Kisho is an information platform, not a medical provider. Nothing on this site constitutes medical advice, diagnosis, or treatment recommendations. All content is aggregated from publicly available sources (including ClinicalTrials.gov, PubMed, FDA.gov, and Orphanet) and is provided for informational purposes only. Clinical trial eligibility, treatment decisions, and any health-related actions should always be discussed with a qualified healthcare professional. Kisho does not endorse any specific therapy, organization, or clinical trial. Terms of use · Privacy policy
Every story we pull is tagged to the disease it’s about — so you can filter to your condition and read only what matters.
20 earlier
targeting type i interferon in lupus panniculitis a case based systematic literature review
Original title: “Targeting type I interferon in lupus panniculitis: a case-based systematic literature review.”
changing aetiology of perforated peptic ulcers rising impact of non steroidal anti inflammatories in western australia
Original title: “Changing Aetiology of Perforated Peptic Ulcers: Rising Impact of Non-Steroidal-Anti-Inflammatories in Western Australia.”
gnb1 related neurodevelopmental disorder due to a pathogenic exon 6 variant nm 002074 5 c239t a p ile80asn inherited from an asymptomatic father with mosaicism
Original title: “GNB1-related neurodevelopmental disorder due to a pathogenic exon 6 variant NM_002074.5:c239T>A (p.Ile80Asn) inherited from an asymptomatic father with mosaicism.”
interpretable fine tuned large language models facilitate making genetic test decisions for rare diseases
Original title: “Interpretable fine-tuned large language models facilitate making genetic test decisions for rare diseases.”
review of the microbial spectrum of mixed respiratory fungal infections
Original title: “Review of the Microbial Spectrum of Mixed Respiratory Fungal Infections.”
futility in adenosquamous pancreatic cancer
Original title: “Futility in adenosquamous pancreatic cancer.”
genetic linkage for bipolar disorder to the distal region of chromosome 19q a large family whole genome sequencing study
Original title: “Genetic Linkage for Bipolar Disorder to the Distal Region of Chromosome 19q: A Large Family Whole Genome Sequencing Study.”
collaboration as a catalyst for advancing rare disease research the experience of the rare diseases clinical research network
Original title: “Collaboration as a Catalyst for Advancing Rare Disease Research: The Experience of the Rare Diseases Clinical Research Network.”
new hope with car t cell therapy for refractory idiopathic inflammatory myopathies a systematic review
Original title: “A new hope with CAR T-cell therapy for refractory idiopathic inflammatory myopathies: a systematic review.”
rare type 1 collagen variants in early onset bicuspid aortic valve disease clinical and genetic overlap with ehlers danlos syndrome and osteogenesis imperfecta
Original title: “Rare Type 1 Collagen Variants in Early-Onset Bicuspid Aortic Valve Disease: Clinical and Genetic Overlap with Ehlers-Danlos Syndrome and Osteogenesis Imperfecta.”
novel frameshift variant in sorl1 gene identified in a eoad family causes app sorting dysfunction and endolysosomal swelling
Original title: “Novel Frameshift Variant in SORL1 Gene Identified in a EOAD Family Causes APP Sorting Dysfunction and Endolysosomal Swelling.”
high dose l serine supplementation during febrile decompensation in sars1 deficiency a case report and review of the literature
Original title: “High-Dose L-Serine Supplementation During Febrile Decompensation in SARS1 Deficiency: A Case Report and Review of the Literature.”
further delineation of the phenotype and genotype in a newly identified pan2 related disorder
Original title: “Further delineation of the phenotype and genotype in a newly identified PAN2-related disorder.”
chainsaw culture cladophialophora bantiana cerebral abscess after chainsaw activity in an immunocompetent host illustrative case
Original title: “Chainsaw culture: Cladophialophora bantiana cerebral abscess after chainsaw activity in an immunocompetent host. Illustrative case.”
safety pharmacokinetics and efficacy of 1 5 ruxolitinib gel hdm3010 in adult patients with prurigo nodularis a phase i ii randomized double blind vehicle controlled multicenter clinical trial
Original title: “Safety, Pharmacokinetics, and Efficacy of 1.5% Ruxolitinib Gel (HDM3010) in Adult Patients with Prurigo Nodularis: A Phase I/II, Randomized, Double-Blind, Vehicle-Controlled Multicenter Clinical Trial.”
primary hepatic neuroendocrine tumor with multifocal liver involvement a case report and review of the literature
Original title: “Primary hepatic neuroendocrine tumor with multifocal liver involvement: A case report and review of the literature.”
rethinking the sphenoparietal sinus implications for lesser sphenoid wing dural arteriovenous fistulas illustrative cases
Original title: “Rethinking the sphenoparietal sinus: implications for lesser sphenoid wing dural arteriovenous fistulas. Illustrative cases.”
two rare cases of fet creb epithelioid mesenchymal tumors displaying atypical immunophenotype myoepithelial like unraveled on next generation sequencing
Original title: “Two rare cases of FET::CREB epithelioid mesenchymal tumors, displaying atypical immunophenotype (myoepithelial-like), unraveled on next-generation sequencing.”
synchronous tumor to tumor metastasis of breast carcinoma to intracranial meningioma illustrative case
Original title: “Synchronous tumor-to-tumor metastasis of breast carcinoma to intracranial meningioma: illustrative case.”
decoding spatial transcriptomics across multicellular and subcellular resolutions
Original title: “Decoding spatial transcriptomics across multicellular and subcellular resolutions.”