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1-12
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Results: 12
Authors:
MATERN D
LANG C
BECK S
BRANDIS M
SEYDEWITZ HH
Citation: D. Matern et al., DIAGNOSIS OF GLYCOGEN-STORAGE-DISEASE TYPE IA - DNA-ANALYSIS OF LEUKOCYTES AS AN ALTERNATIVE TO THE ENZYME ASSAY IN A LIVER-BIOPSY SPECIMEN, Monatsschrift fur Kinderheilkunde, 146(7), 1998, pp. 660-664
Authors:
BOHLEY C
MATERN D
BISCHOFF G
MEISTER WV
KARGOV S
LINDAU S
BARTHEL J
HOFFMANN S
Citation: C. Bohley et al., NUCLEIC-ACID ORGANIZATIONS VISUALIZED BY SCANNING FORCE MICROSCOPY, Surface and interface analysis, 25(7-8), 1997, pp. 614
Authors:
GIBSON KM
CHRISTENSEN E
JAKOBS C
FOWLER B
CLARE MA
HAMMERSEN G
RAAB K
KOBORI J
MOOSA A
VOLLMER B
ROSSIER E
IAFOLLA AK
MATERN D
BROUWER OF
FINELSTEIN J
AKSU F
WEBER HP
BAKKEREN JAJM
GABREELS FJM
BLUESTONE D
BARRON TF
BEAUVAIS P
RABIER D
SANTOS C
UMANSKY R
LEHNERT W
Citation: Km. Gibson et al., THE CLINICAL PHENOTYPE OF SUCCINIC SEMIALDEHYDE DEHYDROGENASE-DEFICIENCY (4-HYDROXYBUTYRIC ACIDURIA) - CASE-REPORTS OF 23 NEW PATIENTS, Pediatrics, 99(4), 1997, pp. 567-574
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:
BLAU N
BECK M
MATERN D
Citation: N. Blau et al., TETRAHYDROBIOPTERIN INDUCED NEONATAL TYROSINEMIA, European journal of pediatrics, 155(9), 1996, pp. 832-832
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:
MATERN D
LEHNERT W
GIBSON KM
KORINTHENBERG R
Citation: D. Matern et al., SEIZURES IN A BOY WITH SUCCINIC SEMIALDEHYDE DEHYDROGENASE-DEFICIENCYTREATED WITH VIGABATRIN (GAMMA-VINYL-GABA), Journal of inherited metabolic disease, 19(3), 1996, pp. 313-318
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:
HEINEN F
MATERN D
PRINGSHEIM W
LEITITIS JU
BRANDIS M
Citation: F. Heinen et al., ZINC-DEFICIENCY IN AN EXCLUSIVELY BREAST-FED PRETERM INFANT, European journal of pediatrics, 154(1), 1995, pp. 71-75
Authors:
MATERN D
HEINEN F
PRINGSHEIM W
BRANDIS M
LEITITIS JU
Citation: D. Matern et al., ZINC-DEFICIENCY SYNDROME IN NEWBORN NOURI SHED ONLY WITH MATERNAL MILK, Monatsschrift fur Kinderheilkunde, 143(12), 1995, pp. 1255-1255
Authors:
KOSEL S
MATERN D
SHIN YS
Citation: S. Kosel et al., PURIFICATION OF HUMAN MICROSOMAL LIVER GLUCOSE-6-PHOSPHATASE SYSTEM BY AFFINITY-CHROMATOGRAPHY AND IMMUNODETECTION, European journal of pediatrics, 152, 1993, pp. 22-25
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