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Year | Number of Results |
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2014 | 1 |
2018 | 2 |
2019 | 1 |
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2023 | 1 |
2024 | 1 |
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Page 1
Treatment of inborn errors of metabolism.
Mol Cytogenet. 2014 Jan 21;7(Suppl 1 Proceedings of the International Conference on Human):I42. doi: 10.1186/1755-8166-7-S1-I42. eCollection 2014.
Mol Cytogenet. 2014.
PMID: 24949099
Free PMC article.
No abstract available.
An integrated multiomic approach as an excellent tool for the diagnosis of metabolic diseases: our first 3720 patients.
Almeida LS, Pereira C, Aanicai R, Schröder S, Bochinski T, Kaune A, Urzi A, Spohr TCLS, Viceconte N, Oppermann S, Alasel M, Ebadat S, Iftikhar S, Jasinge E, Elsayed SM, Tomoum H, Marzouk I, Jalan AB, Cerkauskaite A, Cerkauskiene R, Tkemaladze T, Nadeem AM, El Din Mahmoud IG, Mossad FA, Kamel M, Selim LA, Cheema HA, Paknia O, Cozma C, Juaristi-Manrique C, Guatibonza-Moreno P, Böttcher T, Vogel F, Pinto-Basto J, Bertoli-Avella A, Bauer P.
Almeida LS, et al. Among authors: jalan ab.
Eur J Hum Genet. 2022 Sep;30(9):1029-1035. doi: 10.1038/s41431-022-01119-5. Epub 2022 May 25.
Eur J Hum Genet. 2022.
PMID: 35614200
Free PMC article.
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Nuclear Mitochondrial Disorder Due to a Variant in NAXE in Two Unrelated Indian Children.
Rao SS, Bhavani GS, Jalan AB, Shenoy RD.
Rao SS, et al. Among authors: jalan ab.
Indian J Pediatr. 2024 Feb;91(2):184-187. doi: 10.1007/s12098-023-04495-y. Epub 2023 Feb 11.
Indian J Pediatr. 2024.
PMID: 36773198
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Auxiliary Partial Orthotopic Liver Transplantation for Monogenic Metabolic Liver Diseases: Single-Centre Experience.
Shanmugam NP, Valamparampil JJ, Reddy MS, Al Said KJ, Al-Thihli K, Al-Hashmi N, Al-Jishi E, Isa HMA, Jalan AB, Rela M.
Shanmugam NP, et al. Among authors: jalan ab.
JIMD Rep. 2019;45:29-36. doi: 10.1007/8904_2018_137. Epub 2018 Oct 12.
JIMD Rep. 2019.
PMID: 30311140
Free PMC article.
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Urea cycle disorders in India: clinical course, biochemical and genetic investigations, and prenatal testing.
Bijarnia-Mahay S, Häberle J, Jalan AB, Puri RD, Kohli S, Kudalkar K, Rüfenacht V, Gupta D, Maurya D, Verma J, Shigematsu Y, Yamaguchi S, Saxena R, Verma IC.
Bijarnia-Mahay S, et al. Among authors: jalan ab.
Orphanet J Rare Dis. 2018 Oct 1;13(1):174. doi: 10.1186/s13023-018-0908-1.
Orphanet J Rare Dis. 2018.
PMID: 30285816
Free PMC article.
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Founder effects of the homogentisate 1,2-dioxygenase (HGD) gene in a gypsy population and mutation spectrum in the gene among alkaptonuria patients from India.
Danda S, Mohan S, Devaraj P, Dutta AK, Nampoothiri S, Yesodharan D, Phadke SR, Jalan AB, Thangaraj K, Verma IC, Danda D, Jebaraj I.
Danda S, et al. Among authors: jalan ab.
Clin Rheumatol. 2020 Sep;39(9):2743-2749. doi: 10.1007/s10067-020-05020-8. Epub 2020 Mar 24.
Clin Rheumatol. 2020.
PMID: 32212000
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