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 *

119 related articles for article (PubMed ID: 10323732)

  • 41. Pyruvate-carboxylase deficiency with urea cycle impairment.
    Greter J; Gustafsson J; Holme E
    Acta Paediatr Scand; 1985 Nov; 74(6):982-6. PubMed ID: 3937431
    [TBL] [Abstract][Full Text] [Related]  

  • 42. West syndrome with periventricular leukomalacia: ten-year clinical study.
    Kuzmanić-Samija R; Resić B; Tomasović M; Gabrić Pandurić D; Lozić B; Lozić M; Resić J
    Coll Antropol; 2008 Jan; 32 Suppl 1():105-11. PubMed ID: 18405067
    [TBL] [Abstract][Full Text] [Related]  

  • 43. [Cerebral pathological evaluation following neural stem cells intraventricular transplantation in neonatal rats with periventricular leukomalacia].
    He YQ; Chen HJ; Qian LH; Chen GY
    Zhongguo Dang Dai Er Ke Za Zhi; 2008 Jun; 10(3):362-6. PubMed ID: 18554469
    [TBL] [Abstract][Full Text] [Related]  

  • 44. A novel mutation in the dihydrolipoamide dehydrogenase E3 subunit gene (DLD) resulting in an atypical form of alpha-ketoglutarate dehydrogenase deficiency.
    Odièvre MH; Chretien D; Munnich A; Robinson BH; Dumoulin R; Masmoudi S; Kadhom N; Rötig A; Rustin P; Bonnefont JP
    Hum Mutat; 2005 Mar; 25(3):323-4. PubMed ID: 15712224
    [TBL] [Abstract][Full Text] [Related]  

  • 45. NTP technical report on the toxicity studies of Dibutyl Phthalate (CAS No. 84-74-2) Administered in Feed to F344/N Rats and B6C3F1 Mice.
    Marsman D
    Toxic Rep Ser; 1995 Apr; 30():1-G5. PubMed ID: 12209194
    [TBL] [Abstract][Full Text] [Related]  

  • 46. N-acetylcysteine prevents endotoxin-induced degeneration of oligodendrocyte progenitors and hypomyelination in developing rat brain.
    Paintlia MK; Paintlia AS; Barbosa E; Singh I; Singh AK
    J Neurosci Res; 2004 Nov; 78(3):347-61. PubMed ID: 15389835
    [TBL] [Abstract][Full Text] [Related]  

  • 47. NTP Toxicology and Carcinogenesis Studies of Coumarin (CAS No. 91-64-5) in F344/N Rats and B6C3F1 Mice (Gavage Studies).
    National Toxicology Program
    Natl Toxicol Program Tech Rep Ser; 1993 Sep; 422():1-340. PubMed ID: 12616289
    [TBL] [Abstract][Full Text] [Related]  

  • 48. The molecular basis of pyruvate carboxylase deficiency: mosaicism correlates with prolonged survival.
    Wang D; Yang H; De Braganca KC; Lu J; Yu Shih L; Briones P; Lang T; De Vivo DC
    Mol Genet Metab; 2008; 95(1-2):31-8. PubMed ID: 18676167
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Development of microglia in the cerebral white matter of the human fetus and infant.
    Billiards SS; Haynes RL; Folkerth RD; Trachtenberg FL; Liu LG; Volpe JJ; Kinney HC
    J Comp Neurol; 2006 Jul; 497(2):199-208. PubMed ID: 16705680
    [TBL] [Abstract][Full Text] [Related]  

  • 50. A new case of pyruvate dehydrogenase deficiency due to a novel mutation in the PDX1 gene.
    Dey R; Mine M; Desguerre I; Slama A; Van Den Berghe L; Brivet M; Aral B; Marsac C
    Ann Neurol; 2003 Feb; 53(2):273-7. PubMed ID: 12557299
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Neonatal lactic acidosis, complex I/IV deficiency, and fetal cerebral disruption.
    van Straaten HL; van Tintelen JP; Trijbels JM; van den Heuvel LP; Troost D; Rozemuller JM; Duran M; de Vries LS; Schuelke M; Barth PG
    Neuropediatrics; 2005 Jun; 36(3):193-9. PubMed ID: 15944905
    [TBL] [Abstract][Full Text] [Related]  

  • 52. [Pyruvate carboxylase deficiency].
    Naito E
    Nihon Rinsho; 2002 Apr; 60 Suppl 4():755-8. PubMed ID: 12013992
    [No Abstract]   [Full Text] [Related]  

  • 53. Some biochemical observations on biotin deficiency in the rat as a model for human pyruvate carboxylase deficiency.
    Schrijver J; Dias T; Hommes FA
    Nutr Metab; 1979; 23(3):179-91. PubMed ID: 106342
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Unsuccessful treatment of severe pyruvate carboxylase deficiency with triheptanoin.
    Breen C; White FJ; Scott CA; Heptinstall L; Walter JH; Jones SA; Morris AA
    Eur J Pediatr; 2014 Mar; 173(3):361-6. PubMed ID: 24114256
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Distinguishing Encephaloclastic Lesions Resulting From Primary or Secondary Pyruvate Dehydrogenase Deficiency From Other Neonatal or Infantile Cavitary Brain Lesions.
    Gilani A; Hove JLV; Thomas JA; Kleinschmidt-DeMasters BK
    Pediatr Dev Pathol; 2020; 23(3):189-196. PubMed ID: 31542992
    [TBL] [Abstract][Full Text] [Related]  

  • 56. A Rare Case of Type B Neonatal Pyruvate Carboxylase Enzyme Deficiency Presenting With Refractory Lactic Acidosis in the Early Neonatal Period.
    Sharif S; Velumula PK; Boddu PK; Altinok D; Fernandes N
    Cureus; 2022 Oct; 14(10):e29903. PubMed ID: 36348915
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Pyruvate carboxylase deficiency: An underestimated cause of lactic acidosis.
    Habarou F; Brassier A; Rio M; Chrétien D; Monnot S; Barbier V; Barouki R; Bonnefont JP; Boddaert N; Chadefaux-Vekemans B; Le Moyec L; Bastin J; Ottolenghi C; de Lonlay P
    Mol Genet Metab Rep; 2015 Mar; 2():25-31. PubMed ID: 28649521
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Prolonged survival in pyruvate carboxylase deficiency: lack of correlation with enzyme activity in cultured fibroblasts.
    Stern HJ; Nayar R; Depalma L; Rifai N
    Clin Biochem; 1995 Feb; 28(1):85-9. PubMed ID: 7720232
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Inherited metabolic disorders presenting as hypoxic ischaemic encephalopathy: A case series of patients presenting at a tertiary care hospital in Pakistan.
    Zahid M; Khan AH; Yunus ZM; Chen BC; Steinmann B; Johannes H; Afroze B
    J Pak Med Assoc; 2019 Mar; 69(3):432-436. PubMed ID: 30890842
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Clinical, biochemical and molecular characterization of 12 patients with pyruvate carboxylase deficiency treated with triheptanoin.
    Lasio MLD; Leshinski AC; Ducich NH; Flore LA; Lehman A; Shur N; Jayakar PB; Hainline BE; Basinger AA; Wilson WG; Diaz GA; Erbe RW; Koeberl DD; Vockley J; Bedoyan JK
    Mol Genet Metab; 2023 Jun; 139(2):107605. PubMed ID: 37207470
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.