genetics (bằng tiếng Anh). 48 (9): 602–605. doi:10.1136/jmedgenet-2011-100230. ISSN 0022-2593.
Wehbe, Zeinab; Behringer, Sidney; Alatibi, Khaled; Watkins, David; Rosenblatt, David; Spiekerkoetter, Ute; Tucci, Sara (tháng 11 năm 2019). “The emerging role of the mitochondrial fatty-acid synthase (mtFASII) in the regulation of energy metabolism”. Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids (bằng tiếng Anh). 1864 (11): 1629–1643. doi:10.1016/j.bbalip.2019.07.012.
Levtova, Alina; Waters, Paula J.; Buhas, Daniela; Lévesque, Sébastien; Auray‐Blais, Christiane; Clarke, Joe T.R.; Laframboise, Rachel; Maranda, Bruno; Mitchell, Grant A. (tháng 1 năm 2019). “Combined malonic and methylmalonic aciduria due to ACSF3 mutations: Benign clinical course in an unselected cohort”. Journal of Inherited Metabolic Disease (bằng tiếng Anh). 42 (1): 107–116. doi:10.1002/jimd.12032. ISSN 0141-8955.
Gregg, A. R.; Warman, A. W.; Thorburn, D. R.; O'Brien, W. E. (tháng 6 năm 1998). “Combined malonic and methylmalonic aciduria with normal malonyl-coenzyme A decarboxylase activity: A case supporting multiple aetiologies”. Journal of Inherited Metabolic Disease (bằng tiếng Anh). 21 (4): 382–390. doi:10.1023/A:1005302607897.
Witkowski, Andrzej; Thweatt, Jennifer; Smith, Stuart (tháng 9 năm 2011). “Mammalian ACSF3 Protein Is a Malonyl-CoA Synthetase That Supplies the Chain Extender Units for Mitochondrial Fatty Acid Synthesis”. Journal of Biological Chemistry (bằng tiếng Anh). 286 (39): 33729–33736. doi:10.1074/jbc.M111.291591. PMC 3190830. PMID 21846720.
Gabriel, Marie Cosette; Rice, Stephanie M.; Sloan, Jennifer L.; Mossayebi, Matthew H.; Venditti, Charles P.; Al‐Kouatly, Huda B. (tháng 4 năm 2021). “Considerations of expanded carrier screening: Lessons learned from combined malonic and methylmalonic aciduria”. Molecular Genetics & Genomic Medicine (bằng tiếng Anh). 9 (4). doi:10.1002/mgg3.1621. ISSN 2324-9269. PMC 8123733. PMID 33625768.

elsevier.com

linkinghub.elsevier.com

Sniderman, Lisa C.; Lambert, Marie; Giguère, Robert; Auray-Blais, Christiane; Lemieux, Bernard; Laframboise, Rachel; Rosenblatt, David S.; Treacy, Eileen P. (tháng 6 năm 1999). “Outcome of individuals with low-moderate methylmalonic aciduria detected through a neonatal screening program”. The Journal of Pediatrics (bằng tiếng Anh). 134 (6): 675–680. doi:10.1016/S0022-3476(99)70280-5.
Wehbe, Zeinab; Behringer, Sidney; Alatibi, Khaled; Watkins, David; Rosenblatt, David; Spiekerkoetter, Ute; Tucci, Sara (tháng 11 năm 2019). “The emerging role of the mitochondrial fatty-acid synthase (mtFASII) in the regulation of energy metabolism”. Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids (bằng tiếng Anh). 1864 (11): 1629–1643. doi:10.1016/j.bbalip.2019.07.012.
Witkowski, Andrzej; Thweatt, Jennifer; Smith, Stuart (tháng 9 năm 2011). “Mammalian ACSF3 Protein Is a Malonyl-CoA Synthetase That Supplies the Chain Extender Units for Mitochondrial Fatty Acid Synthesis”. Journal of Biological Chemistry (bằng tiếng Anh). 286 (39): 33729–33736. doi:10.1074/jbc.M111.291591. PMC 3190830. PMID 21846720.

