1. Weyhenmyeye J, Gallman E. Rapid Review Neuroscience. Philadelphia: Mosby. Elsevier; 2007. [
View at Publisher]
2. Zeman A. Persistent vegetative state. The Lancet. 1998; 351(9096): 144. [
View at Publisher] [
DOI:10.1016/S0140-6736(05)78109-5] [
PubMed] [
Google Scholar]
3. Hoflack M, Caruba C, Pitelet G, Haas H, Mas JC, Paquis V, et al. Coma du nourrisson aux urgences: 2 cas de déficit en MCAD [Infant coma in the emergency department: 2 cases of MCAD deficiency. Arch Pediatr. 2010; 17(7): 1074-7. [
View at Publisher] [
DOI:10.1016/j.arcped.2010.03.011] [
Google Scholar]
4. Ghosh S, Chaudhury PK, Goswami HKJIjop. An analysis of six cases of acute intermittent porphyria (AIP). Indian J Psychiatry. 2006;48(3):189. [
View at Publisher] [
DOI:10.4103/0019-5545.31584] [
PubMed] [
Google Scholar]
5. Oizumi J, Ng WG, Koch R, Shaw KN, Sweetman L, Velazquez A, et al. Partial ornithine transcarbamylase deficiency associated with recurrent hyperammonemia, lethargy and depressed sensorium. Clinical genetics. 1984; 25(6): 538-42. [
View at Publisher] [
DOI:10.1111/j.1399-0004.1984.tb00498.x] [
PubMed] [
Google Scholar]
6. De Baulny HO, Saudubray J-M. Branched-chain organic acidurias. Inborn metabolic diseases: Springer. 2000; 196-212. [
View at Publisher] [
DOI:10.1007/978-3-662-04285-4_16]
7. Swaiman KF, Ashwal S, Ferriero DM, Schor NF, Finkel RS, Gropman AL, et al. Swaiman's Pediatric Neurology E-Book: Principles and Practice: Elsevier Health Sciences; 2017. [
View at Publisher]
8. Ducros A, Denier C, Joutel A, Cecillon M, Lescoat C, Vahedi K, et al. The clinical spectrum of familial hemiplegic migraine associated with mutations in a neuronal calcium channel. N Engl J Med. 2001; 345(1): 17-24. [
View at Publisher] [
DOI:10.1056/NEJM200107053450103] [
PubMed] [
Google Scholar]
9. Blumkin L, Michelson M, Leshinsky-Silver E, Kivity S, Lev D, Lerman-Sagie TJJocn. Congenital ataxia, mental retardation, and dyskinesia associated with a novel CACNA1A mutation. J Child Neurol. 2010; 25(7): 892-7. [
View at Publisher] [
DOI:10.1177/0883073809351316] [
PubMed] [
Google Scholar]
10. Pelzer N, Blom D, Stam A, Vijfhuizen L, Hageman A, van Vliet J, et al. Recurrent coma and fever in familial hemiplegic migraine type 2. A prospective 15-year follow-up of a large family with a novel ATP1A2 mutation. Cephalalgia. 2017; 37(8): 737-55. [
View at Publisher] [
DOI:10.1177/0333102416651284] [
PubMed] [
Google Scholar]
11. Stenton SL, Kremer LS, Kopajtich R, Ludwig C, Prokisch H. The diagnosis of inborn errors of metabolism by an integrative "multi‐omics" approach: A perspective encompassing genomics, transcriptomics, and proteomics. Journal of inherited metabolic disease. 2020; 43(1): 25-35. [
View at Publisher] [
DOI:10.1002/jimd.12130] [
PubMed] [
Google Scholar]
12. Guerrero RB, Kloke KM, Salazar D. Inborn Errors of Metabolism and the Gastrointestinal Tract. Gastroenterology Clinics. 2019; 48(2): 183-98. [
View at Publisher] [
DOI:10.1016/j.gtc.2019.02.001] [
PubMed] [
Google Scholar]
13. Ferreira CR, Cassiman D, Blau N. Clinical and biochemical footprints of inherited metabolic diseases. II. Metabolic liver diseases. Molecular genetics and metabolism. 2019; 127(2): 117-21. [
