Nipah virus disease: A rare and intractable disease.

Banerjee S, Gupta N, Kodan P, Mittal A, Ray Y, Nischal N, Soneja M, Biswas A, Wig N

Intractable Rare Dis Res. 2019; 8(1):1-8.

DOI: 10.5582/irdr.2018.01130

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Management strategies in facioscapulohumeral muscular dystrophy.

Lu JR, Yao ZJ, Yang Y, Zhang C, Zhang J, Zhang Y

Intractable Rare Dis Res. 2019; 8(1):9-13.

DOI: 10.5582/irdr.2019.01016

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Novel missense mutation affecting the LIM-A domain of LMX1B in a family with Nail-Patella syndrome.

Claverie-Martin F, Trindade A, Garcia-Gonzalez NC, Callejon Callejon A

Intractable Rare Dis Res. 2019; 8(1):14-19.

DOI: 10.5582/irdr.2018.01131

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The expression of EpCAM in extramammary Paget's disease.

Yamada-Kanazawa S, Tasaki Y, Kajihara I, Sakamoto R, Maeda-Otsuka S, Ihn H

Intractable Rare Dis Res. 2019; 8(1):20-23.

DOI: 10.5582/irdr.2019.01010

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Propranolol and ascorbic acid in control of fibrodysplasia ossificans progressiva flare-ups due to accidental falls.

Palhares DB, Nascimento DR, Palhares MG, Balaniuc SLB, Giuliani LR, Xavier PCN, Brum JMG, Alves F, Vieira FO, Souza-Fagundes EM, Underwood A, Milsted A, Santos RAS, Martins AS

Intractable Rare Dis Res. 2019; 8(1):24-28.

DOI: 10.5582/irdr.2018.01095

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Retroperitoneal fibrosis associated with orbital pseudotumor without evidence of IgG4: A case report with review of literature.

Pérez-Sanz MT, Cervilla-Muñoz E, Alonso-Muñoz J, Marcelo-Ayala A, Pulfer MD, Galeano-Valle F

Intractable Rare Dis Res. 2019; 8(1):29-35.

DOI: 10.5582/irdr.2018.01075

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Hydatid cyst of gall bladder masquerading as carcinoma: A rare case report with review of literature.

Jain G, Kumar C, Meena P, Singh AR, Kumar V, Kumar S, Tanwar P

Intractable Rare Dis Res. 2019; 8(1):36-42.

DOI: 10.5582/irdr.2018.01097

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Guillain-Barré syndrome in a patient of acute Hepatitis E virus infection associated with genotype 1: Case report and literature review.

Choudhary MC, Bajpai V, Anand L, Gupta E

Intractable Rare Dis Res. 2019; 8(1):43-47.

DOI: 10.5582/irdr.2018.01099

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West Nile virus encephalitis in a young immunocompetent female in Omaha Nebraska.

Latif A, Kapoor V, Simmons E, Parekh J, Andukuri V

Intractable Rare Dis Res. 2019; 8(1):48-51.

DOI: 10.5582/irdr.2018.01108

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Leber's hereditary optic neuropathy: Severe vascular pathology in a severe primary mutation.

Asanad S, Meer E, Tian JJ, Fantini M, Nassisi M, Sadun AA

Intractable Rare Dis Res. 2019; 8(1):52-55.

DOI: 10.5582/irdr.2018.01126

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Anesthesia management of arthroscopic ankle arthrodesis for a hemophilia patient after living-donor liver transplantation.

Shibata R, Orii R, Ako R

Intractable Rare Dis Res. 2019; 8(1):56-59.

DOI: 10.5582/irdr.2018.01127

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Budd-Chiari Syndrome in Behçet's Disease successfully managed with immunosuppressive and anticoagulant therapy: A case report and literature review.

Oblitas CM, Galeano-Valle F, Toledo-Samaniego N, Pinilla-Llorente B, Del Toro-Cervera J, Álvarez-Luque A, García-García A, Demelo-Rodriguez P

Intractable Rare Dis Res. 2019; 8(1):60-66.

DOI: 10.5582/irdr.2018.01128

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A novel mutation in CACNA1A gene in a Saudi female with episodic ataxia type 2 with no response to acetazolamide or 4-aminopyridine.

Algahtani H, Shirah B, Algahtani R, Al-Qahtani MH, Abdulkareem AA, Naseer MI

Intractable Rare Dis Res. 2019; 8(1):67-71.

DOI: 10.5582/irdr.2018.01133

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Partial trisomy 9 (9pter->9q22.1) and partial monosomy 14 (14pter- >14q11.2) due to paternal translocation t(9;14)(q22.1;q11.2) in a case of Dysmorphic features.

Dhangar S, Korgaonkar S, Vundinti BR

Intractable Rare Dis Res. 2019; 8(1):72-77.

DOI: 10.5582/irdr.2019.01000

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Network established to collaborate on diagnosis and treatment of rare diseases in China: A strategic alliance backed by tiered healthcare is the key to the future.

Ren QL, Wang JB

Intractable Rare Dis Res. 2019; 8(1):78-79.

DOI: 10.5582/irdr.2019.01024

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