frontiersin.org

Wang, Ping; Shu, Jianbo; Gu, Chunyu; Yu, Xiaoli; Zheng, Jie; Zhang, Chunhua; Cai, Chunquan (ngày 25 tháng 11 năm 2021). “Combined Malonic and Methylmalonic Aciduria Due to ACSF3 Variants Results in Benign Clinical Course in Three Chinese Patients”. Frontiers in Pediatrics. 9: 751895. doi:10.3389/fped.2021.751895. ISSN 2296-2360. PMC 8658908. PMID 34900860.

nature.com

NIH Intramural Sequencing Center Group; Sloan, Jennifer L; Johnston, Jennifer J; Manoli, Irini; Chandler, Randy J; Krause, Caitlin; Carrillo-Carrasco, Nuria; Chandrasekaran, Suma D; Sysol, Justin R (tháng 9 năm 2011). “Exome sequencing identifies ACSF3 as a cause of combined malonic and methylmalonic aciduria”. Nature Genetics (bằng tiếng Anh). 43 (9): 883–886. doi:10.1038/ng.908. ISSN 1061-4036. PMC 3163731. PMID 21841779.

nih.gov

ncbi.nlm.nih.gov

de Sain-van der Velden, Monique G. M.; van der Ham, Maria; Jans, Judith J.; Visser, Gepke; Prinsen, Hubertus C. M. T.; Verhoeven-Duif, Nanda M.; van Gassen, Koen L. I.; van Hasselt, Peter M. (2016), Morava, Eva; Baumgartner, Matthias; Patterson, Marc; Rahman, Shamima (biên tập), “A New Approach for Fast Metabolic Diagnostics in CMAMMA”, JIMD Reports, Volume 30, Berlin, Heidelberg: Springer Berlin Heidelberg, 30, tr. 15–22, doi:10.1007/8904_2016_531, ISBN 978-3-662-53680-3, PMC 5110436, PMID 26915364
NIH Intramural Sequencing Center Group; Sloan, Jennifer L; Johnston, Jennifer J; Manoli, Irini; Chandler, Randy J; Krause, Caitlin; Carrillo-Carrasco, Nuria; Chandrasekaran, Suma D; Sysol, Justin R (tháng 9 năm 2011). “Exome sequencing identifies ACSF3 as a cause of combined malonic and methylmalonic aciduria”. Nature Genetics (bằng tiếng Anh). 43 (9): 883–886. doi:10.1038/ng.908. ISSN 1061-4036. PMC 3163731. PMID 21841779.
Wang, Ping; Shu, Jianbo; Gu, Chunyu; Yu, Xiaoli; Zheng, Jie; Zhang, Chunhua; Cai, Chunquan (ngày 25 tháng 11 năm 2021). “Combined Malonic and Methylmalonic Aciduria Due to ACSF3 Variants Results in Benign Clinical Course in Three Chinese Patients”. Frontiers in Pediatrics. 9: 751895. doi:10.3389/fped.2021.751895. ISSN 2296-2360. PMC 8658908. PMID 34900860.
Witkowski, Andrzej; Thweatt, Jennifer; Smith, Stuart (tháng 9 năm 2011). “Mammalian ACSF3 Protein Is a Malonyl-CoA Synthetase That Supplies the Chain Extender Units for Mitochondrial Fatty Acid Synthesis”. Journal of Biological Chemistry (bằng tiếng Anh). 286 (39): 33729–33736. doi:10.1074/jbc.M111.291591. PMC 3190830. PMID 21846720.
Gabriel, Marie Cosette; Rice, Stephanie M.; Sloan, Jennifer L.; Mossayebi, Matthew H.; Venditti, Charles P.; Al‐Kouatly, Huda B. (tháng 4 năm 2021). “Considerations of expanded carrier screening: Lessons learned from combined malonic and methylmalonic aciduria”. Molecular Genetics & Genomic Medicine (bằng tiếng Anh). 9 (4). doi:10.1002/mgg3.1621. ISSN 2324-9269. PMC 8123733. PMID 33625768.

