MELAS syndrome (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "MELAS syndrome" in English language version.

refsWebsite

Global rank English rank

39nih.gov

4^th place

24doi.org

2^nd place

11worldcat.org

5^th place

4semanticscholar.org

11^th place

8^th place

3elsevier.com

610^th place

704^th place

2wiley.com

222^nd place

297^th place

1creativecommons.org

1,010^th place

612^th place

1imj.ie

low place

1medlineplus.gov

1,581^st place

1,299^th place

creativecommons.org (Global: 1,010^th place; English: 612^th place)

Pia S, Lui F (2020). "Melas Syndrome". Statpearls. Treasure Island (FL): StatPearls Publishing. PMID 30422554. Text was copied from this source, which is available under a Creative Commons Attribution 4.0 International License.

doi.org (Global: 2^nd place; English: 2^nd place)

Pavlakis SG, Phillips PC, DiMauro S, De Vivo DC, Rowland LP (October 1984). "Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes: a distinctive clinical syndrome". Annals of Neurology. 16 (4): 481–488. doi:10.1002/ana.410160409. PMID 6093682. S2CID 41412358.
Hirano M, Pavlakis SG (January 1994). "Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes (MELAS): current concepts". Journal of Child Neurology. 9 (1): 4–13. doi:10.1177/088307389400900102. PMID 8151079. S2CID 31329972.
El-Hattab, Ayman W.; Adesina, Adekunle M.; Jones, Jeremy; Scaglia, Fernando (2015-09-01). "MELAS syndrome: Clinical manifestations, pathogenesis, and treatment options". Molecular Genetics and Metabolism. SI:Therapy. 116 (1): 4–12. doi:10.1016/j.ymgme.2015.06.004. ISSN 1096-7192. PMID 26095523.
Valiente-Pallejà, Alba; Tortajada, Juan; Bulduk, Bengisu K.; Vilella, Elisabet; Garrabou, Glòria; Muntané, Gerard; Martorell, Lourdes (2022). "Comprehensive summary of mitochondrial DNA alterations in the postmortem human brain: A systematic review". eBioMedicine. 76. doi:10.1016/j.ebiom.2022.103815. PMC 8790490. PMID 35085849.
Hirano M, Ricci E, Koenigsberger MR, Defendini R, Pavlakis SG, DeVivo DC, et al. (1992). "Melas: an original case and clinical criteria for diagnosis". Neuromuscular Disorders. 2 (2): 125–135. doi:10.1016/0960-8966(92)90045-8. PMID 1422200. S2CID 45634693.
Abu-Amero KK, Al-Dhalaan H, Bohlega S, Hellani A, Taylor RW (October 2009). "A patient with typical clinical features of mitochondrial encephalopathy, lactic acidosis and stroke-like episodes (MELAS) but without an obvious genetic cause: a case report". Journal of Medical Case Reports. 3: 77. doi:10.1186/1752-1947-3-77. PMC 2783076. PMID 19946553.
Tranchant C, Anheim M (2016). "Movement disorders in mitochondrial diseases". Revue Neurologique. 172 (8–9): 524–529. doi:10.1016/j.neurol.2016.07.003. PMID 27476418.
Yarham, John W.; Elson, Joanna L.; Blakely, Emma L.; McFarland, Robert; Taylor, Robert W. (2010). "Mitochondrial tRNA mutations and disease". WIREs RNA. 1 (2): 304–324. doi:10.1002/wrna.27. ISSN 1757-7012. PMID 21935892.
Bulduk, B.K.; Kiliç, H.B.; Bekircan-Kurt, C.E.; Haliloğlu, G.; Erdem Özdamar, S.; Topaloğlu, H.; Kocaefe, Y.Ç. (2020). "A Novel Amplification-Refractory Mutation System-PCR Strategy to Screen MT-TL1 Pathogenic Variants in Patient Repositories". Genetic Testing and Molecular Biomarkers. 24 (3): 165–170. doi:10.1089/gtmb.2019.0079. PMID 32167396.
Hayman, John; Pavlakis, Steven; Finsterer, Josef (2022-02-17). "Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-Like Episodes (MELAS) in the 18th Century: Mitochondrial Disorders Are Not of Recent Origin". Cureus. 14 (2) e22314. doi:10.7759/cureus.22314. ISSN 2168-8184. PMC 8856639. PMID 35198337.
Na, Ji-Hoon; Lee, Young-Mock (2024-11-28). "Diagnosis and Management of Mitochondrial Encephalopathy, Lactic Acidosis, and Stroke-like Episodes Syndrome". Biomolecules. 14 (12): 1524. doi:10.3390/biom14121524. ISSN 2218-273X. PMC 11672891. PMID 39766231.
