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What's new in your rare disease | Kisho

Not rare diseases news,
news about your rare disease.

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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Research

A recent analysis of the ACCESS randomized trial reveals molecular pathways that enhance the efficacy of clarithromycin in treating community-acquired pneumonia. This study provides insights into the drug's mechanism, potentially guiding future therapeutic strategies.

molecular pathways driving clarithromycin benefit in community acquired pneumonia analysis of the access randomised trial

PubMed Rare Disease·7 months ago·Read at source →

Original title: “Molecular pathways driving clarithromycin benefit in community-acquired pneumonia: analysis of the ACCESS randomised trial.”

cancer esophageal cancerResearch

Dr. Marc Hedrick and Dr. Phil Kantoff discuss the transformative potential of alpha-emitting isotopes in cancer treatment during a recent podcast. They highlight breakthroughs in radiotherapeutics, positioning it as a significant frontier in biotech.

In this episode of Denatured, you'll listen to Dr. Marc Hedrick, President and CEO of Plus Therapeutics and Dr. Phil Kantoff, CEO & Co-founder of Convergent Therapeutics. They discuss breakthroughs like alpha-emitting isotopes, supply chain solutions and why radiotherapeutics is biotech's next big frontier.

BioSpace·7 months ago·Read at source →

Original title: “The Radiotherapeutics Moment: How Isotopes are Changing Cancer Treatment”

cystic fibrosis cystic fibrosis-gastritis-megaloblastic anemia syndromeResearch

A study confirms that elexacaftor/tezacaftor/ivacaftor safely reduces sino-nasal symptoms in cystic fibrosis patients after lung transplantation. This finding supports the drug's efficacy in managing post-transplant complications.

elexacaftor tezacaftor ivacaftor is safe and effectively reduces sino nasal symptoms in people with cystic fibrosis post lung transplantation

PubMed Rare Disease·7 months ago·Read at source →

Original title: “Elexacaftor/tezacaftor/ivacaftor is safe and effectively reduces sino-nasal symptoms in people with cystic fibrosis post lung transplantation.”

Research

Novel LIPC-related recessive form of postural proprioceptive deficits in Brown Swiss cattle.

PubMed Rare Disease·7 months ago·Read at source →

Research

Recent research highlights advancements in understanding neuromyelitis optica spectrum disorder (NMOSD), focusing on its pathophysiology and potential therapeutic targets. This study contributes to the growing body of knowledge aimed at improving treatment options for NMOSD patients.

neuromyelitis optica spectrum disorder

PubMed Rare Disease·7 months ago·Read at source →

Original title: “Neuromyelitis Optica Spectrum Disorder.”

staphylococcal necrotizing pneumoniaResearch

A retrospective analysis highlights the surgical management of necrotizing pneumonia in pediatric patients, providing insights into treatment outcomes at a third-level center. This study contributes to the understanding of surgical interventions for this severe condition.

surgical management of necrotizing pneumonia in pediatric patients a retrospective analysis in a third level center

PubMed Rare Disease·7 months ago·Read at source →

Original title: “Surgical Management of Necrotizing Pneumonia in Pediatric Patients. A Retrospective Analysis in a Third-Level Center.”

Research

Recent research highlights how chromatin remodeling in pericentral hepatocytes influences MASH through CYP450 activity. This study provides insights into the molecular mechanisms that could impact liver function and disease.

chromatin remodeling in pericentral hepatocytes modulates mash through cyp450 activity

PubMed Rare Disease·7 months ago·Read at source →

Original title: “Chromatin remodeling in pericentral hepatocytes modulates MASH through CYP450 activity.”

POEMS syndromeResearch

A recent study highlights the prognostic value of the neutrophil-to-lymphocyte ratio in patients with POEMS syndrome. This research could inform future clinical assessments and treatment strategies for this rare condition.

prognostic value of the neutrophil to lymphocyte ratio in poems syndrome

PubMed Rare Disease·7 months ago·Read at source →

Original title: “Prognostic value of the neutrophil-to-lymphocyte ratio in POEMS syndrome.”

inflammatory bowel disease inflammatory bowel disease 10+1 moreResearch

A study investigates the justification for ordering cytomegalovirus immunohistochemical stains in patients with severe inflammatory bowel disease and ulceration. The findings may influence diagnostic approaches in this patient population.

is it justified to order an upfront cytomegalovirus immunohistochemical stain in patients with severe inflammatory bowel disease and ulceration

PubMed Rare Disease·7 months ago·Read at source →

Original title: “Is It Justified to Order an Upfront Cytomegalovirus Immunohistochemical Stain in Patients with Severe Inflammatory Bowel Disease and Ulceration?”

