Phototherapy sequela in a child with congenital erythropoietic porphyria (letter)

Soylu A; Kavukcu S; Turkmen M

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Phototherapy sequela in a child with congenital erythropoietic porphyria (letter)

机译：先天性红细胞生成性卟啉症患儿的光疗后遗症（字母）

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来源
《European journal of pediatrics》 |1999年第6期|共2页
作者
Soylu A; Kavukcu S; Turkmen M;
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原文格式 PDF
正文语种 eng
中图分类儿科学;
关键词
Photosensitivity Disorders; Porphyria; Erythropoietic; Sunscreening Agents; 光过敏疾患; 卟啉病; 红细胞生成性;

机译：Photosensitivity Disorders;Porphyria;Erythropoietic;Sunscreening Agents;光过敏疾患;卟啉病;红细胞生成性;

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专利

1. Phototherapy sequela in a child with congenital erythropoietic porphyria (letter) [J] . Soylu A, Kavukcu S, Turkmen M European journal of pediatrics . 1999,第6期

机译：先天性红细胞生成性卟啉症患儿的光疗后遗症（字母）
2. Successful hematopoietic stem cell transplantation in a child with congenital erythropoietic porphyria due to a mutation in GATA-1 [J] . Karakurt Neslihan, Tavil Betul, Azik Fatih, Pediatric transplantation. . 2015,第7期

机译：由于GATA-1突变，先天性红细胞卟啉症患儿成功进行造血干细胞移植
3. Congenital erythropoietic porphyria and erythropoietic protoporphyria: Identification of 7 uroporphyrinogen III synthase and 20 ferrochelatase novel mutations [J] . Weiss Yedidyah, Balwani Manisha, Chen Brenden, Molecular genetics and metabolism . 2019,第3期

机译：先天性促红细胞生成斑岩和促红细胞生成卟啉区：鉴定7尿红素素III合成酶和20个铁切酶新突变
4. Recognition of Child Congenital Heart Disease using Electrocardiogram based on Residual of Residual Network [C] . Yunmei Du, Shuai Huang, Canhui Huang, International Conference on Progress in Informatics and Computing . 2020

机译：基于残余网络残余的心电图识别儿童先天性心脏病
5. A Descriptive, Cross-Sectional, Correlational Exploration of Perceived Stress, Quality of Life, and Family Functioning in Parents of a Child with Congenital Heart Disease: The Pinched Study [D] . Gregory, Mary. 2020

机译：对具有先天性心脏病的儿童父母的感知压力，生活质量和家族的描述性，横截面，相关性探索：挤压研究
6. Red Cells: Congenital erythropoietic porphyria due to a mutation in GATA1: the first trans-acting mutation causative for a human porphyria [O] . John D. Phillips, David P. Steensma, Michael A. Pulsipher, -1

机译：红细胞：由于GATA1突变而导致的先天性红细胞卟啉症：人类卟啉症的第一个反式突变
7. Erythropoietic Uroporphyria Associated with Myeloid Malignancy Is Likely Distinct from Autosomal Recessive Congenital Erythropoietic Porphyria [O] . Sarkany, Robert P. E., Ibbotson, Sally H., Whatley, Sharon D., 2011

机译：与常染色体隐性先天性促红细胞生成性卟啉症不同，与骨髓恶性肿瘤相关的促红细胞生成性尿卟啉症

Phototherapy sequela in a child with congenital erythropoietic porphyria (letter)

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