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Journal Abstract Search

362 related items for PubMed ID: 26397944

  • 41. [Newborn screening for congenital adrenal hyperplasia in France].
    Kariyawasam D, Nguyen-Khoa T, Gonzalez Briceño L, Polak M.
    Med Sci (Paris); 2021 May; 37(5):500-506. PubMed ID: 34003096
    [Abstract] [Full Text] [Related]

  • 42. Reverse-hybridization assay for rapid detection of common CYP21A2 mutations in dried blood spots from newborns with elevated 17-OH progesterone.
    Németh S, Riedl S, Kriegshäuser G, Baumgartner-Parzer S, Concolino P, Neocleous V, Phylactou LA, Borucka-Mankiewicz M, Onay H, Tukun A, Oberkanins C.
    Clin Chim Acta; 2012 Dec 24; 414():211-4. PubMed ID: 22985688
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  • 43. Generation of monoclonal antibodies against 17α-hydroxyprogesterone for newborn screening of congenital adrenal hyperplasia.
    Morejón García G, García de la Rosa I, González Reyes EC, Rubio Torres A, Quintana Guerra JM, Hernández Marín M, Pérez Mora PL, Feal Carballo S, Lafita Delfino Y, Pupo Infante M, Castells Martínez EM, Rosabal Poloshkov A, Hernández Pérez L.
    Clin Chim Acta; 2018 Oct 24; 485():311-315. PubMed ID: 30006291
    [Abstract] [Full Text] [Related]

  • 44. Neonatal screening for congenital adrenal hyperplasia.
    White PC.
    Nat Rev Endocrinol; 2009 Sep 24; 5(9):490-8. PubMed ID: 19690561
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  • 45. Neonatal screening for congenital adrenal hyperplasia in Japan.
    Tajima T, Fujikura K, Fukushi M, Hotsubo T, Mitsuhashi Y.
    Pediatr Endocrinol Rev; 2012 Oct 24; 10 Suppl 1():72-8. PubMed ID: 23330248
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  • 46. Newborn Screening and Diagnosis of Infants with Congenital Adrenal Hyperplasia.
    Vats P, Dabas A, Jain V, Seth A, Yadav S, Kabra M, Gupta N, Singh P, Sharma R, Kumar R, Polipalli SK, Batra P, Thelma BK, Kapoor S.
    Indian Pediatr; 2020 Jan 15; 57(1):49-55. PubMed ID: 31937698
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  • 47. Therapy monitoring in congenital adrenal hyperplasia by dried blood samples.
    Wieacker I, Peter M, Borucki K, Empting S, Roehl FW, Mohnike K.
    J Pediatr Endocrinol Metab; 2015 Jul 15; 28(7-8):867-71. PubMed ID: 25781526
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  • 48. Quantitative determination of succinylacetone in dried blood spots for newborn screening of tyrosinemia type I.
    Magera MJ, Gunawardena ND, Hahn SH, Tortorelli S, Mitchell GA, Goodman SI, Rinaldo P, Matern D.
    Mol Genet Metab; 2006 May 15; 88(1):16-21. PubMed ID: 16448836
    [Abstract] [Full Text] [Related]

  • 49. Rapid monitoring assay of congenital adrenal hyperplasia with microbore high-performance liquid chromatography/electrospray ionization tandem mass spectrometry from dried blood spots.
    Lai CC, Tsai CH, Tsai FJ, Lee CC, Lin WD.
    Rapid Commun Mass Spectrom; 2001 May 15; 15(22):2145-51. PubMed ID: 11746879
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  • 50. Evaluation of neonatal screening for congenital adrenal hyperplasia.
    Honour JW, Torresani T.
    Horm Res; 2001 May 15; 55(4):206-11. PubMed ID: 11598376
    [Abstract] [Full Text] [Related]

