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41 . Academic Journal
Angeborene Stoffwechselstörungen: Der österreichische Weg einer Schwerpunktsetzung
저자
by
Sperl, W.
;
Karall, D.
.
소스
Pädiatrie & Pädologie: Österreichische Zeitschrift für Kinder- & Jugendheilkunde
. September 2014 49(4):20-24
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44 . Academic Journal
'Floppy infant' mit besonderem Aussehen und Apnoen. (German)
저자
by
Niedermayr, K.
;
Scholl-Bürgi, S.
;
Albrecht, U.
;
Strobl, R.
;
Müller, F.
, et al.
소스
Monatsschrift Kinderheilkunde; Nov2012, Vol. 160 Issue 11, p1070-1072, 3p
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47 . Academic Journal
With new Portents on proven Ways On the OEGKJ-Presidency 2018 to 2020
저자
by
Karall, D.
.
소스
MONATSSCHRIFT KINDERHEILKUNDE
; JAN 2018, 166 1, p3-p5, 3p.
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43 . Academic Journal
Consensus on nutrition in pediatric palliative medicine. Interdisciplinary and multidisciplinary project
저자
by
Jones, R.
;
Behrens, R.
;
Dilch, A.
;
Brunner-Krainz, M.
;
Heu, V.
, et al.
소스
MONATSSCHRIFT KINDERHEILKUNDE
; SEP 2015, 163 9, p928-p933, 6p.
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47 .
Pädiatrie
저자
by
Karall, D.
;
Meisinger, B.
;
Grissenauer, G.
;
Scholl-Bürgi, S.
;
Heinz-Erian, P.
, et al.
소스
Klinische Ernährungsmedizin
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47 .
Management of phenylketonuria in Europe: Survey results from 19 countries
저자
by
Ozturk, YEŞİM
;
Niinikoski, H.
;
Bonnemains, C.
;
Marioli, S.
;
Barat, P.
, et al.
소스
Molecular Genetics and Metabolism, 99(2), 109-115. ACADEMIC PRESS INC ELSEVIER SCIENCE
Molecular Genetics and Metabolism, 99(2), 109-115. Academic Press Inc.
Full Text (ScienceDirect)
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47 . Academic Journal
Mitochondriopathien: Ein Update
저자
by
Sperl, W.
;
Prokisch, H.
;
Karall, D.
;
Mayr, J.A.
;
Freisinger, P.
.
소스
Monatsschrift Kinderheilkunde: Zeitschrift für Kinder- und Jugendmedizin
. September 2011 159(9):848-854
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47 .
Spectrum of combined respiratory chain defects
저자
by
Mayr, J.A.
;
Haack, T.B.
;
Freisinger, P.
;
Karall, D.
;
Makowski, C.C.
, et al.
소스
J. Inherit. Metab. Dis. 38, 629-640 (2015)
Open Access (OpenAIRE)
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47 .
Proposed guidelines for the diagnosis and management of methylmalonic and propionic acidemia
저자
by
Baumgartner, M.R.
;
Hörster, F.
;
Dionisi-Vici, C.
;
Haliloglu, G.
;
Karall, D.
, et al.
소스
Orphanet Journal of Rare Diseases, vol. 9, no. 1, pp. 130
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47 .
Congenital myopathy Ehlers-Danlos overlap syndrome caused by the deficiency of an enzyme involved in protein folding in the endoplasmic reticulum: identification and characterization of a novel disorder
저자
by
Fauth, C.
;
Baumann, M.
;
Giunta, C.
;
Krabichler, B.
;
Rüschendorf, F.
, et al.
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