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 *

169 related articles for article (PubMed ID: 19277894)

  • 41. [Methylmalonic aciduria. Classification, diagnosis and therapy (author's transl)].
    Leupold D
    Klin Wochenschr; 1977 Jan; 55(2):57-63. PubMed ID: 319293
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Antibiotic therapy for improvement of metabolic control in methylmalonic aciduria.
    Koletzko B; Bachmann C; Wendel U
    J Pediatr; 1990 Jul; 117(1 Pt 1):99-101. PubMed ID: 2370620
    [No Abstract]   [Full Text] [Related]  

  • 43. [Outcomes of patients with combined methylmalonic acidemia and homocystinuria after treatment].
    Huang Z; Han LS; Ye J; Qiu WJ; Zhang HW; Gao XL; Wang Y; Ji WJ; Li XY; Gu XF
    Zhonghua Er Ke Za Zhi; 2013 Mar; 51(3):194-8. PubMed ID: 23751581
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Transcobalamin receptor defect: Identification of two new cases through positive newborn screening for propionic/methylmalonic aciduria and long-term outcome.
    Hannah-Shmouni F; Cruz V; Schulze A; Mercimek-Andrews S
    Am J Med Genet A; 2018 Jun; 176(6):1411-1415. PubMed ID: 29663633
    [TBL] [Abstract][Full Text] [Related]  

  • 45. [Vitamin B 12 responsive methylmalenic aciduria. Apropos of a new case].
    Sann L; Divry P; Rolland MO; Bourgeois J; Bethenod M
    Pediatrie; 1980; 35(3):205-12. PubMed ID: 7393687
    [No Abstract]   [Full Text] [Related]  

  • 46. Spectrum of ocular manifestations in cobalamin C and cobalamin A types of methylmalonic acidemia.
    Ku CA; Ng JK; Karr DJ; Reznick L; Harding CO; Weleber RG; Pennesi ME
    Ophthalmic Genet; 2016 Dec; 37(4):404-414. PubMed ID: 26979128
    [TBL] [Abstract][Full Text] [Related]  

  • 47. N-carbamylglutamate in emergency management of hyperammonemia in neonatal acute onset propionic and methylmalonic aciduria.
    Filippi L; Gozzini E; Fiorini P; Malvagia S; la Marca G; Donati MA
    Neonatology; 2010; 97(3):286-90. PubMed ID: 19887858
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Clinical and molecular heterogeneity in patients with the cblD inborn error of cobalamin metabolism.
    Miousse IR; Watkins D; Coelho D; Rupar T; Crombez EA; Vilain E; Bernstein JA; Cowan T; Lee-Messer C; Enns GM; Fowler B; Rosenblatt DS
    J Pediatr; 2009 Apr; 154(4):551-6. PubMed ID: 19058814
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Modulation of B12 dosage and response in fetal treatment of methylmalonic aciduria (MMA): titration of treatment dose to serum and urine MMA.
    Evans MI; Duquette DA; Rinaldo P; Bawle E; Rosenblatt DS; Whitty J; Quintero RA; Johnson MP
    Fetal Diagn Ther; 1997; 12(1):21-3. PubMed ID: 9101216
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Homozygous nonsense mutation in the MCEE gene and siRNA suppression of methylmalonyl-CoA epimerase expression: a novel cause of mild methylmalonic aciduria.
    Dobson CM; Gradinger A; Longo N; Wu X; Leclerc D; Lerner-Ellis J; Lemieux M; Belair C; Watkins D; Rosenblatt DS; Gravel RA
    Mol Genet Metab; 2006 Aug; 88(4):327-33. PubMed ID: 16697227
    [TBL] [Abstract][Full Text] [Related]  

  • 51. [Methylmalonic aciduria. A case report].
    van Dyk JC; Meiring JL; Prinsloo JG
    S Afr Med J; 1982 Oct; 62(19):700-2. PubMed ID: 7135128
    [TBL] [Abstract][Full Text] [Related]  

  • 52. [Mutation analysis of the MMACHC gene in a pedigree with methylmalonic aciduria].
    Tang H; Hao H; Tang SH; Chen X; Liu F; Cha QB; Li YQ; Li HJ; Sun L; Yu M; Xiao X; Zhou TH
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Feb; 26(1):62-5. PubMed ID: 19199254
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Methylmalonic aciduria due to a new defect in adenosylcobalamin accumulation by cells.
    Cooper BA; Rosenblatt DS; Watkins D
    Am J Hematol; 1990 Jun; 34(2):115-20. PubMed ID: 2339678
    [TBL] [Abstract][Full Text] [Related]  

  • 54. L-Carnitine insufficiency in disorders of organic acid metabolism: response to L-carnitine by patients with methylmalonic aciduria and 3-hydroxy-3-methylglutaric aciduria.
    Chalmers RA; Stacey TE; Tracey BM; de Sousa C; Roe CR; Millington DS; Hoppel CL
    J Inherit Metab Dis; 1984; 7 Suppl 2():109-10. PubMed ID: 6207380
    [No Abstract]   [Full Text] [Related]  

  • 55. [Advances in the clinical and laboratory studies on methylmalonic aciduria combined with homocysteinemia type cblC].
    Liu YP; Yang YL
    Zhonghua Er Ke Za Zhi; 2013 Apr; 51(4):313-6. PubMed ID: 23927810
    [No Abstract]   [Full Text] [Related]  

  • 56. Congenital defect in intracellular cobalamin metabolism resulting in homocysteinuria and methylmalonic aciduria. I. Case report and histopathology.
    Baumgartner ER; Wick H; Maurer R; Egli N; Steinmann B
    Helv Paediatr Acta; 1979; 34(5):465-82. PubMed ID: 528229
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Accumulation of odd-numbered long-chain fatty acids in fetuses and neonates with inherited disorders of propionate metabolism.
    Wendel U; Baumgartner R; van der Meer SB; Spaapen LJ
    Pediatr Res; 1991 Apr; 29(4 Pt 1):403-5. PubMed ID: 1852536
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Congenital defect in intracellular cobalamin metabolism resulting in homocystinuria and methylmalonic aciduria. II. Biochemical investigations.
    Baumgartner ER; Wick H; Linnell JC; Gaull GE; Bachmann C; Steinmann B
    Helv Paediatr Acta; 1979; 34(5):483-96. PubMed ID: 43301
    [TBL] [Abstract][Full Text] [Related]  

  • 59. [Clinical studies on fifty-seven Chinese patients with combined methylmalonic aciduria and homocysteinemia].
    Zhang Y; Song JQ; Liu P; Yan R; Dong JH; Yang YL; Wang LF; Jiang YW; Zhang YH; Qin J; Wu XR
    Zhonghua Er Ke Za Zhi; 2007 Jul; 45(7):513-7. PubMed ID: 17953808
    [TBL] [Abstract][Full Text] [Related]  

  • 60. The natural history of the inherited methylmalonic acidemias.
    Matsui SM; Mahoney MJ; Rosenberg LE
    N Engl J Med; 1983 Apr; 308(15):857-61. PubMed ID: 6132336
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.