Zschocke, Johannes Prof. Dr. Dr. med.Universität HeidelbergHeidelberg
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Recent publications in heiBIB 
(In total there are 11 publications catalogued)
- Schossig, Anna Sarah: Mutations in ROGDI cause Kohlschütter-Tönz syndrome / Anna Schossig, Nicole I. Wolf, Christine Fischer, Maria Fischer, Gernot Stocker, Stephan Pabinger, A… , March 15, 2012. - 7 S.
In: The American journal of human genetics, ISSN 1537-6605. 90(2012), 4, Seite 701-707
DOI: 10.1016/j.ajhg.2012.02.012
- Gan-Schreier, Hongying: Newborn population screening for classic homocystinuria by determination of total homocysteine from guthrie cards / Hongying Gan-Schreier, PhD, Moustafa Kebbewar, Junmin Fang-Hoffmann, MD, Julia Wilrich, MD, Ghassan … , March 2010. - 6 S.
In: The journal of pediatrics, ISSN 1097-6833. 156(2010), 3 vom: März, Seite 427-432
DOI: 10.1016/j.jpeds.2009.09.054
- Janssen, Bart: Carnosine as a protective factor in diabetic nephropathy : association with a leucine repeat of the carnosinase gene CNDP1 / Bart Janssen, Daniela Hohenadel, Paul Brinkkoetter, Verena Peters, Nina Rind, Christine Fischer, Iva… , 2005. - 8 S.
In: Diabetes, ISSN 1939-327X. 54(2005), 8, Seite 2320-2327
DOI: 10.2337/diabetes.54.8.2320
- Wolf, Nicole: Leukoencephalopathy with ataxia, hypodontia, and hypomyelination / N.I. Wolf, I. Harting, E. Boltshauser, G. Wiegand, M.J. Koch, T. Schmitt-Mechelke, E. Martin, J. Zsc… , April 25, 2005. - 4 S.
In: Neurology, ISSN 1526-632X. 64(2005), 8, Seite 1461-1464
DOI: 10.1212/01.WNL.0000158615.56071.E3
- Bandmann, Oliver: The phenylalanine loading test in the differential diagnosis of dystonia / O. Bandmann, M. Goertz, J. Zschocke, G. Deuschl, W. Jost, H. Hefter, U. Müller, P. Zöfel, G. Hoffman… , February 25, 2003. - 3 S.
In: Neurology, ISSN 1526-632X. 60(2003), 4, Seite 700-702
DOI: 10.1212/01.WNL.0000048205.18445.98
- Zschocke, Johannes: The molecular basis of phenylalanine hydroxylase deficiency in Croatia / Johannes Zschocke, Astrid Preusse, Vladimir Sarnavka, Ksenija Fumic, Duško Mardešic, Georg F. Hoffma… , 19 March 2003. - 6 S.
In: Human mutation, ISSN 1098-1004. 21(2003), 4, Artikel-ID 399
DOI: 10.1002/humu.9115
- Ly-Hartig, Thi Bach Nga: Mutations in the AUH gene cause 3-methylglutaconic aciduria type I / T.B. Nga Ly, Verena Peters, K. Michael Gibson, Michael Liesert, Wolfgang Buckel, Bridget Wilcken, Ke… , 19 March 2003. - 7 S.
In: Human mutation, ISSN 1098-1004. 21(2003), 4, Seite 401-407
DOI: 10.1002/humu.10202
- Zschocke, Johannes: Genetische Determinanten phänotypischer Variabilität bei erblichen Störungen des Intermediärstoffwechsels im Kindesalter / vorgelegt von Johannes Zschocke, 2003. - Getr. Zählung : Ill., graph. Darst.
- Zschocke, Johannes: Nature and nurture in vitamin B12 deficiency / J. Zschocke, S. Schindler, G.F. Hoffmann, M. Albani, July 01, 2002. - 2 S.
In: Archives of disease in childhood, ISSN 1468-2044. 87(2002), 1, Seite 75-76
DOI: 10.1136/adc.87.1.75
- Zschocke, Johannes: The diagnosis of mitochondrial HMG-CoA synthase deficiency / Johannes Zschocke, Johannes M. Penzien, Rainer Bielen, Núria Casals, Rosa Aledo, Juan Pié, Georg F. … , 11 July 2002. - 3 S.
In: The journal of pediatrics, ISSN 1097-6833. 140(2002), 6, Seite 778-780
DOI: 10.1067/mpd.2002.123854