Schapira, Anthony HV (2006-07-01). "Mitochondrial disease". The Lancet. 368 (9529): 70–82. doi:10.1016/S0140-6736(06)68970-8. ISSN 0140-6736. PMID 16815381.
Khasminsky, Vadim; Auriel, Eitan; Luckman, Judith; Eliahou, Ruth; Inbar, Edna; Pardo, Keshet; Landau, Yuval; Barnea, Rani; Mermelstein, Maor; Shelly, Shahar; Naftali, Jonathan; Peretz, Shlomi (August 2023). "Clinicoradiologic Criteria for the Diagnosis of Stroke-like Episodes in MELAS". Neurology Genetics. 9 (4) e200082. doi:10.1212/NXG.0000000000200082. PMC 10323819. PMID 37426458.
Wong-Riley, Margaret (July 2010). "Energy metabolism of the visual system". Eye and Brain. 2: 99–116. doi:10.2147/EB.S9078. ISSN 1179-2744. PMC 3515641. PMID 23226947.
Muñoz-Guillén N, León-López R, Ferrer-Higueras MJ, Vargas-Vaserot FJ, Dueñas-Jurado JM (August 2009). "[Arreflexic coma and MELAS syndrome]" [Arreflexic coma and MELAS syndrome]. Revista Clinica Espanola (in Spanish). 209 (7): 337–341. doi:10.1016/s0014-2565(09)71818-1. PMID 19709537.
Kang, Hoon-Chul; Lee, Young-Mock; Kim, Heung Dong; Lee, Joon Soo; Slama, Abdelhamid (2007). "Safe and Effective Use of the Ketogenic Diet in Children with Epilepsy and Mitochondrial Respiratory Chain Complex Defects". Epilepsia. 48 (1): 82–88. doi:10.1111/j.1528-1167.2006.00906.x. ISSN 1528-1167. PMID 17241212.
Na, Ji-Hoon; Kim, Heung-Dong; Lee, Young-Mock (2020-01-01). "Effective and safe diet therapies for Lennox-Gastaut syndrome with mitochondrial dysfunction". Therapeutic Advances in Neurological Disorders. 13 1756286419897813. doi:10.1177/1756286419897813. ISSN 1756-2864. PMC 7005978. PMID 32082420.
Zweers, Heidi; van Wegberg, Annemiek M. J.; Janssen, Mirian C. H.; Wortmann, Saskia B. (2021-07-03). "Ketogenic diet for mitochondrial disease: a systematic review on efficacy and safety". Orphanet Journal of Rare Diseases. 16 (1): 295. doi:10.1186/s13023-021-01927-w. ISSN 1750-1172. PMC 8254320. PMID 34217336.
Rodriguez MC, MacDonald JR, Mahoney DJ, Parise G, Beal MF, Tarnopolsky MA (February 2007). "Beneficial effects of creatine, CoQ10, and lipoic acid in mitochondrial disorders". Muscle & Nerve. 35 (2): 235–242. doi:10.1002/mus.20688. PMID 17080429. S2CID 28962906.
Koga Y, Akita Y, Nishioka J, Yatsuga S, Povalko N, Katayama K, Matsuishi T (2007). "MELAS and L-arginine therapy". Mitochondrion. 7 (1–2): 133–139. doi:10.1016/j.mito.2006.11.006. PMID 17276739.
Ohsawa, Yutaka; Hagiwara, Hiroki; Nishimatsu, Shin-ichiro; Hirakawa, Akihiro; Kamimura, Naomi; Ohtsubo, Hideaki; Fukai, Yuta; Murakami, Tatsufumi; Koga, Yasutoshi; Goto, Yu-ichi; Ohta, Shigeo; Sunada, Yoshihide (May 2019). "Taurine supplementation for prevention of stroke-like episodes in MELAS: a multicentre, open-label, 52-week phase III trial". Journal of Neurology, Neurosurgery & Psychiatry. 90 (5): 529–536. doi:10.1136/jnnp-2018-317964. ISSN 0022-3050. PMC 6581075. PMID 29666206.
Schaffer, Stephen; Kim, Ha Won (2018-05-01). "Effects and Mechanisms of Taurine as a Therapeutic Agent". Biomolecules & Therapeutics. 26 (3): 225–241. doi:10.4062/biomolther.2017.251. ISSN 2005-4483. PMC 5933890. PMID 29631391.
Yatsuga, Shuichi; Povalko, Nataliya; Nishioka, Junko; Katayama, Koju; Kakimoto, Noriko; Matsuishi, Toyojiro; Kakuma, Tatsuyuki; Koga, Yasutoshi (May 2012). "MELAS: A nationwide prospective cohort study of 96 patients in Japan". Biochimica et Biophysica Acta (BBA) - General Subjects. 1820 (5): 619–624. doi:10.1016/j.bbagen.2011.03.015. PMID 21443929.
Majamaa, Kari; Moilanen, Jukka S.; Uimonen, Seija; Remes, Anne M.; Salmela, Pasi I.; Kärppä, Mikko; Majamaa-Voltti, Kirsi A.M.; Rusanen, Harri; Sorri, Martti; Peuhkurinen, Keijo J.; Hassinen, Ilmo E. (August 1998). "Epidemiology of A3243G, the Mutation for Mitochondrial Encephalomyopathy, Lactic Acidosis, and Strokelike Episodes: Prevalence of the Mutation in an Adult Population". The American Journal of Human Genetics. 63 (2): 447–454. doi:10.1086/301959. PMC 1377301. PMID 9683591.

