An update on China's national policies regarding rare diseases

Ying ZY, Gong L, Li CY

Intractable Rare Dis Res. 2021; 10(3):148-153.

DOI: 10.5582/irdr.2021.01027

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Immunopathogenic mechanisms of rheumatoid arthritis and the use of anti-inflammatory drugs

Zhang L, Zhang YH, Pan JH

Intractable Rare Dis Res. 2021; 10(3):154-164.

DOI: 10.5582/irdr.2021.01022

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Integrative overview of IFITMs family based on Bioinformatics analysis

Liu P, Zhang Y, Zhang S, Peng C, Yang W, Li X, Zhang C, Li M, Han J, Lu Y

Intractable Rare Dis Res. 2021; 10(3):165-172.

DOI: 10.5582/irdr.2021.01041

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Myoblast differentiation of C2C12 cell may related with oxidative stress

Li X, Zhang S, Zhang Y, Liu P, Li M, Lu Y, Han J

Intractable Rare Dis Res. 2021; 10(3):173-178.

DOI: 10.5582/irdr.2021.01058

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Rare and intractable fibrodysplasia ossificans progressiva shows different PBMC phenotype possibly modulated by ascorbic acid and propranolol treatment

Nascimento DR, Balaniuc SLB, Palhares DB, Underwood A, Palhares MG, Alves F, Vieira FO, Souza-Fagundes EM,Giuliani LDR, Xavier PCN, Del Puerto HL, Santos RAS, Milsted A, Brum JM, Silva IS, Martins AS

Intractable Rare Dis Res. 2021; 10(3):179-189.

DOI: 10.5582/irdr.2021.01012

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The usage of enzyme replacement treatments, economic burden, and quality of life of patients with four lysosomal storage diseases in Shanghai, China

Hu JH, Zhu L, He JJ, Li DG, Kang Q, Jin CL

Intractable Rare Dis Res. 2021; 10(3):190-197.

DOI: 10.5582/irdr.2021.01091

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One-year follow-up of thyroid function in 23 infants with Prader- Willi syndrome at a single center in China

Yang M, Ye J, Han LS, Qiu WJ, Yu YG, Gu XF, Zhang HW

Intractable Rare Dis Res. 2021; 10(3):198-201.

DOI: 10.5582/irdr.2021.01055

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The coincidence of two ultra-rare hereditary eye diseases: gyrate atrophy and Kjer optic atrophy - a surprising diagnosis based on next-generation sequencing

Skorczyk-Werner A, Raczynska D, Wawrocka A, Zholdybayeva D, Yakhiyayeva N, Krawczynski MR

Intractable Rare Dis Res. 2021; 10(3):202-206.

DOI: 10.5582/irdr.2021.01042

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Familial SDHB gene mutation in disseminated non-hypoxiarelated malignant paraganglioma treated with [⁹⁰Y]Y/[¹⁷⁷Lu]Lu- DOTATATE

Łoń I, Kunikowska J, Jędrusik P, Góra J, Toutounchi S, Placha P, Gaciong Z

Intractable Rare Dis Res. 2021; 10(3):207-213.

DOI: 10.5582/irdr.2021.01047

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Mediastinal lymph node metastasis as a single expression of disease relapse in Ewing's sarcoma: multidisciplinary approach of two consecutive cases

Gallina FT, Ferraresi V, Annovazzi A, Vari S, Visca P,Forcella D, Assisi D, Melis E, Facciolo F

Intractable Rare Dis Res. 2021; 10(3):214-219.

DOI: 10.5582/irdr.2021.01063

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Mild congenital myopathy due to a novel variation in SPEG gene

Yildirim M, Balasar O, Kose E, Dogan MT

Intractable Rare Dis Res. 2021; 10(3):220-222.

DOI: 10.5582/irdr.2021.01034

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