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 *

121 related articles for article (PubMed ID: 6244624)

  • 21. [Propionic acidemia].
    Ohura T
    Ryoikibetsu Shokogun Shirizu; 1998; (18 Pt 1):276-9. PubMed ID: 9590046
    [No Abstract]   [Full Text] [Related]  

  • 22. Association of intracranial hemorrhages with organic acidemias.
    Weisse ME; Wiswell TE; Cunningham BE; Faleski EJ
    Tex Med; 1988 Jan; 84(1):42-5. PubMed ID: 3347912
    [No Abstract]   [Full Text] [Related]  

  • 23. Inborn errors of biotin metabolism. Clinical and laboratory features of eight cases.
    Coşkun T; Tokatli A; Ozalp I
    Turk J Pediatr; 1994; 36(4):267-78. PubMed ID: 7825232
    [TBL] [Abstract][Full Text] [Related]  

  • 24. 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]  

  • 25. The implications of hyperammonemia in rare and common disorders, including migraine.
    Russell A
    Mt Sinai J Med; 1973; 40(6):723-35. PubMed ID: 4202440
    [No Abstract]   [Full Text] [Related]  

  • 26. Protein and essential amino acid requirements in a child with propionic acidemia.
    Queen PM; Fernhoff PM; Acosta PB
    J Am Diet Assoc; 1981 Nov; 79(5):562-5. PubMed ID: 7288063
    [No Abstract]   [Full Text] [Related]  

  • 27. Propionic acidemia--biochemical studies.
    Barash V; Elpeleg O; Amit R; Gottfried S; Yatziv S; Gutman A
    Isr J Med Sci; 1989 Feb; 25(2):103-6. PubMed ID: 2495260
    [TBL] [Abstract][Full Text] [Related]  

  • 28. A new case of malonic aciduria with a presymptomatic diagnosis and an early treatment.
    Celato A; Mitola C; Tolve M; Giannini MT; De Leo S; Carducci C; Carducci C; Leuzzi V
    Brain Dev; 2013 Aug; 35(7):675-80. PubMed ID: 23177061
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Hyperglycinemia with ketoacidosis and leukopenia. Metabolic studies on the nature of the defect.
    Soriano JR; Taitz LS; Finberg L; Edelmann CM
    Pediatrics; 1967 Jun; 39(6):818-28. PubMed ID: 6026548
    [No Abstract]   [Full Text] [Related]  

  • 30. Neonatal type of nonketotic hyperglycinemia.
    Lu FL; Wang PJ; Hwu WL; Tsou Yau KI; Wang TR
    Pediatr Neurol; 1999 Apr; 20(4):295-300. PubMed ID: 10328279
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Antenatal diagnosis of propianicacidaemia.
    Gompertz D; Goodey PA; Thom H; Russell G; MacLean MV; Ferguson-Smith ME; Ferguson-Smith MA
    Lancet; 1973 May; 1(7810):1009-10. PubMed ID: 4121578
    [No Abstract]   [Full Text] [Related]  

  • 32. [Propionic acidemia with myelination disorders of the CNS].
    Behbehani AW; Lehnert W; Langenbeck U; Luthe H; Baumgartner R
    Klin Padiatr; 1984; 196(2):106-10. PubMed ID: 6737946
    [TBL] [Abstract][Full Text] [Related]  

  • 33. [Hyperglycinuria induced by n-dipropylacetate. Possible model of propionic acidemia].
    Kamoun P; Parvy P; Debray-Ritzen P
    Nouv Presse Med; 1977 Jun; 6(24):2162. PubMed ID: 333384
    [No Abstract]   [Full Text] [Related]  

  • 34. 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]  

  • 35. [Congenital disorders of metabolism].
    Bulovich D; Filipovich D; Khaĭdukovich R; Zagorka S
    Vopr Okhr Materin Det; 1975 Jun; 20(6):37-40. PubMed ID: 1136318
    [No Abstract]   [Full Text] [Related]  

  • 36. Citrin deficiency: a novel cause of failure to thrive that responds to a high-protein, low-carbohydrate diet.
    Dimmock D; Kobayashi K; Iijima M; Tabata A; Wong LJ; Saheki T; Lee B; Scaglia F
    Pediatrics; 2007 Mar; 119(3):e773-7. PubMed ID: 17332192
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Absence of acidosis in the initial presentation of propionic acidaemia.
    Walter JH; Wraith JE; Cleary MA
    Arch Dis Child Fetal Neonatal Ed; 1995 May; 72(3):F197-9. PubMed ID: 7796239
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Protein-bound biotin: a consideration in multiple carboxylase deficiency.
    Suchy SF; Wolf B
    Lancet; 1982 Jan; 1(8263):108. PubMed ID: 6119473
    [No Abstract]   [Full Text] [Related]  

  • 39. [Laboratory diagnosis of inborn metabolic disorders: a method for early detection of mental retardation (author's transl)].
    Zimolo A
    Lijec Vjesn; 1978 Jan; 100(1):75-6. PubMed ID: 642698
    [No Abstract]   [Full Text] [Related]  

  • 40. Beta-ketothiolase deficiency. A case report.
    Altintaş B; Teziç T; Coşkun T; Ozalp I; Kükner S; Kaya A
    Turk J Pediatr; 1992; 34(1):43-6. PubMed ID: 1509529
    [TBL] [Abstract][Full Text] [Related]  

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