elsevier.com (Global: 610^th place; English: 704^th place)

linkinghub.elsevier.com

El-Hattab, Ayman W.; Adesina, Adekunle M.; Jones, Jeremy; Scaglia, Fernando (2015-09-01). "MELAS syndrome: Clinical manifestations, pathogenesis, and treatment options". Molecular Genetics and Metabolism. SI:Therapy. 116 (1): 4–12. doi:10.1016/j.ymgme.2015.06.004. ISSN 1096-7192. PMID 26095523.
Schapira, Anthony HV (2006-07-01). "Mitochondrial disease". The Lancet. 368 (9529): 70–82. doi:10.1016/S0140-6736(06)68970-8. ISSN 0140-6736. PMID 16815381.
Yatsuga, Shuichi; Povalko, Nataliya; Nishioka, Junko; Katayama, Koju; Kakimoto, Noriko; Matsuishi, Toyojiro; Kakuma, Tatsuyuki; Koga, Yasutoshi (May 2012). "MELAS: A nationwide prospective cohort study of 96 patients in Japan". Biochimica et Biophysica Acta (BBA) - General Subjects. 1820 (5): 619–624. doi:10.1016/j.bbagen.2011.03.015. PMID 21443929.

imj.ie (Global: low place; English: low place)

Quinn NM, Stone G, Brett F, Caro-Dominguez P, Neylon O, Lynch B (September 2016). "MELAS (Mitochondrial Encephalomyopathy, Lactic Acidosis, Stroke) - a Diagnosis Not to be Missed". Irish Medical Journal. 109 (8): 455. PMID 28124854.

medlineplus.gov (Global: 1,581^st place; English: 1,299^th place)

"MELAS". Genetics Home Reference. December 2013. Retrieved 11 April 2017. This article incorporates text from this source, which is in the public domain.

