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Items: 3

1.
The clinico‐radiological findings of MSUD in a group of Egyptian children: Contribution to early diagnosis and outcome
Montaser M. Mohamed, Mohamed A. Bakheet, Rofaida M. Magdy, Heba S. El‐Abd, Mohamad Hasan Alam‐Eldeen, Hany M. Abo‐Haded
Mol Genet Genomic Med. 2021 Oct; 9(10): e1790. Published online 2021 Aug 25. doi: 10.1002/mgg3.1790
PMCID:
PMC8580081
AbstractArticlePDF–926K
2.
Higher Branched-chain Amino Acids and Lower Serine Exist in the Plasma of Nondiabetic Mice: A Comparison Between High- and Low-protein Diet Conditions
EMI ARIMURA, MIHARU USHIKAI, MASAHISA HORIUCHI
In Vivo. 2021 May-Jun; 35(3): 1555–1560. Published online 2021 May 3. doi: 10.21873/invivo.12410
PMCID:
PMC8193297
AbstractArticlePDF–114K
3.
A Novel Syndrome Affecting Multiple Mitochondrial Functions, Located by Microcell-Mediated Transfer to Chromosome 2p14-2p13
Agnieszka Seyda, Robert F. Newbold, Thomas J. Hudson, Andrei Verner, Neviana MacKay, Susan Winter, Annette Feigenbaum, Suzann Malaney, Diego Gonzalez-Halphen, Andrew P. Cuthbert, Brian H. Robinson
Am J Hum Genet. 2001 Feb; 68(2): 386–396. Published online 2001 Jan 10. doi: 10.1086/318196
PMCID:
PMC1235272
AbstractArticlePDF–488K

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