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Bodamer, O.
65
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Online (65)
Mediatypes
Articles (Online) (52)
OpenAccess-fulltext (13)
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1
PRO68 THE USE OF A PATIENT REGISTRY TO BETTER INFORM HEALTH..:
Blakely, E.
;
Brown, C.
;
Bodamer, O.
...
Value in Health. 22 (2019) - p. S348 , 2019
Link:
https://doi.org/10.1016/..
?
2
Expanding the clinical spectrum of biallelic ZNF335 variant:
Stouffs, K.
;
Stergachis, A.B.
;
Vanderhasselt, T.
...
Clinical Genetics. 94 (2018) 2 - p. 246-251 , 2018
Link:
https://doi.org/10.1111/..
?
3
Mutations inRIT1cause Noonan syndrome - additional function..:
Koenighofer, M.
;
Hung, C. Y.
;
McCauley, J. L.
...
Clinical Genetics. 89 (2015) 3 - p. 359-366 , 2015
Link:
https://doi.org/10.1111/..
?
4
Liver, Pancreas and Kidney Transplantation for the Treatmen..:
Tzakis, A.G.
;
Nunnelley, M.J.
;
Tekin, A.
...
American Journal of Transplantation. 15 (2015) 2 - p. 565-567 , 2015
Link:
https://doi.org/10.1111/..
?
5
Update on transcobalamin deficiency: clinical presentation,..:
Trakadis, Y. J.
;
Alfares, A.
;
Bodamer, O. A.
...
Journal of Inherited Metabolic Disease. 37 (2013) 3 - p. 461-473 , 2013
Link:
https://doi.org/10.1007/..
?
6
Expert recommendations for the laboratory diagnosis of MPS ..:
Wood, T.
;
Bodamer, O.A.
;
Burin, M.G.
...
Molecular Genetics and Metabolism. 106 (2012) 1 - p. 73-82 , 2012
Link:
https://doi.org/10.1016/..
?
7
Free asymmetric dimethylarginine (ADMA) is low in children ..:
Huemer, M.
;
Simma, B.
;
Mayr, D.
...
Journal of Inherited Metabolic Disease. 35 (2012) 5 - p. 817-821 , 2012
Link:
https://doi.org/10.1007/..
?
8
Neugeborene mit Herpes-simplex-Virus-Infektionen: Folgen ei..:
Bodamer, O.A.
Monatsschrift Kinderheilkunde. 160 (2012) 4 - p. 325-328 , 2012
Link:
https://doi.org/10.1007/..
?
9
Propionic acidemia: neonatal versus selective metabolic scr..:
Grünert, S. C.
;
Müllerleile, S.
;
de Silva, L.
...
Journal of Inherited Metabolic Disease. 35 (2011) 1 - p. 41-49 , 2011
Link:
https://doi.org/10.1007/..
?
10
Mutation analysis in 54 propionic acidemia patients:
Kraus, J. P.
;
Spector, E.
;
Venezia, S.
...
Journal of Inherited Metabolic Disease. 35 (2011) 1 - p. 51-63 , 2011
Link:
https://doi.org/10.1007/..
?
11
Erratum zu: Angeborene Stoffwechselstörungen: Akute Präsent..:
Bodamer, O.
Monatsschrift Kinderheilkunde. 159 (2011) 1 - p. 24-24 , 2011
Link:
https://doi.org/10.1007/..
?
12
Magnetic resonance spectroscopy in patients with Fabry and ..:
Gruber, S.
;
Bogner, W.
;
Stadlbauer, A.
..
European Journal of Radiology. 79 (2011) 2 - p. 295-298 , 2011
Link:
https://doi.org/10.1016/..
?
13
Angeborene Stoffwechselstörungen: Akute Präsentation und Di..:
Bodamer, O.
Monatsschrift Kinderheilkunde. 158 (2010) 10 - p. 987-996 , 2010
Link:
https://doi.org/10.1007/..
?
14
147 Compound heterozygosity for mutations in TMEM70:
Sperl, W.
;
Bodamer, O.
;
Möslinger, D.
...
Mitochondrion. 10 (2010) 2 - p. 241 , 2010
Link:
https://doi.org/10.1016/..
?
15
P317 Cerebral creatine deficiency syndromes: clinical and l..:
Haliloglu, G.
;
Oguz, K. Karlı
;
Dursun, A.
...
European Journal of Paediatric Neurology. 13 (2009) - p. S119 , 2009
Link:
https://doi.org/10.1016/..
1-15