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 *

105 related articles for article (PubMed ID: 22784324)

  • 1. Urea cycle disorder--argininosuccinic lyase deficiency.
    Mehta N; Kirk PC; Holder R; Precheur HV
    Spec Care Dentist; 2012; 32(4):155-9. PubMed ID: 22784324
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Urea cycle disorders: clinical presentation outside the newborn period.
    Smith W; Kishnani PS; Lee B; Singh RH; Rhead WJ; Sniderman King L; Smith M; Summar M
    Crit Care Clin; 2005 Oct; 21(4 Suppl):S9-17. PubMed ID: 16227115
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A neonatal screening test for argininosuccinic acid lyase deficiency and other urea cycle disorders.
    Talbot HW; Sumlin AB; Naylor EW; Guthrie R
    Pediatrics; 1982 Oct; 70(4):526-31. PubMed ID: 7122151
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Aciduria argininosuccĂ­nica: informe de un caso de inicio neonatal].
    P Zuza M; Gerbaudo G; O Molina S; Pereyra M
    Arch Argent Pediatr; 2021 Oct; 119(5):e508-e512. PubMed ID: 34569752
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Neonatal hyperammonemia].
    Jaeken J; Devlieger H; Evens M; Casaer P; Eggermont E
    Tijdschr Kindergeneeskd; 1983 Jun; 51(3):101-4. PubMed ID: 6636106
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Argininosuccinic aciduria: clinical and biochemical phenotype findings in Malaysian children.
    Chen BC; Ngu LH; Zabedah MY
    Malays J Pathol; 2010 Dec; 32(2):87-95. PubMed ID: 21329179
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Leukocyte urea cycle enzymes in hyperammonemia.
    Wolfe DM; Gatfield PD
    Pediatr Res; 1975 Jun; 9(6):531-5. PubMed ID: 1161340
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Natural history of epilepsy in argininosuccinic aciduria provides new insights into pathophysiology: A retrospective international study.
    Elkhateeb N; Olivieri G; Siri B; Boyd S; Stepien KM; Sharma R; Morris AAM; Hartley T; Crowther L; Grunewald S; Cleary M; Mundy H; Chakrapani A; Lachmann R; Murphy E; Santra S; Uudelepp ML; Yeo M; Bernhardt I; Sudakhar S; Chan A; Mills P; Ridout D; Gissen P; Dionisi-Vici C; Baruteau J
    Epilepsia; 2023 Jun; 64(6):1612-1626. PubMed ID: 36994644
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Essential medical issues related to HIV in dentistry.
    Moswin AH; Epstein JB
    J Can Dent Assoc; 2007 Dec; 73(10):945-8. PubMed ID: 18275697
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Hyperammonemia in pediatric diseases].
    Cathelineau L
    Arch Fr Pediatr; 1979; 36(7):724-35. PubMed ID: 394697
    [No Abstract]   [Full Text] [Related]  

  • 12. Dental health and management for children with congenital heart disease.
    FitzGerald K; Fleming P; Franklin O
    Prim Dent Care; 2010 Jan; 17(1):21-5. PubMed ID: 20067687
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Argininosuccinic Aciduria-A Rare Indication for Liver Transplant: Report of Two Cases.
    Yankol Y; Mecit N; Kanmaz T; Acarli K; Kalayoglu M
    Exp Clin Transplant; 2017 Oct; 15(5):581-584. PubMed ID: 26768012
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Hereditary urea cycle diseases in Finland.
    Keskinen P; Siitonen A; Salo M
    Acta Paediatr; 2008 Oct; 97(10):1412-9. PubMed ID: 18616627
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Long-term follow-up of 12 patients with the late-onset variant of argininosuccinic acid lyase deficiency: no impairment of intellectual and psychomotor development during therapy.
    Widhalm K; Koch S; Scheibenreiter S; Knoll E; Colombo JP; Bachmann C; Thalhammer O
    Pediatrics; 1992 Jun; 89(6 Pt 2):1182-4. PubMed ID: 1594374
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Blood levels of ammonia and nitrogen scavenging amino acids in patients with inherited hyperammonemia.
    Tuchman M; Yudkoff M
    Mol Genet Metab; 1999 Jan; 66(1):10-5. PubMed ID: 9973542
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Hyperammonemia in review: pathophysiology, diagnosis, and treatment.
    Auron A; Brophy PD
    Pediatr Nephrol; 2012 Feb; 27(2):207-22. PubMed ID: 21431427
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The differences between providing oral health care to HIV-infected children and HIV-infected adults: a general dentist's guide.
    Gonzales CB; Smith S; Galvan A; Mabry J
    Gen Dent; 2010; 58(5):424-32; quiz 733-4. PubMed ID: 20829168
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Hereditary diseases related to a disorder of the enzymatic activity of the urea formation cycle].
    Kazanskaia NS; Alekseenko LP
    Vopr Med Khim; 1976; 22(4):435-43. PubMed ID: 800301
    [No Abstract]   [Full Text] [Related]  

  • 20. [Molecular basis of urea cycle disorders].
    Matsuda I; Matsuura T; Hoshide R; Uchino T; Matsubasa T
    Nihon Rinsho; 1993 Feb; 51(2):520-4. PubMed ID: 8464164
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.