Bi-allelic variants in INTS11 are associated with a complex neurological disorder.

SPTSSA variants alter sphingolipid synthesis and cause a complex hereditary spastic paraplegia.

Participation in a national diagnostic research study: assessing the patient experience.

A concurrent dual analysis of genomic data augments diagnoses: Experiences of 2 clinical sites in the Undiagnosed Diseases Network.

Potential of siRNA-Bearing Subtilosomes in the Treatment of Diethylnitrosamine-Induced Hepatocellular Carcinoma.

Bi-allelic ATG4D variants are associated with a neurodevelopmental disorder characterized by speech and motor impairment.

Innovations in the synthesis of graphene nanostructures for bio and gas sensors.

Continuing a search for a diagnosis: the impact of adolescence and family dynamics.

Amphotericin B Nano-Assemblies Circumvent Intrinsic Toxicity and Ensure Superior Protection in Experimental Visceral Leishmaniasis with Feeble Toxic Manifestation.

A pilot study of olfactory function in veterans with a history of deployment-related mild traumatic brain injury.

Corrigendum to "Exploring new immunological insight on SP15 (∟14 kDa) family protein in saliva of Indian sand-fly (Phlebotomus argentipes) in experimental visceral leishmaniasis". [Cellular Immunology 332 (2018) 51-57].

Efficient Photocatalytic Dye Degradation and Bacterial Inactivation by Graphitic Carbon Nitride and Starch-Doped Magnesium Hydroxide Nanostructures.

Deciphering the role of precursor miR-12136 and miR-8485 in the progression of intellectual disability (ID).

Endocannabinoid dysfunction in neurological disease: neuro-ocular DAGLA-related syndrome.

Gain-of-function mutations in ALPK1 cause an NF-ÎşB-mediated autoinflammatory disease: functional assessment, clinical phenotyping and disease course of patients with ROSAH syndrome.