A basic understanding of mucopolysaccharidosis: Incidence, clinical features, diagnosis, and management

Zhou J, Lin J, Leung WT, Wang L

Intractable Rare Dis Res. 2020; 9(1):1-9.

DOI: 10.5582/irdr.2020.01011

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Advances in stem cell therapy for the treatment of Peyronie's disease

Moussa M, Abou Chakra M, Moussa Y

Intractable Rare Dis Res. 2020; 9(1):10-13.

DOI: 10.5582/irdr.2019.01130

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Comprehensive bioinformatic analysis of Wnt1 and Wnt1-associated diseases

Peng C, Lu Y, Ren X, Wang Y, Zhang S, Chen M, Liu J, Fang F, Li T, Han J

Intractable Rare Dis Res. 2020; 9(1):14-22.

DOI: 10.5582/irdr.2020.01018

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TXNDC5 protects synovial fibroblasts of rheumatoid arthritis from the detrimental effects of endoplasmic reticulum stress

Lu Q, Wang J, Zhang X, Tian R, Qiao L, Ge L, Pan J, Wang L

Intractable Rare Dis Res. 2020; 9(1):23-29.

DOI: 10.5582/irdr.2019.01139

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Identification and clinical implications of a novel pathogenic variant in the GJB2 gene causes autosomal recessive non-syndromic hearing loss in a consanguineous Iranian family

Koohiyan M

Intractable Rare Dis Res. 2020; 9(1):30-34.

DOI: 10.5582/irdr.2019.01112

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Health assessment of patients with achondroplasia, pseudoachondroplasia, and rickets based on 3D non-linear diagnostics

Zhang J, Lu Y, Wang Y, Li T, Peng C, Zhang S, Gao Q, Liu W, Liu C, Han J

Intractable Rare Dis Res. 2020; 9(1):35-39.

DOI: 10.5582/irdr.2020.01019

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Replication study of four keloid-associated polymorphisms in patients of European descent - a single centre study

Dmytrzak A, Boroń A, Łoniewska B, Clark JSC, Kaczmarczyk M, Ciechanowicz A

Intractable Rare Dis Res. 2020; 9(1):40-42.

DOI: 10.5582/irdr.2020.01013

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Minor blood group incompatibility due to blood groups other than Rh(D) leading to hemolytic disease of fetus and newborn: a need for routine antibody screening during pregnancy

Agrawal A, Hussain KS, Kumar A

Intractable Rare Dis Res. 2020; 9(1):43-47.

DOI: 10.5582/irdr.2019.01094

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Characterization of a novel pathogenic variation c.1237T>G in the FZD4 gene presenting new inheritance from an Iranian individual suffering vitreoretinopathy

Zamani M, Shariati G, Seifi T, Sedaghat A, Galehdari H

Intractable Rare Dis Res. 2020; 9(1):48-53.

DOI: 10.5582/irdr.2019.01109

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Nitrous oxide recreational abuse presenting with myeloneuropathy and mimicking Guillain-Barre syndrome

Algahtani H, Shirah B, Abdelghaffar N, Abuhawi O, Alqahtani A

Intractable Rare Dis Res. 2020; 9(1):54-57.

DOI: 10.5582/irdr.2020.01007

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High prevalence of congenital generalized lipodystrophy in Piura, Peru

Purizaca-Rosillo N, Benites-Cóndor Y, Abarca H, Del Águila C, Chávez M, Franco L, Olea R, Rejas J, Martinez L, Chavesta F, Gamarra J, Arámbulo S, Ávila A

Intractable Rare Dis Res. 2020; 9(1):58-60.

DOI: 10.5582/irdr.2020.01004

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Multiphasic acute disseminated encephalomyelitis and differential with early onset multiple sclerosis

Stokes Brackett AC, Hernández-Fustes OJ, Arteaga Rodríguez C, Hernandez Fustes OJ

Intractable Rare Dis Res. 2020; 9(1):61-63.

DOI: 10.5582/irdr.2020.01009

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