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Page 1
Newborn screening programs for spinal muscular atrophy worldwide: Where we stand and where to go.
Neuromuscul Disord. 2021 Jun;31(6):574-582. doi: 10.1016/j.nmd.2021.03.007. Epub 2021 Apr 7.
Neuromuscul Disord. 2021.
PMID: 33985857
Expert Group Consensus on early diagnosis and management of infantile-onset pompe disease in the Gulf Region.
Al-Hassnan Z, Hashmi NA, Makhseed N, Omran TB, Al Jasmi F, Teneiji AA.
Al-Hassnan Z, et al. Among authors: omran tb.
Orphanet J Rare Dis. 2022 Oct 27;17(1):388. doi: 10.1186/s13023-022-02545-w.
Orphanet J Rare Dis. 2022.
PMID: 36303251
Free PMC article.
Review.
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The re-occurrence of dilated cardiomyopathy in propionic acidemia after liver transplantation requiring heart transplant, first case from Middle East.
Hejazi Y, Hijazi ZM, Al-Saloos H, Omran TB.
Hejazi Y, et al. Among authors: omran tb.
Cardiol Young. 2022 Feb 16:1-4. doi: 10.1017/S104795112200035X. Online ahead of print.
Cardiol Young. 2022.
PMID: 35170426
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Point of Care Exome Sequencing Reveals Allelic and Phenotypic Heterogeneity Underlying Mendelian disease in Qatar.
Fakhro KA, Robay A, Rodrigues-Flores JL, Mezey JG, Al-Shakaki AA, Chidiac O, Stadler D, Malek JA, Imam AB, Sheikh A, Azzam A, Janahi I, Khanjar I, Osman K, Ziki MA, Mahmah MA, Selim M, Numeiri N, Ali R, Lakhani S, Butt F, Omran TB, Crystal RG.
Fakhro KA, et al. Among authors: omran tb.
Hum Mol Genet. 2019 Dec 1;28(23):3970-3981. doi: 10.1093/hmg/ddz134.
Hum Mol Genet. 2019.
PMID: 31625567
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Correction: Expert Group Consensus on early diagnosis and management of infantile-onset pompe disease in the Gulf Region.
Al-Hassnan Z, Al Hashmi N, Makhseed N, Omran TB, Al Jasmi F, Al Teneiji A.
Al-Hassnan Z, et al. Among authors: omran tb.
Orphanet J Rare Dis. 2023 Nov 23;18(1):365. doi: 10.1186/s13023-023-02967-0.
Orphanet J Rare Dis. 2023.
PMID: 37996946
Free PMC article.
No abstract available.
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Human heterologous liver cells transiently improve hyperammonemia and ureagenesis in individuals with severe urea cycle disorders.
Meyburg J, Opladen T, Spiekerkötter U, Schlune A, Schenk JP, Schmidt J, Weitz J, Okun J, Bürger F, Omran TB, Abdoh G, Al Rifai H, Monavari A, Konstantopoulou V, Kölker S, Yudkoff M, Hoffmann GF.
Meyburg J, et al. Among authors: omran tb.
J Inherit Metab Dis. 2018 Jan;41(1):81-90. doi: 10.1007/s10545-017-0097-4. Epub 2017 Oct 12.
J Inherit Metab Dis. 2018.
PMID: 29027067
Clinical Trial.
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