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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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glioblastoma adult glioblastoma+1 moreResearch

Recent research highlights the development of magneto-NIR-II-programmed cascade nanozymes that facilitate blood-brain barrier translocation and enhance autophagic resistance in glioblastoma. This innovative approach could pave the way for more effective treatments targeting this aggressive brain tumor.

magneto nir ii programmed cascade nanozymes unlocking blood brain barrier translocation and autophagic resistance in glioblastoma

PubMed Rare Disease·3 months ago·Read at source →

Original title: “Magneto-NIR-II-Programmed Cascade Nanozymes Unlocking Blood-Brain Barrier Translocation and Autophagic Resistance in Glioblastoma.”

Research

A study published in PubMed examines the species composition and seasonal variation of medically important mosquitoes in Bajaur, Khyber Pakhtunkhwa, Pakistan. This research contributes to understanding vector dynamics that may impact disease transmission.

species composition relative abundance and seasonal variation of medically important mosquitoes in district bajaur khyber pakhtunkhwa pakistan

PubMed Rare Disease·3 months ago·Read at source →

Original title: “Species composition, relative abundance and seasonal variation of medically important mosquitoes in district Bajaur, Khyber Pakhtunkhwa, Pakistan.”

autosomal recessive juvenile Parkinson disease 2 juvenile onset Parkinson disease 19AResearch

A recent study highlights the significant symptom burden and treatment challenges faced by patients with juvenile Parkinson's disease. The findings underscore the need for targeted research and improved therapeutic strategies for this rare condition.

juvenile parkinson s disease symptom burden and treatment challenges

PubMed Rare Disease·3 months ago·Read at source →

Original title: “Juvenile Parkinson's disease: Symptom burden and treatment challenges.”

Moyamoya disease moyamoya disease 7+1 moreResearch

A study investigates the influence of the VEGFA rs2010963 variant on the severity of bilaterality and posterior artery stenosis in moyamoya disease patients. This research could enhance understanding of genetic factors in disease progression.

impact of vegfa rs2010963 on bilaterality and posterior artery stenosis in patients with moyamoya disease

PubMed Rare Disease·3 months ago·Read at source →

Original title: “The Impact of VEGFA rs2010963 on Bilaterality and Posterior Artery Stenosis in Patients with Moyamoya Disease.”

Research

A comprehensive review highlights safety considerations in blepharoplasty, emphasizing the need for careful patient selection and surgical technique to minimize complications. This study provides valuable insights for practitioners involved in cosmetic and reconstructive surgery.

safety considerations in blepharoplasty a comprehensive review

PubMed Rare Disease·3 months ago·Read at source →

Original title: “Safety Considerations in Blepharoplasty: A Comprehensive Review.”

osteonecrosis osteonecrosis of genetic origin+1 moreResearch

A case report suggests a potential link between COVID-19 and Kienböck's disease, a rare form of osteonecrosis. This finding may prompt further investigation into the long-term effects of COVID-19 on bone health.

rare osteonecrosis kienb ck s disease potentially linked to covid 19 a case report

PubMed Rare Disease·3 months ago·Read at source →

Original title: “A rare osteonecrosis Kienböck's disease potentially linked to COVID-19: a case report.”

acquired aneurysmal subarachnoid hemorrhageResearch

A recent study published in PubMed examines the morbidity and mortality associated with pediatric endovascularly treated aneurysmal subarachnoid hemorrhage over a twenty-year period. The findings contribute valuable insights into the long-term outcomes of this rare condition in children.

pediatric endovascularly treated aneurysmal subarachnoid hemorrhage a twenty year national inpatient sample study of morbidity and mortality

PubMed Rare Disease·3 months ago·Read at source →

Original title: “Pediatric Endovascularly Treated Aneurysmal Subarachnoid Hemorrhage: A Twenty-Year National Inpatient Sample Study of Morbidity and Mortality.”

myasthenia gravis transient neonatal myasthenia gravisResearch

A nationwide cohort study in South Korea reveals the rate of autoimmune diseases in the decade before a myasthenia gravis diagnosis. This research provides insights into potential comorbidities that may influence patient management.

rate of autoimmune diseases in the 10 years preceding myasthenia gravis diagnosis a nationwide cohort study in south korea

PubMed Rare Disease·3 months ago·Read at source →

Original title: “Rate of Autoimmune Diseases in the 10 Years Preceding Myasthenia Gravis Diagnosis: A Nationwide Cohort Study in South Korea.”

gallbladder pleomorphic giant cell adenocarcinoma prostate cancer+1 moreResearch

A study published in PubMed highlights the treatment of pleomorphic giant cell carcinoma of the prostate using Lutetium-177 PSMA. This research contributes to the understanding of targeted therapies for rare prostate cancer variants.

pleomorphic giant cell carcinoma of the prostate treated with lutetium 177 psma

PubMed Rare Disease·3 months ago·Read at source →

Original title: “Pleomorphic Giant Cell Carcinoma of the Prostate Treated With Lutetium-177 PSMA.”

