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 *

272 related articles for article (PubMed ID: 11986039)

  • 41. Essential polyunsaturated fatty acids in plasma and erythrocytes of children with inborn errors of amino acid metabolism.
    Vlaardingerbroek H; Hornstra G; de Koning TJ; Smeitink JA; Bakker HD; de Klerk HB; Rubio-Gozalbo ME
    Mol Genet Metab; 2006 Jun; 88(2):159-65. PubMed ID: 16530443
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Urea cycle disorders in Thai infants: a report of 5 cases.
    Wasant P; Srisomsap C; Liammongkolkul S; Svasti J
    J Med Assoc Thai; 2002 Aug; 85 Suppl 2():S720-31. PubMed ID: 12403252
    [TBL] [Abstract][Full Text] [Related]  

  • 43. [Perioperative management of the child with a known metabolic disease].
    Grosu I; Scholtes JL; Veyckemans F
    Arch Pediatr; 2010 Jun; 17(6):949-50. PubMed ID: 20654975
    [No Abstract]   [Full Text] [Related]  

  • 44. Hazards associated with pregnancies and deliveries in lysinuric protein intolerance.
    Tanner L; Näntö-Salonen K; Niinikoski H; Erkkola R; Huoponen K; Simell O
    Metabolism; 2006 Feb; 55(2):224-31. PubMed ID: 16423630
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Metabolic myopathies: update 2009.
    van Adel BA; Tarnopolsky MA
    J Clin Neuromuscul Dis; 2009 Mar; 10(3):97-121. PubMed ID: 19258857
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Cardiac manifestations of inborn errors of metabolism.
    Evangeliou A; Papadopoulou-Legbelou K; Daphnis E; Ganotakis E; Vavouranakis I; Michailidou H; Hitoglou-Makedou A; Nicolaidou P; Wevers R; Varlamis G
    Minerva Pediatr; 2007 Jun; 59(3):215-8. PubMed ID: 17519866
    [TBL] [Abstract][Full Text] [Related]  

  • 47. [Inborn errors of metabolism: transition from childhood to adulthood].
    Tran C; Barbey F; Pitteloud N; Philippe J; Kern I; Bonafé L
    Rev Med Suisse; 2015 Feb; 11(462):445-9. PubMed ID: 25915985
    [TBL] [Abstract][Full Text] [Related]  

  • 48. [The Austrian Metabolic Register].
    Fang-Kircher S
    Wien Klin Wochenschr; 1997 Feb; 109(3):89-92. PubMed ID: 9139465
    [TBL] [Abstract][Full Text] [Related]  

  • 49. [Combined use of tandem mass spectrometry with urine gas chromatography/mass spectrometry is useful for diagnosis of inborn errors of metabolism in children].
    Xie LJ; Zhu JX; Zhu XD; Li HJ; Han LS; Gu XF
    Zhongguo Dang Dai Er Ke Za Zhi; 2008 Feb; 10(1):31-4. PubMed ID: 18289467
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Clinical evaluation and emergency management of inborn errors of metabolism presenting in the newborn.
    Christodoulou J
    Southeast Asian J Trop Med Public Health; 2003; 34 Suppl 3():189-97. PubMed ID: 15906734
    [TBL] [Abstract][Full Text] [Related]  

  • 51. [Genetics and metabolic disorders].
    Albasanz Gallan JL
    Med Trop (Madr); 1966; 42(6):434-51. PubMed ID: 5998995
    [No Abstract]   [Full Text] [Related]  

  • 52. [Clinical issues of adult patients with genetic and metabolic disorders diagnosed in childhood].
    Ida H
    Nihon Rinsho; 2010 Jan; 68(1):19-25. PubMed ID: 20077785
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Biochemical aspects of urea cycle disorders.
    Snodgrass PJ
    Pediatrics; 1981 Aug; 68(2):273-83, 295-7. PubMed ID: 7267238
    [No Abstract]   [Full Text] [Related]  

  • 54. Gastrointestinal motility disorders in adolescent patients: transitioning to adult care.
    Sood MR; Rudolph CD
    Gastroenterol Clin North Am; 2007 Sep; 36(3):749-63, xi. PubMed ID: 17950447
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Therapy insight: inborn errors of metabolism in adult neurology--a clinical approach focused on treatable diseases.
    Sedel F; Lyon-Caen O; Saudubray JM
    Nat Clin Pract Neurol; 2007 May; 3(5):279-90. PubMed ID: 17479075
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Approach to the patient with a fatty acid oxidation disorder.
    Saudubray JM; Mitchell G; Bonnefont JP; Schwartz G; Nuttin C; Munnich A; Brivet M; Vassault A; Demaugre F; Rabier D
    Prog Clin Biol Res; 1992; 375():271-88. PubMed ID: 1438373
    [No Abstract]   [Full Text] [Related]  

  • 57. [Mitochondrial beta-oxidation defects].
    Woldseth B; Rootwelt T
    Tidsskr Nor Laegeforen; 2006 Mar; 126(6):756-9. PubMed ID: 16541168
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Inherited metabolic disorders in Thailand.
    Wasant P; Svasti J; Srisomsap C; Liammongkolkul S
    J Med Assoc Thai; 2002 Aug; 85 Suppl 2():S700-9. PubMed ID: 12403250
    [TBL] [Abstract][Full Text] [Related]  

  • 59. [Care continuity for patients with myopathy during transition of childhood to adulthood].
    Yoshioka M; Tsuji M; Kawamoto M; Kouhara N
    Nihon Rinsho; 2010 Jan; 68(1):53-6. PubMed ID: 20077790
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Clinical approach to inherited metabolic disorders in neonates: an overview.
    Saudubray JM; Nassogne MC; de Lonlay P; Touati G
    Semin Neonatol; 2002 Feb; 7(1):3-15. PubMed ID: 12069534
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 14.