Das AM - Search Results

1

3-Methylglutaconic aciduria type I redefined: a syndrome with late-onset leukoencephalopathy.

Wortmann SB, Kremer BH, Graham A, Willemsen MA, Loupatty FJ, Hogg SL, Engelke UF, Kluijtmans LA, Wanders RJ, Illsinger S, Wilcken B, Cruysberg JR, Das AM, Morava E, Wevers RA. Wortmann SB, et al. Among authors: das am. Neurology. 2010 Sep 21;75(12):1079-83. doi: 10.1212/WNL.0b013e3181f39a8a. Neurology. 2010. PMID: 20855850

2

Secondary respiratory chain defect in a boy with long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: possible diagnostic pitfalls.

Das AM, Fingerhut R, Wanders RJ, Ullrich K. Das AM, et al. Eur J Pediatr. 2000 Apr;159(4):243-6. doi: 10.1007/s004310050063. Eur J Pediatr. 2000. PMID: 10789927

3

BH4-sensitive hyperphenylalaninemia: new case and review of literature.

Lücke T, Illsinger S, Aulehla-Scholz C, Sander J, Das AM. Lücke T, et al. Among authors: das am. Pediatr Neurol. 2003 Mar;28(3):228-30. doi: 10.1016/s0887-8994(02)00516-7. Pediatr Neurol. 2003. PMID: 12770680 Review.

4

3-methylglutaconic aciduria type I in a boy with fever-associated seizures.

Illsinger S, Lücke T, Zschocke J, Gibson KM, Das AM. Illsinger S, et al. Among authors: das am. Pediatr Neurol. 2004 Mar;30(3):213-5. doi: 10.1016/j.pediatrneurol.2003.09.016. Pediatr Neurol. 2004. PMID: 15033206

5

Two cases of isolated glycerol kinase deficiency with heterogeneous neurological symptoms.

Illsinger S, Marquardt I, Lücke T, Hellerud C, Korenke C, Das AM. Illsinger S, et al. Among authors: das am. Dev Med Child Neurol. 2007 May;49(5):396-7. doi: 10.1111/j.1469-8749.2007.00396.x. Dev Med Child Neurol. 2007. PMID: 17489818 Free article. No abstract available.

6

Diagnostic work-up and management of patients with isolated methylmalonic acidurias in European metabolic centres.

Zwickler T, Lindner M, Aydin HI, Baumgartner MR, Bodamer OA, Burlina AB, Das AM, DeKlerk JB, Gökcay G, Grünewald S, Guffon N, Maier EM, Morava E, Geb S, Schwahn B, Walter JH, Wendel U, Wijburg FA, Müller E, Kölker S, Hörster F. Zwickler T, et al. Among authors: das am. J Inherit Metab Dis. 2008 Jun;31(3):361-7. doi: 10.1007/s10545-008-0804-2. Epub 2008 May 27. J Inherit Metab Dis. 2008. PMID: 18563634

7

Carnitine-palmitoyltransferase 2 deficiency: novel mutations and relevance of newborn screening.

Illsinger S, Lücke T, Peter M, Ruiter JP, Wanders RJ, Deschauer M, Handig I, Wuyts W, Das AM. Illsinger S, et al. Among authors: das am. Am J Med Genet A. 2008 Nov 15;146A(22):2925-8. doi: 10.1002/ajmg.a.32545. Am J Med Genet A. 2008. PMID: 18925671

8

Developmental changes of oxalate excretion in enterally fed preterm infants.

Illsinger S, Lücke T, Vaske B, Schmidt KH, Bohnhorst B, Das AM. Illsinger S, et al. Among authors: das am. J Inherit Metab Dis. 2009 Feb;32(1):102-8. doi: 10.1007/s10545-008-1024-5. Epub 2008 Dec 12. J Inherit Metab Dis. 2009. PMID: 19067228

9

Plasma and urine amino acid pattern in preterm infants on enteral nutrition: impact of gestational age.

Illsinger S, Schmidt KH, Lücke T, Vaske B, Bohnhorst B, Das AM. Illsinger S, et al. Among authors: das am. Amino Acids. 2010 Mar;38(3):959-72. doi: 10.1007/s00726-009-0305-0. Epub 2009 May 26. Amino Acids. 2010. PMID: 19468821 Clinical Trial.

10

Prediction of outcome in isolated methylmalonic acidurias: combined use of clinical and biochemical parameters.

Hörster F, Garbade SF, Zwickler T, Aydin HI, Bodamer OA, Burlina AB, Das AM, De Klerk JBC, Dionisi-Vici C, Geb S, Gökcay G, Guffon N, Maier EM, Morava E, Walter JH, Schwahn B, Wijburg FA, Lindner M, Grünewald S, Baumgartner MR, Kölker S. Hörster F, et al. Among authors: das am. J Inherit Metab Dis. 2009 Oct;32(5):630. doi: 10.1007/s10545-009-1189-6. Epub 2009 Jul 31. J Inherit Metab Dis. 2009. PMID: 19642010

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