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Results of search for 'au:"Mönch, E"', page 3 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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41.
Phenylketonuria and hyperphenylalaninemia in eastern Germany: a characteristic molecular profile and 15 novel mutations.
[electronic resource]
by
Hennermann, J B
Vetter, B
Wolf, C
Windt, E
Bührdel, P
Seidel, J
Mönch, E
Kulozik, A E
Producer:
20000504
In:
Human mutation
vol. 15
Online resources:
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42.
[Comparative determination of syphilis-specific antibodies in the blood of newborn infants in various regions of West Germany].
[electronic resource]
by
Sander, J
Niehaus, C
von Reuss, K
Hoffmann, K
Husmann, K H
Lacombe, M
Mönch, E
Werner, W
Producer:
19820924
In:
Das Offentliche Gesundheitswesen
vol. 44
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43.
Experimental evaluation of a cell module for hybrid liver support.
[electronic resource]
by
Gerlach, J C
Botsch, M
Kardassis, D
Lemmens, P
Schön, M
Janke, J
Puhl, G
Unger, J
Kraemer, M
Busse, B
Böhmer, C
Belal, R
Ingenlath, M
Kosan, M
Kosan, B
Sültmann, J
Patzold, A
Tietze, S
Rossaint, R
Müller, C
Mönch, E
Sauer, I M
Neuhaus, P
Producer:
20020625
In:
The International journal of artificial organs
vol. 24
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44.
Tyrosinemia type II: Mutation update, 11 novel mutations and description of 5 independent subjects with a novel founder mutation.
[electronic resource]
by
Peña-Quintana, L
Scherer, G
Curbelo-Estévez, M L
Jiménez-Acosta, F
Hartmann, B
La Roche, F
Meavilla-Olivas, S
Pérez-Cerdá, C
García-Segarra, N
Giguère, Y
Huppke, P
Mitchell, G A
Mönch, E
Trump, D
Vianey-Saban, C
Trimble, E R
Vitoria-Miñana, I
Reyes-Suárez, D
Ramírez-Lorenzo, T
Tugores, A
Producer:
20180430
In:
Clinical genetics
vol. 92
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