Warning: Undefined array key "mm" in /www/wwwroot/www.ai-bt.com/si.php on line 10 Deprecated: trim(): Passing null to parameter #1 ($string) of type string is deprecated in /www/wwwroot/www.ai-bt.com/si.php on line 10 Phenylketonuria. Mass screening of newborns in Ireland.

Literature DB >> 5645686

Phenylketonuria. Mass screening of newborns in Ireland.

S F Cahalane.

Abstract

Entities: Disease

Mesh：

Substances：
Tyrosine
Phenylalanine

Year: 1968 PMID： 5645686 PMCID： PMC2019828 DOI： 10.1136/adc.43.228.141

Source DB: PubMed Journal: Arch Dis Child ISSN： 0003-9888 Impact factor: 3.791

× No keyword cloud information.

15 in total

1. MATERNAL PHENYLKETONURIA. A CAUSE OF MENTAL RETARDATION IN CHILDREN WITHOUT THE METABOLIC DEFECT.

Authors: C C MABRY; J C DENNISTON; T L NELSON; C D SON
Journal: N Engl J Med Date: 1963-12-26 Impact factor: 91.245

2. A SIMPLE PHENYLALANINE METHOD FOR DETECTING PHENYLKETONURIA IN LARGE POPULATIONS OF NEWBORN INFANTS.

Authors: R GUTHRIE; A SUSI
Journal: Pediatrics Date: 1963-09 Impact factor: 7.124

3. PHENYLKETONURIA: A REPORT ON THE GUTHRIE SCREENING TEST.

Authors: S F CAHALANE
Journal: J Ir Med Assoc Date: 1964-03

4. Atypical phenylketonuria in sisters with normal offspring.

Authors: L I WOOLF; C OUNSTED; D LEE; M HUMPHREY; N M CHESHIRE; G R STEED
Journal: Lancet Date: 1961-08-26 Impact factor: 79.321

5. The birthplaces of parents and grandparents of a series of patients with phenylketonuria in in south-east England.

Authors: C O CARTER; L I WOOLF
Journal: Ann Hum Genet Date: 1961-05 Impact factor: 1.670

6. Variations in intelligence in phenylktonuria.

Authors: M W PARTINGTON
Journal: Can Med Assoc J Date: 1962-04-21 Impact factor: 8.262

7. Diagnosis and treatment: interpreting the positive screening test in the newborn infant.

Authors: C R Scriver
Journal: Pediatrics Date: 1967-05 Impact factor: 7.124

8. Screening program for early detection of phenylketonuria in the newborn in Israel.

Authors: B E Cohen; A Szeinberg; I Peled; B Szeinberg; R Bar-Or
Journal: Isr J Med Sci Date: 1966 Mar-Apr

9. Atypical phenylketonuric heterozygote. Deficiency in phenylalanine hydroxylase and transaminase activity.

Authors: J A Anderson; R Fisch; E Miller; D Doeden
Journal: J Pediatr Date: 1966-03 Impact factor: 4.406

10. Diagnostic and therapeutic implications of persistent hyperphenylalaninemia in an infant heterozygous for the gene of phenylketonuria.

Authors: A J Schneider; S D Garrard
Journal: J Pediatr Date: 1966-05 Impact factor: 4.406

13 in total

1. Screening for phenylketonuria.

Authors:
Journal: Can Med Assoc J Date: 1968-07-27 Impact factor: 8.262

2. Phenylketonuria: outcome and problems in a "diet-for-life" clinic.

Authors: E R Naughten; B Kiely; I Saul; D Murphy
Journal: Eur J Pediatr Date: 1987 Impact factor: 3.183

3. The heterozygote advantage in phenylketonuria.

Authors: L I Woolf
Journal: Am J Hum Genet Date: 1986-05 Impact factor: 11.025

Review 4. Phenylketonuria and its variations. A review of recent developments.

Authors: M E Blaskovics; T L Nelson
Journal: Calif Med Date: 1971-07

5. Problems of phenylketonuria.

Authors:
Journal: Br Med J Date: 1971-12-18

6. Mass screening of the newborn for metabolic disease.

Authors: L I Woolf
Journal: Arch Dis Child Date: 1968-04 Impact factor: 3.791

7. The search for phenylketonuria.

Authors:
Journal: Can Med Assoc J Date: 1969-08-23 Impact factor: 8.262

8. Ethnic variation in genetic disease: possible roles of hitchhiking and epistasis.

Authors: D K Wagener; L L Cavalli-Sforza
Journal: Am J Hum Genet Date: 1975-05 Impact factor: 11.025

9. Liver phenylalanine hydroxylase activity in relation to blood concentrations of tyrosine and phenylalanine in the rat.

Authors: M M McGee; O Greengard; W E Knox
Journal: Biochem J Date: 1972-05 Impact factor: 3.857

10. Screening for congenital hypothyroidism in the Republic of Ireland.

Authors: S Dockeray; S F Cahalane; M Brody; C Mullins; M J Cullen
Journal: Br Med J Date: 1980-12-06