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Dermatologica
|
January 1, 1989
Familial porphyria cutanea tarda with normal erythrocytic urodecarboxylase: an exception to the rule?
L D'Alessandro Gandolfo, D Griso, A Macri, et al.
Dermatology (Basel, Switzerland)
|
August 19, 2004
A case of variegate porphyria with coeliac disease and beta-thalassaemia minor
D Dal Sacco, A Parodi, E Cozzani, et al.
The British Journal of Dermatology
|
December 16, 2014
Long-term observational study of afamelanotide in 115 patients with erythropoietic protoporphyria
G Biolcati, E Marchesini, F Sorge, et al.
Cellular and Molecular Biology (Noisy-Le-Grand, France)
|
February 1, 1997
Iron and porphyria cutanea tarda
L D'Alessandro Gandolfo, D Griso, A Macrì, et al.
Cellular and Molecular Biology (Noisy-Le-Grand, France)
|
March 10, 2009
Four novel mutations of the coproporphyrinogen III oxidase gene
C Aurizi, G Lupia Palmieri, L Barbieri, et al.
Recenti Progressi in Medicina
|
March 1, 1989
[An unusual mechanism of lead poisoning. Presentation of a case]
L D'Alessandro Gandolfo, A Macrì, G Biolcati, et al.
Biochimica Et Biophysica Acta
|
August 16, 2016
Glutathione S-transferase ϴ-subunit as a phenotypic suppressor of pmr1Δ strain, the Kluyveromyces lactis model for Hailey-Hailey disease
G Ficociello, E Zanni, S Cialfi, et al.
Human Mutation
|
May 2, 2000
Molecular analysis of the hydroxymethylbilane synthase (HMBS) gene in Italian patients with acute intermittent porphyria: report of four novel mutations
F Martinez di Montemuros, E Di Pierro, S Fargion, et al.
Blood Cells, Molecules & Diseases
|
February 8, 2002
Acute intermittent porphyria: heterogeneity of mutations in the hydroxymethylbilane synthase gene in Italy
F Martinez di Montemuros, E Di Pierro, G Biolcati, et al.
European Journal of Gastroenterology & Hepatology
|
August 17, 2001
Non-alcoholic steatohepatitis induced by carbamazepine and variegate porphyria
A Grieco, B Alfei, P Di Rocco, et al.
Page
of 3
Search research articles
Search
Showing results (11-20 of 26) with videos related to
Sort By:
Page
of 3
Dermatologica
|
January 1, 1989
Familial porphyria cutanea tarda with normal erythrocytic urodecarboxylase: an exception to the rule?
L D'Alessandro Gandolfo, D Griso, A Macri, et al.
Dermatology (Basel, Switzerland)
|
August 19, 2004
A case of variegate porphyria with coeliac disease and beta-thalassaemia minor
D Dal Sacco, A Parodi, E Cozzani, et al.
The British Journal of Dermatology
|
December 16, 2014
Long-term observational study of afamelanotide in 115 patients with erythropoietic protoporphyria
G Biolcati, E Marchesini, F Sorge, et al.
Cellular and Molecular Biology (Noisy-Le-Grand, France)
|
February 1, 1997
Iron and porphyria cutanea tarda
L D'Alessandro Gandolfo, D Griso, A Macrì, et al.
Cellular and Molecular Biology (Noisy-Le-Grand, France)
|
March 10, 2009
Four novel mutations of the coproporphyrinogen III oxidase gene
C Aurizi, G Lupia Palmieri, L Barbieri, et al.
Recenti Progressi in Medicina
|
March 1, 1989
[An unusual mechanism of lead poisoning. Presentation of a case]
L D'Alessandro Gandolfo, A Macrì, G Biolcati, et al.
Biochimica Et Biophysica Acta
|
August 16, 2016
Glutathione S-transferase ϴ-subunit as a phenotypic suppressor of pmr1Δ strain, the Kluyveromyces lactis model for Hailey-Hailey disease
G Ficociello, E Zanni, S Cialfi, et al.
Human Mutation
|
May 2, 2000
Molecular analysis of the hydroxymethylbilane synthase (HMBS) gene in Italian patients with acute intermittent porphyria: report of four novel mutations
F Martinez di Montemuros, E Di Pierro, S Fargion, et al.
Blood Cells, Molecules & Diseases
|
February 8, 2002
Acute intermittent porphyria: heterogeneity of mutations in the hydroxymethylbilane synthase gene in Italy
F Martinez di Montemuros, E Di Pierro, G Biolcati, et al.
European Journal of Gastroenterology & Hepatology
|
August 17, 2001
Non-alcoholic steatohepatitis induced by carbamazepine and variegate porphyria
A Grieco, B Alfei, P Di Rocco, et al.
Page
of 3