Opladen T - Search Results

1

Consensus guideline for the diagnosis and treatment of aromatic l-amino acid decarboxylase (AADC) deficiency.

Wassenberg T, Molero-Luis M, Jeltsch K, Hoffmann GF, Assmann B, Blau N, Garcia-Cazorla A, Artuch R, Pons R, Pearson TS, Leuzzi V, Mastrangelo M, Pearl PL, Lee WT, Kurian MA, Heales S, Flint L, Verbeek M, Willemsen M, Opladen T. Wassenberg T, et al. Among authors: opladen t. Orphanet J Rare Dis. 2017 Jan 18;12(1):12. doi: 10.1186/s13023-016-0522-z. Orphanet J Rare Dis. 2017. PMID: 28100251 Free PMC article. Review.

2

Autoantibodies to folate receptors in the cerebral folate deficiency syndrome.

Ramaekers VT, Rothenberg SP, Sequeira JM, Opladen T, Blau N, Quadros EV, Selhub J. Ramaekers VT, et al. Among authors: opladen t. N Engl J Med. 2005 May 12;352(19):1985-91. doi: 10.1056/NEJMoa043160. N Engl J Med. 2005. PMID: 15888699 Free article.

3

Analysis of 5-methyltetrahydrofolate in serum of healthy children.

Opladen T, Ramaekers VT, Heimann G, Blau N. Opladen T, et al. Mol Genet Metab. 2006 Jan;87(1):61-5. doi: 10.1016/j.ymgme.2005.08.011. Epub 2005 Nov 28. Mol Genet Metab. 2006. PMID: 16310391

4

Effect of antiepileptic drugs and reactive oxygen species on folate receptor 1 (FOLR1)-dependent 5-methyltetrahydrofolate transport.

Opladen T, Blau N, Ramaekers VT. Opladen T, et al. Mol Genet Metab. 2010 Sep;101(1):48-54. doi: 10.1016/j.ymgme.2010.05.006. Epub 2010 Jun 16. Mol Genet Metab. 2010. PMID: 20619709 Free article.

5

Phenylalanine loading in pediatric patients with dopa-responsive dystonia: revised test protocol and pediatric cutoff values.

Opladen T, Okun JG, Burgard P, Blau N, Hoffmann GF. Opladen T, et al. J Inherit Metab Dis. 2010 Dec;33(6):697-703. doi: 10.1007/s10545-010-9164-9. Epub 2010 Jul 29. J Inherit Metab Dis. 2010. PMID: 20668943 Clinical Trial.

6

Clinical and biochemical characterization of patients with early infantile onset of autosomal recessive GTP cyclohydrolase I deficiency without hyperphenylalaninemia.

Opladen T, Hoffmann G, Hörster F, Hinz AB, Neidhardt K, Klein C, Wolf N. Opladen T, et al. Mov Disord. 2011 Jan;26(1):157-61. doi: 10.1002/mds.23329. Epub 2010 Sep 3. Mov Disord. 2011. PMID: 20818608

7

Diagnosis of tetrahydrobiopterin deficiency using filter paper blood spots: further development of the method and 5 years experience.

Opladen T, Abu Seda B, Rassi A, Thöny B, Hoffmann GF, Blau N. Opladen T, et al. J Inherit Metab Dis. 2011 Jun;34(3):819-26. doi: 10.1007/s10545-011-9300-1. Epub 2011 Mar 17. J Inherit Metab Dis. 2011. PMID: 21416196

8

Neuropsychiatric symptoms and intelligence quotient in autosomal dominant Segawa disease.

López-Laso E, Sánchez-Raya A, Moriana JA, Martínez-Gual E, Camino-León R, Mateos-González ME, Pérez-Navero JL, Ochoa-Sepúlveda JJ, Ormazabal A, Opladen T, Klein C, Lao-Villadóniga JI, Beyer K, Artuch R. López-Laso E, et al. Among authors: opladen t. J Neurol. 2011 Dec;258(12):2155-62. doi: 10.1007/s00415-011-6079-9. Epub 2011 May 10. J Neurol. 2011. PMID: 21556877

9

Cerebral folate deficiency: a neurometabolic syndrome?

Mangold S, Blau N, Opladen T, Steinfeld R, Wessling B, Zerres K, Häusler M. Mangold S, et al. Among authors: opladen t. Mol Genet Metab. 2011 Nov;104(3):369-72. doi: 10.1016/j.ymgme.2011.06.004. Epub 2011 Jun 14. Mol Genet Metab. 2011. PMID: 21737328

10

Does the aromatic L-amino acid decarboxylase contribute to thyronamine biosynthesis?

Hoefig CS, Renko K, Piehl S, Scanlan TS, Bertoldi M, Opladen T, Hoffmann GF, Klein J, Blankenstein O, Schweizer U, Köhrle J. Hoefig CS, et al. Among authors: opladen t. Mol Cell Endocrinol. 2012 Feb 26;349(2):195-201. doi: 10.1016/j.mce.2011.10.024. Epub 2011 Oct 28. Mol Cell Endocrinol. 2012. PMID: 22061622

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