Alport syndrome X-linked Alport syndromeResearch

A recent study published in PubMed outlines the epidemiological characteristics and treatment patterns of Alport syndrome in Korea. This research provides valuable insights into the disease's prevalence and management strategies within the region.

epidemiological characteristics and treatment patterns of alport syndrome in korea

PubMed Rare Disease·7 months ago·Read at source →

Original title: “Epidemiological characteristics and treatment patterns of Alport syndrome in Korea.”

oncocytic breast carcinoma parotid gland cancer+1 moreResearch

A case study published in PubMed highlights the use of (18)F-FDG PET/CT imaging in diagnosing progressive oncocytic carcinoma of the parotid gland. This research contributes to understanding imaging techniques in rare cancers.

18 f fdg pet ct in progressive oncocytic carcinoma of the parotid gland case study

PubMed Rare Disease·7 months ago·Read at source →

Original title: “(18)F-FDG PET/CT in Progressive Oncocytic Carcinoma of the Parotid Gland-Case Study.”

Research

Research highlights the potential of bone marrow organoids as innovative models for studying blood formation and failure. These organoids could advance understanding of hematological conditions and improve therapeutic strategies.

rise of bone marrow organoids as next generation models for blood formation and failure

PubMed Rare Disease·7 months ago·Read at source →

Original title: “The rise of bone marrow organoids as next-generation models for blood formation and failure.”

propionic acidemia PCCB-related propionic acidemia+1 moreResearch

A new study explores the use of antisense oligonucleotides to skip a pseudoexon in the PCCA gene, offering potential versatility in treating propionic acidemia. This research could pave the way for innovative therapeutic strategies for this rare metabolic disorder.

from n of 1 to versatility in propionic acidemia antisense oligonucleotide mediated skipping of a constitutive pcca pseudoexon

PubMed Rare Disease·7 months ago·Read at source →

Original title: “From N-of-1 to versatility in propionic acidemia: Antisense oligonucleotide-mediated skipping of a constitutive PCCA pseudoexon.”

Research

A recent publication discusses the current management strategies for cerebral venous thrombosis, highlighting the importance of timely diagnosis and treatment. The review emphasizes the evolving understanding of this condition and its implications for patient care.

current management of cerebral venous thrombosis

PubMed Rare Disease·7 months ago·Read at source →

Original title: “Current Management of Cerebral Venous Thrombosis.”

primary localized amyloidosis amyloidosisResearch

A case report details a decade-long progression of localized amyloidosis from the larynx to the nasal cavity, highlighting the disease's potential for significant anatomical impact. This study contributes to the understanding of amyloidosis and its clinical implications.

decade long progression of localized amyloidosis from the larynx to the nasal cavity a case report

PubMed Rare Disease·7 months ago·Read at source →

Original title: “Decade-Long Progression of Localized Amyloidosis from the Larynx to the Nasal Cavity-A Case Report.”

Research

A recent study published in PubMed investigates patient preferences and priorities in advanced Parkinson's disease using a discrete choice experiment. The findings aim to inform treatment decisions and improve patient-centered care.

exploring preferences and priorities in advanced parkinson s disease a discrete choice experiment

PubMed Rare Disease·7 months ago·Read at source →

Original title: “Exploring Preferences and Priorities in Advanced Parkinson's Disease: A Discrete Choice Experiment.”

Research

A French multicenter study investigates the incidence and risk factors of smoking post-lung transplantation. The findings contribute to understanding patient behaviors that may impact transplant outcomes.

smoking after lung transplantation incidence and risk factors in the french multicenter prospective tabatransplant cohort study

PubMed Rare Disease·7 months ago·Read at source →

Original title: “Smoking after lung transplantation: Incidence and risk factors in the French multicenter prospective tabatransplant cohort study.”

