Das AM - Search Results

1

ALG1-CDG: a new case with early fatal outcome.

Rohlfing AK, Rust S, Reunert J, Tirre M, Du Chesne I, Wemhoff S, Meinhardt F, Hartmann H, Das AM, Marquardt T. Rohlfing AK, et al. Among authors: das am. Gene. 2014 Jan 25;534(2):345-51. doi: 10.1016/j.gene.2013.10.013. Epub 2013 Oct 21. Gene. 2014. PMID: 24157261

2

Isolated mitochondrial long-chain ketoacyl-CoA thiolase deficiency resulting from mutations in the HADHB gene.

Das AM, Illsinger S, Lücke T, Hartmann H, Ruiter JP, Steuerwald U, Waterham HR, Duran M, Wanders RJ. Das AM, et al. Clin Chem. 2006 Mar;52(3):530-4. doi: 10.1373/clinchem.2005.062000. Epub 2006 Jan 19. Clin Chem. 2006. PMID: 16423905

3

Pitfalls in paediatric gait disturbances: painless bone diseases.

Lücke T, Illsinger S, Das AM, Schirg E, Hartmann H. Lücke T, et al. Among authors: das am. Eur J Pediatr. 2006 Dec;165(12):909-12. doi: 10.1007/s00431-006-0180-6. Epub 2006 Jul 21. Eur J Pediatr. 2006. PMID: 16858582

4

Developmental outcome in five children with Hurler syndrome after stem cell transplantation: a pilot study.

Lücke T, Das AM, Hartmann H, Sykora KW, Donnerstag F, Schmid-Ott G, Grigull L. Lücke T, et al. Among authors: das am. Dev Med Child Neurol. 2007 Sep;49(9):693-6. doi: 10.1111/j.1469-8749.2007.00693.x. Dev Med Child Neurol. 2007. PMID: 17718826 Free article.

5

[Maternal vitamin B12 deficiency: cause for neurological symptoms in infancy].

Lücke T, Korenke GC, Poggenburg I, Bentele KH, Das AM, Hartmann H. Lücke T, et al. Among authors: das am. Z Geburtshilfe Neonatol. 2007 Aug;211(4):157-61. doi: 10.1055/s-2007-981249. Z Geburtshilfe Neonatol. 2007. PMID: 17729202 German.

6

Novel mutations in exon 6 of the GFAP gene affect a highly conserved if motif in the rod domain 2B and are associated with early onset infantile Alexander disease.

Hartmann H, Herchenbach J, Stephani U, Ledaal P, Donnerstag F, Lücke T, Das AM, Christen HJ, Hagedorn M, Meins M. Hartmann H, et al. Among authors: das am. Neuropediatrics. 2007 Jun;38(3):143-7. doi: 10.1055/s-2007-985902. Neuropediatrics. 2007. PMID: 17985264

7

Correspondence (letter to the editor): Risk group includes infants.

Hartmann H, Das AM, Lücke T. Hartmann H, et al. Among authors: das am. Dtsch Arztebl Int. 2009 Apr;106(17):290-1; author reply 291. doi: 10.3238/arztebl.2009.0291. Epub 2009 Apr 24. Dtsch Arztebl Int. 2009. PMID: 19547633 Free PMC article. No abstract available.

8

Scheie syndrome: enzyme replacement therapy does not prevent progression of cervical myelopathy due to spinal cord compression.

Illsinger S, Lücke T, Hartmann H, Mengel E, Müller-Forell W, Donnerstag F, Das AM. Illsinger S, et al. Among authors: das am. J Inherit Metab Dis. 2009 Dec;32 Suppl 1:S321-5. doi: 10.1007/s10545-009-1265-y. Epub 2009 Nov 4. J Inherit Metab Dis. 2009. PMID: 19894140

9

Glycogen storage disease type 1: impact of medium-chain triglycerides on metabolic control and growth.

Das AM, Lücke T, Meyer U, Hartmann H, Illsinger S. Das AM, et al. Ann Nutr Metab. 2010;56(3):225-32. doi: 10.1159/000283242. Epub 2010 Mar 30. Ann Nutr Metab. 2010. PMID: 20357432

10

Dietary habits and metabolic control in adolescents and young adults with phenylketonuria: self-imposed protein restriction may be harmful.

Das AM, Goedecke K, Meyer U, Kanzelmeyer N, Koch S, Illsinger S, Lücke T, Hartmann H, Lange K, Lanfermann H, Hoy L, Ding XQ. Das AM, et al. JIMD Rep. 2014;13:149-58. doi: 10.1007/8904_2013_273. Epub 2013 Nov 13. JIMD Rep. 2014. PMID: 24222493 Free PMC article.

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