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 *

132 related articles for article (PubMed ID: 2066863)

  • 41. Response to dietary therapy in B 12 unresponsive methylmalonic acidemia.
    Nyhan WL; Fawcett N; Ando T; Rennert OM; Julius RL
    Pediatrics; 1973 Mar; 51(3):539-48. PubMed ID: 4707869
    [No Abstract]   [Full Text] [Related]  

  • 42. Symmetrical necrosis of the basal ganglia in methylmalonic acidaemia.
    Roodhooft AM; Baumgartner ER; Martin JJ; Blom W; Van Acker KJ
    Eur J Pediatr; 1990 May; 149(8):582-4. PubMed ID: 2189733
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Methylmalonic aciduria. An inborn error of metabolism leading to chronic metabolic acidosis.
    Oberholzer VG; Levin B; Burgess EA; Young WF
    Arch Dis Child; 1967 Oct; 42(225):492-504. PubMed ID: 6061291
    [No Abstract]   [Full Text] [Related]  

  • 44. [Encephalopathy and congenital lactic acidosis (apropos of an anatomo-clinical case)].
    Peytel J; Salle B; Tommasi M; Mathieu M; Antener I; Rosenberg D; Monnet P
    Arch Fr Pediatr; 1969 Mar; 26(3):321-36. PubMed ID: 5797344
    [No Abstract]   [Full Text] [Related]  

  • 45. [Combined methylmalonic acidemia and homocystinuria; a case report].
    Jiménez Varo I; Bueno Delgado M; Dios Fuentes E; Delgado Pecellin C; González Meneses A; Soto Moreno A; Venegas Moreno E
    Nutr Hosp; 2015 Apr; 31(4):1885-8. PubMed ID: 25795986
    [TBL] [Abstract][Full Text] [Related]  

  • 46. [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]  

  • 47. Cobalamin C mutation (methylmalonic aciduria and homocystinuria) in adolescence. A treatable cause of dementia and myelopathy.
    Shinnar S; Singer HS
    N Engl J Med; 1984 Aug; 311(7):451-4. PubMed ID: 6749192
    [No Abstract]   [Full Text] [Related]  

  • 48. Cobalamin C disease presenting with hemophagocytic lymphohistiocytosis.
    Wu S; Gonzalez-Gomez I; Coates T; Yano S
    Pediatr Hematol Oncol; 2005 Dec; 22(8):717-21. PubMed ID: 16251179
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Biochemical and clinical response to hydroxocobalamin versus cyanocobalamin treatment in patients with methylmalonic acidemia and homocystinuria (cblC).
    Andersson HC; Shapira E
    J Pediatr; 1998 Jan; 132(1):121-4. PubMed ID: 9470012
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Reversible dementia in an adolescent with cblC disease: clinical heterogeneity within the same family.
    Augoustides-Savvopoulou P; Mylonas I; Sewell AC; Rosenblatt DS
    J Inherit Metab Dis; 1999 Aug; 22(6):756-8. PubMed ID: 10472537
    [No Abstract]   [Full Text] [Related]  

  • 51. Gene discovery in methylmalonic aciduria and homocystinuria.
    Thiele J; Van Raamsdonk JM
    Clin Genet; 2006 May; 69(5):402-3. PubMed ID: 16650077
    [No Abstract]   [Full Text] [Related]  

  • 52. Citrullinemia: a new case, with implications concerning adaptation to defective urea synthesis.
    Scott-Emuakpor A; Higgins JV; Kohrman AF
    Pediatr Res; 1972 Jul; 6(7):626-33. PubMed ID: 5057291
    [No Abstract]   [Full Text] [Related]  

  • 53. Mechanism of vitamin B12-responsiveness in cblC methylmalonic aciduria with homocystinuria.
    Froese DS; Zhang J; Healy S; Gravel RA
    Mol Genet Metab; 2009 Dec; 98(4):338-43. PubMed ID: 19700356
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Screening for metabolic disease in a metropolitan hospital.
    Krieger I; Nigro M; Taqi Q
    Am J Dis Child; 1982 Feb; 136(2):125-8. PubMed ID: 7064926
    [TBL] [Abstract][Full Text] [Related]  

  • 55. [Human fibroblast bank for studying amino acid disorders and organic acidemias].
    del Valle JA; Merinero B; Pérez-Cerdá C; Ugarte M
    Rev Esp Fisiol; 1982; 38 Suppl():207-10. PubMed ID: 7146578
    [TBL] [Abstract][Full Text] [Related]  

  • 56. [Congenital metabolic acidosis in the postnatal period].
    Schreier K; Porath U
    Dtsch Med Wochenschr; 1978 Jun; 103(22):943-7. PubMed ID: 207503
    [No Abstract]   [Full Text] [Related]  

  • 57. [Letter: Sudden infant death syndrome (SIDS)].
    Vaandrager GJ
    Ned Tijdschr Geneeskd; 1975 Jul; 119(29):1156. PubMed ID: 808742
    [No Abstract]   [Full Text] [Related]  

  • 58. Renal transplantation in a 14-year-old girl with vitamin B12-responsive cblA-type methylmalonic acidaemia.
    Coman D; Huang J; McTaggart S; Sakamoto O; Ohura T; McGill J; Burke J
    Pediatr Nephrol; 2006 Feb; 21(2):270-3. PubMed ID: 16247646
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Methylmalonic aciduria articles.
    Fowler B
    J Inherit Metab Dis; 2008 Feb; 31(1):4. PubMed ID: 18196472
    [No Abstract]   [Full Text] [Related]  

  • 60. Lethal neonatal deficiency of carbamyl phosphate synthetase.
    Gelehrter TD; Snodgrass PJ
    N Engl J Med; 1974 Feb; 290(8):430-3. PubMed ID: 4811018
    [No Abstract]   [Full Text] [Related]  

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