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🧠 Blue Rubber Bleb Nevus Syndrome

πŸ–Š BRBNS is also known as Bean syndrome. It is a rare syndrome of venous malformations that arise in the skin and gastrointestinal tract.

πŸ–Š Patients present with multiple venous malformations in various organ systems including the liver, spleen, heart, eye, and central nervous system.

πŸ–Š Patients with BRBNS are at increased risk for gastrointestinal hemorrhage and severe iron deficiency anemia. They require a multifaceted medical management approach with hematology, dermatology, gastroenterology, and other specialties involved in their care

πŸ–Š Treatment is largely supportive and involves managing potential complications such as volvulus, intussusception, infarction, and gastrointestinal bleeding.

πŸ”ŽSource:
- Blue Rubber Bleb Nevus Syndrome, StatPearls

#MCQ #Neurology
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πŸ“Œ8th Annual Neuroscience Innovation Forum (NIF)

πŸ“† 12 January, 2025
πŸ“ San Francisco, USA

πŸ”†Key features:

πŸ”·οΈFocus on Neuroscience Developments: The forum will concentrate on the latest advancements in neuroscience, covering therapeutic innovations, neurotechnology, and diagnostic tools.

πŸ”ΆοΈHigh-Level Discussions: Attendees can expect over eight hours of keynotes and panel discussions led by industry leaders, addressing critical topics in the field.


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πŸ“ŒANT Neuromeeting Berlin 2025

πŸ“† January 16-18, 2025
πŸ“ Berlin, Germany

πŸ”†Key features:

πŸ”·οΈScientific Presentations and Workshops: The event will feature presentations by renowned experts, hands-on showcases, workshops, and demonstrations of innovative neurotechnology.


πŸ”ΆοΈNetworking Opportunities: Attendees will have the chance to connect with international peers, researchers, clinicians, and industry leaders, fostering collaboration and knowledge exchange.

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🧠 Friedreich’s ataxia

πŸ–Š Friedreich’s ataxia (FRDA) is an autosomal recessive spinocerebellar ataxia.
πŸ–Š In the majority of cases the disease is caused by a homozygous GAA triplet repeat expansion in the frataxin (FXN) gene, and the shorter repeat expansion length correlates with age at onset and disease severity.
πŸ–Š The clinical phenotype is broad, but consistently involves gait and limb ataxia, dysarthria and loss of lower limb reflexes.
πŸ–Š Our understanding of the genetic aetiology, pathophysiology and clinical phenotype has progressed significantly.

πŸ”ŽSource:
- Neurosurgery Board Review, Third Edition
- Friedreich’s ataxia: clinical features, pathogenesis and management


#MCQ #Neuroradiology
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πŸ“Œ7th International Virtual Conference on Neuroscience, Brain Disorders & Therapeutics

πŸ“† January 25-26, 2025
πŸ“ online

πŸ”†Key features:

πŸ”·οΈFocus on Advancements and Challenges: The conference will explore recent treatment techniques and novel approaches in neuroscience and brain disorders, providing a platform for discussing advancements and addressing challenges in the field.


πŸ”ΆοΈDiverse Participation: It aims to bring together neuroscientists, neurobiologists, neurological surgeons, neurologists, neuropathologists, neurophysiologists, neuropsychologists, and psychiatrists from various countries to share their ideas and views.



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πŸ“ŒKeystone Symposia: Neural Influence on Cancer, Tumor Microenvironment, and Cancer Immunology

πŸ“† January 18–21, 2025
πŸ“ Alberta, Canada

πŸ”†Key features:

πŸ”·οΈFocus Areas:

- Exploring how nerves contribute to cancer initiation, growth, and metastasis.
- Investigating neuro-immune interactions that shape the tumor microenvironment.
- Evaluating current neuron-targeted therapeutics that could be repurposed as adjuvant cancer therapies.

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πŸ“ŒJanuary 2025 fMRI Speaker Series

πŸ“† January 21, 2025
πŸ“ Ann Arbor, USA

πŸ”†Key features:

πŸ”·οΈThis event is part of the University of Michigan's Functional MRI Laboratory Speaker Series, which provides opportunities for researchers and students to learn about advancements in functional MRI and related fields.

