BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

121 related articles for article (PubMed ID: 6629607)

  • 1. Pseudoscleroderma and phenylketonuria.
    Guillet GY; Dore N; Hehunstre JP; Maleville J; Battin J
    Int J Dermatol; 1983 Sep; 22(7):422-6. PubMed ID: 6629607
    [TBL] [Abstract][Full Text] [Related]  

  • 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]  

  • 7. Phenylketonuria and scleroderma.
    Lasser AE; Schultz BC; Beaff D; Bielinski S; Kirschenbaum B
    Arch Dermatol; 1978 Aug; 114(8):1215-7. PubMed ID: 677922
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Scleroderma-like skin lesions in two patients with phenylketonuria.
    Coşkun T; Ozalp I; Kale G; Göğüş S
    Eur J Pediatr; 1990 Dec; 150(2):109-10. PubMed ID: 2279504
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Pinocchio syndrome. Scleroderma-like lesions in phenylketonuria].
    Lebioda J; Nowińska-Lebioda H
    Przegl Dermatol; 1973; 60(1):49-56. PubMed ID: 4789828
    [No Abstract]   [Full Text] [Related]  

  • 10. Diagnosis of phenylalanine hydroxylase deficiency (phenylketonuria).
    Berry HK; Hsieh MH; Bofinger MK; Schubert WK
    Am J Dis Child; 1982 Feb; 136(2):111-4. PubMed ID: 7064923
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Phenylketonuria and scleroderma.
    Brown EH; Berry HK; Olson J; Levinson J
    J Inherit Metab Dis; 1986; 9(4):405-6. PubMed ID: 3104681
    [No 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]  

  • 14. [Pseudoscleroderma and scleroderma-like states].
    Thivolet J
    Rev Prat; 1975 May; 25(25):1959-63. PubMed ID: 1135585
    [No 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]
    of 7.