nih.gov (Global: 4^th place; English: 4^th place)

pubmed.ncbi.nlm.nih.gov

Pia S, Lui F (2020). "Melas Syndrome". Statpearls. Treasure Island (FL): StatPearls Publishing. PMID 30422554. Text was copied from this source, which is available under a Creative Commons Attribution 4.0 International License.
Pavlakis SG, Phillips PC, DiMauro S, De Vivo DC, Rowland LP (October 1984). "Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes: a distinctive clinical syndrome". Annals of Neurology. 16 (4): 481–488. doi:10.1002/ana.410160409. PMID 6093682. S2CID 41412358.
Hirano M, Pavlakis SG (January 1994). "Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes (MELAS): current concepts". Journal of Child Neurology. 9 (1): 4–13. doi:10.1177/088307389400900102. PMID 8151079. S2CID 31329972.
El-Hattab, Ayman W.; Adesina, Adekunle M.; Jones, Jeremy; Scaglia, Fernando (2015-09-01). "MELAS syndrome: Clinical manifestations, pathogenesis, and treatment options". Molecular Genetics and Metabolism. SI:Therapy. 116 (1): 4–12. doi:10.1016/j.ymgme.2015.06.004. ISSN 1096-7192. PMID 26095523.
Valiente-Pallejà, Alba; Tortajada, Juan; Bulduk, Bengisu K.; Vilella, Elisabet; Garrabou, Glòria; Muntané, Gerard; Martorell, Lourdes (2022). "Comprehensive summary of mitochondrial DNA alterations in the postmortem human brain: A systematic review". eBioMedicine. 76. doi:10.1016/j.ebiom.2022.103815. PMC 8790490. PMID 35085849.
Hirano M, Ricci E, Koenigsberger MR, Defendini R, Pavlakis SG, DeVivo DC, et al. (1992). "Melas: an original case and clinical criteria for diagnosis". Neuromuscular Disorders. 2 (2): 125–135. doi:10.1016/0960-8966(92)90045-8. PMID 1422200. S2CID 45634693.
Abu-Amero KK, Al-Dhalaan H, Bohlega S, Hellani A, Taylor RW (October 2009). "A patient with typical clinical features of mitochondrial encephalopathy, lactic acidosis and stroke-like episodes (MELAS) but without an obvious genetic cause: a case report". Journal of Medical Case Reports. 3: 77. doi:10.1186/1752-1947-3-77. PMC 2783076. PMID 19946553.
Tranchant C, Anheim M (2016). "Movement disorders in mitochondrial diseases". Revue Neurologique. 172 (8–9): 524–529. doi:10.1016/j.neurol.2016.07.003. PMID 27476418.
Yarham, John W.; Elson, Joanna L.; Blakely, Emma L.; McFarland, Robert; Taylor, Robert W. (2010). "Mitochondrial tRNA mutations and disease". WIREs RNA. 1 (2): 304–324. doi:10.1002/wrna.27. ISSN 1757-7012. PMID 21935892.
Bulduk, B.K.; Kiliç, H.B.; Bekircan-Kurt, C.E.; Haliloğlu, G.; Erdem Özdamar, S.; Topaloğlu, H.; Kocaefe, Y.Ç. (2020). "A Novel Amplification-Refractory Mutation System-PCR Strategy to Screen MT-TL1 Pathogenic Variants in Patient Repositories". Genetic Testing and Molecular Biomarkers. 24 (3): 165–170. doi:10.1089/gtmb.2019.0079. PMID 32167396.
Hayman, John; Pavlakis, Steven; Finsterer, Josef (2022-02-17). "Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-Like Episodes (MELAS) in the 18th Century: Mitochondrial Disorders Are Not of Recent Origin". Cureus. 14 (2) e22314. doi:10.7759/cureus.22314. ISSN 2168-8184. PMC 8856639. PMID 35198337.
Na, Ji-Hoon; Lee, Young-Mock (2024-11-28). "Diagnosis and Management of Mitochondrial Encephalopathy, Lactic Acidosis, and Stroke-like Episodes Syndrome". Biomolecules. 14 (12): 1524. doi:10.3390/biom14121524. ISSN 2218-273X. PMC 11672891. PMID 39766231.
Schapira, Anthony HV (2006-07-01). "Mitochondrial disease". The Lancet. 368 (9529): 70–82. doi:10.1016/S0140-6736(06)68970-8. ISSN 0140-6736. PMID 16815381.
Khasminsky, Vadim; Auriel, Eitan; Luckman, Judith; Eliahou, Ruth; Inbar, Edna; Pardo, Keshet; Landau, Yuval; Barnea, Rani; Mermelstein, Maor; Shelly, Shahar; Naftali, Jonathan; Peretz, Shlomi (August 2023). "Clinicoradiologic Criteria for the Diagnosis of Stroke-like Episodes in MELAS". Neurology Genetics. 9 (4) e200082. doi:10.1212/NXG.0000000000200082. PMC 10323819. PMID 37426458.
