129 related articles for article (PubMed ID: 7132849)
1. Genetic screening of newborn in Australia: results for 1980.
Pitt D; Connelly J; Francis I; Wilcken B; Brown DA; Robertson E; Hill G; Masters P; Tucker RG; Raby J; McFarlane J; Hancock J
Med J Aust; 1982 Feb; 1(3):119-20. PubMed ID: 7132849
[TBL] [Abstract][Full Text] [Related]
2. Genetic screening of newborn in Australia. Results for 1981.
Pitt D; Connelly J; Francis I; Wilcken B; Brown DA; Robertson E; Hill G; Masters P; Raby J; McFarlane J; Bowling F; Hancock J
Med J Aust; 1983 Apr; 1(7):333-5. PubMed ID: 6835136
[TBL] [Abstract][Full Text] [Related]
3. Genetic screening of newborn in Australia: results for 1979.
Pitt D; Connelly J; Francis I; Wilcken B; Brown DA; Robertson E; Hill G; Masters P; Tucker RG; Raby J; McFarlane J; Hancock J
Med J Aust; 1981 Jan; 1(1):39-40. PubMed ID: 7207294
[TBL] [Abstract][Full Text] [Related]
4. Genetic screening of the newborn in Australia. Results for 1978.
Pitt D; Connelly J; Francis I; Wilcken B; Brown DA; Hill G; Masters P; Tucker RG; Raby J; McFarlane J
Med J Aust; 1979 Sep; 2(5):272-3. PubMed ID: 514173
[TBL] [Abstract][Full Text] [Related]
5. Newborn phenylketonuria (PKU) Guthrie (BIA) screening and early hospital discharge.
Hanley WB; Demshar H; Preston MA; Borczyk A; Schoonheyt WE; Clarke JT; Feigenbaum A
Early Hum Dev; 1997 Jan; 47(1):87-96. PubMed ID: 9118832
[TBL] [Abstract][Full Text] [Related]
6. Neonatal screening for congenital hypothyroidism and phenylketonuria at Siriraj Hospital, Mahidol University, Bangkok, Thailand--a pilot study.
Wasant P; Liammongkolkul S; Srisawat C
Southeast Asian J Trop Med Public Health; 1999; 30 Suppl 2():33-7. PubMed ID: 11400774
[TBL] [Abstract][Full Text] [Related]
7. Neonatal screening program in Rajavithi Hospital, Thailand.
Ratrisawadi V; Horpaopan S; Chotigeat U; Sangtawesin V; Kanjanapattanakul W; Ningsanond V; Sunthornthepvarakul T; Khooarmompatana S; Charoensiriwatana W
Southeast Asian J Trop Med Public Health; 1999; 30 Suppl 2():28-32. PubMed ID: 11400773
[TBL] [Abstract][Full Text] [Related]
8. Receiver operating characteristic plots to evaluate Guthrie, Wallac, and Isolab phenylalanine kit performance for newborn phenylketonuria screening.
Wang ST; Pizzolato S; Demshar HP
Clin Chem; 1997 Oct; 43(10):1838-42. PubMed ID: 9342001
[TBL] [Abstract][Full Text] [Related]
9. Neonatal biochemical screening for disease.
Clague A; Thomas A
Clin Chim Acta; 2002 Jan; 315(1-2):99-110. PubMed ID: 11728413
[TBL] [Abstract][Full Text] [Related]
10. Hyperphenylalaninemia (PKU) and hypothyroid testing.
Stanage WF; Gregg JB
S D J Med; 1982 Jul; 35(7):8. PubMed ID: 6958065
[No Abstract] [Full Text] [Related]
11. [Evolution of the screening program for congenital hypothyroidism and phenylketonuria in the Sergipe State from 1995 to 2003].
Ramalho RJ; Ramalho AR; Oliveira CR; Aguiar-Oliveira MH
Arq Bras Endocrinol Metabol; 2004 Dec; 48(6):890-6. PubMed ID: 15761565
[TBL] [Abstract][Full Text] [Related]
12. On indications for treatment of the hyperphenylalaninemic neonate.
Güttler F; Wamberg E
Acta Paediatr Scand; 1977 May; 66(3):339-44. PubMed ID: 868515
[TBL] [Abstract][Full Text] [Related]
13. Neonatal screening in Italy for congenital hypothyroidism and metabolic disorders: hyperphenylalaninemia, maple syrup urine disease and homocystinuria.
Antonozzi I; Dominici R; Andreoli M; Monaco F
J Endocrinol Invest; 1980; 3(4):357-63. PubMed ID: 7204885
[TBL] [Abstract][Full Text] [Related]
14. Newborn screening for PKU and congenital hypothyroidism in Latvia.
Lugovska R; Vevere P; Andrusaite R; Kornejeva A
Southeast Asian J Trop Med Public Health; 1999; 30 Suppl 2():52-3. PubMed ID: 11400783
[TBL] [Abstract][Full Text] [Related]
15. Issues in newborn screening for phenylketonuria.
Koch RK
Am Fam Physician; 1999 Oct; 60(5):1462-6. PubMed ID: 10524490
[TBL] [Abstract][Full Text] [Related]
16. The diagnosis of phenylketonuria: a report from the Collaborative Study of Children Treated for Phenylketonuria.
O'Flynn ME; Holtzman NA; Blaskovics M; Azen C; Williamson ML
Am J Dis Child; 1980 Aug; 134(8):769-74. PubMed ID: 7405915
[TBL] [Abstract][Full Text] [Related]
17. Newborn screening for phenylketonuria: predictive validity as a function of age.
McCabe ER; McCabe L; Mosher GA; Allen RJ; Berman JL
Pediatrics; 1983 Sep; 72(3):390-8. PubMed ID: 6889045
[TBL] [Abstract][Full Text] [Related]
18. [Did the change of technique of screening investigations influence on improvement of test credibility in recognizing and differentiating diagnostics of hiperphenylalaninemias?].
Didycz B; Lemańska D; Słuszniak A
Przegl Lek; 2009; 66(1-2):11-3. PubMed ID: 19485249
[TBL] [Abstract][Full Text] [Related]
19. Economic evaluation of neonatal screening for phenylketonuria and congenital hypothyroidism.
Geelhoed EA; Lewis B; Hounsome D; O'leary P
J Paediatr Child Health; 2005 Nov; 41(11):575-9. PubMed ID: 16398841
[TBL] [Abstract][Full Text] [Related]
20. Evaluation of 6-year application of the enzymatic colorimetric phenylalanine assay in the setting of neonatal screening for phenylketonuria.
Schulze A; Mayatepek E; Hoffmann GF
Clin Chim Acta; 2002 Mar; 317(1-2):27-37. PubMed ID: 11814455
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
