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Journal Abstract Search

138 related items for PubMed ID: 8490057

  • 21. Aminolaevulinate dehydratase porphyria in infancy. A clinical and biochemical study.
    Thunell S, Holmberg L, Lundgren J.
    J Clin Chem Clin Biochem; 1987 Jan; 25(1):5-14. PubMed ID: 3559484
    [Abstract] [Full Text] [Related]

  • 22. Hb H hydrops foetalis syndrome: a case report and review of literature.
    Lorey F, Charoenkwan P, Witkowska HE, Lafferty J, Patterson M, Eng B, Waye JS, Finklestein JZ, Chui DH.
    Br J Haematol; 2001 Oct; 115(1):72-8. PubMed ID: 11722414
    [Abstract] [Full Text] [Related]

  • 23. Congenital Erythropoietic Porphyria: A Rare Inherited Disorder.
    Saikrishna P, Palaniswamy G, Pillikunte Doddareddy N, Ishfaq L, Zargar MN, Wafa Eranhikkal F, Sahu S.
    Cureus; 2024 Mar; 16(3):e55558. PubMed ID: 38576642
    [Abstract] [Full Text] [Related]

  • 24. Hydrops foetalis caused by hepatic haemangioma.
    Albano G, Pugliese A, Stabile M, Sirimarco F, Arsieri R.
    Acta Paediatr; 1998 Dec; 87(12):1307-9. PubMed ID: 9894836
    [Abstract] [Full Text] [Related]

  • 25. Late onset erythropoietic porphyria (Gunther's disease).
    Rao SU, Dar NR, Abbas M, Mumtaz J.
    J Coll Physicians Surg Pak; 2011 Sep; 21(9):564-6. PubMed ID: 21914417
    [Abstract] [Full Text] [Related]

  • 26. Identification of two new mutations in congenital erythropoietic porphyria.
    Bensidhoum M, Ged C, Hombrados I, Moreau-Gaudry F, Hift RS, Meissner P, Sturrock ED, de Verneuil H.
    Eur J Hum Genet; 1995 Sep; 3(2):102-7. PubMed ID: 7552139
    [Abstract] [Full Text] [Related]

  • 27. The third case of Doss porphyria (delta-amino-levulinic acid dehydratase deficiency) in Germany.
    Doss MO, Stauch T, Gross U, Renz M, Akagi R, Doss-Frank M, Seelig HP, Sassa S.
    J Inherit Metab Dis; 2004 Sep; 27(4):529-36. PubMed ID: 15303011
    [Abstract] [Full Text] [Related]

  • 28. Nonimmune hydrops fetalis and bilateral pulmonary hypoplasia in a newborn infant with nuchal vascular hamartoma.
    Ozkan H, Gülen H, Demir N, Ozer E, Haberal S, Erçal D, Cevik NT.
    Turk J Pediatr; 1997 Sep; 39(4):557-60. PubMed ID: 9433160
    [Abstract] [Full Text] [Related]

  • 29. Homozygous acute intermittent porphyria in a 7-year-old boy with massive excretions of porphyrins and porphyrin precursors.
    Hessels J, Voortman G, van der Wagen A, van der Elzen C, Scheffer H, Zuijderhoudt FM.
    J Inherit Metab Dis; 2004 Sep; 27(1):19-27. PubMed ID: 14970743
    [Abstract] [Full Text] [Related]

  • 30. The prenatal presentation of congenital erythropoietic porphyria: report of two siblings with elevated maternal serum alpha-fetoprotein.
    Lazebnik N, Lazebnik RS.
    Prenat Diagn; 2004 Apr; 24(4):282-6. PubMed ID: 15065102
    [Abstract] [Full Text] [Related]

  • 31. [Severe light dermatosis following photo therapy in a newborn infant with congenital erythropoietic urophyria].
    Tönz O, Vogt J, Filippini L, Simmler F, Wachsmuth ED, Winterhalter KH.
    Helv Paediatr Acta; 1975 May; 30(1):47-56. PubMed ID: 1099056
    [Abstract] [Full Text] [Related]

  • 32. Evaluation and clinical application of the Enterotest for the determination of human biliary porphyrin composition.
    Beukeveld GJ, Bijleveld CM, Kuipers F, Kreeftenberg HG, Huizenga JR, te Velde K, Wolthers BG.
    Eur J Clin Chem Clin Biochem; 1995 Jul; 33(7):453-62. PubMed ID: 7548456
    [Abstract] [Full Text] [Related]

  • 33. Bullous lesions following phototherapy in a newborn.
    Toscano MM, Cintra FF, Resende LO, Casteleti P, Moraes LHA, Rivitti-Machado MCDM, Nico MMS, Del Bigio JZ, Carvalho WB.
    Einstein (Sao Paulo); 2023 Jul; 21():eRC0256. PubMed ID: 37255061
    [Abstract] [Full Text] [Related]

  • 34. Congenital erythropoietic porphyria in an African hedgehog (Atelerix albiventris).
    Wolff C, Corradini P, Cortés G.
    J Zoo Wildl Med; 2005 Jun; 36(2):323-5. PubMed ID: 17323578
    [Abstract] [Full Text] [Related]

  • 35. [Erythropoietic porphyria. Report of the 1st case in Costa Rica].
    Castro-Coto A, Rojas-Solano LF, Hidalgo-Hidalgo H, Solano-Aguilar E, Esquivel-Chinchilla JM.
    Med Cutan Ibero Lat Am; 1983 Jun; 11(1):39-44. PubMed ID: 6348439
    [Abstract] [Full Text] [Related]

  • 36. Advances in understanding the pathogenesis of congenital erythropoietic porphyria.
    Di Pierro E, Brancaleoni V, Granata F.
    Br J Haematol; 2016 May; 173(3):365-79. PubMed ID: 26969896
    [Abstract] [Full Text] [Related]

  • 37. Excretion pattern of faecal coproporphyrin isomers I-IV in human porphyrias.
    Jacob K, Doss MO.
    Eur J Clin Chem Clin Biochem; 1995 Dec; 33(12):893-901. PubMed ID: 8845420
    [Abstract] [Full Text] [Related]

  • 38. [Gunther's erythropoietic porphyria].
    Durieu C, Mazereeuw-Hautier J, Bonafé JL.
    Ann Dermatol Venereol; 2002 Apr; 129(4 Pt 1):455-6. PubMed ID: 12055557
    [No Abstract] [Full Text] [Related]

  • 39. Urinary excretion of porphyrins, porphobilinogen and δ-aminolaevulinic acid following an attack of acute intermittent porphyria.
    Marsden JT, Rees DC.
    J Clin Pathol; 2014 Jan; 67(1):60-5. PubMed ID: 23908454
    [Abstract] [Full Text] [Related]

  • 40. Age-dependent reference values of urinary porphyrins in children.
    Minder EI, Schneider-Yin X.
    Eur J Clin Chem Clin Biochem; 1996 May; 34(5):439-43. PubMed ID: 8790980
    [Abstract] [Full Text] [Related]

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