  • 51. Streamlined determination of lysophosphatidylcholines in dried blood spots for newborn screening of X-linked adrenoleukodystrophy.
    Turgeon CT, Moser AB, Mørkrid L, Magera MJ, Gavrilov DK, Oglesbee D, Raymond K, Rinaldo P, Matern D, Tortorelli S.
    Mol Genet Metab; 2015 Jan 15; 114(1):46-50. PubMed ID: 25481105
    [Abstract] [Full Text] [Related]

  • 52. Wisconsin's Screening Algorithm for the Identification of Newborns with Congenital Adrenal Hyperplasia.
    Bialk ER, Lasarev MR, Held PK.
    Int J Neonatal Screen; 2019 Sep 15; 5(3):33. PubMed ID: 33072992
    [Abstract] [Full Text] [Related]

  • 53. Diagnosis of congenital adrenal hyperplasia by rapid determination of 17alpha-hydroxyprogesterone in dried blood spots by gas chromatography/mass spectrometry following microwave-assisted silylation.
    Deng C, Ji J, Zhang L, Zhang X.
    Rapid Commun Mass Spectrom; 2005 Sep 15; 19(20):2974-8. PubMed ID: 16178052
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  • 54. Screening for adenylosuccinate lyase deficiency using tandem mass spectrometry analysis of succinylpurines in neonatal dried blood spots.
    Zikanova M, Krijt J, Skopova V, Krijt M, Baresova V, Kmoch S.
    Clin Biochem; 2015 Jan 15; 48(1-2):2-7. PubMed ID: 25445730
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  • 55. Steroid profiling for the diagnosis of congenital adrenal hyperplasia by microbore ultra-performance liquid chromatography-tandem mass spectrometry.
    Feng D, Wang Z, Li H, Shi X, Zou L, Kong H, Xu Z, Yu C, Hu C, Xu G.
    Clin Chim Acta; 2023 Mar 15; 543():117304. PubMed ID: 36958425
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  • 56. Confirmation of congenital adrenal hyperplasia by adrenal steroid profiling of filter paper dried blood samples using ultra-performance liquid chromatography-tandem mass spectrometry.
    Rossi C, Calton L, Brown HA, Gillingwater S, Wallace AM, Petrucci F, Ciavardelli D, Urbani A, Sacchetta P, Morris M.
    Clin Chem Lab Med; 2011 Apr 15; 49(4):677-84. PubMed ID: 21288182
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  • 57. The use of mass spectrometry to analyze dried blood spots.
    Wagner M, Tonoli D, Varesio E, Hopfgartner G.
    Mass Spectrom Rev; 2016 Apr 15; 35(3):361-438. PubMed ID: 25252132
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  • 58. LC-MS/MS improves screening towards 21-hydroxylase deficiency.
    Ambroziak U, Kępczyńska-Nyk A, Kuryłowicz A, Wysłouch-Cieszyńska A, Małunowicz EM, Bartoszewicz Z, Kondracka A, Jaźwiec R, Pawłowska E, Szcześniak M, Dadlez M, Bednarczuk T.
    Gynecol Endocrinol; 2015 Apr 15; 31(4):296-300. PubMed ID: 25539143
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  • 59. Simultaneous determination of 17alpha-hydroxypregnenolone and 17alpha-hydroxyprogesterone in dried blood spots from low birth weight infants using LC-MS/MS.
    Higashi T, Nishio T, Uchida S, Shimada K, Fukushi M, Maeda M.
    J Pharm Biomed Anal; 2008 Sep 10; 48(1):177-82. PubMed ID: 18571354
    [Abstract] [Full Text] [Related]

  • 60. Comparison of one-tier and two-tier newborn screening metrics for congenital adrenal hyperplasia.
    Sarafoglou K, Banks K, Gaviglio A, Hietala A, McCann M, Thomas W.
    Pediatrics; 2012 Nov 10; 130(5):e1261-8. PubMed ID: 23071209
    [Abstract] [Full Text] [Related]

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