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Results of search for 'au:"Mönch, E"', page 2 of 3
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Authors
Ahnert-Hilger, G
Arnold, M
Bachmann, C
Bassir, C
Brösicke, H G
Burgard, P
Busse, B
Bührdel, P
Falkenberg, N
Gerlach, J C
Geyer, G
Herrmann, M E
Jakobs, C
Keller, M
Kulozik, A E
Mönch, E
Müller, C
Neuhaus, P
Siemes, H
Vetter, B
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Topics
Adolescent
Adult
Amino Acid Metabolism, Inborn Errors
Amino Acids
Animals
Child
Child, Preschool
Creatinine
Female
Humans
Infant
Infant, Newborn
Male
Phenylalanine
Phenylketonurias
analysis
blood
complications
diagnosis
metabolism
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Languages
English
g d
German
Your search returned 44 results.
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21.
Propionacidaemia and immunodeficiency.
[electronic resource]
by
Müller, S
Falkenberg, N
Mönch, E
Jakobs, C
Producer:
19800530
In:
Lancet (London, England)
vol. 1
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22.
Phenotypic heterogeneity and adverse effects of serine treatment in 3-phosphoglycerate dehydrogenase deficiency: report on two siblings.
[electronic resource]
by
Häusler, M G
Jaeken, J
Mönch, E
Ramaekers, V T
Producer:
20011101
In:
Neuropediatrics
vol. 32
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23.
Diurnal changes in plasma amino acids in maple syrup urine disease.
[electronic resource]
by
Schwahn, B
Wendel, U
Schadewaldt, P
Falkenberg, N
Mönch, E
Producer:
19990318
In:
Acta paediatrica (Oslo, Norway : 1992)
vol. 87
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24.
Inherited metabolic disorders in Turkey.
[electronic resource]
by
Ozalp, I
Coskun, T
Tokol, S
Demircin, G
Mönch, E
Producer:
19910110
In:
Journal of inherited metabolic disease
vol. 13
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25.
Development of Metabolic Phenotype in Phenylketonuria: Evaluation of the Blaskovics Protein Loading Test at 5 Years of Age.
[electronic resource]
by
Burgard, P
Mönch, E
Zschocke, J
Wendel, U
Langenbeck, U
Publication details:
JIMD reports
2016
In:
JIMD reports
vol. 29
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26.
Glutaraldehyde mediated echinocyte/discocyte transformation is Ca2+ dependent.
[electronic resource]
by
Mönch, E
Halbhuber, K J
Fröber, R
Unger, J
Geyer, G
Producer:
19790626
In:
Folia haematologica (Leipzig, Germany : 1928)
vol. 105
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27.
HFE gene mutation and transferrin saturation in very low birthweight infants.
[electronic resource]
by
Maier, R F
Witt, H
Bührer, C
Mönch, E
Köttgen, E
Producer:
19990924
In:
Archives of disease in childhood. Fetal and neonatal edition
vol. 81
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28.
Utilisation of amino acid mixtures in adolescents with phenylketonuria.
[electronic resource]
by
Mönch, E
Herrmann, M E
Brösicke, H
Schöffer, A
Keller, M
Producer:
19970113
In:
European journal of pediatrics
vol. 155 Suppl 1
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29.
Dependence of the utilization of a phenylalanine-free amino acid mixture on different amounts of single dose ingested. A case report.
[electronic resource]
by
Herrmann, M E
Brösicke, H G
Keller, M
Mönch, E
Helge, H
Producer:
19941213
In:
European journal of pediatrics
vol. 153
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30.
Spread of HIV infection in the general population in Germany.
[electronic resource]
by
Vettermann, W
Siedler, A
Voss, L
Mönch, E
Heckler, R
Pauli, G
Producer:
20010614
In:
AIDS (London, England)
vol. 14
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31.
Examination of urine metabolites in the newborn period and during protein loading tests at 6 months of age--Part 1.
[electronic resource]
by
Mönch, E
Kneer, J
Jakobs, C
Arnold, M
Diehl, H
Batzler, U
Producer:
19910613
In:
European journal of pediatrics
vol. 149 Suppl 1
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32.
[Phenylalanine-free amino acid mixture: metabolic effects in relation to a single dose].
[electronic resource]
by
Hermann, M E
Mönch, E
Reinbacher, M
Kohlen, W
Brösicke, H G
Producer:
19920109
In:
Monatsschrift Kinderheilkunde : Organ der Deutschen Gesellschaft fur Kinderheilkunde
vol. 139
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33.
Urinary excretion of gamma-hydroxybutyric acid in a patient with neurological abnormalities. The probability of a new inborn error of metabolism.
[electronic resource]
by
Jakobs, C
Bojasch, M
Mönch, E
Rating, D
Siemes, H
Hanefeld, F
Producer:
19810709
In:
Clinica chimica acta; international journal of clinical chemistry
vol. 111
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34.
[Drug influence on screening tests for inborn errors of metabolism].
[electronic resource]
by
Mönch, E
Röhnelt, M
Siemes, H
Lison, H
Friedrich, R
Fuhr, H
Producer:
19740114
In:
Monatsschrift fur Kinderheilkunde
vol. 121
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35.
Clinical features and diagnostic approach in type I tyrosinaemia in an infant with cytomegaly virus infection and bacterial sepsis.
[electronic resource]
by
Wabitsch, M
Pohlandt, F
Leupold, D
Berger, R
Mönch, E
Heinze, E
Teller, W
Producer:
19930601
In:
European journal of pediatrics
vol. 152
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36.
Liver pathology in transient neonatal hyperammonemia.
[electronic resource]
by
Zimmermann, A
Bachmann, C
Högger, I
Gehler, J
Mielfried, A
Mönch, E
Peters, H
Producer:
19840214
In:
Virchows Archiv. A, Pathological anatomy and histopathology
vol. 402
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37.
Biochemical characterization of bioreactors for hybrid liver support: serum-free liver cell coculture of nonparenchymal and parenchymal cells.
[electronic resource]
by
Obermayer, N
Busse, B
Grünwald, A
Mönch, E
Müller, C
Neuhaus, P
Gerlach, J C
Producer:
20010628
In:
Transplantation proceedings
vol. 33
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38.
Design of a prospective neonatal cohort study of homozygous and double heterozygous factor V Leiden and factor II G20210A.
[electronic resource]
by
Hundsdoerfer, P
Vetter, B
Stöver, B
Bassir, C
Mönch, E
Ziemer, S
Kulozik, A E
Producer:
20001017
In:
Klinische Padiatrie
vol. 212
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39.
Gastroenteropancreatic neuroendocrine tumours contain a common set of synaptic vesicle proteins and amino acid neurotransmitters.
[electronic resource]
by
Ahnert-Hilger, G
Grube, K
Kvols, L
Lee, I
Mönch, E
Riecken, E O
Schmitt, L
Wiedenmann, B
Producer:
19940216
In:
European journal of cancer (Oxford, England : 1990)
vol. 29A
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40.
Rationale for the German recommendations for phenylalanine level control in phenylketonuria 1997.
[electronic resource]
by
Burgard, P
Bremer, H J
Bührdel, P
Clemens, P C
Mönch, E
Przyrembel, H
Trefz, F K
Ullrich, K
Producer:
19990323
In:
European journal of pediatrics
vol. 158
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