pubmed.ncbi.nlm.nih.gov

de Sain-van der Velden, Monique G. M.; van der Ham, Maria; Jans, Judith J.; Visser, Gepke; Prinsen, Hubertus C. M. T.; Verhoeven-Duif, Nanda M.; van Gassen, Koen L. I.; van Hasselt, Peter M. (2016), Morava, Eva; Baumgartner, Matthias; Patterson, Marc; Rahman, Shamima (biên tập), “A New Approach for Fast Metabolic Diagnostics in CMAMMA”, JIMD Reports, Volume 30, Berlin, Heidelberg: Springer Berlin Heidelberg, 30, tr. 15–22, doi:10.1007/8904_2016_531, ISBN 978-3-662-53680-3, PMC 5110436, PMID 26915364
NIH Intramural Sequencing Center Group; Sloan, Jennifer L; Johnston, Jennifer J; Manoli, Irini; Chandler, Randy J; Krause, Caitlin; Carrillo-Carrasco, Nuria; Chandrasekaran, Suma D; Sysol, Justin R (tháng 9 năm 2011). “Exome sequencing identifies ACSF3 as a cause of combined malonic and methylmalonic aciduria”. Nature Genetics (bằng tiếng Anh). 43 (9): 883–886. doi:10.1038/ng.908. ISSN 1061-4036. PMC 3163731. PMID 21841779.
Wang, Ping; Shu, Jianbo; Gu, Chunyu; Yu, Xiaoli; Zheng, Jie; Zhang, Chunhua; Cai, Chunquan (ngày 25 tháng 11 năm 2021). “Combined Malonic and Methylmalonic Aciduria Due to ACSF3 Variants Results in Benign Clinical Course in Three Chinese Patients”. Frontiers in Pediatrics. 9: 751895. doi:10.3389/fped.2021.751895. ISSN 2296-2360. PMC 8658908. PMID 34900860.
Witkowski, Andrzej; Thweatt, Jennifer; Smith, Stuart (tháng 9 năm 2011). “Mammalian ACSF3 Protein Is a Malonyl-CoA Synthetase That Supplies the Chain Extender Units for Mitochondrial Fatty Acid Synthesis”. Journal of Biological Chemistry (bằng tiếng Anh). 286 (39): 33729–33736. doi:10.1074/jbc.M111.291591. PMC 3190830. PMID 21846720.
Gabriel, Marie Cosette; Rice, Stephanie M.; Sloan, Jennifer L.; Mossayebi, Matthew H.; Venditti, Charles P.; Al‐Kouatly, Huda B. (tháng 4 năm 2021). “Considerations of expanded carrier screening: Lessons learned from combined malonic and methylmalonic aciduria”. Molecular Genetics & Genomic Medicine (bằng tiếng Anh). 9 (4). doi:10.1002/mgg3.1621. ISSN 2324-9269. PMC 8123733. PMID 33625768.

springer.com

link.springer.com

de Sain-van der Velden, Monique G. M.; van der Ham, Maria; Jans, Judith J.; Visser, Gepke; Prinsen, Hubertus C. M. T.; Verhoeven-Duif, Nanda M.; van Gassen, Koen L. I.; van Hasselt, Peter M. (2016), Morava, Eva; Baumgartner, Matthias; Patterson, Marc; Rahman, Shamima (biên tập), “A New Approach for Fast Metabolic Diagnostics in CMAMMA”, JIMD Reports, Volume 30, Berlin, Heidelberg: Springer Berlin Heidelberg, 30, tr. 15–22, doi:10.1007/8904_2016_531, ISBN 978-3-662-53680-3, PMC 5110436, PMID 26915364