Wong-Riley, Margaret (July 2010). "Energy metabolism of the visual system". Eye and Brain. 2: 99–116. doi:10.2147/EB.S9078. ISSN 1179-2744. PMC 3515641. PMID 23226947.
Quinn NM, Stone G, Brett F, Caro-Dominguez P, Neylon O, Lynch B (September 2016). "MELAS (Mitochondrial Encephalomyopathy, Lactic Acidosis, Stroke) - a Diagnosis Not to be Missed". Irish Medical Journal. 109 (8): 455. PMID 28124854.
Muñoz-Guillén N, León-López R, Ferrer-Higueras MJ, Vargas-Vaserot FJ, Dueñas-Jurado JM (August 2009). "[Arreflexic coma and MELAS syndrome]" [Arreflexic coma and MELAS syndrome]. Revista Clinica Espanola (in Spanish). 209 (7): 337–341. doi:10.1016/s0014-2565(09)71818-1. PMID 19709537.
Kang, Hoon-Chul; Lee, Young-Mock; Kim, Heung Dong; Lee, Joon Soo; Slama, Abdelhamid (2007). "Safe and Effective Use of the Ketogenic Diet in Children with Epilepsy and Mitochondrial Respiratory Chain Complex Defects". Epilepsia. 48 (1): 82–88. doi:10.1111/j.1528-1167.2006.00906.x. ISSN 1528-1167. PMID 17241212.
Na, Ji-Hoon; Kim, Heung-Dong; Lee, Young-Mock (2020-01-01). "Effective and safe diet therapies for Lennox-Gastaut syndrome with mitochondrial dysfunction". Therapeutic Advances in Neurological Disorders. 13 1756286419897813. doi:10.1177/1756286419897813. ISSN 1756-2864. PMC 7005978. PMID 32082420.
Zweers, Heidi; van Wegberg, Annemiek M. J.; Janssen, Mirian C. H.; Wortmann, Saskia B. (2021-07-03). "Ketogenic diet for mitochondrial disease: a systematic review on efficacy and safety". Orphanet Journal of Rare Diseases. 16 (1): 295. doi:10.1186/s13023-021-01927-w. ISSN 1750-1172. PMC 8254320. PMID 34217336.
Rodriguez MC, MacDonald JR, Mahoney DJ, Parise G, Beal MF, Tarnopolsky MA (February 2007). "Beneficial effects of creatine, CoQ10, and lipoic acid in mitochondrial disorders". Muscle & Nerve. 35 (2): 235–242. doi:10.1002/mus.20688. PMID 17080429. S2CID 28962906.
Koga Y, Akita Y, Nishioka J, Yatsuga S, Povalko N, Katayama K, Matsuishi T (2007). "MELAS and L-arginine therapy". Mitochondrion. 7 (1–2): 133–139. doi:10.1016/j.mito.2006.11.006. PMID 17276739.
Ohsawa, Yutaka; Hagiwara, Hiroki; Nishimatsu, Shin-ichiro; Hirakawa, Akihiro; Kamimura, Naomi; Ohtsubo, Hideaki; Fukai, Yuta; Murakami, Tatsufumi; Koga, Yasutoshi; Goto, Yu-ichi; Ohta, Shigeo; Sunada, Yoshihide (May 2019). "Taurine supplementation for prevention of stroke-like episodes in MELAS: a multicentre, open-label, 52-week phase III trial". Journal of Neurology, Neurosurgery & Psychiatry. 90 (5): 529–536. doi:10.1136/jnnp-2018-317964. ISSN 0022-3050. PMC 6581075. PMID 29666206.
Schaffer, Stephen; Kim, Ha Won (2018-05-01). "Effects and Mechanisms of Taurine as a Therapeutic Agent". Biomolecules & Therapeutics. 26 (3): 225–241. doi:10.4062/biomolther.2017.251. ISSN 2005-4483. PMC 5933890. PMID 29631391.
Yatsuga, Shuichi; Povalko, Nataliya; Nishioka, Junko; Katayama, Koju; Kakimoto, Noriko; Matsuishi, Toyojiro; Kakuma, Tatsuyuki; Koga, Yasutoshi (May 2012). "MELAS: A nationwide prospective cohort study of 96 patients in Japan". Biochimica et Biophysica Acta (BBA) - General Subjects. 1820 (5): 619–624. doi:10.1016/j.bbagen.2011.03.015. PMID 21443929.
Majamaa, Kari; Moilanen, Jukka S.; Uimonen, Seija; Remes, Anne M.; Salmela, Pasi I.; Kärppä, Mikko; Majamaa-Voltti, Kirsi A.M.; Rusanen, Harri; Sorri, Martti; Peuhkurinen, Keijo J.; Hassinen, Ilmo E. (August 1998). "Epidemiology of A3243G, the Mutation for Mitochondrial Encephalomyopathy, Lactic Acidosis, and Strokelike Episodes: Prevalence of the Mutation in an Adult Population". The American Journal of Human Genetics. 63 (2): 447–454. doi:10.1086/301959. PMC 1377301. PMID 9683591.

