Klee D - Search Results

1

Increase of CSF tyrosine and impaired serotonin turnover in tyrosinemia type I.

Thimm E, Herebian D, Assmann B, Klee D, Mayatepek E, Spiekerkoetter U. Thimm E, et al. Among authors: klee d. Mol Genet Metab. 2011 Feb;102(2):122-5. doi: 10.1016/j.ymgme.2010.11.003. Epub 2010 Nov 10. Mol Genet Metab. 2011. PMID: 21112803

2

Cystic renal dysplasia as a leading sign of inherited metabolic disease.

Distelmaier F, Vogel M, Spiekerkötter U, Gempel K, Klee D, Braunstein S, Groneck HP, Mayatepek E, Wendel U, Schwahn B. Distelmaier F, et al. Among authors: klee d. Pediatr Nephrol. 2007 Dec;22(12):2119-24. doi: 10.1007/s00467-007-0536-9. Epub 2007 Jul 19. Pediatr Nephrol. 2007. PMID: 17638024

3

Bloody nipple discharge (BND) in an 8 months old girl and a 9 months old male--rational diagnostic approach.

Harmsen S, Mayatepek E, Klee D, Meissner T. Harmsen S, et al. Among authors: klee d. Klin Padiatr. 2010 Mar;222(2):79-83. doi: 10.1055/s-0029-1234075. Epub 2010 Feb 17. Klin Padiatr. 2010. PMID: 20166010

4

Chronic pancreatitis in branched-chain organic acidurias--a case of methylmalonic aciduria and an overview of the literature.

Marquard J, El Scheich T, Klee D, Schmitt M, Meissner T, Mayatepek E, Oh J. Marquard J, et al. Among authors: klee d. Eur J Pediatr. 2011 Feb;170(2):241-5. doi: 10.1007/s00431-010-1313-5. Epub 2010 Oct 6. Eur J Pediatr. 2011. PMID: 20924605 Review.

5

Neurocognitive outcome in patients with hypertyrosinemia type I after long-term treatment with NTBC.

Thimm E, Richter-Werkle R, Kamp G, Molke B, Herebian D, Klee D, Mayatepek E, Spiekerkoetter U. Thimm E, et al. Among authors: klee d. J Inherit Metab Dis. 2012 Mar;35(2):263-8. doi: 10.1007/s10545-011-9394-5. Epub 2011 Nov 9. J Inherit Metab Dis. 2012. PMID: 22069142

6

Non-enhanced ECG-gated respiratory-triggered 3-D steady-state free-precession MR angiography with slab-selective inversion: initial experience in visualisation of renal arteries in free-breathing children without renal artery abnormality.

Klee D, Lanzman RS, Blondin D, Schmitt P, Oh J, Salgin B, Mayatepek E, Antoch G, Schaper J. Klee D, et al. Pediatr Radiol. 2012 Jul;42(7):785-90. doi: 10.1007/s00247-011-2343-5. Epub 2012 Mar 31. Pediatr Radiol. 2012. PMID: 22466749

7

Crossed cerebellar diaschisis after status epilepticus in a young child.

Koy A, Klee D, Weber AA, Karenfort M, Mayatepek E. Koy A, et al. Among authors: klee d. Neuropediatrics. 2012 Apr;43(2):55-8. doi: 10.1055/s-0032-1309306. Epub 2012 Apr 3. Neuropediatrics. 2012. PMID: 22473242

8

Brown-Vialetto-Van Laere syndrome: a riboflavin-unresponsive patient with a novel mutation in the C20orf54 gene.

Koy A, Pillekamp F, Hoehn T, Waterham H, Klee D, Mayatepek E, Assmann B. Koy A, et al. Among authors: klee d. Pediatr Neurol. 2012 Jun;46(6):407-9. doi: 10.1016/j.pediatrneurol.2012.03.008. Pediatr Neurol. 2012. PMID: 22633641

9

Approach to the management of slipped capital femoral epiphysis and primary hyperparathyroidism.

El Scheich T, Marquard J, Westhoff B, Schneider A, Cupisti K, Oh J, Meissner T, Mayatepek E, Klee D. El Scheich T, et al. Among authors: klee d. J Pediatr Endocrinol Metab. 2012;25(3-4):239-44. J Pediatr Endocrinol Metab. 2012. PMID: 22768650 Review.

10

Approach to the management of slipped capital femoral epiphysis and primary hyperparathyroidism.

El Scheich T, Marquard J, Westhoff B, Krauspe R, Schneider A, Cupisti K, Oh J, Meissner T, Mayatepek E, Klee D. El Scheich T, et al. Among authors: klee d. J Pediatr Endocrinol Metab. 2012;25(5-6):407-12. J Pediatr Endocrinol Metab. 2012. PMID: 22876531 Review.

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