Хайлтын үр дүнгүүд - Enns, Gregory M.
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Profound neonatal lactic acidosis and renal tubulopathy in a patient with glycogen storage disease type IXɑ2 secondary to a de novo pathogenic variant in PHKA2 -н Morales, J. Andres, Tise, Christina G., Narang, Amrita, Grimm, Paul C., Enns, Gregory M., Lee, Chung U.
Хэвлэсэн 2021текст -
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Inherited disorders affecting mitochondrial function are associated with glutathione deficiency and hypocitrullinemia -н Atkuri, Kondala R., Cowan, Tina M., Kwan, Tony, Ng, Angelina, Herzenberg, Leonard A., Herzenberg, Leonore A., Enns, Gregory M.
Хэвлэсэн 2009текст -
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Line intensities and temperature-dependent line broadening coefficients of Q-branch transitions in the v(2) band of ammonia near 10.4 μm -н Sur, Ritobrata, Spearrin, R. Mitchell, Peng, Wen Y., Strand, Christopher L., Jeffries, Jay B., Enns, Gregory M., Hanson, Ronald K.
Хэвлэсэн 2016текст -
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Degree of Glutathione Deficiency and Redox Imbalance Depend on Subtype of Mitochondrial Disease and Clinical Status -н Enns, Gregory M., Moore, Tereza, Le, Anthony, Atkuri, Kondala, Shah, Monisha K., Cusmano-Ozog, Kristina, Niemi, Anna-Kaisa, Cowan, Tina M.
Хэвлэсэн 2014текст -
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A congenital disorder of deglycosylation: Biochemical characterization of N-glycanase 1 deficiency in patient fibroblasts -н He, Ping, Grotzke, Jeff E, Ng, Bobby G, Gunel, Murat, Jafar-Nejad, Hamed, Cresswell, Peter, Enns, Gregory M, Freeze, Hudson H
Хэвлэсэн 2015текст -
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A Novel Mutation in the HSD17B10 Gene of a 10-Year-Old Boy with Refractory Epilepsy, Choreoathetosis and Learning Disability -н Seaver, Laurie H., He, Xue-Ying, Abe, Keith, Cowan, Tina, Enns, Gregory M., Sweetman, Lawrence, Philipp, Manfred, Lee, Sansan, Malik, Mazhar, Yang, Song-Yu
Хэвлэсэн 2011текст -
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The Present and Future of Mitochondrial-Based Therapeutics for Eye Disease -н Ji, Marco H., Kreymerman, Alexander, Belle, Kinsley, Ghiam, Benjamin K., Muscat, Stephanie R., Mahajan, Vinit B., Enns, Gregory M., Mercola, Mark, Wood, Edward H.
Хэвлэсэн 2021текст -
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High-quality DNA sequence capture of 524 disease candidate genes -н Shen, Peidong, Wang, Wenyi, Krishnakumar, Sujatha, Palm, Curtis, Chi, Aung-Kyaw, Enns, Gregory M., Davis, Ronald W., Speed, Terence P., Mindrinos, Michael N., Scharfe, Curt
Хэвлэсэн 2011текст -
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A New Approach to Rare Diseases of Children: The Undiagnosed Diseases Network -н Reuter, Chloe M., Brimble, Elise, DeFilippo, Colette, Dries, Annika M., Enns, Gregory M., Ashley, Euan A., Bernstein, Jonathan A., Fisher, Paul Graham, Wheeler, Matthew T.
Хэвлэсэн 2018текст -
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Hypoglycemia in CDG patients due to PMM2 mutations: Follow up on hyperinsulinemic patients -н Moravej, Hossein, Altassan, Ruqaiah, Jaeken, Jaak, Enns, Gregory M., Ellaway, Carolyn, Balasubramaniam, Shanti, De Lonlay, Pascale, Coman, David, Mercimek‐Andrews, Saadet, Witters, Peter, Morava, Eva
Хэвлэсэн 2019текст