ncbi.nlm.nih.gov

Pia S, Lui F (2020). "Melas Syndrome". Statpearls. Treasure Island (FL): StatPearls Publishing. PMID 30422554. Text was copied from this source, which is available under a Creative Commons Attribution 4.0 International License.
Valiente-Pallejà, Alba; Tortajada, Juan; Bulduk, Bengisu K.; Vilella, Elisabet; Garrabou, Glòria; Muntané, Gerard; Martorell, Lourdes (2022). "Comprehensive summary of mitochondrial DNA alterations in the postmortem human brain: A systematic review". eBioMedicine. 76. doi:10.1016/j.ebiom.2022.103815. PMC 8790490. PMID 35085849.
Abu-Amero KK, Al-Dhalaan H, Bohlega S, Hellani A, Taylor RW (October 2009). "A patient with typical clinical features of mitochondrial encephalopathy, lactic acidosis and stroke-like episodes (MELAS) but without an obvious genetic cause: a case report". Journal of Medical Case Reports. 3: 77. doi:10.1186/1752-1947-3-77. PMC 2783076. PMID 19946553.
Hayman, John; Pavlakis, Steven; Finsterer, Josef (2022-02-17). "Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-Like Episodes (MELAS) in the 18th Century: Mitochondrial Disorders Are Not of Recent Origin". Cureus. 14 (2) e22314. doi:10.7759/cureus.22314. ISSN 2168-8184. PMC 8856639. PMID 35198337.
Na, Ji-Hoon; Lee, Young-Mock (2024-11-28). "Diagnosis and Management of Mitochondrial Encephalopathy, Lactic Acidosis, and Stroke-like Episodes Syndrome". Biomolecules. 14 (12): 1524. doi:10.3390/biom14121524. ISSN 2218-273X. PMC 11672891. PMID 39766231.
Khasminsky, Vadim; Auriel, Eitan; Luckman, Judith; Eliahou, Ruth; Inbar, Edna; Pardo, Keshet; Landau, Yuval; Barnea, Rani; Mermelstein, Maor; Shelly, Shahar; Naftali, Jonathan; Peretz, Shlomi (August 2023). "Clinicoradiologic Criteria for the Diagnosis of Stroke-like Episodes in MELAS". Neurology Genetics. 9 (4) e200082. doi:10.1212/NXG.0000000000200082. PMC 10323819. PMID 37426458.
Wong-Riley, Margaret (July 2010). "Energy metabolism of the visual system". Eye and Brain. 2: 99–116. doi:10.2147/EB.S9078. ISSN 1179-2744. PMC 3515641. PMID 23226947.
Na, Ji-Hoon; Kim, Heung-Dong; Lee, Young-Mock (2020-01-01). "Effective and safe diet therapies for Lennox-Gastaut syndrome with mitochondrial dysfunction". Therapeutic Advances in Neurological Disorders. 13 1756286419897813. doi:10.1177/1756286419897813. ISSN 1756-2864. PMC 7005978. PMID 32082420.
Zweers, Heidi; van Wegberg, Annemiek M. J.; Janssen, Mirian C. H.; Wortmann, Saskia B. (2021-07-03). "Ketogenic diet for mitochondrial disease: a systematic review on efficacy and safety". Orphanet Journal of Rare Diseases. 16 (1): 295. doi:10.1186/s13023-021-01927-w. ISSN 1750-1172. PMC 8254320. PMID 34217336.
