Global frailty screening tools: Review and application of frailty screening tools from 2001 to 2023

Deng Y, Sato N

Intractable Rare Dis Res. 2024; 13(1):1-11.

DOI: 10.5582/irdr.2023.01113

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The use of artificial intelligence in the treatment of rare diseases: A scoping review

He D, Wang R, Xu ZL, Wang JN, Song PP, Wang HY, Su JY

Intractable Rare Dis Res. 2024; 13(1):12-22.

DOI: 10.5582/irdr.2023.01111

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Situs viscerum inversus and abdominal aortic aneurysm: A systematic review of a rare association

Ossola P, Mascioli F, Luzzi AP, Epis L, Coletta D

Intractable Rare Dis Res. 2024; 13(1):23-28.

DOI: 10.5582/irdr.2023.01081

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Systematic analysis and evaluation of chromosome aberrations in major birth defects associated with infertility

Lan FY, Chen ZZ, Lin XL

Intractable Rare Dis Res. 2024; 13(1):29-35.

DOI: 10.5582/irdr.2023.01100

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Haploinsufficiency of NKX2-1 is likely to contribute to developmental delay involving 14q13 microdeletions

Machida O, Sakamoto H, Shimojima Yamamoto K, Hasegawa Y, Nii S, Okada H, Nishikawa K, Sumimoto S, Nishi E, Okamoto N, Yamamoto T

Intractable Rare Dis Res. 2024; 13(1):36-41.

DOI: 10.5582/irdr.2023.01119

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Role of IFITM2 in osteogenic differentiation of C3H10T1/2 mesenchymal stem cells

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

Intractable Rare Dis Res. 2024; 13(1):42-50.

DOI: 10.5582/irdr.2023.01108

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Surgical outcomes of locally advanced gastrointestinal stromal tumors after multivisceral resection: A retrospective study of 64 patients at a single institution

Qiu H, Wang Z, Liu BN, Sun RZ, Tian XY, Hao CY

Intractable Rare Dis Res. 2024; 13(1):51-56.

DOI: 10.5582/irdr.2023.01112

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Emotional journey of patients with specified intractable diseases in Japan

Tanaka H, Shimaoka M

Intractable Rare Dis Res. 2024; 13(1):57-62.

DOI: 10.5582/irdr.2023.01115

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Clinical features of extrahepatic portal vein obstruction: Myeloproliferative neoplasms eliminate hypersplenic hematologic changes in extrahepatic portal vein obstruction

Shimizu T, Yoshida H, Taniai N, Yoshioka M, Kawano Y, Matsushita A, Ueda J, Iwai T, Murokawa T, Ono T, Hamaguchi A

Intractable Rare Dis Res. 2024; 13(1):63-68.

DOI: 10.5582/irdr.2023.01106

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Wiskott-Aldrich syndrome: A new synonym mutation in the WAS gene

Sun YX, Song XM, Pan H, Li XX, Sun LR, Song L, Ma F, Hao JN

Intractable Rare Dis Res. 2024; 13(1):69-72.

DOI: 10.5582/irdr.2023.01102

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