Works matching DE "HEREDITARY coproporphyria"

Results: 12

Is non-alcoholic steatohepatitis a predisposing factor to porphyria cutanea tarda?

Published in:

Photodermatology, Photoimmunology & Photomedicine, 2013, v. 29, n. 2, p. 106, doi. 10.1111/phpp.12032

By:

Ergen, Elizabeth N.;
Seidler, Elizabeth;
Parekh, Samir;
Parker, Sareeta R. S.

Publication type:

Article

Haem arginate as effective maintenance therapy for hereditary coproporphyria.

Published in:

Australasian Journal of Dermatology, 2011, v. 52, n. 2, p. 135, doi. 10.1111/j.1440-0960.2011.00747.x

By:

Ma, Ellen;
Mar, Victoria;
Varigos, George;
Nicoll, Amanda;
Ross, Gayle

Publication type:

Article

Systemic Lupus Erythematosus and Hereditary Coproporphyria: Two Different Entities Diagnosed by WES in the Same Patient.

Published in:

BioMed Research International, 2022, p. 1, doi. 10.1155/2022/9096999

By:

Liu, Anlei;
Zhou, Lingli;
Zhu, Huadong;
Li, Yi;
Yang, Jing

Publication type:

Article

HEREDITARNA KOPROPORFIRIJA SA ASPEKTA KLINIČARA -- PRIKAZ SLUČAJA.

Published in:

Medical Review / Medicinski Pregled, 2013, v. 66, n. 9/10, p. 411, doi. 10.2298/MPNS1310411S

By:

SAVIĆ, Željka;
VRAČARIĆ, Vladimir;
HADNAÐEV, Ljiljana;
PETROVIĆ, Zora;
DAMJANOV, Dragomir

Publication type:

Article

Neuropathic pain in hereditary coproporphyria.

Published in:

Pakistan Journal of Medical Sciences, 2013, v. 29, n. 2, p. 672, doi. 10.12669/pjms.292.3202

By:

Guan-Liang Chen;
Deng-Ho Yang;
Jeng-Yuau Wu;
Chia-Wen Kuo;
Wen-Hsiu Hsu

Publication type:

Article

The nature of King James VI/I’s medical conditions: new approaches to the diagnosis.

Published in:

History of Psychiatry, 2012, v. 23, n. 3, p. 277, doi. 10.1177/0957154X11428413

By:

Peters, Timothy;
Garrard, Peter;
Ganesan, Vijeya;
Stephenson, John

Publication type:

Article

The enzyme engineering of mutant homodimer and heterodimer of coproporphyinogen oxidase contributes to new insight into hereditary coproporphyria and harderoporphyria.

Published in:

Journal of Biochemistry, 2013, v. 154, n. 6, p. 551, doi. 10.1093/jb/mvt086

By:

Kim, Dao Hoang Thien;
Hino, Ryoko;
Adachi, Yuka;
Kobori, Akio;
Taketani, Shigeru

Publication type:

Article

Increased Porphyrins in Primary Liver Cancer Mainly Reflect a Parallel Liver Disease.

Published in:

Gastroenterology Research & Practice, 2009, v. 2009, p. 1, doi. 10.1155/2009/402394

By:

Kaczynski, Jerzy;
Hansson, Göran;
Wallerstedt, Sven

Publication type:

Article

Update review of the acute porphyrias.

Published in:

British Journal of Haematology, 2017, v. 176, n. 4, p. 527, doi. 10.1111/bjh.14459

By:

Stein, Penelope E.;
Badminton, Michael N.;
Rees, David C.

Publication type:

Article

Digenic Inheritance of Mutations in the Coproporphyrinogen Oxidase and Protoporphyrinogen Oxidase Genes in a Unique Type of Porphyria.

Published in:

Journal of Investigative Dermatology, 2011, v. 131, n. 11, p. 2249, doi. 10.1038/jid.2011.186

By:

van Tuyll van Serooskerken, Anne Moniek;
de Rooij, Felix W;
Edixhoven, Annie;
Bladergroen, Reno S;
Baron, Jens M;
Joussen, Sylvia;
Merk, Hans F;
Steijlen, Peter M;
Poblete-Gutiérrez, Pamela;
te Velde, Kornelis;
Wilson, J H Paul;
Koole, Rita H;
van Geel, Michel;
Frank, Jorge

Publication type:

Article

A case of hereditary coproporphyria with posterior reversible encephalopathy and novel coproporphyrinogen oxidase gene mutation c.863T>G (p.Leu288Trp).

Published in:

2018

By:

Lambie, Deborah;
Florkowski, Chris;
Sies, Chris;
Raizis, Anthony;
Siu, Wai-Kwan;
Towns, Cindy

Publication type:

journal article

Establishing a network of specialist Porphyria centres - effects on diagnostic activities and services.

Published in:

Orphanet Journal of Rare Diseases, 2012, v. 7, n. 1, p. 1, doi. 10.1186/1750-1172-7-93

By:

Tollånes, Mette C.;
Aarsand, Aasne K.;
Villanger, Jørild Haugen;
Støle, Egil;
Deybach, Jean-Charles;
Marsden, Joanne;
To-Figueras, Jordi;
Sandberg, Sverre

Publication type:

Article