Results 111 to 120 of about 17,878 (259)

ACUTE PORPHYRIA [PDF]

The Lancet, 1947
C H, GRAY, C, RIMINGTON
openaire   +6 more sources

Dental Treatment of the Patient with Porphyria [PDF]

, 2005
Porfirije su skupina nasljednih bolesti uzrokovanih defektnim enzimima na biosintetskom putu hema. Ovisno o defektu pojedinog enzima razlikujemo i razne vrste porfirija.
Berislav Perić, Niko Krakar
core   +1 more source

Diagnostic Dilemmas in Hepatitis C Virus Infection for Hemodialysis Patients

Folia Medica, 2017
Background: Hepatitis C virus (HCV) is a leading cause of chronic hepatitis in dialysis patients. The diagnosis of HCV infection in these patients is predominantly based on laboratory tests because of the specificity of the clinical course of the disease.
Komitova Radka T., Atanasova Maria V., Pavlova Toska A., Nyagolov Monica Sh., Ivanova Aneta V.   +4 more
doaj   +1 more source

Feasibility of Photofrin II as a radiosensitizing agent in solid tumors - Preliminary results [PDF]

, 2006
Background: Photofrin II has been demonstrated to serve as a specific and selective radiosensitizing agent in in vitro and in vivo tumor models. We aimed to investigate the feasibility of a clinical application of Photofrin II.
Byrne CJ, Cohen L, Dougherty TJ, Foote CS, Gomer CJ, Kostron H, Kulka U, McDonald IJ, Miller RA, O'Hara JA, Orenstein A, Schaffer M, Schaffer M, Schaffer M, Schaffer M, Schaffer M, Schmidt-Erfurth U, Schwartz S, Schwartz S, Sessler JL, Shikowitz MJ, Stewart F, Vogeser M   +22 more
core   +1 more source

Microelements and Inherited Metabolic Diseases

Acta Medica, 2002
In addition to the main groups of inherited metabolic diseases, including mitochondrial, peroxisomal and lysosomal defects, organic acidurias, porphyrias, defects of amino acids, saccharides and fatty acids metabolism, disorders of transport and ...
Eliška Marklová
doaj   +1 more source

Biochemical and molecular diagnosis of erythropoietic protoporphyria in an Ashkenazi Jewish family [PDF]

, 2018
Summary: Erythropoietic protoporphyria (EPP) is a rare hereditary disorder due to a partial deficiency of ferrochelatase (FECH). The genotype of EPP patients features a mutation on one allele of the FECH gene and a common hypomorphic FECH IVS3-48c on the
Mamet, R., Minder, E., Schneider-Yin, X., Schoenfeld, N.   +3 more
core  

Porphyrias [PDF]

British Journal of Anaesthesia, 2000
M F, James, R J, Hift
openaire   +2 more sources

Acute porphyrias and porphyric neuropathy

Southwest Respiratory and Critical Care Chronicles, 2016
The porphyrias are a group of uncommon inherited metabolic disorders of heme biosynthesis. Acute porphyrias are specific types of porphyrias characterized by the presence of acute attacks that usually present with abdominal pain, psychiatric symptoms ...
Doungporn Ruthirago, Parunyou Julayanont, Supannee Rassameehiran   +2 more
doaj  

LABRAD : Vol 34, Issue 3 - October 2009 [PDF]

, 2009
Detection of Amoebic Meningitis by Wet Film of Cerebrospinal Fluid (CSF) Biochemical Tests in the Diagnosis of Anaemia Pathophysiology and Laboratory Investigation in Anaemia of Chronic Disease Haematogones: A pitfall in the Diagnosis of Leukemias ...
Aga Khan University Hospital, Karachi
core   +1 more source

Variegate porphyria onset as neurovisceral manifestation and unusual sensory impairment distribution. Case report

Brain Disorders
Background: Acute hepatic porphyrias are heme metabolism disorders presenting with a broad clinical spectrum, including neurovisceral manifestations. Peripheral neuropathy is one of the most frequent complications in porphyrias and can correspond about ...
Lucas Grobério Moulim de Moraes, Caroline Colnago Demoner, Amanda Ambrosini Cipriano, Giselle Alves de Oliveira, Raphael de Paula Doyle Maia, Paula Zago Melo Dias, Mariana Lacerda Reis Grenfell, Renann Nunes Pirola, Marcelo Ramos Muniz   +8 more
doaj   +1 more source