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 *

115 related articles for article (PubMed ID: 8905994)

  • 1. [A case report of mild from of phenylketonuria].
    Komada S; Masuzugawa S; Taniguchi A; Narita Y; Kuzuhara S
    Rinsho Shinkeigaku; 1996 May; 36(5):699-701. PubMed ID: 8905994
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Phenylketonuria with adult-onset neurological manifestation].
    Ishimaru K; Tamasawa N; Baba M; Matsunaga M; Takebe K
    Rinsho Shinkeigaku; 1993 Sep; 33(9):961-5. PubMed ID: 8299276
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Prenatal brain damage in maternal, untreated phenylketonuria].
    Peters WH; Lubs H; Machill G; Knapp A; Pietsch P; Wiechert P
    Zentralbl Gynakol; 1975; 97(15):905-17. PubMed ID: 1189770
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Letter: Screening for phenylketonuria in mental retardates in Hyderabad using Guthrie's test.
    Sharada D; Polasa H
    Indian Pediatr; 1974 Apr; 11(4):331. PubMed ID: 4213861
    [No Abstract]   [Full Text] [Related]  

  • 5. [Brain white matter lesions of children with phenylketonuria before and after treatment].
    Wang ZX; Zhou ZS; Yu WM
    Zhongguo Dang Dai Er Ke Za Zhi; 2006 Feb; 8(1):13-6. PubMed ID: 16522231
    [TBL] [Abstract][Full Text] [Related]  

  • 6. An exceptional Albanian family with seven children presenting with dysmorphic features and mental retardation: maternal phenylketonuria.
    Knerr I; Zschocke J; Schellmoser S; Topf HG; Weigel C; Dötsch J; Rascher W
    BMC Pediatr; 2005 Apr; 5(1):5. PubMed ID: 15811181
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Phenylketonuria with acute myeloblastic leukemia in a 9-year-old boy: reporting a rare case.
    Patiroglu T; Unal E; Kardas F; Ozdemir MA; Karakukcu M; Sayilmaz O
    J Pediatr Hematol Oncol; 2011 Aug; 33(6):e256-7. PubMed ID: 21792031
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Delayed diagnosis of phenylketonuria as the cause of mental retardation in an adolescent].
    Villaverde R; Escribano JB; Salmerón P; Tortosa D; Meca J; Fernández-Barreiro A
    Rev Neurol; 1997 Dec; 25(148):1911-6. PubMed ID: 9528029
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Impact of neonatal protein metabolism and nutrition on screening for phenylketonuria.
    Ponzone A; Spada M; Roasio L; Porta F; Mussa A; Ferraris S
    J Pediatr Gastroenterol Nutr; 2008 May; 46(5):561-9. PubMed ID: 18493213
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. 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]  

  • 12. [A 60-year-old man with intention tremor as an initial symptom followed by cerebellar ataxia, peripheral neuropathy and dementia].
    Machida Y; Lijima M; Nakamura K; Ota S; Hattori N; Mizuno Y
    No To Shinkei; 2005 Aug; 57(8):710-9. PubMed ID: 16146216
    [TBL] [Abstract][Full Text] [Related]  

  • 13. The use of Guthrie's test to detect phenylketonuria in a population of mentally retarded individuals.
    Krasnopol'skaya KD; Martinson AE
    Sov Genet; 1974 May; 8(4):526-33. PubMed ID: 4213489
    [No Abstract]   [Full Text] [Related]  

  • 14. Treating phenylketonuria by a phenylalanine-free diet.
    Start K
    Prof Care Mother Child; 1998; 8(4):109-10. PubMed ID: 9814366
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Neonatal screening for phenylketonuria.
    Netzloff ML
    Ann Clin Lab Sci; 1982; 12(5):368-71. PubMed ID: 7137934
    [No Abstract]   [Full Text] [Related]  

  • 16. [Modification of Guthrie's quantitative selection technic for the diagnosis of phenylketonuria].
    Balcázar de Astegui M; Garrido Lozada E
    Rev Latinoam Microbiol Parasitol (Mex); 1968; 10(2):71-8. PubMed ID: 4984898
    [No Abstract]   [Full Text] [Related]  

  • 17. Phenylketonuria, a family study. Borderline intelligence in two siblings with mentally retarded children.
    Colombo JP; Vassella F; Humbel R; Rossi E
    Helv Paediatr Acta; 1967 Jul; 22(3):243-51. PubMed ID: 5592735
    [No Abstract]   [Full Text] [Related]  

  • 18. Impact of the phenylalanine hydroxylase gene on maternal phenylketonuria outcome.
    Güttler F; Azen C; Guldberg P; Romstad A; Hanley WB; Levy HL; Matalon R; Rouse BM; Trefz F; de la Cruz F; Koch R
    Pediatrics; 2003 Dec; 112(6 Pt 2):1530-3. PubMed ID: 14654659
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 6-pyruvoyl-tetrahydropterin synthase deficiency with mild hyperphenylalaninemia.
    Demos MK; Waters PJ; Vallance HD; Lillquist Y; Makhseed N; Hyland K; Blau N; Connolly MB
    Ann Neurol; 2005 Jul; 58(1):164-7. PubMed ID: 15984017
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Atypical phenylketonuria in a seven-year-old profoundly retarded girl: development of phenylalanine tolerance, in spite of apparently continued failure to convert phenylalanine to tyrosine.
    Cohn GH; Ouellette EM; Moser HW; Efron ML
    Neurology; 1968 Mar; 18(3):310-1. PubMed ID: 5690427
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 6.