(1) In other words, children with phenylketonuria can and should have a normal productive life.

(2) Samples obtained through screening programme for phenylketonuria and congenital hypothyroidism.

(3) The management of phenylketonuria in childhood requires a multidisciplinary approach across the hospital community interface.

(4) Other trace elements have been observed with phenylketonuria, an inherited metabolic disorder, and kwashiorkor, a severe form of malnutrition that occurs mainly in developing nations.

(5) Objective To describe the incidence of congenital hypothyroidism(CH)and phenylketonuria(PKU)in Maanshan city.

(6) To explore the morbidity of Congenital hypothyroidism(CH) and phenylketonuria(PKU) among newborn in Heze city.

(7) To understand the prevalence of thyroid hypofunction(CH) and phenylketonuria(PKU) among newborn in Penglai in order to find and treat them in time.

(8) The EEG in 94 patients with phenylketonuria was analyzed. The abnormality rate of EEG was 65%, mainly showing epileptiform discharges(80%), partly showing background activity abnormality(20%).

(9) Take the gene mutation that causes phenylketonuria or PKU. People with the disease can't break down the amino acid phenylalanine a problem that can lead to severe cognitive damage.

(10) Conclusion:The special bone changes in phenylketonuria were important X-ray signs suggestive of phenylketonuria.

(11) Objective To establish a simple, accurate and rapid method for screening of the mutant genes in phenylketonuria.

(12) Tragically, their daughter Carol was born in 1920 with a genetic birth defect called phenylketonuria, which led to mental impairment.

(13) Separating Amino Acids in Blood and Urine by Microcrystalline Cellulose Film Chromatography - To ldentify Phenylketonuria.

(14) Maternal teratogens that hae been reported in association with cleft lip and palate include alcohol, maternal phenylketonuria , hyperthermia, hydantoin, trimethadione, aminopterin, and methotrexate.

(15) This result showed that PCR-SSCP analysis could be effectively used for the direct gene diagnosis of phenylketonuria.

(16) Objective To study the method for gene diagnosis of phenylketonuria.

(17) To explore the morbidity Congenital hypothyroidism ( CH ) and phenylketonuria ( PKU ) among newborn in Heze city.

(18) Objective To investigate the point mutation features of exon 11 and 12 in phenylalanine hydroxylase( PAH )gene of the patients with phenylketonuria(PKU)in Xinjiang.

(19) Objective To establish a method with high efficiency in detecting phenylalanine hydroxylase(PAH) gene mutations and hence to rapidly diagnose prenatal fetals with phenylketonuria .

(20) Objective To explore the incidence and distribution features of neonatal phenylketonuria(PKU) and congenital hypothyroidism(CH) in Lianyungang area.

(21) Objective To establish a simple[sentence dictionary], accurate and rapid method for screening of the mutant genes in phenylketonuria (PKU).

(22) The comparison of ABR changes at the beginning of therapy against congenital hypothyroidism and phenylketonuria and later could serve as an objective criteria for follow-up of therapeutic efficiency.

(23) Objective To report the bone X ray changes in phenylketonuria.