Ohsawa, Yutaka; Hagiwara, Hiroki; Nishimatsu, Shin-ichiro; Hirakawa, Akihiro; Kamimura, Naomi; Ohtsubo, Hideaki; Fukai, Yuta; Murakami, Tatsufumi; Koga, Yasutoshi; Goto, Yu-ichi; Ohta, Shigeo; Sunada, Yoshihide (May 2019). "Taurine supplementation for prevention of stroke-like episodes in MELAS: a multicentre, open-label, 52-week phase III trial". Journal of Neurology, Neurosurgery & Psychiatry. 90 (5): 529–536. doi:10.1136/jnnp-2018-317964. ISSN 0022-3050. PMC 6581075. PMID 29666206.
Schaffer, Stephen; Kim, Ha Won (2018-05-01). "Effects and Mechanisms of Taurine as a Therapeutic Agent". Biomolecules & Therapeutics. 26 (3): 225–241. doi:10.4062/biomolther.2017.251. ISSN 2005-4483. PMC 5933890. PMID 29631391.
Majamaa, Kari; Moilanen, Jukka S.; Uimonen, Seija; Remes, Anne M.; Salmela, Pasi I.; Kärppä, Mikko; Majamaa-Voltti, Kirsi A.M.; Rusanen, Harri; Sorri, Martti; Peuhkurinen, Keijo J.; Hassinen, Ilmo E. (August 1998). "Epidemiology of A3243G, the Mutation for Mitochondrial Encephalomyopathy, Lactic Acidosis, and Strokelike Episodes: Prevalence of the Mutation in an Adult Population". The American Journal of Human Genetics. 63 (2): 447–454. doi:10.1086/301959. PMC 1377301. PMID 9683591.

ghr.nlm.nih.gov

MELAS syndrome at NLM Genetics Home Reference

semanticscholar.org (Global: 11^th place; English: 8^th place)

api.semanticscholar.org

Pavlakis SG, Phillips PC, DiMauro S, De Vivo DC, Rowland LP (October 1984). "Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes: a distinctive clinical syndrome". Annals of Neurology. 16 (4): 481–488. doi:10.1002/ana.410160409. PMID 6093682. S2CID 41412358.
Hirano M, Pavlakis SG (January 1994). "Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes (MELAS): current concepts". Journal of Child Neurology. 9 (1): 4–13. doi:10.1177/088307389400900102. PMID 8151079. S2CID 31329972.
Hirano M, Ricci E, Koenigsberger MR, Defendini R, Pavlakis SG, DeVivo DC, et al. (1992). "Melas: an original case and clinical criteria for diagnosis". Neuromuscular Disorders. 2 (2): 125–135. doi:10.1016/0960-8966(92)90045-8. PMID 1422200. S2CID 45634693.
Rodriguez MC, MacDonald JR, Mahoney DJ, Parise G, Beal MF, Tarnopolsky MA (February 2007). "Beneficial effects of creatine, CoQ10, and lipoic acid in mitochondrial disorders". Muscle & Nerve. 35 (2): 235–242. doi:10.1002/mus.20688. PMID 17080429. S2CID 28962906.

