These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

210 related articles for article (PubMed ID: 8648535)

  • 21. [Maternal phenylketonuria: dietary treatment of a 2 generation illness].
    Möslinger D; Scheibenreiter S; Spoula E; Stöckler-Ipsiroglu S
    Z Geburtshilfe Neonatol; 2000; 204(5):181-6. PubMed ID: 11126803
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Maternal phenylketonuria syndrome: congenital heart defects, microcephaly, and developmental outcomes.
    Rouse B; Matalon R; Koch R; Azen C; Levy H; Hanley W; Trefz F; de la Cruz F
    J Pediatr; 2000 Jan; 136(1):57-61. PubMed ID: 10636975
    [TBL] [Abstract][Full Text] [Related]  

  • 23. [Diagnosis of phenylketonuria in a 35-year-old mother in relation to prenatal diagnosis of intrauterine growth retardation with microcephaly].
    Thibaud D; Ploussard JP; Vaquant PO; Chemouny S; Kleitz T
    Arch Pediatr; 1998 Nov; 5(11):1229-31. PubMed ID: 9853062
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Phenylketonuria: variable phenotypic outcomes of the R261Q mutation and maternal PKU in the offspring of a healthy homozygote.
    Kleiman S; Vanagaite L; Bernstein J; Schwartz G; Brand N; Elitzur A; Woo SL; Shiloh Y
    J Med Genet; 1993 Apr; 30(4):284-8. PubMed ID: 8487271
    [TBL] [Abstract][Full Text] [Related]  

  • 25. [An eighteen-year study on phenylketonuria].
    Yu WM; Xu L; Li XW; He C; Shen M; Zhang ZX; Jin YY; Zhou ZS; Qiao F
    Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 2003 Apr; 25(2):218-22. PubMed ID: 12905726
    [TBL] [Abstract][Full Text] [Related]  

  • 26. [Maternal phenylketonuria].
    Rittinger O; Plöchl E; Jarosch E
    Padiatr Padol; 1984; 19(1):87-92. PubMed ID: 6701000
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Phenylketonuria and the brain.
    Rovelli V; Longo N
    Mol Genet Metab; 2023 May; 139(1):107583. PubMed ID: 37105048
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Unbalanced X; autosome translocation.
    Gupta N; Goel H; Phadke SR
    Indian J Pediatr; 2006 Sep; 73(9):840-2. PubMed ID: 17006048
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Brain white matter abnormalities associated with copy number variants.
    Vigdorovich N; Ben-Sira L; Blumkin L; Precel R; Nezer I; Yosovich K; Cross Z; Vanderver A; Lev D; Lerman-Sagie T; Zerem A
    Am J Med Genet A; 2020 Jan; 182(1):93-103. PubMed ID: 31622028
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Familial white matter hypoplasia, agenesis of the corpus callosum, mental retardation and growth deficiency: a new distinctive syndrome.
    Curatolo P; Cilio MR; Del Giudice E; Romano A; Gaggero R; Pessagno A
    Neuropediatrics; 1993 Apr; 24(2):77-82. PubMed ID: 8327066
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Nasomaxillary hypoplasia and severe orofacial clefting in a child of a mother with phenylketonuria.
    Sweeney E; Fryer A
    J Inherit Metab Dis; 2002 Feb; 25(1):77-9. PubMed ID: 11999984
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Pregnancy experiences in the woman with mild hyperphenylalaninemia.
    Levy HL; Waisbren SE; Güttler F; Hanley WB; Matalon R; Rouse B; Trefz FK; de la Cruz F; Azen CG; Koch R
    Pediatrics; 2003 Dec; 112(6 Pt 2):1548-52. PubMed ID: 14654663
    [TBL] [Abstract][Full Text] [Related]  

  • 33. The North American Maternal Phenylketonuria Collaborative Study, developmental assessment of the offspring: preliminary report.
    Hanley WB; Koch R; Levy HL; Matalon R; Rouse B; Azen C; de la Cruz F
    Eur J Pediatr; 1996 Jul; 155 Suppl 1():S169-72. PubMed ID: 8828638
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Role of nutrition in pregnancy with phenylketonuria and birth defects.
    Matalon KM; Acosta PB; Azen C
    Pediatrics; 2003 Dec; 112(6 Pt 2):1534-6. PubMed ID: 14654660
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Congenital heart disease in maternal phenylketonuria: report from the Maternal PKU Collaborative Study.
    Levy HL; Guldberg P; Güttler F; Hanley WB; Matalon R; Rouse BM; Trefz F; Azen C; Allred EN; de la Cruz F; Koch R
    Pediatr Res; 2001 May; 49(5):636-42. PubMed ID: 11328945
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Maternal mild hyperphenylalaninaemia: an international survey of offspring outcome.
    Levy HL; Waisbren SE; Lobbregt D; Allred E; Schuler A; Trefz FK; Schweitzer SM; Sardharwalla IB; Walter JH; Barwell BE
    Lancet; 1994 Dec; 344(8937):1589-94. PubMed ID: 7983992
    [TBL] [Abstract][Full Text] [Related]  

  • 37. A Chinese family with phenylketonuria and maternal phenylketonuria detected by family screening.
    Hsiao KJ; Chen CH; Chiu PC; Huang SC; Wuu KD
    Eur J Pediatr; 1986 Oct; 145(5):409-12. PubMed ID: 3792388
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Maternal phenylketonuria and hyperphenylalaninemia. An international survey of the outcome of untreated and treated pregnancies.
    Lenke RR; Levy HL
    N Engl J Med; 1980 Nov; 303(21):1202-8. PubMed ID: 7421947
    [TBL] [Abstract][Full Text] [Related]  

  • 39. [Magnetic resonance imaging of the brain in phenylketonuria].
    Izumi M; Yamazaki H; Nakabayashi H; Owada M
    No To Hattatsu; 2006 Jan; 38(1):27-31. PubMed ID: 16447793
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Prevention of fetal damage through dietary control of maternal hyperphenylalaninemia.
    Ghavami M; Levy HL; Erbe RW
    Clin Obstet Gynecol; 1986 Sep; 29(3):580-5. PubMed ID: 3757336
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 11.