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2. [Pseudoscleroderma or scleroderma coexisting with phenylketonuria]. Jablonska S; Stachow A Ann Dermatol Syphiligr (Paris); 1972; 99(3):257-62. PubMed ID: 4654109 [No Abstract] [Full Text] [Related]
3. [Scleroderma-like skin and muscle changes in children with phenylketonuria]. Stachów A; Rowecka-Trzebicka K; Cabalska B; Skiendzielewska A Pediatr Pol; 1975 Dec; 50(12):1441-6. PubMed ID: 1196715 [No Abstract] [Full Text] [Related]
4. [Scleroderma-like lesions and phenylketonuria (PKU). Role of hyperphenylalaninemia, efficacy of diet (3 cases)]. Bodemer C; Bonnefont JP; Saudubray JM; Teillac D; De Prost Y Ann Dermatol Venereol; 1989; 116(11):798-800. PubMed ID: 2619165 [No Abstract] [Full Text] [Related]
5. [Pseudosclerodermatous lesions of the skin and muscles in a 19-month-old girl with phenylketonuria]. Krauze M; Marszał E; Jamroz E; Kajor M Pol Tyg Lek; 1989 Jan; 44(4):99-100. PubMed ID: 2798215 [No Abstract] [Full Text] [Related]
6. Scleroderma-like skin indurations in a child with phenylketonuria: a clinicopathologic correlation and review of the literature. Nova MP; Kaufman M; Halperin A J Am Acad Dermatol; 1992 Feb; 26(2 Pt 2):329-33. PubMed ID: 1569253 [TBL] [Abstract][Full Text] [Related]
12. Late diagnosis of phenylketonuria in a Bedouin mother. Usha R; Uma R; Farag TI; Girish Y; al-Ghanim MM; al-Najdi K; al-Awadi SA; el-Badramany MH Am J Med Genet; 1992 Dec; 44(6):713-5. PubMed ID: 1481837 [TBL] [Abstract][Full Text] [Related]
13. Tryptophan metabolism in a patient with phenylketonuria and scleroderma: a proposed explanation of the indole defect in phenylketonuria. Drummond KN; Michael AF; Good RA Can Med Assoc J; 1966 Apr; 94(16):834-8. PubMed ID: 5929533 [TBL] [Abstract][Full Text] [Related]
15. [Importance of the diagnoses and treatment of phenylketonuria]. Mira NV; Marquez UM Rev Saude Publica; 2000 Feb; 34(1):86-96. PubMed ID: 10769367 [TBL] [Abstract][Full Text] [Related]
16. [Serum tyrosine in children with phenylketonuria and mild hyperphenylalaninemia]. Cabalska B; Nowacka M; Laskowska-Klita T; Nowaczewska I; Zorska K; Taljański W Med Wieku Rozwoj; 2000; 4(1):5-12. PubMed ID: 11013857 [TBL] [Abstract][Full Text] [Related]
17. [Treatment of phenylketonuria coexisting with scleroderma]. Goncerzewicz M; Socha J; Chobot-Maciejewska H; Orzeszko-Spaczyńska A Pediatr Pol; 1977 Apr; 52(4):441-4. PubMed ID: 865931 [No Abstract] [Full Text] [Related]
18. Hyperphenylalaninemia in a premature infant with heterozygosity for phenylketonuria. Hennermann JB; Loui A; Weber A; Mönch E J Perinat Med; 2004; 32(4):383-5. PubMed ID: 15346830 [TBL] [Abstract][Full Text] [Related]
19. [Phenylalanine tolerance and results of oral phenylalanine load in children with phenylketonuria in various ages]. Bührdel P; Theile H Kinderarztl Prax; 1975 Nov; 43(11):501-8. PubMed ID: 1214334 [No Abstract] [Full Text] [Related]
20. 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] [Next] [New Search]