Research

A study provides empirical evidence of a trade-off between reproduction and tumor dynamics in the freshwater cnidarian Hydra oligactis. This research could have implications for understanding cancer biology and regenerative processes.

empirical evidence for a trade off between reproduction and tumour dynamics in the freshwater cnidarian hydra oligactis

PubMed Rare Disease·3 months ago·Read at source →

Original title: “Empirical evidence for a trade-off between reproduction and tumour dynamics in the freshwater cnidarian Hydra oligactis.”

cancer esophageal cancerResearch

A new study demonstrates that integrative cfDNA profiling from low-pass whole-genome sequencing can accurately predict the tissue of origin in cancer. This advancement could enhance diagnostic precision and personalized treatment strategies.

integrative cfdna profiling from low pass whole genome sequencing enables tissue of origin prediction in cancer

PubMed Rare Disease·3 months ago·Read at source →

Original title: “Integrative cfDNA profiling from low-pass whole-genome sequencing enables tissue-of-origin prediction in cancer.”

group B streptococcal infectionResearch

The European Society for Pediatric Infectious Diseases has released guidelines for managing invasive Group A Streptococcal infections in children. These guidelines aim to standardize treatment approaches and improve outcomes for affected pediatric patients.

management of invasive group a streptococcal four infections in children the european society for pediatric infectious disease guidelines

PubMed Rare Disease·3 months ago·Read at source →

Original title: “Management of Invasive Group A Streptococcal Four Infections in Children: The European Society for Pediatric Infectious Disease Guidelines.”

Research

A recent study highlights pediatric hematuria as a critical indicator for initiating family genetic investigations in type IV collagen nephropathies. This research emphasizes the importance of early detection and genetic screening in managing these rare kidney disorders.

pediatric hematuria as a gateway to family genetic investigation in type iv collagen nephropathies experience from a regional cohort

PubMed Rare Disease·3 months ago·Read at source →

Original title: “Pediatric hematuria as a gateway to family genetic investigation in type IV collagen nephropathies: experience from a regional cohort.”

progressive familial intrahepatic cholestasis type 2Research

A recent study published in PubMed highlights the differing effects of two ABCB11 variants on patients with progressive familial intrahepatic cholestasis type 2. This research provides insights into the genetic underpinnings of the disease, which could inform future therapeutic strategies.

contrasting impacts of two abcb11 variants affecting the same residue in progressive familial intrahepatic cholestasis type 2

PubMed Rare Disease·3 months ago·Read at source →

Original title: “Contrasting Impacts of Two ABCB11 Variants Affecting the Same Residue in Progressive Familial Intrahepatic Cholestasis Type 2.”

Research

A recent study highlights a case of anterior rib malformation leading to hepatic compression in an adolescent. This discovery may provide insights into the complexities of rib malformations and their systemic effects.

beyond the chest wall anterior rib malformation causing hepatic compression in an adolescent

PubMed Rare Disease·3 months ago·Read at source →

Original title: “Beyond the chest wall: anterior rib malformation causing hepatic compression in an adolescent.”

Research

New research utilizes serum elemental profiles and machine learning to identify Alzheimer's disease and predict cognitive scores. This study highlights the potential for innovative diagnostic approaches in neurodegenerative diseases.

serum elemental profile based machine learning models for alzheimer s disease identification and cognitive score prediction

PubMed Rare Disease·3 months ago·Read at source →

Original title: “Serum elemental profile-based machine learning models for Alzheimer's disease identification and cognitive score prediction.”

Research

A new study explores the toxic and immunoglobulin E-mediated effects of processionary moth exposure in Europe, highlighting the need for improved diagnosis and management strategies. The findings may inform future research and clinical practices related to allergic responses.

processionary moth exposure in europe toxic irritant and immunoglobulin e mediated endotypes diagnosis and management

PubMed Rare Disease·3 months ago·Read at source →

Original title: “Processionary Moth Exposure in Europe: Toxic-Irritant and Immunoglobulin E-Mediated Endotypes, Diagnosis and Management.”

appendiceal neoplasmResearch

A recent case presentation highlights a rare instance of low-grade appendiceal mucinous neoplasm, contributing to the understanding of this uncommon condition. This case may provide insights for future research and clinical considerations.

low grade appendiceal mucinous neoplasm a rare case presentation

PubMed Rare Disease·3 months ago·Read at source →

Original title: “Low-grade Appendiceal Mucinous Neoplasm: A Rare Case Presentation.”

