المؤلفون: Zheng, G. Y., Chu, G. M., Li, P. P., He, R.^{Aff1, IDs40618023020208_cor4}

المصدر: Journal of Endocrinological Investigation: Official Journal of Italian Society of Endocrinology (SIE). 46(8):1613-1622

المؤلفون: Zheng, Wanqi, Duan, Ying, Xia, Yu, Liang, Lili, Gong, Zhuwen, Wang, Ruifang, Lu, Deyun, Zhang, Kaichuang, Yang, Yi, Sun, Yuning, Zhang, Huiwen, Han, Lianshu, Gong, Zizhen, Xiao, Bing^{Aff1, IDs1302302302737y_cor14}, Qiu, Wenjuan^{Aff1, IDs1302302302737y_cor15}

المصدر: Orphanet Journal of Rare Diseases. 18(1)

المؤلفون: Wanqi Zheng, Ying Duan, Yu Xia, Lili Liang, Zhuwen Gong, Ruifang Wang, Deyun Lu, Kaichuang Zhang, Yi Yang, Yuning Sun, Huiwen Zhang, Lianshu Han, Zizhen Gong, Bing Xiao, Wenjuan Qiu

المصدر: Orphanet Journal of Rare Diseases, Vol 18, Iss 1, Pp 1-14 (2023)

مصطلحات موضوعية: Adrenal hypoplasia congenita, Hypogonadotropic hypogonadism, DAX1, NR0B1, Children, Variant, Medicine

وصف الملف: electronic resource

Relation: https://doaj.org/toc/1750-1172

URL الوصول: https://doaj.org/article/f9707ff88ac3441c84a4bef5ede3aeb3

المؤلفون: Bravo Nieto Daniel, García Fernández Alba S., Diaz Troyano Noelia, Giralt Arnaiz Marina, Arias García Andrea, Fernández Álvarez Paula, Campos Martorell Ariadna, Ferrer Costa Roser, Clemente León María

المصدر: Advances in Laboratory Medicine, Vol 4, Iss 2, Pp 199-202 (2023)

مصطلحات موضوعية: hipoplasia adrenal congénita, insuficiencia suprarrenal, nr0b1, Medical technology, R855-855.5

وصف الملف: electronic resource

Relation: https://doaj.org/toc/2628-491X

URL الوصول: https://doaj.org/article/6a2bdaace9d84b4085940e41dd341934

المؤلفون: Bravo Nieto Daniel, García Fernández Alba S., Díaz Troyano Noelia, Arnaiz Marina Giralt, Arias García Andrea, Fernández Álvarez Paula, Campos Martorell Ariadna, Ferrer Costa Roser, Clemente León María

المصدر: Advances in Laboratory Medicine, Vol 4, Iss 2, Pp 195-198 (2023)

مصطلحات موضوعية: adrenal insufficiency, congenital adrenal hypoplasia, nr0b1, Medical technology, R855-855.5

وصف الملف: electronic resource

Relation: https://doaj.org/toc/2628-491X

URL الوصول: https://doaj.org/article/9e0413265b3141d0a1d7f37f6abfa7df

المؤلفون: Yuqing Jiang, Huifang Peng, Rui Zhao, Yina Chang, Jie Liu, Liujun Fu, Liping Li, Yujin Ma, Wei Li, Hongwei Jiang

المصدر: Molecular Genetics & Genomic Medicine, Vol 11, Iss 6, Pp n/a-n/a (2023)

مصطلحات موضوعية: CT image change of adrenal, infertility issue, minigene, NR0B1 (nuclear receptor subfamily 0 group B member 1), splice‐site variant, X‐linked AHC, Genetics, QH426-470

وصف الملف: electronic resource

Relation: https://doaj.org/toc/2324-9269

URL الوصول: https://doaj.org/article/776f5eb26a8d4605991c172afafc022a

المؤلفون: Gupta, Priyanka, Sharma, Rajni, Jain, Vandana^{Aff2, IDs12098021040552_cor3}

المصدر: Indian Journal of Pediatrics. 89(6):587-590

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المؤلفون: Xiaohui Tao, Tian Xu, Li Liu, Xiaoyun Lin, Zhenlin Zhang, Hua Yue

المصدر: Frontiers in Endocrinology, Vol 13 (2022)

مصطلحات موضوعية: secondary osteoporosis, X-linked congenital adrenocortical hypoplasia, gene mutation, NR0B1 gene, efficacy of treatment, Diseases of the endocrine glands. Clinical endocrinology, RC648-665

وصف الملف: electronic resource

Relation: https://www.frontiersin.org/articles/10.3389/fendo.2022.961322/full; https://doaj.org/toc/1664-2392

URL الوصول: https://doaj.org/article/0340e5bacdf448bc89d9d05bc1fb9f64