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STARCH GEL ELECTROPHORESIS FOR GALACTOSE-1-PHOSPHATE URIDYLYL-TRANSFERASE APPLIED TO DRIED FILTER PAPER BLOOD SPECIMENS.HAMMERSEN G; LEVY HL.1977; CLIN. CHIM. ACTA; PAYS-BAS; DA. 1977; VOL. 77; NO 3; PP. 295-299; BIBL. 17 REF.Article

ANGEBORENER FAKTOR-VII-MANGEL IM KINDESALTER = DEFICIT CONGENITAL EN FACTEUR VII CHEZ L'ENFANTWAHN U; HAMMERSEN G; ZIMMERMANN K et al.1979; THERAPIEWOCHE; DEU; DA. 1979; VOL. 29; NO 50; PP. 8709-8711; BIBL. 11 REF.Article

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ZUR BEDEUTUNG DES FAKTOR VII-MANGELS IM KINDESALTER. = L'IMPORTANCE DU DEFICIT EN FACTEUR VII CHEZ L'ENFANTHAMMERSEN G; WAHN U; ZIMMERMANN R et al.1978; MONATSSCHR. KINDERHEILKDE; DTSCH.; DA. 1978; VOL. 126; NO 6; PP. 366-370; ABS. ANGL.; BIBL. 1 P. 1/2Article

COMPARISON OF GALACTOSE-1-PHOSPHATE URIDYLTRANSFERASE IN FETAL AND ADULT TISSUES = COMPARAISON DE LA GALACTOSE-1-PHOSPHATE URIDYLTRANSFERASE DANS LES TISSUS DES FOETUS ET ADULTESHAMMERSEN G; LEVY HL; FRIGOLETTO F et al.1975; CLIN. CHIM. ACTA; PAYS-BAS; DA. 1975; VOL. 60; NO 3; PP. 281-284; BIBL. 17REF.Article

OCULO-NEURAL INVOLVEMENT IN AN ENZYMATICALLY PROVEN CASE OF NIEMANN-PICK DISEASE TYPE BHAMMERSEN G; OPPERMANN HC; HARMS E et al.1979; EUROP. J. PEDIATR.; DEU; DA. 1979; VOL. 132; NO 2; PP. 77-84; BIBL. 12 REF.Article

MAPLE SYRUP URINE DISEASE: TREATMENT OF THE ACUTELY ILL NEWBORNHAMMERSEN G; WILLE L; SCHMIDT H et al.1978; EUROP. J. PEDIATR.; DEU; DA. 1978; VOL. 129; NO 3; PP. 157-165; BIBL. 31 REF.Article

GROUP B STREPTOCOCCI: A NEW THREAT TO THE NEWBORN.HAMMERSEN G; BARTHOLOME K; OPPERMANN HC et al.1977; EUROP. J. PEDIATR.; GERM.; DA. 1977; VOL. 126; NO 3; PP. 189-197; BIBL. 1 P. 1/2Article

GALACTOSE-I-PHOSPHATE URIDYL TRANSFERASE DEFICIENCY DUE TO DUARTE/GALACTOSEMIA COMBINED VARIATION: CLINICAL AND BIOCHEMICAL STUDIES.LEVY HL; SEPE SJ; WALTON DS et al.1978; J. PEDIATR.; USA; DA. 1978; VOL. 92; NO 3; PP. 390-393; BIBL. 21 REF.Article

Echokardiographische Diagnose von kongenitalen Divertikeln des rechten und des linken Ventrikels = Echocardiographic diagnosis of congenital cardiac diverticulumWILD, F; HOFBECK, M; SINGER, H et al.Klinische Pädiatrie. 1993, Vol 205, Num 3, pp 167-169, issn 0300-8630Article

Intestinal amino acid absorption in the Fanconi syndrome: studies in patients and in rats with the maleic acid induced syndromeNÜTZENADEL, W; FAHR, K; HAMMERSEN, G et al.Pediatric research. 1983, Vol 17, Num 9, pp 710-713, issn 0031-3998Article

IMPROVED PRENATAL DIAGNOSIS OF METHYLMALONIC ACIDEMIA: MASS FRAGMENTOGRAPHY OF METHYLMALONIC ACID IN AMNIOTIC FLUID AND MATERNAL URINETREFZ FK; SCHMIDT H; TAUSCHER B et al.1981; EUR. J. PEDIATR.; ISSN 0340-6199; DEU; DA. 1981; VOL. 137; NO 3; PP. 261-266; BIBL. 15 REF.Article

Klinik und Genetik des Ito-Syndroms = Clinical and genetic features of ITO syndromeROTT, H.-D; BASSL, V; HAMMERSEN, G et al.Monatsschrift für Kinderheilkunde. 1994, Vol 142, Num 6, pp 396-401, issn 0026-9298Article

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Overwhelming postsplenectomy infection with vaccine-type Streptococcus pneumoniae in a 12-year-old girl despite vaccination and antibiotic prophylaxisKLINGE, J; HAMMERSEN, G; SCHARF, J et al.Infection. 1997, Vol 25, Num 6, pp 368-371, issn 0300-8126Article

Lethal cutis laxa with contractural arachnodactyly, overgrowth and soft tissue bleeding due to a novel homozygous fibulin-4 gene mutationHOYER, J; KRAUS, C; HAMMERSEN, G et al.Clinical genetics. 2009, Vol 76, Num 3, pp 276-281, issn 0009-9163, 6 p.Article

Fetal Adrenal Haemorrhage -Two-Dimensional and Three-Dimensional ImagingSCHRAUDER, M. G; HAMMERSEN, G; SIEMER, J et al.Fetal diagnosis and therapy. 2008, Vol 23, Num 1, pp 72-75, issn 1015-3837, 4 p.Article

The clinical phenotype of succinic semialdehyde dehydrogenase deficiency (4-hydroxybutyric aciduria) : Case reports of 23 new patientsGIBSON, K. M; CHRISTENSEN, E; ROSSIER, E et al.Pediatrics (Evanston). 1997, Vol 99, Num 4, pp 567-574, issn 0031-4005Article