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Page 1
Lipoprotein (a): its role in childhood thromboembolism.
Nowak-Göttl U, Debus O, Findeisen M, Kassenböhmer R, Koch HG, Pollmann H, Postler C, Weber P, Vielhaber H. Nowak-Göttl U, et al. Among authors: debus o. Pediatrics. 1997 Jun;99(6):E11. doi: 10.1542/peds.99.6.e11. Pediatrics. 1997. PMID: 9164807
Expanding the clinical and molecular spectrum of thiamine pyrophosphokinase deficiency: a treatable neurological disorder caused by TPK1 mutations.
Banka S, de Goede C, Yue WW, Morris AA, von Bremen B, Chandler KE, Feichtinger RG, Hart C, Khan N, Lunzer V, Mataković L, Marquardt T, Makowski C, Prokisch H, Debus O, Nosaka K, Sonwalkar H, Zimmermann FA, Sperl W, Mayr JA. Banka S, et al. Among authors: debus o. Mol Genet Metab. 2014 Dec;113(4):301-6. doi: 10.1016/j.ymgme.2014.09.010. Epub 2014 Oct 5. Mol Genet Metab. 2014. PMID: 25458521
Dextromethorphan in molybdenum cofactor deficiency.
Kurlemann G, Debus O, Schuierer G. Kurlemann G, et al. Among authors: debus o. Eur J Pediatr. 1996 May;155(5):422-3. doi: 10.1007/BF01955280. Eur J Pediatr. 1996. PMID: 8741046 No abstract available.
A Medical Mystery.
Kurlemann G, Debus O. Kurlemann G, et al. Among authors: debus o. N Engl J Med. 2000 Oct 5;343(14):1019. doi: 10.1056/NEJM200010053431406. N Engl J Med. 2000. PMID: 11018169 Free article. No abstract available.
Medical mystery: the answer.
Kurlemann G, Debus O. Kurlemann G, et al. Among authors: debus o. N Engl J Med. 2000 Nov 23;343(21):1573. doi: 10.1056/NEJM200011233432114. N Engl J Med. 2000. PMID: 11184752 No abstract available.
[Cockayne syndrome with marked cerebral symptoms].
Menges-Wenzel EM, Debus O, Sträter R, Schuierer G, Kurlemann G. Menges-Wenzel EM, et al. Among authors: debus o. Klin Padiatr. 2001 May-Jun;213(3):134-8. doi: 10.1055/s-2001-15864. Klin Padiatr. 2001. PMID: 11417366 German.
35 results