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 *

142 related articles for article (PubMed ID: 5684701)

  • 61. [Early diagnosis and diet therapy of phenylpyruvic idiocy].
    Schwarz-Tiene E
    Minerva Med; 1969 Apr; 60(31):1491-2. PubMed ID: 5783937
    [No Abstract]   [Full Text] [Related]  

  • 62. [Mental retardation in children: prevention and early screening. Introduction].
    Etienne JP
    Arch Fr Pediatr; 1978 May; 35 Suppl 1():III. PubMed ID: 686954
    [No Abstract]   [Full Text] [Related]  

  • 63. [Etiology and prevention of severe mental handicaps].
    Willard D; Gandhour R; Ebtinger B; Messer J
    Arch Fr Pediatr; 1982; 39(7):471-5. PubMed ID: 7149893
    [TBL] [Abstract][Full Text] [Related]  

  • 64. [Growth and nutrition: long term follow-up in early treated phenylketonuric and hyperphenylalaninemic children (author's transl)].
    Koepp P; Hinze G; Held KR
    Monatsschr Kinderheilkd; 1981 Mar; 129(3):154-9. PubMed ID: 6112681
    [TBL] [Abstract][Full Text] [Related]  

  • 65. Phenylketonuric mother without mental retardation and her two phenylketonuric children.
    Onisawa J; Suzuki Y; Nakamura N; Kurumada T
    Paediatr Univ Tokyo; 1968 Jan; 15():17-21. PubMed ID: 5674458
    [No Abstract]   [Full Text] [Related]  

  • 66. Hyperphenylalaninemia: diagnosis and classification of the various types of phenylalanine hydroxylase deficiency in childhood.
    Güttler F
    Acta Paediatr Scand Suppl; 1980; 280():1-80. PubMed ID: 7006308
    [No Abstract]   [Full Text] [Related]  

  • 67. [Problems of the discovery and eary biological diagnosis of phenylketonuria].
    Boniface L; Dubois B; Biserte G; Fontaine G
    Lille Med; 1966; 11(6):719-25. PubMed ID: 5942192
    [No Abstract]   [Full Text] [Related]  

  • 68. Screening for the fragile X syndrome: the necessity of international guidelines for molecular genetics predictive testing in general.
    Fryns JP
    Genet Couns; 1995; 6(4):293-6. PubMed ID: 8775414
    [No Abstract]   [Full Text] [Related]  

  • 69. [Phenylketonuria, from neonatal screening to adulthood].
    Abadie V
    Arch Pediatr; 2007 Jun; 14(6):607-9. PubMed ID: 17391941
    [No Abstract]   [Full Text] [Related]  

  • 70. Mental retardation due to congenital hypothyroidism and its prevention.
    Sutan Assin M
    Paediatr Indones; 1984; 24(3-4):57-63. PubMed ID: 6527885
    [No Abstract]   [Full Text] [Related]  

  • 71. [Patterns of mental development in phenylketonuric children who started dietetic treatment in the second part of childhood].
    Grossi-Bianchi ML; Baldaro-Verde J
    Minerva Pediatr; 1967 Aug; 19(34):1579-82. PubMed ID: 5610732
    [No Abstract]   [Full Text] [Related]  

  • 72. [The biochemical diagnosis of phenylpyruvic oligophrenia].
    Humbel R; Bernhard P
    Encephale; 1966; 55(2):170-88. PubMed ID: 5933607
    [No Abstract]   [Full Text] [Related]  

  • 73. PKU laws, a model for the future?
    Bessman SP
    Md State Med J; 1966 Jul; 15(7):145-6. PubMed ID: 5943133
    [No Abstract]   [Full Text] [Related]  

  • 74. Phenylketonuria: detection, biological study and treatment (43 cases).
    Romano C; Grossi-Bianchi ML; Sietti C
    Panminerva Med; 1968 Nov; 10(11):436-40. PubMed ID: 5704945
    [No Abstract]   [Full Text] [Related]  

  • 75. The National Institute of Child Health and Human Development and phenylketonuria.
    Alexander D
    Pediatrics; 2003 Dec; 112(6 Pt 2):1514-5. PubMed ID: 14654655
    [TBL] [Abstract][Full Text] [Related]  

  • 76. NIH consensus statement on phenylketonuria.
    Hellekson KL;
    Am Fam Physician; 2001 Apr; 63(7):1430-2. PubMed ID: 11310654
    [No Abstract]   [Full Text] [Related]  

  • 77. [Our experiences with treatment of phenylketonuria].
    Tresohlavá Z; Brachfeld K; Svatý J
    Cesk Pediatr; 1969 Jun; 24(6):522-8. PubMed ID: 5792287
    [No Abstract]   [Full Text] [Related]  

  • 78. [Hyperphenylalaninemia in 1981. A diagnostic approach (author's transl)].
    Dhondt JL; Farriaux JP
    Arch Fr Pediatr; 1981 Oct; 38(8):573-8. PubMed ID: 7316669
    [TBL] [Abstract][Full Text] [Related]  

  • 79. [Atypical forms of phenylketonuria (PKU), cause of mental deficiency].
    Repciuc E; Mogoş-Tănase I; Ionescu S; Ionescu D
    Neurol Psihiatr Neurochir; 1965; 10(5):453-61. PubMed ID: 5862295
    [No Abstract]   [Full Text] [Related]  

  • 80. [Preliminary data on the detection of phenylketonuria in the Cluj district].
    Popescu A; Butnariu J; Toma C; Scurtu C; Milcu M; Bojan O; Muschievici D
    Rev Pediatr Obstet Ginecol Pediatr; 1980; 29(2):139-45. PubMed ID: 6776607
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.