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Page 1
Treatment of inborn errors of metabolism.
Jalan AB. Jalan AB. 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.
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