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Results:
1-7
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Results: 7
Authors:
SEWELL AC
HERWIG J
WIEGRATZ I
LEHNERT W
NIEDERHOFF H
SONG XQ
KONDO N
FUKAO T
Citation: Ac. Sewell et al., MITOCHONDRIAL ACETOACETYL-COA THIOLASE (BETA-KETOTHIOLASE) DEFICIENCYAND PREGNANCY, Journal of inherited metabolic disease, 21(4), 1998, pp. 441-442
Authors:
ERMISCH B
HILDEBRANDT F
ZIMMERHACKL LB
POHL M
GORDJANI N
NIEDERHOFF H
MATERN D
SEYDEWITZ HH
LEHNERT W
LEITITIS JU
BRANDIS M
Citation: B. Ermisch et al., HEMODIALYSIS OR HEMOFILTRATION AS TREATME NT OF ACUTE HYPERAMMONEMIC COMA CAUSED BY INBORN-ERRORS OF METABOLISM IN NEONATES AND INFANTS, Monatsschrift fur Kinderheilkunde, 145(7), 1997, pp. 714-718
Authors:
MATERN D
SEYDEWITZ H
NIEDERHOFF H
WIEBUSCH H
BRANDIS M
Citation: D. Matern et al., DYSLIPIDEMIA IN A BOY WITH RECURRENT ABDOMINAL-PAIN, HYPERSALIVATION AND DECREASED LIPOPROTEIN-LIPASE ACTIVITY, European journal of pediatrics, 155(8), 1996, pp. 660-664
Authors:
LEHNERT W
NIEDERHOFF H
SUORMALA T
BAUMGARTNER ER
Citation: W. Lehnert et al., ISOLATED BIOTIN-RESISTANT 3-METHYLCROTONYL-COA CARBOXYLASE DEFICIENCY- LONG-TERM OUTCOME IN A CASE WITH NEONATAL ONSET, European journal of pediatrics, 155(7), 1996, pp. 568-572
Authors:
MATERN D
NIEDERHOFF H
BRANDIS M
CHOU JY
Citation: D. Matern et al., VERIFICATION OF DIAGNOSIS IN A 17-YEAR-OLD BOY WITH CLINICAL GLYCOGEN-STORAGE-DISEASE TYPE IA BY MUTATION SCREENING, Journal of inherited metabolic disease, 19(2), 1996, pp. 205-208
Authors:
MATERN D
SEYDEWITZ HH
LEHNERT W
NIEDERHOFF H
LEITITIS JU
BRANDIS M
Citation: D. Matern et al., PRIMARY-TREATMENT OF PROPIONIC ACIDEMIA COMPLICATED BY ACUTE THIAMINE-DEFICIENCY, The Journal of pediatrics, 129(5), 1996, pp. 758-760
Authors:
SUTOR AH
DAGRES N
NIEDERHOFF H
Citation: Ah. Sutor et al., LATE FORM OF VITAMIN-K-DEFICIENCY BLEEDING IN GERMANY, Klinische Padiatrie, 207(3), 1995, pp. 89-97
Risultati:
1-7
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