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Results: 1 to 20 of 100

1.

Vertical sandwich-type continuous/evaporative TLC with fixed mobile phase volume for separating sugars of clinical relevance in paper-borne urine and blood samples in newborn screening.

Alonso-Fernandez JR, Carpinteiro MI, Baleato J, Fidalgo J.

J Clin Lab Anal. 2010;24(2):106-12. doi: 10.1002/jcla.20371.

PMID:
20333764
[PubMed - indexed for MEDLINE]
2.

Detection of some clinically important carbohydrates in plasma and urine by means of thin-layer chromatography.

Szustkiewicz C, Demetriou J.

Clin Chim Acta. 1971 May;32(3):355-9. No abstract available.

PMID:
5096949
[PubMed - indexed for MEDLINE]
3.

Sugars in blood and urine of milk-fed normal young infants.

Tengström B, Wranne L.

Scand J Clin Lab Invest. 1968;22(2):137-41. No abstract available.

PMID:
5710159
[PubMed - indexed for MEDLINE]
4.

Development of a protocol for newborn screening for disorders of the galactose metabolic pathway.

Bowling FG, Brown AR.

J Inherit Metab Dis. 1986;9(1):99-104.

PMID:
3014213
[PubMed - indexed for MEDLINE]
5.

[Effectiveness of the screening programme for galactosemia. New strategy in Poland].

Radomyska B.

Med Wieku Rozwoj. 2001 Jan-Mar;5(1):51-8.

PMID:
11276504
[PubMed - indexed for MEDLINE]
6.

[Detection of sugars in the urine of premature infants, using a thin-layer chromatographic method].

Romagnoli S, Bargero L, Giordano C.

Minerva Pediatr. 1971 Sep 15;23(37):1507-8. Italian. No abstract available.

PMID:
5131913
[PubMed - indexed for MEDLINE]
7.

Automated blood galactose analysis as a screening method for galactosaemia in milk-fed newborns.

Tengström B.

Scand J Clin Lab Invest. 1969 May;23(3):197-200. No abstract available.

PMID:
5395999
[PubMed - indexed for MEDLINE]
8.
9.

Transient galactosemia detected by neonatal mass screening.

Ono H, Mawatari H, Mizoguchi N, Eguchi T, Sakura N, Hamakawa M.

Pediatr Int. 1999 Jun;41(3):281-4.

PMID:
10365579
[PubMed - indexed for MEDLINE]
10.

[The advisory report 'Neonatal screening' from the Health Council of The Netherlands].

Bolhuis PA, Page-Christiaens GC.

Ned Tijdschr Geneeskd. 2005 Dec 17;149(51):2857-60. Dutch.

PMID:
16398167
[PubMed - indexed for MEDLINE]
11.

Screening for galactosemia: Philippines experience. Newborn Screening Study Group.

Lee JY, Padilla CD, Chua EL.

Southeast Asian J Trop Med Public Health. 1999;30 Suppl 2:66-8.

PMID:
11405207
[PubMed - indexed for MEDLINE]
12.

[Galactosemia urine--screening with test paper].

Johansson S, Thalme B, Werner B.

Lakartidningen. 1970 Sep 30;67(40):4502-4. Swedish. No abstract available.

PMID:
5477770
[PubMed - indexed for MEDLINE]
13.

Results of newborn screening for galactose metabolic disorders.

Inoue B, Hata M, Ichiba Y, Wada H, Misumi H, Mori T.

J Inherit Metab Dis. 1990;13(1):93-101.

PMID:
2109152
[PubMed - indexed for MEDLINE]
14.

A case of uridine diphosphate galactose-4-epimerase deficiency detected by neonatal screening for galactosaemia.

Bowling FG, Fraser DK, Clague AE, Hayes A, Morris DJ.

Med J Aust. 1986 Feb 3;144(3):150-1.

PMID:
3945203
[PubMed - indexed for MEDLINE]
15.

Quantitative Beutler test for newborn mass screening of galactosemia using a fluorometric microplate reader.

Fujimoto A, Okano Y, Miyagi T, Isshiki G, Oura T.

Clin Chem. 2000 Jun;46(6 Pt 1):806-10.

PMID:
10839768
[PubMed - indexed for MEDLINE]
Free Article
16.

Simple and rapid system for screening and identification of reducing sugars in urine.

Auray-Blais C, Giguere R, Draper P, Shapcott D, Lemieux B.

Clin Biochem. 1978 Dec;11(6):235-7.

PMID:
737847
[PubMed - indexed for MEDLINE]
17.

Neonatal screening for galactosemia by quantitative analysis of hexose monophosphates using tandem mass spectrometry: a retrospective study.

Jensen UG, Brandt NJ, Christensen E, Skovby F, Nørgaard-Pedersen B, Simonsen H.

Clin Chem. 2001 Aug;47(8):1364-72.

PMID:
11468223
[PubMed - indexed for MEDLINE]
Free Article
18.

Newborn screening.

Wilcken B, Wiley V.

Pathology. 2008 Feb;40(2):104-15. doi: 10.1080/00313020701813743. Review.

PMID:
18203033
[PubMed - indexed for MEDLINE]
19.

[Determination of total phenylalanine and galactose from a sample of dry blood on paper filter: its application on neonatal screening].

Torres E, Baloy A, Frómeta A, Fernández L.

Biomedica. 2002 Mar;22(1):22-9. Spanish.

PMID:
11957360
[PubMed - indexed for MEDLINE]
20.

Screening for galactosaemia in Greece.

Schulpis K, Papakonstantinou ED, Michelakakis H, Podskarbi T, Patsouras A, Shin Y.

Paediatr Perinat Epidemiol. 1997 Oct;11(4):436-40.

PMID:
9373865
[PubMed - indexed for MEDLINE]

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