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Journal Abstract Search

247 related items for PubMed ID: 5820611

  • 21. Diagnostic significance of amniotic fluid amino acids.
    O'Neill RT, Morrow G, Hammel D, Auerbach VH, Barness LA.
    Obstet Gynecol; 1971 Apr; 37(4):550-4. PubMed ID: 5547853
    [No Abstract] [Full Text] [Related]

  • 22. [The intermediate form of maple syrup disease].
    Rittinger O, Bachmann C, Irnberger T, Pilz P, Walter GF, Wendel U, Plöchl E.
    Klin Padiatr; 1986 Apr; 198(1):37-43. PubMed ID: 3959487
    [Abstract] [Full Text] [Related]

  • 23. Simple biochemical methods for the study of lipidoses and aminoacidopathies.
    Adriaenssens K, Karcher D.
    Riv Patol Nerv Ment; 1970 Oct; 91(5):274-6. PubMed ID: 5525772
    [No Abstract] [Full Text] [Related]

  • 24. Maple syrup urine disease: response to dietary modifications.
    Marshall JR, Gracy RW, Kester MV.
    J Am Osteopath Assoc; 1979 Sep; 79(1):98-104. PubMed ID: 489438
    [No Abstract] [Full Text] [Related]

  • 25. [Diagnosis of inborn amino acid metabolism errors. Important symptoms and laboratory methods].
    Kroll S, Zebisch P, Toussaint W.
    Fortschr Med; 1972 Apr 13; 90(11):430-1. PubMed ID: 4681731
    [No Abstract] [Full Text] [Related]

  • 26. [Diagnosis of inborn errors of metabolism. (principles and results of investigation of 3,000 persons)].
    Farriaux JP, Adam E, Fontaine G, Delecour M.
    Lille Med; 1968 Oct 13; 13(8):864-72. PubMed ID: 5743598
    [No Abstract] [Full Text] [Related]

  • 27. [Neonatal diagnosis of maple syrup urine disease and trial of exchange transfusion].
    Statter M, Ben-Zvi A, Russell A.
    Harefuah; 1976 Oct 01; 91(7):167-9. PubMed ID: 1002028
    [No Abstract] [Full Text] [Related]

  • 28. A rapid ultra performance liquid chromatography tandem mass spectrometric method for measuring amino acids associated with maple syrup urine disease, tyrosinaemia and phenylketonuria.
    Freeto S, Mason D, Chen J, Scott RH, Narayan SB, Bennett MJ.
    Ann Clin Biochem; 2007 Sep 01; 44(Pt 5):474-81. PubMed ID: 17761035
    [Abstract] [Full Text] [Related]

  • 29. [Brain atrophy and disorders of the amino acid metabolism].
    Bickel H.
    Monatsschr Kinderheilkd (1902); 1967 Apr 01; 115(4):254-8. PubMed ID: 5592531
    [No Abstract] [Full Text] [Related]

  • 30. [Simultaneous thin-layer chromatography of blood and urine samples for the diagnosis of hereditary amino acid metabolism disorders].
    Peters WH, Lubs H, Knapp A.
    Z Arztl Fortbild (Jena); 1974 Jul 15; 68(14):716-25. PubMed ID: 4216183
    [No Abstract] [Full Text] [Related]

  • 31. Inborn errors of metabolism (IEM) -- an Indian perspective.
    Kumta NB.
    Indian J Pediatr; 2005 Apr 15; 72(4):325-32. PubMed ID: 15876762
    [Abstract] [Full Text] [Related]

  • 32. [Brain damage in infants--brain lesions in several cases of inborn errors of metabolism].
    Kamoshita S.
    Shinkei Kenkyu No Shimpo; 1972 Jun 15; 16(3):438-46. PubMed ID: 5066186
    [No Abstract] [Full Text] [Related]

  • 33. Perinatal diagnosis of the inborn errors of metabolism.
    Elsas LJ.
    J Med Assoc Ga; 1971 Sep 15; 60(9):308-11. PubMed ID: 5093796
    [No Abstract] [Full Text] [Related]

  • 34. [A screening test for phenylketonuria using a paper chromatography method].
    Halvorsen S, Skjelkvåle L.
    Lakartidningen; 1974 Mar 20; 71(12):1166-7. PubMed ID: 4821497
    [No Abstract] [Full Text] [Related]

  • 35. Maple syrup urine disease presenting with neonatal status epilepticus: report of one case.
    Wang IJ, Chu SY, Wang CY, Wang PJ, Hwu WL.
    Acta Paediatr Taiwan; 2003 Mar 20; 44(4):246-8. PubMed ID: 14674232
    [Abstract] [Full Text] [Related]

  • 36. [Disorders of amino acids].
    Aoki K.
    Nihon Rinsho; 1993 Jan 20; 51 Suppl():332-9. PubMed ID: 8459561
    [No Abstract] [Full Text] [Related]

  • 37. M aple syrup urine disease. A review with a report of an additional case.
    Schwartz JF, Kolendrianos ET.
    Dev Med Child Neurol; 1969 Aug 20; 11(4):460-70. PubMed ID: 5805351
    [No Abstract] [Full Text] [Related]

  • 38. [3 patients with maple syrup urine disease].
    Merinero B, del Valle JA, García MJ, García Miguel MJ, Barrio MI, García Hortelano J, Morales E, González F, García Aparicio J, Sáez Pérez E.
    An Esp Pediatr; 1983 Nov 20; 19(5):393-400. PubMed ID: 6660657
    [Abstract] [Full Text] [Related]

  • 39. [Paper chromatography in the detection of aminoacidopathies].
    Sietti C.
    Minerva Pediatr; 1971 Dec 22; 23(51):2123-4. PubMed ID: 5136311
    [No Abstract] [Full Text] [Related]

  • 40. Differential response to renal replacement therapy in neonatal-onset inborn errors of metabolism.
    Porta F, Peruzzi L, Bonaudo R, Pieretti S, Busso M, Cocchi E, Conio A, Pagliardini V, Spada M.
    Nephrology (Carlton); 2018 Oct 22; 23(10):957-961. PubMed ID: 29888426
    [Abstract] [Full Text] [Related]

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