Research

A joint consensus statement has been published on the management of thyroid storm, providing updated guidelines for clinicians. This document aims to standardize treatment approaches and improve patient outcomes in thyroid emergencies.

management of thyroid emergencies joint consensus statement on management of thyroid storm

PubMed Rare Disease·3 months ago·Read at source →

Original title: “Management of Thyroid Emergencies: Joint Consensus Statement on Management of Thyroid Storm.”

Pseudomonas aeruginosa infectious disease Pseudomonas aeruginosa PA14 infectionResearch

Research reveals that the mgtC gene in Pseudomonas aeruginosa is regulated by PhoP and CbrAB, with its expression observable in macrophages. This discovery could enhance understanding of bacterial pathogenesis and immune response.

pseudomonas aeruginosa mgtc gene is under the control of phop and cbrab regulators and its expression can be visualized in macrophages

PubMed Rare Disease·3 months ago·Read at source →

Original title: “Pseudomonas aeruginosa mgtC gene is under the control of PhoP and CbrAB regulators, and its expression can be visualized in macrophages.”

Previous184 / 483Next

Daily Briefings

Not rare diseases news,news about your rare disease.

Earlier

A study published in PubMed examines the species composition and seasonal variation of medically important mosquitoes in Bajaur, Khyber Pakhtunkhwa, Pakistan. This research contributes to understanding vector dynamics that may impact disease transmission.

A recent study highlights the significant symptom burden and treatment challenges faced by patients with juvenile Parkinson's disease. The findings underscore the need for targeted research and improved therapeutic strategies for this rare condition.

A study investigates the influence of the VEGFA rs2010963 variant on the severity of bilaterality and posterior artery stenosis in moyamoya disease patients. This research could enhance understanding of genetic factors in disease progression.

A comprehensive review highlights safety considerations in blepharoplasty, emphasizing the need for careful patient selection and surgical technique to minimize complications. This study provides valuable insights for practitioners involved in cosmetic and reconstructive surgery.

A case report suggests a potential link between COVID-19 and Kienböck's disease, a rare form of osteonecrosis. This finding may prompt further investigation into the long-term effects of COVID-19 on bone health.

A recent study published in PubMed examines the morbidity and mortality associated with pediatric endovascularly treated aneurysmal subarachnoid hemorrhage over a twenty-year period. The findings contribute valuable insights into the long-term outcomes of this rare condition in children.

A nationwide cohort study in South Korea reveals the rate of autoimmune diseases in the decade before a myasthenia gravis diagnosis. This research provides insights into potential comorbidities that may influence patient management.

A study published in PubMed highlights the treatment of pleomorphic giant cell carcinoma of the prostate using Lutetium-177 PSMA. This research contributes to the understanding of targeted therapies for rare prostate cancer variants.

A study provides empirical evidence of a trade-off between reproduction and tumor dynamics in the freshwater cnidarian Hydra oligactis. This research could have implications for understanding cancer biology and regenerative processes.

A new study demonstrates that integrative cfDNA profiling from low-pass whole-genome sequencing can accurately predict the tissue of origin in cancer. This advancement could enhance diagnostic precision and personalized treatment strategies.

The European Society for Pediatric Infectious Diseases has released guidelines for managing invasive Group A Streptococcal infections in children. These guidelines aim to standardize treatment approaches and improve outcomes for affected pediatric patients.

A recent study highlights pediatric hematuria as a critical indicator for initiating family genetic investigations in type IV collagen nephropathies. This research emphasizes the importance of early detection and genetic screening in managing these rare kidney disorders.

A recent study published in PubMed highlights the differing effects of two ABCB11 variants on patients with progressive familial intrahepatic cholestasis type 2. This research provides insights into the genetic underpinnings of the disease, which could inform future therapeutic strategies.

A recent study highlights a case of anterior rib malformation leading to hepatic compression in an adolescent. This discovery may provide insights into the complexities of rib malformations and their systemic effects.

New research utilizes serum elemental profiles and machine learning to identify Alzheimer's disease and predict cognitive scores. This study highlights the potential for innovative diagnostic approaches in neurodegenerative diseases.

A new study explores the toxic and immunoglobulin E-mediated effects of processionary moth exposure in Europe, highlighting the need for improved diagnosis and management strategies. The findings may inform future research and clinical practices related to allergic responses.

A recent case presentation highlights a rare instance of low-grade appendiceal mucinous neoplasm, contributing to the understanding of this uncommon condition. This case may provide insights for future research and clinical considerations.

A joint consensus statement has been published on the management of thyroid storm, providing updated guidelines for clinicians. This document aims to standardize treatment approaches and improve patient outcomes in thyroid emergencies.

Research reveals that the mgtC gene in Pseudomonas aeruginosa is regulated by PhoP and CbrAB, with its expression observable in macrophages. This discovery could enhance understanding of bacterial pathogenesis and immune response.

Not rare diseases news,
news about your rare disease.