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Exploration of treatment in childhood Langerhans cell histiocytosis based on inflammatory and malignant symptoms: a pilot study.

• Authors : Lin, Hui-ling¹ (AUTHOR); Zheng, Qing-qing¹ (AUTHOR); Huang, Ru-lin¹ (AUTHOR)

• Source: Orphanet Journal of Rare Diseases. 4/23/2024, Vol. 19 Issue 1, p1-9. 9p.

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Exploration of treatment in childhood Langerhans cell histiocytosis based on inflammatory and malignant symptoms: a pilot study

• Authors : Hui-ling Lin; Qing-qing Zheng; Ru-lin Huang

Subjects: Langerhans cell histiocytosis; Inflammatory; Malignant

• Source: Orphanet Journal of Rare Diseases, Vol 19, Iss 1, Pp 1-9 (2024)

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Birt-Hogg-Dubé syndrome encountered at rare lung disease clinic in Anhui province, China.

• Authors : Zhang, Guofeng^1,2 (AUTHOR); Liu, Jinli³ (AUTHOR); Wang, Yushuo^1,2 (AUTHOR)

• Source: Orphanet Journal of Rare Diseases. 5/16/2022, Vol. 17 Issue 1, p1-9. 9p.

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Multidisciplinary approach to screening and management of children with Fabry disease: practice at a Tertiary Children's Hospital in China.

• Authors : Shen, Qian¹ (AUTHOR); Liu, Jialu¹ (AUTHOR); Chen, Jing¹ (AUTHOR)

• Source: Orphanet Journal of Rare Diseases. 12/14/2021, Vol. 16 Issue 1, p1-9. 9p.

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Unusual sites of bone involvement in Langerhans cell histiocytosis: a systematic review of the literature.

• Authors : Reisi, Nahid¹ (AUTHOR) ; Raeissi, Pouran² (AUTHOR); Harati Khalilabad, Touraj³ (AUTHOR)

• Source: Orphanet Journal of Rare Diseases. 1/2/2021, Vol. 16 Issue 1, p1-13. 13p.

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Australian children living with rare diseases: experiences of diagnosis and perceived consequences of diagnostic delays.

• Authors : Zurynski, Yvonne^1,2 ; Deverell, Marie^1,2; Dalkeith, Troy^1,3

• Source: Orphanet Journal of Rare Diseases. 4/11/2017, Vol. 12, p1-9. 9p.

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Impulse oscillometry identifies peripheral airway dysfunction in children with adenosine deaminase deficiency.

• Authors : Komarow, Hirsh D.¹ ; Sokolic, Robert²; Hershfield, Michael S.³

• Source: Orphanet Journal of Rare Diseases. 12/18/2015, Vol. 10 Issue 1, p1-5. 5p.

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