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Results of search for 'au:"Mönch, E"', page 1 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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1.
[A simple method to shorten the freeze drying time].
[electronic resource]
by
Mönch, E
Producer:
19680928
In:
Zeitschrift fur klinische Chemie und klinische Biochemie
vol. 5
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2.
[Enzymatic methods for the diagnosis of galactosemia and galactose deficiency].
[electronic resource]
by
Kruas, H
Mönch, E
Producer:
19720102
In:
Klinische Wochenschrift
vol. 48
Online resources:
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3.
[Weight curves of phenylketonuric newborns and children under phenylalanine-free diet].
[electronic resource]
by
Mönch, E
Loidolt, M
Producer:
19711130
In:
Monatsschrift fur Kinderheilkunde
vol. 118
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4.
[Increased epidemic incidence of hepatitis B in a district hospital].
[electronic resource]
by
Jakob, A
Mönch, E
Producer:
19780517
In:
Zeitschrift fur die gesamte innere Medizin und ihre Grenzgebiete
vol. 33
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5.
[Screening for cystinuria and homocystinuria. Manual and semiautomatic quantitative determination of urinary aliphatic compounds with SH groups and S-S bridges].
[electronic resource]
by
Mönch, E
Siemes, H
Producer:
19710916
In:
Zeitschrift fur klinische Chemie und klinische Biochemie
vol. 8
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6.
[A simple method for diagnosis of galactosemia and its heterozygotic gene carriers].
[electronic resource]
by
Kraus, H
Mönch, E
Producer:
19720306
In:
Monatsschrift fur Kinderheilkunde
vol. 118
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7.
[Screening of newborns].
[electronic resource]
by
Mönch, E
Grüters, A
Producer:
19930415
In:
Deutsche Krankenpflegezeitschrift
vol. 46
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8.
[Sweat phenylalanine concentration in healthy and phenylketonuric subjects].
[electronic resource]
by
Herrmann, G
Mönch, E
Producer:
19740114
In:
Monatsschrift fur Kinderheilkunde
vol. 121
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9.
[Hyperaminoaciduria during infancy and childhood: a semiautomatic test for congenital metabolic errors].
[electronic resource]
by
Siemes, H
Mönch, E
Producer:
19711130
In:
Monatsschrift fur Kinderheilkunde
vol. 118
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10.
[Semi automatic urine screening test for mucopolysaccharidoses].
[electronic resource]
by
Richter, C H
Mönch, E
Producer:
19760510
In:
Monatsschrift fur Kinderheilkunde
vol. 123
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11.
[Free amino acids in the skeletal muscles, blood and urine of healthy persons and of patients with progressive muscular dystrophy].
[electronic resource]
by
Mönch, E
Kirsten, E
Heyck, H
Producer:
19680906
In:
Monatsschrift fur Kinderheilkunde
vol. 115
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12.
[Screening test for hyperphenylalaninemias and tyrosinemias : fluorometric micromethods for quantitative determination of phenylalanine and tyrosine by means of the same auto-analyzer system].
[electronic resource]
by
Mönch, E
Winkelmann, M
Stäblein, W
Producer:
19770825
In:
Monatsschrift fur Kinderheilkunde
vol. 125
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13.
Plasma taurine levels in healthy cats and cats with cardiac disorders.
[electronic resource]
by
Skrodzki, M
Trautvetter, E
Mönch, E
Producer:
19911125
In:
The Journal of nutrition
vol. 121
Online resources:
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14.
[Pepper type neuroblastoma with homocystinuria. Diagnosis, biochemistry and therapy].
[electronic resource]
by
Mönch, E
Stefan, H
Käser, H
Producer:
19710227
In:
Helvetica paediatrica acta
vol. 25
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15.
[Creatinine concentration, osmolar concentration and blank color as basis for concentration dependent values in urine (author's transl)].
[electronic resource]
by
Mönch, E
Wollweber, M
Reich, M
Producer:
19770415
In:
Monatsschrift fur Kinderheilkunde
vol. 125
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16.
Penylalanine hydroxylation in phenylketonuria.
[electronic resource]
by
Hoffbauer, R W
Schrempf, G
Mönch, E
Producer:
19770103
In:
Lancet (London, England)
vol. 2
Online resources:
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17.
[Thin layer chromatographic test for the indirect and direct detection of the enzyme defect in histidinemia].
[electronic resource]
by
Mönch, E
Weissenbach-Wollweber, M
Jäckel, R
Producer:
19830617
In:
Monatsschrift Kinderheilkunde : Organ der Deutschen Gesellschaft fur Kinderheilkunde
vol. 131
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18.
[Medium-chain acyl-CoA dehydrogenase defect. Acute cerebral episodes and nonketotic hypoglycemia in children].
[electronic resource]
by
von Mühlendahl, K E
Lehnert, W
Mönch, E
Producer:
19900921
In:
Deutsche medizinische Wochenschrift (1946)
vol. 115
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19.
Hypotonic unmasking of erythrocyte receptor sites.
[electronic resource]
by
Geyer, G
Linss, W
Mönch, E
Feuerstein, H
Producer:
19800228
In:
Experimentelle Pathologie
vol. 17
Online resources:
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20.
Haplotype analysis of the phenylalanine hydroxylase gene in Turkish phenylketonuria families.
[electronic resource]
by
Stuhrmann, M
Riess, O
Mönch, E
Kurdoglu, G
Producer:
19891004
In:
Clinical genetics
vol. 36
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