View at Publisher] [
DOI:10.1016/j.ymgme.2019.04.002] [
PubMed] [
Google Scholar]
14. Huang D, Zhou Q, Chao Y-Q, Zou C-C. Clinical features and genetic analysis of childhood sitosterolemia: Two case reports and literature review. Medicine. 2019;98(15). [
DOI:10.1097/MD.0000000000015013] [
PubMed] [
Google Scholar]
15. Saudubray J-M, Garcia-Cazorla A. An overview of inborn errors of metabolism affecting the brain: from neurodevelopment to neurodegenerative disorders. Dialogues in clinical neuroscience. 2018;20(4):301. [
DOI:10.31887/DCNS.2018.20.4/jmsaudubray] [
PubMed] [
Google Scholar]
16. Maestri NE, Brusilow SW, Clissold DB, Bassett SS. Long-term treatment of girls with ornithine transcarbamylase deficiency. New England Journal of Medicine. 1996; 335(12): 855-60. [
View at Publisher] [
DOI:10.1056/NEJM199609193351204] [
PubMed] [
Google Scholar]
17. Caldovic L, Abdikarim I, Narain S, Tuchman M, Morizono H. Genotype-phenotype correlations in ornithine transcarbamylase deficiency: A mutation update. Journal of Genetics and Genomics. 2015; 42(5): 181-94. [
View at Publisher] [
DOI:10.1016/j.jgg.2015.04.003] [
PubMed] [
Google Scholar]
18. Seegmiller JE, Rosenbloom FM, Kelley WN. Enzyme defect associated with a sex-linked human neurological disorder and excessive purine synthesis. Science. 1967;155(3770):1682-4. [
View at Publisher] [
DOI:10.1126/science.155.3770.1682] [
PubMed] [
Google Scholar]
19. Cusumano FJ, Penna KJ, Panossian G. Prevention of self-mutilation in patients with Lesch-Nyhan syndrome: review of literature. Journal of Dentistry for Children. 2001; 68(3): 175-8. [
PubMed] [
Google Scholar]
20. Lynch BJ, Noetzel MJ. Recurrent coma and Lesch-Nyhan syndrome. Pediatric neurology. 1991; 7(5): 389-91. [
View at Publisher] [
DOI:10.1016/0887-8994(91)90073-T] [
PubMed] [
Google Scholar]
21. Strauss KA, Wardley B, Robinson D, Hendrickson C, Rider NL, Puffenberger EG, et al. Classical maple syrup urine disease and brain development: principles of management and formula design. Molecular genetics and metabolism. 2010; 99(4): 333-45. [
View at Publisher] [
DOI:10.1016/j.ymgme.2009.12.007] [
PubMed] [
Google Scholar]
22. Blackburn PR, Gass JM, e Vairo FP, Farnham KM, Atwal HK, Macklin S, et al. Maple syrup urine disease: mechanisms and management. The application of clinical genetics. 2017;10:57. [
DOI:10.2147/TACG.S125962] [
PubMed] [
Google Scholar]
23. Andresen BS, Dobrowolski SF, O'Reilly L, Muenzer J, McCandless SE, Frazier DM, et al. Medium-chain acyl-CoA dehydrogenase (MCAD) mutations identified by MS/MS-based prospective screening of newborns differ from those observed in patients with clinical symptoms: identification and characterization of a new, prevalent mutation that results in mild MCAD deficiency. The American Journal of Human Genetics. 2001; 68(6):1408-18. [
View at Publisher] [
DOI:10.1086/320602] [
PubMed] [
Google Scholar]
24. Roomets E, Lundbom N, Pihko H, Heikkinen S, Tyni T. Lipids detected by brain MRS during coma caused by carnitine palmitoyltransferase 1 deficiency. Neurology. 2006;67(8):1516-7. [
DOI:10.1212/01.wnl.0000240118.82937.ed] [
Google Scholar]
