Results 161 to 170 of about 17,994 (195)

RESULTS OF TREATMENT AND TERMINATION OF THE DIET IN PHENYLKETONURIA (PKU)

Pediatrics, 1970
The mean I.Q. of 27 PKU patients at the mean age of 3 years 10 months treated before 3 weeks of age was comparable to that of their unaffected siblings. The mean I.Q., of 12 patients at the mean age of 5 years 6 months treated between 3 and 6 weeks of age fell significantly below the mean I.Q. of their unaffected siblings.
E S, Kang, N D, Sollee, P S, Gerald
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Hyperphenylalaninemia or phenylketonuria (PKU)?

Zeitschrift f�r Kinderheilkunde, 1972
Early differential diagnosis between PKU and prolonged Hyperphenylalaninemia is an important but difficult problem. No clear-cut differences between the two conditions occur with respect to blood level, results of the usual 5 hrs loading test and the urinary excretion of metabolites.
S, Scheibenreiter, O, Thalhammer
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?PKU Bodies?: Characteristic inclusions in the brain in phenylketonuria

Acta Neuropathologica, 1976
The ultrastructure of various inclusions within oligodendroglial cells in the brains from two phenylketonuric patients was studied. Characteristic lamellar, oval, slightly irregular inclusions measured between 0.5 and 2 micra in diameter and were bounded by a single membrane.
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Screening for phenylketonuria (PKU) in the Netherlands

1990
In the period 1st September 1974 to 1st Januari 1989 2,511,000 infants (99.3 of all livebirths) were screened for PKU. Treatment was required in 158 of the 330 referred infants. The diagnosis of these 158 patients was PKU (137), hyperphenylalaninaemia (HPA) (19) and malignant HPA (2). Three cases had a false-negative screening result. The prevalence of
Verkerk, P.H., Vaandrager, G.J., Sengers, R.C.A.   +2 more
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Phenylketonuria (PKU) in Israel

2015
B E, Cohen, A, Szeinberg, Y, Levine, I, Peled, S, Pollack, M, Crispin, M, Normand   +6 more
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PKU: Phenylketonuria

The American Journal of Nursing, 1975
Parvin Justice, George F. Smith
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Phenylketonuria (PKU)

2019
  +4 more sources

Phenylketonuria (PKU): screening and management.

NIH consensus statement, 2002
To provide health care providers, patients, and the general public with a responsible assessment of currently available data regarding screening for, and management of. phenylketonuria (PKU).A non-Federal, non-advocate, 14-member panel representing the fields of pediatrics, genetics, human development, public policy, nursing, molecular physiology, and ...
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Health Status and Comorbidities of Adult Patients With Phenylketonuria (PKU) in France With a Focus on Early-Diagnosed Patients – A Nationwide Study of Health Insurance Claims Data

Molecular Genetics and Metabolism, 2023
Christian Jacob, François Maillot
exaly  

Therapeutic targets for phenylketonuria (PKU)

Drugs of the Future, 2020
null Sorbera, L.A., null Dulsat, C., null Graul, A.I.   +2 more
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