Ibel H - Search Results

1

Multiple respiratory chain abnormalities associated with hypertrophic cardiomyopathy and 3-methylglutaconic aciduria.

Ibel H, Endres W, Hadorn HB, Deufel T, Paetzke I, Duran M, Kennaway NG, Gibson KM. Ibel H, et al. Eur J Pediatr. 1993 Aug;152(8):665-70. doi: 10.1007/BF01955244. Eur J Pediatr. 1993. PMID: 7691603

2

Hartnup syndrome, progressive encephalopathy and allo-albuminaemia. A clinico-pathological case study.

Schmidtke K, Endres W, Roscher A, Ibel H, Herschkowitz N, Bachmann C, Plöchl E, Hadorn HB. Schmidtke K, et al. Among authors: ibel h. Eur J Pediatr. 1992 Dec;151(12):899-903. doi: 10.1007/BF01954126. Eur J Pediatr. 1992. PMID: 1473543

3

Fatal infantile mitochondrial cardiomyopathy and myopathy with heterogeneous tissue expression of combined respiratory chain deficiencies.

Müller-Höcker J, Ibel H, Paetzke I, Deufel T, Endres W, Kadenbach B, Gokel JM, Hübner G. Müller-Höcker J, et al. Among authors: ibel h. Virchows Arch A Pathol Anat Histopathol. 1991;419(4):355-62. doi: 10.1007/BF01606527. Virchows Arch A Pathol Anat Histopathol. 1991. PMID: 1659034

4

Report on a new patient with combined deficiencies of sulphite oxidase and xanthine dehydrogenase due to molybdenum cofactor deficiency.

Endres W, Shin YS, Günther R, Ibel H, Duran M, Wadman SK. Endres W, et al. Among authors: ibel h. Eur J Pediatr. 1988 Dec;148(3):246-9. doi: 10.1007/BF00441412. Eur J Pediatr. 1988. PMID: 3215199

5

Bone marrow transplantation in Lesch-Nyhan disease.

Endres W, Helmig M, Shin YS, Albert E, Wank R, Ibel H, Weiss M, Hadorn HB, Hass R. Endres W, et al. Among authors: ibel h. J Inherit Metab Dis. 1991;14(2):270-1. doi: 10.1007/BF01800605. J Inherit Metab Dis. 1991. PMID: 1886412 No abstract available.

6

[D-penicillamine-induced IgA deficiency in the therapy of Wilson's disease].

Ibel H, Feist D, Endres W, Belohradsky BH. Ibel H, et al. Klin Padiatr. 1990 Nov-Dec;202(6):427-9. doi: 10.1055/s-2007-1025560. Klin Padiatr. 1990. PMID: 2266710 German.

7

Tetrahydrobiopterin and "non-responsive" dihydropteridine reductase deficiency.

Endres W, Ibel H, Kierat L, Blau N, Curtius HC. Endres W, et al. Among authors: ibel h. Lancet. 1987 Jul 25;2(8552):223. doi: 10.1016/s0140-6736(87)90813-0. Lancet. 1987. PMID: 2885683 No abstract available.

8

Outcome and long-term follow-up of 36 patients with tetrahydrobiopterin deficiency.

Jäggi L, Zurflüh MR, Schuler A, Ponzone A, Porta F, Fiori L, Giovannini M, Santer R, Hoffmann GF, Ibel H, Wendel U, Ballhausen D, Baumgartner MR, Blau N. Jäggi L, et al. Among authors: ibel h. Mol Genet Metab. 2008 Mar;93(3):295-305. doi: 10.1016/j.ymgme.2007.10.004. Epub 2007 Dec 3. Mol Genet Metab. 2008. PMID: 18060820

9

Colour Doppler imaging of intracranial vasculopathy in severe infantile sialidosis.

Ries M, Deeg KH, Wölfel D, Ibel H, Maier B, Buheitel G. Ries M, et al. Among authors: ibel h. Pediatr Radiol. 1992;22(3):179-81. doi: 10.1007/BF02012489. Pediatr Radiol. 1992. PMID: 1508583

10

Imitation behavior and subsequent complications.

Noll T, Sattler JB, Ibel H. Noll T, et al. Among authors: ibel h. Dtsch Arztebl Int. 2012 Jul;109(27-28):490; author reply 490-1. doi: 10.3238/arztebl.2012.0490a. Epub 2012 Jul 9. Dtsch Arztebl Int. 2012. PMID: 22833763 Free PMC article. No abstract available.

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