25. Wieser T. Carnitine Palmitoyltransferase II Deficiency. 2004 Aug 27 [updated 2019 Jan 3]. In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Mirzaa G, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2021. [
PubMed]
26. Vanderver A, Prust M, Tonduti D, Mochel F, Hussey HM, Helman G, et al. Case definition and classification of leukodystrophies and leukoencephalopathies. Molecular genetics and metabolism. 2015;114(4):494-500. [
View at Publisher] [
DOI:10.1016/j.ymgme.2015.01.006] [
PubMed] [
Google Scholar]
27. Chabriat H, Vahedi K, Bousser M, Iba-Zizen M, Joutel A, Nibbio A, et al. Clinical spectrum of CADASIL: a study of 7 families. The Lancet. 1995;346(8980):934-9. [
View at Publisher] [
DOI:10.1016/S0140-6736(95)91557-5] [
Google Scholar]
28. Eswaradass V, Ramasamy B, Kalidoss R, Gnanagurusamy G. Cadasil coma: Unusual cause for acute encephalopathy. Annals of Indian Academy of Neurology. 2015;18(4). [
View at Publisher] [
DOI:10.4103/0972-2327.160072] [
PubMed] [
Google Scholar]
29. Ophoff RA, Terwindt GM, Vergouwe MN, Van Eijk R, Oefner PJ, Hoffman SM, et al. Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca 2+ channel gene CACNL1A4. Cell. 1996;87(3):543-52. [
View at Publisher] [
DOI:10.1016/S0092-8674(00)81373-2] [
PubMed] [
Google Scholar]
30. Smith MA, Katsouri L, Virtue S, Choudhury AI, Vidal-Puig A, Ashford ML, et al. Calcium channel CaV2. 3 subunits regulate hepatic glucose production by modulating leptin-induced excitation of arcuate pro-opiomelanocortin neurons. Cell reports. 2018;25(2):278-87. e4. [
View at Publisher] [
DOI:10.1016/j.celrep.2018.09.024] [
PubMed] [
Google Scholar]
31. Fouad Y, Waked I, Bollipo S, Gomaa A, Ajlouni Y, Attia D. What's in a name? Renaming 'NAFLD'to 'MAFLD'. Liver International. 2020. [
View at Publisher] [
DOI:10.1111/liv.14478] [
PubMed] [
Google Scholar]
32. Hadinia A, Doustimotlagh AH, Goodarzi HR, Arya A, Jafarinia M. Circulating levels of pro-inflammatory cytokines in patients with nonalcoholic fatty liver disease and non-alcoholic steatohepatitis. Iranian Journal of Immunology. 2019;16(4):327-33. [
View at Publisher] [
PubMed] [
Google Scholar]
33. Borrelli A, Bonelli P, Tuccillo FM, Goldfine ID, Evans JL, Buonaguro FM, et al. Role of gut microbiota and oxidative stress in the progression of non-alcoholic fatty liver disease to hepatocarcinoma: Current and innovative therapeutic approaches. Redox biology. 2018;15:467-79. [
View at Publisher] [
DOI:10.1016/j.redox.2018.01.009] [
PubMed] [
Google Scholar]
34. Trépo E, Romeo S, Zucman-Rossi J, Nahon P. PNPLA3 gene in liver diseases. Journal of hepatology. 2016; 65(2): 399-412. [
View at Publisher] [
DOI:10.1016/j.jhep.2016.03.011] [
Google Scholar]
35. Mardis ER. The impact of next-generation sequencing technology on genetics. Trends in genetics. 2008;24(3):133-41. [
View at Publisher] [
DOI:10.1016/j.tig.2007.12.007] [
Google Scholar]
36. Illumina I. An introduction to next-generation sequencing technology. 2015. [
View at Publisher]
37. Kuroda M, Ohta T, Uchiyama I, Baba T, Yuzawa H, Kobayashi I, et al. Whole genome sequencing of meticillin-resistant Staphylococcus aureus. The Lancet. 2001;357(9264):1225-40. [
View at Publisher] [
DOI:10.1016/S0140-6736(00)04403-2] [
PubMed] [
