Pascal and Francis Bibliographic Databases

Help

Search results

Your search

au.\*:("BLASKOVICS M")

Publication Year[py]

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Discipline (document) [di]

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Author Country

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Results 1 to 8 of 8

  • Page / 1
Export

Selection :

  • and

FOUR CASES OF HYPERPHENYLALANINAEMIA: STUDIES DURING PREGNANCY AND OF THE OFFSPRING PRODUCEDKOCH R; BLASKOVICS M.1982; J. INHERIT. METAB. DIS.; ISSN 0141-8955; GBR; DA. 1982; VOL. 5; NO 1; PP. 11-15; BIBL. 12 REF.Article

EEG PATTERN IN PHENYLKETONURIA UNDER EARLY INITIATED DIETARY TREATMENTBLASKOVICS M; ENGEL R; PODOSIN RL et al.1981; AM. J. DIS. CHILD. (1960); ISSN 0002-922X; USA; DA. 1981; VOL. 135; NO 9; PP. 802-808; BIBL. 17 REF.Article

NESIDIOBLASTOSIS AND OTHER ISLET CELL ABNORMALITIES IN HYPERINSULINEMIC HYPOGLYCEMIA OF CHILDHOODDAHMS BB; LANDLING BH; BLASKOVICS M et al.1980; HUM. PATHOL.; ISSN 0046-8177; USA; DA. 1980; VOL. 11; NO 6; PP. 641-649; BIBL. 22 REF.Article

THE DIAGNOSIS OF PHENYLKETONURIA: A REPORT FROM THE COLLABORATIVE STUDY OF CHILDREN TREATED FOR PHENYLKETONURIAO'FLYNN ME; HOLTZMAN NA; BLASKOVICS M et al.1980; AM. J. DIS. CHILD. (1960); ISSN 0002-922X; USA; DA. 1980; VOL. 134; NO 8; PP. 769-774; BIBL. 22 REF.Article

Diagnostic screening for mucopolysaccharidoses type I-VII by fluorophore-labelled carbohydrate PAGEGIUDICI, T. A; SUNICO, H; BLASKOVICS, M et al.Journal of inherited metabolic disease. 1996, Vol 19, Num 2, pp 263-266, issn 0141-8955Article

96. Pterin chemistry. Part 921 : Loading experiments with 6α,β-tetrahydro-L-[3'-2H1]biopterinADLER, C; CURTIUS, H.-C; WETZEL, E et al.Helvetica chimica acta. 1992, Vol 75, Num 4, pp 1237-1244, issn 0018-019XArticle

Primapterinuria: a new variant of atypical phenylketonuriaBLAU, N; CURTIUS, H. C; KUSTER, T et al.Journal of inherited metabolic disease. 1989, Vol 12, pp 335-338, issn 0141-8955, suppl. 2Article

Hyperphenylalaninemia with high levels of 7-biopterin is associated with mutations in the PCBD gene encoding the bifunctional protein pterin-4a-carbinolamine dehydratase and transcriptional coactivator (DCoH)THÖNY, B; NEUHEISER, F; KIERAT, L et al.American journal of human genetics. 1998, Vol 62, Num 6, pp 1302-1311, issn 0002-9297Article

  • Page / 1