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Every story we pull is tagged to the disease it’s about — so you can filter to your condition and read only what matters.
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fasciitis like primary breast pyoderma gangrenosum a rare case report
Original title: “[Fasciitis-like primary breast pyoderma gangrenosum: A rare case report].”
exploring global cfdna fragmentomics as a biomarker in real world melanoma patients
Original title: “Exploring global cfDNA fragmentomics as a biomarker in real-world melanoma patients.”
management of adverse events in patients with pediatric low grade glioma treated with mapk directed therapies delphi consensus recommendations and unmet needs
Original title: “Management of adverse events in patients with pediatric low-grade glioma treated with MAPK-directed therapies: Delphi consensus recommendations and unmet needs.”
frontal cholesterol granuloma in a pediatric patient a case report
Original title: “Frontal Cholesterol Granuloma in a Pediatric Patient: A Case Report.”
In this episode of Denatured, Jennifer C. Smith-Parker speaks to Erik Digman Wiklund, CEO of Circio and Jacob Becraft, Co-founder and CEO of Strand Therapeutics. They discuss how post-COVID, emerging platforms like circular and logic circuit RNA are expanding the field's therapeutic horizons.
Original title: “Programmable RNA 2.0: Beyond the First mRNA Revolution”
epithelioid and spindle cell rhabdomyosarcoma of the rib with fus tfcp2 fusion a case report and literature review
Original title: “Epithelioid and spindle cell rhabdomyosarcoma of the rib with FUS-TFCP2 fusion: A case report and literature review.”
massive non functioning adrenocortical carcinoma presenting as acute abdomen without rupture a case report
Original title: “Massive non-functioning Adrenocortical carcinoma presenting as acute abdomen without rupture: A case report.”
Data-driven, patient-first: using insights in striving to transform cancer care
Original title: “Patient-centric oncology trials”
editing the skin in place in vivo genome correction of rare skin disease
Original title: “Editing the skin in place: In vivo genome correction of rare skin disease.”
long term ala pdt for giant extramammary paget s disease in a centenarian a 5 year case study with 58 sessions
Original title: “Long-term ALA-PDT for Giant Extramammary Paget's Disease in a Centenarian: A 5-Year Case Study with 58 Sessions.”
neurodegeneration in langerhans cell histiocytosis beyond a sequela
Original title: “Neurodegeneration in Langerhans Cell Histiocytosis: beyond a Sequela.”
genetic diagnosis of macrotia in pik3ca related overgrowth spectrum pros and long term outcome of otoplasty a case report and literature review
Original title: “Genetic diagnosis of macrotia in PIK3CA-Related Overgrowth Spectrum (PROS) and long-term outcome of otoplasty: a case report and literature review.”
activity of chemotherapy in mesenchymal chondrosarcoma a multicentre retrospective analysis within the italian sarcoma group network
Original title: “Activity of chemotherapy in mesenchymal chondrosarcoma: a multicentre retrospective analysis within the Italian Sarcoma Group network.”
mismatch repair deficiency and microsatellite instability in adrenocortical carcinoma
Original title: “Mismatch repair deficiency and microsatellite instability in adrenocortical carcinoma.”
shared pathogenic pathways between rem sleep behavior disorder and neurodegenerative and psychiatric disorders
Original title: “Shared Pathogenic Pathways Between REM Sleep Behavior Disorder and Neurodegenerative and Psychiatric Disorders.”
targeted deep sequencing identifies mosaicism in patients with immune dysregulation
Original title: “Targeted deep sequencing identifies mosaicism in patients with immune dysregulation.”
clinical characteristics and treatment outcomes of autoimmune like hepatitis after allogeneic hematopoietic stem cell transplantation
Original title: “Clinical characteristics and treatment outcomes of autoimmune-like hepatitis after allogeneic hematopoietic stem cell transplantation.”
single cell transcriptomic profiling of peripheral blood mononuclear cells reveals monocyte heterogeneity in patients with moyamoya disease
Original title: “Single-cell transcriptomic profiling of peripheral blood mononuclear cells reveals monocyte heterogeneity in patients with Moyamoya disease.”
patient experience of hereditary angioedema findings from a racially diverse sample of adult patients
Original title: “The patient experience of hereditary angioedema: findings from a racially diverse sample of adult patients.”
enamel renal syndrome due to fam20a mutations challenging kidney management in view of nephrocalcinosis hypophosphatemia and hypocalciuria
Original title: “Enamel renal syndrome due to FAM20A mutations: challenging kidney management in view of nephrocalcinosis, hypophosphatemia and hypocalciuria.”