Google Scholar]
38. Van Dijk EL, Auger H, Jaszczyszyn Y, Thermes C. Ten years of next-generation sequencing technology. Trends in genetics. 2014; 30(9): 418-26. [
View at Publisher] [
DOI:10.1016/j.tig.2014.07.001] [
Google Scholar]
39. Adhikari AN, Gallagher RC, Wang Y, Currier RJ, Amatuni G, Bassaganyas L, et al. The role of exome sequencing in newborn screening for inborn errors of metabolism. Nature Medicine. 2020;26(9):1392-7. [
View at Publisher] [
DOI:10.1038/s41591-020-0966-5] [
PubMed] [
Google Scholar]
40. Li R, Zhu H, Ruan J, Qian W, Fang X, Shi Z, et al. De novo assembly of human genomes with massively parallel short read sequencing. Genome research. 2010;20(2):265-72. [
View at Publisher] [
DOI:10.1101/gr.097261.109] [
PubMed]
41. Damodaran S, Berger MF, Roychowdhury S. Clinical tumor sequencing: opportunities and challenges for precision cancer medicine. American Society of Clinical Oncology Educational Book. 2015;35(1):e175-e82. [
View at Publisher] [
DOI:10.14694/EdBook_AM.2015.35.e175] [
PubMed] [
Google Scholar]
42. Ponzi E, Maiorana A, Lepri FR, Mucciolo M, Semeraro M, Taurisano R, et al. Persistent hypoglycemia in children: Targeted gene panel improves the diagnosis of hypoglycemia due to inborn errors of metabolism. The Journal of pediatrics. 2018;202:272-8. e4. [
View at Publisher] [
DOI:10.1016/j.jpeds.2018.06.050] [
PubMed] [
Google Scholar]
43. Bevilacqua J, Hesse A, Cormier B, Davey J, Patel D, Shankar K, et al. Clinical utility of a 377 gene custom next-generation sequencing epilepsy panel. Journal of genetics. 2017;96(4):681-5. [
View at Publisher] [
DOI:10.1007/s12041-017-0791-x] [
PubMed] [
Google Scholar]
44. Xu Y, Gao S, Yang Y, Huang M, Cheng L, Wei Q, et al. Transcriptome sequencing and whole genome expression profiling of chrysanthemum under dehydration stress. BMC genomics. 2013;14(1):662. [
View at Publisher] [
DOI:10.1186/1471-2164-14-662] [
PubMed] [
Google Scholar]
45. Jen JC. Familial hemiplegic migraine. GeneReviews®[Internet]: University of Washington, Seattle; 2015. [
PubMed]
46. Maksemous N, Smith RA, Haupt LM, Griffiths LR. Targeted next generation sequencing identifies novel NOTCH3 gene mutations in CADASIL diagnostics patients. Human genomics. 2016; 10(1): 1-12. [
View at Publisher] [
DOI:10.1186/s40246-016-0093-z] [
PubMed] [
Google Scholar]
47. Alameri M, Shakra M, Alsaadi T. Fatal coma in a young adult due to late-onset urea cycle deficiency presenting with a prolonged seizure: a case report. Journal of medical case reports. 2015;9(1):1-6. [
View at Publisher] [
DOI:10.1186/s13256-015-0741-2] [
PubMed] [
Google Scholar]
48. Ghorbani MJ, Razmi N, Tabei SMB, Zibaeenezhad MJ, Goodarzi HR. Genetic analysis of early onset familial coronary artery diseases. Archives of Medical Sciences Atherosclerotic Diseases. 2019;4:e1. [
View at Publisher] [
DOI:10.5114/amsad.2019.83149] [
PubMed] [
Google Scholar]
49. Maksemous N, Smith RA, Sutherland HG, Maher BH, Ibrahim O, Nicholson GA, et al. Targeted next generation sequencing identifies a genetic spectrum of DNA variants in patients with hemiplegic migraine. Cephalalgia Reports. 2019; 2: 1-9. [
View at Publisher] [
DOI:10.1177/2515816319881630] [
Google Scholar]