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πŸ“ŒBig Ten Neuroscience Seminar Series

πŸ“† January 27, 2025
πŸ“ Virtual Event

πŸ”†Key features:

πŸ”·οΈShowcases neuroscience research from postdoctoral fellows and early career faculty.

πŸ”ΆοΈProvides a platform for interdisciplinary collaboration and knowledge exchange.

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The most appropriate treatment for a patient with multiple ischemic events and the accompanying angiogram is?
Anonymous Quiz
35%
Carotid endarterectomy
5%
Encephalomyosynangiosis
30%
Heparinization
25%
Superficial temporal artery to middle cerebral artery bypass
5%
No treatment
πŸ•―Prof. Vinko V. Dolenc
(1940-2025)

β–ͺ️Born on June 29, 1940, in SestrΕΎe near Ptuj, Slovenia.
▫️Dedicated his life to advancing the field of neurosurgery, particularly through his groundbreaking work in microsurgical techniques.
β–ͺ️Among the first surgeons worldwide to perform ruptured aneurism surgery in the acute phase.
▫️His most significant contributions came in the early 1990s with his pioneering research in parasellar space neuro-anatomy and groundbreaking surgeries on aneurysms and tumours in the cavernous sinus.
β–ͺ️His pioneering spirit, innovative approaches, and dedication to teaching have left an indelible mark on our field.

πŸ•― May his sole rest in peace.
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🧠 Heparinization in multiple ischemic events

πŸ–Š Pharmacologic efforts to improve outcomes following aneurysmal subarachnoid hemorrhage (aSAH) remain disappointing, likely owing to the complex nature of post-hemorrhage brain injury.
πŸ–Š Previous work suggests that heparin, due to the multimodal nature of its actions, reduces the incidence of clinical vasospasm and delayed cerebral ischemia that accompany the disease.
πŸ–Š How heparin may mitigate the non-vasospastic pathological aspects of aSAH, particularly those related to neuroinflammation.

πŸ”ŽSource:
- Neurosurgery Board Review, Third Edition
- Heparin and Heparin-Derivatives in Post-Subarachnoid Hemorrhage Brain Injury


#MCQ #Neuroradiology
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🧠 Neurofibromatosis type 2

πŸ–Š Neurofibromatosis type 2 is an autosomal-dominant multiple neoplasia syndrome that results from mutations in the NF2 tumour suppressor gene located on chromosome 22q.
πŸ–Š It has a frequency of one in 25,000 livebirths and nearly 100% penetrance by 60 years of age.
πŸ–Š Half of patients inherit a germline mutation from an affected parent and the remainder acquire a de novo mutation for neurofibromatosis type 2.
πŸ–Š Patients develop nervous system tumours (schwannomas, meningiomas, ependymomas, astrocytomas, and neurofibromas), peripheral neuropathy, ophthalmological lesions (cataracts, epiretinal membranes, and retinal hamartomas), and cutaneous lesions (skin tumours).

πŸ”ŽSource:
- Neurosurgery Board Review, Third Edition
- Neurofibromatosis type 2: A Review study


#MCQ #Neuroradiology
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#Neuroanatomy

Most of the fibers of the stria terminalis originate from the...
Anonymous Quiz
31%
Amygdala
13%
Anterior hypothalamus
31%
Arcuate nucleus
19%
Habenula
6%
Septal nuclei
🧠 Amygdala

πŸ–Š The amygdala is a hub of subcortical region that is crucial in a wide array of affective and motivation-related behaviors.
πŸ–Š While early research contributed significantly to our understanding of this region's extensive connections to other subcortical and cortical regions, recent methodological advances have enabled researchers to better understand the details of these circuits and their behavioral contributions.
πŸ–Š Much of this work has focused specifically on investigating the role of amygdala circuits in social cognition. In this chapter, we review both long-standing knowledge and novel research on the amygdala's structure, function, and involvement in social cognition.

πŸ”ŽSource:
- Neurosurgery Board Review, Third Edition
- Amygdala connectivity and implications for social cognition and disorders

#MCQ #Neuroanatomy
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2025/02/01 10:13:02
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