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Journal Abstract Search

161 related items for PubMed ID: 38255745

  • 1. Severe Perinatal Presentations of Günther's Disease: Series of 20 Cases and Perspectives.
    Goudet C, Ged C, Petit A, Desage C, Mahe P, Salhi A, Harzallah I, Blouin JM, Mercie P, Schmitt C, Poli A, Gouya L, Barlogis V, Richard E.
    Life (Basel); 2024 Jan 17; 14(1):. PubMed ID: 38255745
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  • 2. Successful treatment of congenital erythropoietic porphyria using matched unrelated hematopoietic stem cell transplantation.
    Martinez Peinado C, Díaz de Heredia C, To-Figueras J, Arias-Santiago S, Nogueras P, Elorza I, Olivé T, Bádenas C, Moreno MJ, Tercedor J, Herrero C.
    Pediatr Dermatol; 2013 Jan 17; 30(4):484-9. PubMed ID: 23557135
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  • 6. Erythrodontia in congenital erythropoietic porphyria.
    Bhavasar R, Santoshkumar G, Prakash BR.
    J Oral Maxillofac Pathol; 2011 Jan 17; 15(1):69-73. PubMed ID: 21731282
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  • 9. Interdependence between degree of porphyrin excess and disease severity in congenital erythropoietic porphyria (Günther's disease).
    Freesemann AG, Bhutani LK, Jacob K, Doss MO.
    Arch Dermatol Res; 1997 Apr 17; 289(5):272-6. PubMed ID: 9164637
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  • 10. Late onset erythropoietic porphyria (Gunther's disease).
    Rao SU, Dar NR, Abbas M, Mumtaz J.
    J Coll Physicians Surg Pak; 2011 Sep 17; 21(9):564-6. PubMed ID: 21914417
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  • 12. A Case of Congenital Erythropoietic Porphyria without Haemolysis.
    Garg KK, Singh H.
    Eur J Case Rep Intern Med; 2016 Sep 17; 3(7):000497. PubMed ID: 30755899
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  • 15. Bone Marrow Transplantation in Congenital Erythropoietic Porphyria: Sustained Efficacy but Unexpected Liver Dysfunction.
    Besnard C, Schmitt C, Galmiche-Rolland L, Debray D, Fabre M, Molina T, Gouya L, Ged C, Castelle M, Cavazzana M, Magrin E, Neven B, Moshous D, Blanche S, Frémond ML.
    Biol Blood Marrow Transplant; 2020 Apr 17; 26(4):704-711. PubMed ID: 31843562
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  • 16. Congenital erythropoietic porphyria.
    To-Figueras J, Erwin AL, Aguilera P, Millet O, Desnick RJ.
    Liver Int; 2024 Aug 17; 44(8):1842-1855. PubMed ID: 38717058
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  • 17. Biochemical diagnosis of a fatal case of Günther's disease in a newborn with hydrops foetalis.
    Verstraeten L, Van Regemorter N, Pardou A, de Verneuil H, Da Silva V, Rodesch F, Vermeylen D, Donner C, Noël JC, Nordmann Y.
    Eur J Clin Chem Clin Biochem; 1993 Mar 17; 31(3):121-8. PubMed ID: 8490057
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  • 18. Congenital Erythropoietic Porphyria: A Rare Case of Photosensitivity with Hemolytic Anaemia and Mental Retardation.
    Shirazi N, Chauhan P, Jindal R, Ahmad S.
    J Coll Physicians Surg Pak; 2019 Jun 17; 29(6):S23-S25. PubMed ID: 31142411
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  • 19. Neonatal hemolytic anemia does not always indicate thalassemia: a case report.
    Al-Harazi AA, Al-Eryani BM, Al-Sharafi BA.
    BMC Res Notes; 2017 Sep 12; 10(1):476. PubMed ID: 28899405
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  • 20. Very Early Diagnosis and Management of Congenital Erythropoietic Porphyria.
    Desjardins MP, Naccache L, Hébert A, Auger I, Teira P, Pelland-Marcotte MC.
    Clin Pediatr (Phila); 2023 Jun 12; 62(5):399-403. PubMed ID: 36217751
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