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 *

125 related articles for article (PubMed ID: 4973015)

  • 21. Bone changes in homocystinuria.
    MacCarthy JM; Carey MC
    Clin Radiol; 1968 Apr; 19(2):128-34. PubMed ID: 5648071
    [No Abstract]   [Full Text] [Related]  

  • 22. Neurologic outcome in children with inborn errors of urea synthesis. Outcome of urea-cycle enzymopathies.
    Msall M; Batshaw ML; Suss R; Brusilow SW; Mellits ED
    N Engl J Med; 1984 Jun; 310(23):1500-5. PubMed ID: 6717540
    [TBL] [Abstract][Full Text] [Related]  

  • 23. [Aspects of the biochemistry of the urine in mental deficiency in children].
    Tănase I
    Physiologie; 1975; 12(3):211-4. PubMed ID: 812122
    [No Abstract]   [Full Text] [Related]  

  • 24. Non-ketotic hyperglycinaemia: a new case with late onset.
    Leuzzi V; Morano S; Moretti F; Fabbrizi F; Antonozzi I
    J Inherit Metab Dis; 1990; 13(2):238. PubMed ID: 2116560
    [No Abstract]   [Full Text] [Related]  

  • 25. Letter: Homocarnosinosis: a new metabolic disorder associated with spasticity and mental retardation.
    Gjessing LR; Sjaastad O
    Lancet; 1974 Oct; 2(7887):1028. PubMed ID: 4138320
    [No Abstract]   [Full Text] [Related]  

  • 26. Familial hyperprolinemia and mental retardation. A second metabolic type.
    Selkoe DJ
    Neurology; 1969 May; 19(5):494-502. PubMed ID: 5815222
    [No Abstract]   [Full Text] [Related]  

  • 27. HOMOCYSTINURIA: A NEW INBORN ERROR OF METABOLISM ASSOCIATED WITH MENTAL DEFICIENCY.
    CARSON NA; CUSWORTH DC; DENT CE; FIELD CM; NEILL DW; WESTALL RG
    Arch Dis Child; 1963 Oct; 38(201):425-36. PubMed ID: 14065982
    [No Abstract]   [Full Text] [Related]  

  • 28. Routine newborn screening for histidinemia. Clinical and biochemical results.
    Levy HL; Shih VE; Madigan PM
    N Engl J Med; 1974 Dec; 291(23):1214-9. PubMed ID: 4421298
    [No Abstract]   [Full Text] [Related]  

  • 29. [Amino acid imbalance as a pathogenetic factor in mental retardation (author's transl)].
    Fekete G
    Klin Wochenschr; 1974 May; 52(6):276-82. PubMed ID: 4408538
    [No Abstract]   [Full Text] [Related]  

  • 30. Upregulation of AGAT as a Possible Target in Molecular Nutrition.
    Ostojic SM
    Ann Nutr Metab; 2020; 76(3):207-208. PubMed ID: 32580202
    [No Abstract]   [Full Text] [Related]  

  • 31. Aminoaciduria in familial mental retardation.
    POSER CM; BUNCH L
    Arch Neurol; 1963 Jul; 9():35-46. PubMed ID: 13985642
    [No Abstract]   [Full Text] [Related]  

  • 32. Hyperornithinemia, hyperammonemia, and homocitrullinuria. A new disorder of amino acid metabolism associated with myoclonic seizures and mental retardation.
    Shih VE; Efron ML; Moser HW
    Am J Dis Child; 1969 Jan; 117(1):83-92. PubMed ID: 5782534
    [No Abstract]   [Full Text] [Related]  

  • 33. Beta mercaptolactate-cysteine disulfide: analog of cystine in the urine of a mentally retarded patient.
    Crawhall JC; Parker R; Sneddon W; Young EP; Ampola MG; Efron ML; Bixby EM
    Science; 1968 Apr; 160(3826):419-20. PubMed ID: 5644041
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Argininosuccinic aciduria in adult: a clinical, electrophysiological and biochemical study.
    Grisar T
    Adv Exp Med Biol; 1982; 153():83-93. PubMed ID: 7164925
    [No Abstract]   [Full Text] [Related]  

  • 35. Type I hyperprolinemia in a family suffering from aniridia and severe dystrophia of ocular tissues.
    Fusco G; Carlomagno S; Romano A; Rinaldi E; Cedrola G; Cianciaruso L; Curto A; Rosolia S; Auricchio G
    Ophthalmologica; 1976; 173(1):1-10. PubMed ID: 958671
    [No Abstract]   [Full Text] [Related]  

  • 36. Hyperlysinuria with hyperammonemia. A new metabolic disorder.
    Brown JH; Fabre LF; Farrell GL; Adams ED
    Am J Dis Child; 1972 Jul; 124(1):127-32. PubMed ID: 5033744
    [No Abstract]   [Full Text] [Related]  

  • 37. Roentgen findings in homocystinuria.
    Smith SW
    Am J Roentgenol Radium Ther Nucl Med; 1967 May; 100(1):147-54. PubMed ID: 6023889
    [No Abstract]   [Full Text] [Related]  

  • 38. Transient mental deficits associated with recurrent prolonged epileptic clouded state.
    Rennick M; Perez-Borja C; Rodin EA
    Epilepsia; 1969 Sep; 10(3):397-405. PubMed ID: 4979083
    [No Abstract]   [Full Text] [Related]  

  • 39. A Woman With Intellectual Disability, Amenorrhoea, Seizures, and Balance Problems.
    Hughes AJ; Steele HE; Pyle A; Hart Y; Quinton R; Chinnery PF
    JAMA Neurol; 2016 Dec; 73(12):1494-1495. PubMed ID: 27775760
    [No Abstract]   [Full Text] [Related]  

  • 40. 3-Phosphoglycerate dehydrogenase deficiency: description of two new cases in Tunisia and review of the literature.
    Kraoua I; Wiame E; Kraoua L; Nasrallah F; Benrhouma H; Rouissi A; Turki I; Chaabouni H; Briand G; Kaabachi N; Van Schaftingen E; Gouider-Khouja N
    Neuropediatrics; 2013 Oct; 44(5):281-5. PubMed ID: 23564319
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.