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Lysine-Restricted Diet as Adjunct Therapy for Pyridoxine-Dependent Epilepsy: The PDE Consortium Consensus Recommendations.
JIMD Rep. 2014;15:1-11. doi: 10.1007/8904_2014_296. Epub 2014 Apr 19.
JIMD Rep. 2014.
PMID: 24748525
Free PMC article.
Lysine restricted diet for pyridoxine-dependent epilepsy: first evidence and future trials.
van Karnebeek CD, Hartmann H, Jaggumantri S, Bok LA, Cheng B, Connolly M, Coughlin CR 2nd, Das AM, Gospe SM Jr, Jakobs C, van der Lee JH, Mercimek-Mahmutoglu S, Meyer U, Struys E, Sinclair G, Van Hove J, Collet JP, Plecko BR, Stockler S.
van Karnebeek CD, et al.
Mol Genet Metab. 2012 Nov;107(3):335-44. doi: 10.1016/j.ymgme.2012.09.006. Epub 2012 Sep 10.
Mol Genet Metab. 2012.
PMID: 23022070
Free article.
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Biochemical signatures mimicking multiple carboxylase deficiency in children with mutations in MT-ATP6.
Larson AA, Balasubramaniam S, Christodoulou J, Burrage LC, Marom R, Graham BH, Diaz GA, Glamuzina E, Hauser N, Heese B, Horvath G, Mattman A, van Karnebeek C, Lane Rutledge S, Williamson A, Estrella L, Van Hove JKL, Weisfeld-Adams JD.
Larson AA, et al. Among authors: van hove jkl.
Mitochondrion. 2019 Jan;44:58-64. doi: 10.1016/j.mito.2018.01.001. Epub 2018 Jan 4.
Mitochondrion. 2019.
PMID: 29307858
Free PMC article.
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Neutrophils in Barth syndrome (BTHS) avidly bind annexin-V in the absence of apoptosis.
Kuijpers TW, Maianski NA, Tool AT, Becker K, Plecko B, Valianpour F, Wanders RJ, Pereira R, Van Hove J, Verhoeven AJ, Roos D, Baas F, Barth PG.
Kuijpers TW, et al.
Blood. 2004 May 15;103(10):3915-23. doi: 10.1182/blood-2003-11-3940. Epub 2004 Feb 5.
Blood. 2004.
PMID: 14764526
Free article.
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Practice patterns of mitochondrial disease physicians in North America. Part 1: diagnostic and clinical challenges.
Parikh S, Goldstein A, Koenig MK, Scaglia F, Enns GM, Saneto R; Mitochondrial Medicine Society Clinical Directors Working Group; MMS Clinical Director's Work Group; Anselm I, Collins A, Cohen BH, DeBrosse SD, Dimmock D, Falk MJ, Ganesh J, Greene C, Gropman AL, Haas R, Kahler SG, Kamholz J, Kendall F, Korson MS, Mattman A, Milone M, Niyazov D, Pearl PL, Reimschisel T, Salvarinova-Zivkovic R, Sims K, Tarnopolsky M, Tsao CY, van Hove J, Walsh L, Wolfe LA.
Parikh S, et al.
Mitochondrion. 2014 Jan;14(1):26-33. doi: 10.1016/j.mito.2013.07.116. Epub 2013 Jul 26.
Mitochondrion. 2014.
PMID: 23891656
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MRI of the brain and cervical spinal cord in rhizomelic chondrodysplasia punctata.
Bams-Mengerink AM, Majoie CB, Duran M, Wanders RJ, Van Hove J, Scheurer CD, Barth PG, Poll-The BT.
Bams-Mengerink AM, et al.
Neurology. 2006 Mar 28;66(6):798-803; discussion 789. doi: 10.1212/01.wnl.0000205594.34647.d0.
Neurology. 2006.
PMID: 16567694
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A novel POLG gene mutation in 4 children with Alpers-like hepatocerebral syndromes.
Kurt B, Jaeken J, Van Hove J, Lagae L, Löfgren A, Everman DB, Jayakar P, Naini A, Wierenga KJ, Van Goethem G, Copeland WC, DiMauro S.
Kurt B, et al.
Arch Neurol. 2010 Feb;67(2):239-44. doi: 10.1001/archneurol.2009.332.
Arch Neurol. 2010.
PMID: 20142534
Free PMC article.
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Purification and cellulolytic activity of cellvibrio.
VOETS JP, VAN HOVE JK.
VOETS JP, et al. Among authors: van hove jk.
Nature. 1953 Jun 13;171(4363):1073-4. doi: 10.1038/1711073b0.
Nature. 1953.
PMID: 13063537
No abstract available.
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