Results 171 to 180 of about 11,286 (212)

Prevalence of HFE gene mutation in patients with porphyria cutanea tarda University Hospital Pedro Ernesto-UERJ

, 2013
Roberto Gomes; Programa de Pós-Graduação em Sistemas e Processos Agroindustriais (PPGSPA) -Universidade Federal do Rio Grande (FURG) Silva
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Acute Hepatic Porphyria in Denmark; a retrospective study [PDF]

Magnus Emil Ulrich Wagner, Morten Frost, Jan Frystyk   +2 more
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Phycoerythrocyanin [PDF]

, 1993
Hong, Q., Scheer, Hugo, Shima, A., Siebzehnrübl, S., Zhao, K. H.   +4 more
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Dorsal Hand Involvement in Porphyria Cutanea Tarda

Gilberto Pires da Rosa, MA Costa, Alberto Mota   +2 more
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Abdominal pain in a patient with acute lymphoblastic leukaemia [PDF]

, 2018
Breitenstein, Alexander, Goede, Jeroen, Kühne, Reto, Marek, Aleksandra, Minder, Elisabeth, Renner, Christoph, Schanz, Urs   +6 more
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Porphyria cutanea tarda, Polyneuropathie und Myopathie bei kleinzelligem Bronchialkarzinom [PDF]

, 1982
Born, J. A., Hartmann, A., Krause, Klaus-Henning, Schmitt, H.-P.   +3 more
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[Mixed porphyria (porphyria variegata)].

Srpski arhiv za celokupno lekarstvo, 1979
M, Ljaljević, M, Savić-Perisić, V, Zamurović   +2 more
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Hydroxymethylbilane Synthase Gene Mutation: The Hidden Driver of Abdominal Pain and Neurological Symptoms in Acute Intermittent Porphyria

Abeer Zakariyah, Rahaf Khaled AL-Zahrani, Iman Alhazmi, Alia Abotaleb, Mohammed Alasmari, Abdulrahim Basendwah, Rasha Alsubaie, Muhammad Sohaib Khan, Leena Alnajjar, Sultan Altouri   +9 more
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Acute intermittent porphyria and early hematin treatment

, 2014
Viroj Wiwanitkit
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Porphyrias

The Lancet, 2010
Hereditary porphyrias are a group of eight metabolic disorders of the haem biosynthesis pathway that are characterised by acute neurovisceral symptoms, skin lesions, or both. Every porphyria is caused by abnormal function of a separate enzymatic step, resulting in a specific accumulation of haem precursors.
Hervé, Puy, Laurent, Gouya, Jean-Charles, Deybach   +2 more
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