Müller-Berghaus J - Search Results

1

Neonatal haemochromatosis: report of a patient with favourable outcome.

Müller-Berghaus J, Knisely AS, Zaum R, Vierzig A, Kirn E, Michalk DV, Roth B. Müller-Berghaus J, et al. Eur J Pediatr. 1997 Apr;156(4):296-8. doi: 10.1007/s004310050604. Eur J Pediatr. 1997. PMID: 9128815

2

Diagnosis and treatment of a child with the syndrome of apparent mineralocorticoid excess type 1.

Müller-Berghaus J, Homoki J, Michalk DV, Querfeld U. Müller-Berghaus J, et al. Acta Paediatr. 1996 Jan;85(1):111-3. doi: 10.1111/j.1651-2227.1996.tb13903.x. Acta Paediatr. 1996. PMID: 8834992

3

Intravenous iron treatment of renal anemia in children on hemodialysis.

Tenbrock K, Müller-Berghaus J, Michalk D, Querfeld U. Tenbrock K, et al. Pediatr Nephrol. 1999 Sep;13(7):580-2. doi: 10.1007/s004670050747. Pediatr Nephrol. 1999. PMID: 10460505 Clinical Trial.

4

Artificial abdominal hernia for the treatment of hepatomegaly in a neonate with stage 4S neuroblastoma.

Müller-Berghaus J, Kurowski C, Gharib M, Engelskirchen R, Roth B, Berthold F. Müller-Berghaus J, et al. Pediatr Hematol Oncol. 1999 Sep-Oct;16(5):453-8. doi: 10.1080/088800199277010. Pediatr Hematol Oncol. 1999. PMID: 10505322

5

Levamisole treatment in steroid-sensitive and steroid-resistant nephrotic syndrome.

Tenbrock K, Müller-Berghaus J, Fuchshuber A, Michalk D, Querfeld U. Tenbrock K, et al. Pediatr Nephrol. 1998 Aug;12(6):459-62. doi: 10.1007/s004670050487. Pediatr Nephrol. 1998. PMID: 9745868 Clinical Trial.

6

Cerebral complications in Schimke immuno-osseous dysplasia.

Schmidt B, Christen HJ, Herkenrath P, Benz-Bohm G, Müller-Berghaus J, Querfeld U. Schmidt B, et al. Eur J Pediatr. 1997 Oct;156(10):789-91. doi: 10.1007/s004310050714. Eur J Pediatr. 1997. PMID: 9365070

7

A transplanted child with severe hypercalcaemic hyperparathyroidism despite only modest bone lesions.

Müller-Berghaus J, Hoppe B, Schmidt R, Wagner M, Querfeld U. Müller-Berghaus J, et al. Nephrol Dial Transplant. 1997 Nov;12(11):2445-6. doi: 10.1093/ndt/12.11.2445. Nephrol Dial Transplant. 1997. PMID: 9394345 No abstract available.

8

The clinical course of steroid-sensitive childhood nephrotic syndrome is associated with a functional IL12B promoter polymorphism.

Müller-Berghaus J, Kemper MJ, Hoppe B, Querfeld U, Müller-Wiefel DE, Morahan G, Schadendorf D, Tenbrock K. Müller-Berghaus J, et al. Nephrol Dial Transplant. 2008 Dec;23(12):3841-4. doi: 10.1093/ndt/gfn395. Epub 2008 Jul 15. Nephrol Dial Transplant. 2008. PMID: 18632587

9

No association of IL-12p40 pro1.1 polymorphism with juvenile idiopathic arthritis.

Eberhardt CS, Haas JP, Girschick H, Schwarz T, Morbach H, Rösen-Wolff A, Foell D, Dannecker G, Schepp C, Ganser G, Honke N, Eggermann T, Müller-Berghaus J, Wagner N, Ohl K, Tenbrock K. Eberhardt CS, et al. Among authors: muller berghaus j. Pediatr Rheumatol Online J. 2015 Dec 15;13:61. doi: 10.1186/s12969-015-0059-z. Pediatr Rheumatol Online J. 2015. PMID: 26667304 Free PMC article.

10

Human herpesvirus-6 (HHV-6)-associated necrotizing encephalitis in Griscelli's syndrome.

Wagner M, Müller-Berghaus J, Schroeder R, Sollberg S, Luka J, Leyssens N, Schneider B, Krueger GR. Wagner M, et al. J Med Virol. 1997 Nov;53(3):306-12. doi: 10.1002/(sici)1096-9071(199711)53:3<306::aid-jmv21>3.0.co;2-d. J Med Virol. 1997. PMID: 9365900

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