wiley.com

onlinelibrary.wiley.com

Levtova, Alina; Waters, Paula J.; Buhas, Daniela; Lévesque, Sébastien; Auray‐Blais, Christiane; Clarke, Joe T.R.; Laframboise, Rachel; Maranda, Bruno; Mitchell, Grant A. (tháng 1 năm 2019). “Combined malonic and methylmalonic aciduria due to ACSF3 mutations: Benign clinical course in an unselected cohort”. Journal of Inherited Metabolic Disease (bằng tiếng Anh). 42 (1): 107–116. doi:10.1002/jimd.12032. ISSN 0141-8955.
Gabriel, Marie Cosette; Rice, Stephanie M.; Sloan, Jennifer L.; Mossayebi, Matthew H.; Venditti, Charles P.; Al‐Kouatly, Huda B. (tháng 4 năm 2021). “Considerations of expanded carrier screening: Lessons learned from combined malonic and methylmalonic aciduria”. Molecular Genetics & Genomic Medicine (bằng tiếng Anh). 9 (4). doi:10.1002/mgg3.1621. ISSN 2324-9269. PMC 8123733. PMID 33625768.

doi.wiley.com

Gregg, A. R.; Warman, A. W.; Thorburn, D. R.; O'Brien, W. E. (tháng 6 năm 1998). “Combined malonic and methylmalonic aciduria with normal malonyl-coenzyme A decarboxylase activity: A case supporting multiple aetiologies”. Journal of Inherited Metabolic Disease (bằng tiếng Anh). 21 (4): 382–390. doi:10.1023/A:1005302607897.

worldcat.org

NIH Intramural Sequencing Center Group; Sloan, Jennifer L; Johnston, Jennifer J; Manoli, Irini; Chandler, Randy J; Krause, Caitlin; Carrillo-Carrasco, Nuria; Chandrasekaran, Suma D; Sysol, Justin R (tháng 9 năm 2011). “Exome sequencing identifies ACSF3 as a cause of combined malonic and methylmalonic aciduria”. Nature Genetics (bằng tiếng Anh). 43 (9): 883–886. doi:10.1038/ng.908. ISSN 1061-4036. PMC 3163731. PMID 21841779.
Wang, Ping; Shu, Jianbo; Gu, Chunyu; Yu, Xiaoli; Zheng, Jie; Zhang, Chunhua; Cai, Chunquan (ngày 25 tháng 11 năm 2021). “Combined Malonic and Methylmalonic Aciduria Due to ACSF3 Variants Results in Benign Clinical Course in Three Chinese Patients”. Frontiers in Pediatrics. 9: 751895. doi:10.3389/fped.2021.751895. ISSN 2296-2360. PMC 8658908. PMID 34900860.
Alfares, A.; Nunez, L. D.; Al-Thihli, K.; Mitchell, J.; Melancon, S.; Anastasio, N.; Ha, K. C. H.; Majewski, J.; Rosenblatt, D. S. (ngày 1 tháng 9 năm 2011). “Combined malonic and methylmalonic aciduria: exome sequencing reveals mutations in the ACSF3 gene in patients with a non-classic phenotype”. Journal of Medical Genetics (bằng tiếng Anh). 48 (9): 602–605. doi:10.1136/jmedgenet-2011-100230. ISSN 0022-2593.
Levtova, Alina; Waters, Paula J.; Buhas, Daniela; Lévesque, Sébastien; Auray‐Blais, Christiane; Clarke, Joe T.R.; Laframboise, Rachel; Maranda, Bruno; Mitchell, Grant A. (tháng 1 năm 2019). “Combined malonic and methylmalonic aciduria due to ACSF3 mutations: Benign clinical course in an unselected cohort”. Journal of Inherited Metabolic Disease (bằng tiếng Anh). 42 (1): 107–116. doi:10.1002/jimd.12032. ISSN 0141-8955.
Gabriel, Marie Cosette; Rice, Stephanie M.; Sloan, Jennifer L.; Mossayebi, Matthew H.; Venditti, Charles P.; Al‐Kouatly, Huda B. (tháng 4 năm 2021). “Considerations of expanded carrier screening: Lessons learned from combined malonic and methylmalonic aciduria”. Molecular Genetics & Genomic Medicine (bằng tiếng Anh). 9 (4). doi:10.1002/mgg3.1621. ISSN 2324-9269. PMC 8123733. PMID 33625768.