Opladen T - Search Results

1

The continuously evolving phenotype of succinic semialdehyde dehydrogenase deficiency.

Julia-Palacios NA, Kuseyri Hübschmann O, Olivella M, Pons R, Horvath G, Lücke T, Fung CW, Wong SN, Cortès-Saladelafont E, Rovira-Remisa MM, Yıldız Y, Mercimek-Andrews S, Assmann B, Stevanović G, Manti F, Brennenstuhl H, Jung-Klawitter S, Jeltsch K, Sivri HS, Garbade SF, García-Cazorla À, Opladen T. Julia-Palacios NA, et al. Among authors: opladen t. J Inherit Metab Dis. 2024 May;47(3):447-462. doi: 10.1002/jimd.12723. Epub 2024 Mar 18. J Inherit Metab Dis. 2024. PMID: 38499966

2

Flow cytometric cerebrospinal fluid analysis in children.

Häusler M, Sellhaus B, Schweizer K, Ramaekers VT, Opladen T, Kleines M. Häusler M, et al. Among authors: opladen t. Pathol Res Pract. 2003;199(10):667-75. doi: 10.1078/0344-0338-00478. Pathol Res Pract. 2003. PMID: 14666969

3

Clinical and genetic studies in a family with a novel mutation in the sepiapterin reductase gene.

Koht J, Rengmark A, Opladen T, Bjørnarå KA, Selberg T, Tallaksen CM, Blau N, Toft M. Koht J, et al. Among authors: opladen t. Acta Neurol Scand Suppl. 2014;(198):7-12. doi: 10.1111/ane.12230. Acta Neurol Scand Suppl. 2014. PMID: 24588500

4

Psychomotor retardation, spastic paraplegia, cerebellar ataxia and dyskinesia associated with low 5-methyltetrahydrofolate in cerebrospinal fluid: a novel neurometabolic condition responding to folinic acid substitution.

Ramaekers VT, Häusler M, Opladen T, Heimann G, Blau N. Ramaekers VT, et al. Among authors: opladen t. Neuropediatrics. 2002 Dec;33(6):301-8. doi: 10.1055/s-2002-37082. Neuropediatrics. 2002. PMID: 12571785 Free article.

5

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

6

Congenital null mutations of the FOLR1 gene: a progressive neurologic disease and its treatment.

Cario H, Bode H, Debatin KM, Opladen T, Schwarz K. Cario H, et al. Among authors: opladen t. Neurology. 2009 Dec 15;73(24):2127-9. doi: 10.1212/WNL.0b013e3181c679df. Neurology. 2009. PMID: 20018644 No abstract available.

7

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

8

Peripheral decrease and pulmonary homing of CD4+CD45RO+ helper memory T cells in cystic fibrosis.

Häusler M, Schweizer K, Biesterfel S, Opladen T, Heimann G. Häusler M, et al. Among authors: opladen t. Respir Med. 2002 Feb;96(2):87-94. doi: 10.1053/rmed.2001.1217. Respir Med. 2002. PMID: 11860174 Free article.

9

Severe mucitis after sublingual administration of tetrahydrobiopterin in a patient with tetrahydrobiopterin-responsive phenylketonuria.

Opladen T, Zurflüh M, Kern I, Kierat L, Thöny B, Blau N. Opladen T, et al. Eur J Pediatr. 2005 Jun;164(6):395-6. doi: 10.1007/s00431-005-1638-7. Epub 2005 Feb 22. Eur J Pediatr. 2005. PMID: 15726407 Free article. Clinical Trial. No abstract available.

10

A novel mutation (c.64_65delGGinsAACC [p.G21fsX66]) in the GTP cyclohydrolase 1 gene that causes Segawa disease.

von Mering M, Gabriel H, Opladen T, Hoffmann GF, Storch A. von Mering M, et al. Among authors: opladen t. J Neurol Neurosurg Psychiatry. 2008 Feb;79(2):229. doi: 10.1136/jnnp.2007.130849. J Neurol Neurosurg Psychiatry. 2008. PMID: 18202219 No abstract available.

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