wiley.com (Global: 222^nd place; English: 297^th place)

wires.onlinelibrary.wiley.com

Yarham, John W.; Elson, Joanna L.; Blakely, Emma L.; McFarland, Robert; Taylor, Robert W. (2010). "Mitochondrial tRNA mutations and disease". WIREs RNA. 1 (2): 304–324. doi:10.1002/wrna.27. ISSN 1757-7012. PMID 21935892.

onlinelibrary.wiley.com

Kang, Hoon-Chul; Lee, Young-Mock; Kim, Heung Dong; Lee, Joon Soo; Slama, Abdelhamid (2007). "Safe and Effective Use of the Ketogenic Diet in Children with Epilepsy and Mitochondrial Respiratory Chain Complex Defects". Epilepsia. 48 (1): 82–88. doi:10.1111/j.1528-1167.2006.00906.x. ISSN 1528-1167. PMID 17241212.

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El-Hattab, Ayman W.; Adesina, Adekunle M.; Jones, Jeremy; Scaglia, Fernando (2015-09-01). "MELAS syndrome: Clinical manifestations, pathogenesis, and treatment options". Molecular Genetics and Metabolism. SI:Therapy. 116 (1): 4–12. doi:10.1016/j.ymgme.2015.06.004. ISSN 1096-7192. PMID 26095523.
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Hayman, John; Pavlakis, Steven; Finsterer, Josef (2022-02-17). "Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-Like Episodes (MELAS) in the 18th Century: Mitochondrial Disorders Are Not of Recent Origin". Cureus. 14 (2) e22314. doi:10.7759/cureus.22314. ISSN 2168-8184. PMC 8856639. PMID 35198337.
Na, Ji-Hoon; Lee, Young-Mock (2024-11-28). "Diagnosis and Management of Mitochondrial Encephalopathy, Lactic Acidosis, and Stroke-like Episodes Syndrome". Biomolecules. 14 (12): 1524. doi:10.3390/biom14121524. ISSN 2218-273X. PMC 11672891. PMID 39766231.
Schapira, Anthony HV (2006-07-01). "Mitochondrial disease". The Lancet. 368 (9529): 70–82. doi:10.1016/S0140-6736(06)68970-8. ISSN 0140-6736. PMID 16815381.
Wong-Riley, Margaret (July 2010). "Energy metabolism of the visual system". Eye and Brain. 2: 99–116. doi:10.2147/EB.S9078. ISSN 1179-2744. PMC 3515641. PMID 23226947.
Kang, Hoon-Chul; Lee, Young-Mock; Kim, Heung Dong; Lee, Joon Soo; Slama, Abdelhamid (2007). "Safe and Effective Use of the Ketogenic Diet in Children with Epilepsy and Mitochondrial Respiratory Chain Complex Defects". Epilepsia. 48 (1): 82–88. doi:10.1111/j.1528-1167.2006.00906.x. ISSN 1528-1167. PMID 17241212.
Na, Ji-Hoon; Kim, Heung-Dong; Lee, Young-Mock (2020-01-01). "Effective and safe diet therapies for Lennox-Gastaut syndrome with mitochondrial dysfunction". Therapeutic Advances in Neurological Disorders. 13 1756286419897813. doi:10.1177/1756286419897813. ISSN 1756-2864. PMC 7005978. PMID 32082420.
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Ohsawa, Yutaka; Hagiwara, Hiroki; Nishimatsu, Shin-ichiro; Hirakawa, Akihiro; Kamimura, Naomi; Ohtsubo, Hideaki; Fukai, Yuta; Murakami, Tatsufumi; Koga, Yasutoshi; Goto, Yu-ichi; Ohta, Shigeo; Sunada, Yoshihide (May 2019). "Taurine supplementation for prevention of stroke-like episodes in MELAS: a multicentre, open-label, 52-week phase III trial". Journal of Neurology, Neurosurgery & Psychiatry. 90 (5): 529–536. doi:10.1136/jnnp-2018-317964. ISSN 0022-3050. PMC 6581075. PMID 29666206.
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MELAS syndrome (English Wikipedia)

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