Research

Recent research highlights how genetic variation at the MECOM locus influences the pathogenesis of various human diseases. This discovery could pave the way for targeted therapies and better understanding of disease mechanisms.

genetic variation at the mecom locus shaping human disease pathogenesis

PubMed Rare Disease·7 months ago·Read at source →

Original title: “Genetic variation at the MECOM locus shaping human disease pathogenesis.”

herpes zoster geniculate herpes zosterResearch

A new study highlights segmental anhidrosis as a rare autonomic complication resulting from herpes zoster. This research adds to the understanding of the diverse manifestations of herpes zoster.

segmental anhidrosis secondary to herpes zoster a rare autonomic complication

PubMed Rare Disease·7 months ago·Read at source →

Original title: “Segmental Anhidrosis Secondary to Herpes Zoster: A Rare Autonomic Complication.”

osteoarthritis osteoarthritis, spine+1 moreResearch

Research identifies PIEZO1 gene variants that decrease open channel probability as linked to familial osteoarthritis. This discovery could inform future genetic studies and therapeutic approaches for the disease.

piezo1 variants that reduce open channel probability are associated with familial osteoarthritis

PubMed Rare Disease·7 months ago·Read at source →

Original title: “PIEZO1 variants that reduce open channel probability are associated with familial osteoarthritis.”

Previous381 / 488Next

Daily Briefings

Not rare diseases news,news about your rare disease.

Earlier

A recent analysis of the ACCESS randomized trial reveals molecular pathways that enhance the efficacy of clarithromycin in treating community-acquired pneumonia. This study provides insights into the drug's mechanism, potentially guiding future therapeutic strategies.

Dr. Marc Hedrick and Dr. Phil Kantoff discuss the transformative potential of alpha-emitting isotopes in cancer treatment during a recent podcast. They highlight breakthroughs in radiotherapeutics, positioning it as a significant frontier in biotech.

A study confirms that elexacaftor/tezacaftor/ivacaftor safely reduces sino-nasal symptoms in cystic fibrosis patients after lung transplantation. This finding supports the drug's efficacy in managing post-transplant complications.

Novel LIPC-related recessive form of postural proprioceptive deficits in Brown Swiss cattle.

Recent research highlights advancements in understanding neuromyelitis optica spectrum disorder (NMOSD), focusing on its pathophysiology and potential therapeutic targets. This study contributes to the growing body of knowledge aimed at improving treatment options for NMOSD patients.

A retrospective analysis highlights the surgical management of necrotizing pneumonia in pediatric patients, providing insights into treatment outcomes at a third-level center. This study contributes to the understanding of surgical interventions for this severe condition.

Recent research highlights how chromatin remodeling in pericentral hepatocytes influences MASH through CYP450 activity. This study provides insights into the molecular mechanisms that could impact liver function and disease.

A recent study highlights the prognostic value of the neutrophil-to-lymphocyte ratio in patients with POEMS syndrome. This research could inform future clinical assessments and treatment strategies for this rare condition.

A study investigates the justification for ordering cytomegalovirus immunohistochemical stains in patients with severe inflammatory bowel disease and ulceration. The findings may influence diagnostic approaches in this patient population.

A recent study published in PubMed outlines the epidemiological characteristics and treatment patterns of Alport syndrome in Korea. This research provides valuable insights into the disease's prevalence and management strategies within the region.

A case study published in PubMed highlights the use of (18)F-FDG PET/CT imaging in diagnosing progressive oncocytic carcinoma of the parotid gland. This research contributes to understanding imaging techniques in rare cancers.

Research highlights the potential of bone marrow organoids as innovative models for studying blood formation and failure. These organoids could advance understanding of hematological conditions and improve therapeutic strategies.

A new study explores the use of antisense oligonucleotides to skip a pseudoexon in the PCCA gene, offering potential versatility in treating propionic acidemia. This research could pave the way for innovative therapeutic strategies for this rare metabolic disorder.

A recent publication discusses the current management strategies for cerebral venous thrombosis, highlighting the importance of timely diagnosis and treatment. The review emphasizes the evolving understanding of this condition and its implications for patient care.

A case report details a decade-long progression of localized amyloidosis from the larynx to the nasal cavity, highlighting the disease's potential for significant anatomical impact. This study contributes to the understanding of amyloidosis and its clinical implications.

A recent study published in PubMed investigates patient preferences and priorities in advanced Parkinson's disease using a discrete choice experiment. The findings aim to inform treatment decisions and improve patient-centered care.

A French multicenter study investigates the incidence and risk factors of smoking post-lung transplantation. The findings contribute to understanding patient behaviors that may impact transplant outcomes.

Recent research highlights how genetic variation at the MECOM locus influences the pathogenesis of various human diseases. This discovery could pave the way for targeted therapies and better understanding of disease mechanisms.

A new study highlights segmental anhidrosis as a rare autonomic complication resulting from herpes zoster. This research adds to the understanding of the diverse manifestations of herpes zoster.

Research identifies PIEZO1 gene variants that decrease open channel probability as linked to familial osteoarthritis. This discovery could inform future genetic studies and therapeutic approaches for the disease.

Not rare diseases news,
news about your rare disease.