keyword
https://read.qxmd.com/read/38802173/amyotrophic-lateral-sclerosis-clinical-features-differential-diagnosis-and-pathology
#21
REVIEW
Michael A Van Es
Amyotrophic lateral sclerosis (ALS) is a late-onset syndrome characterized by the progressive degeneration of both upper motor neurons (UMN) and lower motor neurons (LMN). ALS forms a clinical continuum with frontotemporal dementia (FTD), in which there are progressive language deficits or behavioral changes. The genetics and pathology underlying both ALS and FTD overlap as well, with cytoplasmatic misvocalization of TDP-43 as the hallmark. ALS is diagnosed by exclusion. Over the years several diagnostic criteria have been proposed, which in essence all require a history of slowly progressive motor symptoms, with UMN and LMN signs on neurological examination, clear spread of symptoms through the body, the exclusion of other disorder that cause similar symptoms and an EMG that it is compatible with LMN loss...
2024: International Review of Neurobiology
https://read.qxmd.com/read/38801998/effects-of-housing-condition-on-the-development-and-persistence-of-addictive-like-behavior-induced-by-toluene
#22
JOURNAL ARTICLE
David García-Jácome, Lucía Martínez-Mota, Nayeli Páez-Martínez
Environmental factors can modify addictive responses induced by drugs of abuse; however, little is known about the impact of environmental conditions on behavioral responses induced by inhalants. In this study, we analyzed the effects of housing conditions, considering environmental enrichment (EE; n = 10), social isolation (SI; n = 10), and standard housing (STD; n = 10), as positive, negative, and control environments, respectively, on the development and persistence of behavioral sensitization induced by toluene...
May 25, 2024: Neurotoxicology
https://read.qxmd.com/read/38801762/mobile-electrocardiograms-in-the-detection-of-subclinical-atrial-fibrillation-in-high-risk-outpatient-populations-protocol-for-an-observational-study
#23
JOURNAL ARTICLE
Ajay Mittal, Yasmine Elkaldi, Susana Shih, Riken Nathu, Mark Segal
BACKGROUND: Single-lead, smartphone-based mobile electrocardiograms (ECGs) have the potential to provide a noninvasive, rapid, and cost-effective means of screening for atrial fibrillation (AFib) in outpatient settings. AFib has been associated with various comorbid diseases that prompt further investigation and screening methodologies for at-risk populations. A simple 30-second sinus rhythm strip from the KardiaMobile ECG (AliveCor) can provide an effective screen for cardiac rhythm abnormalities...
May 27, 2024: JMIR Research Protocols
https://read.qxmd.com/read/38800683/the-psychophysiology-of-music-based-interventions-and-the-experience-of-pain
#24
REVIEW
Carolyn A Arnold, Matthew K Bagg, Alan R Harvey
In modern times there is increasing acceptance that music-based interventions are useful aids in the clinical treatment of a range of neurological and psychiatric conditions, including helping to reduce the perception of pain. Indeed, the belief that music, whether listening or performing, can alter human pain experiences has a long history, dating back to the ancient Greeks, and its potential healing properties have long been appreciated by indigenous cultures around the world. The subjective experience of acute or chronic pain is complex, influenced by many intersecting physiological and psychological factors, and it is therefore to be expected that the impact of music therapy on the pain experience may vary from one situation to another, and from one person to another...
2024: Frontiers in Psychology
https://read.qxmd.com/read/38800238/the-delayed-presentation-of-bilateral-subdural-hematoma-secondary-to-epidural-anesthesia-for-elective-vaginal-delivery-a-case-report-and-review-of-the-literature
#25
Ahmad Awwad, Rawan A Daraghma, Mohammed M Hajhamad, Diya M Asad, Omar R Khalil
Epidural anesthesia (EA) involves reaching the spinal epidural space with an anesthetic drug injection. This procedure provides pain relief during labor. Although EA can lead to some complications, subdural hemorrhage (SDH) is a rare adverse event associated with it. We report the case of a 25-year-old female patient who presented to our emergency department with a one-month history of headaches and associated blurred vision following a normal vaginal delivery with EA. She was initially treated as a case of post-dural puncture headache (PDPH), with no improvement...
April 2024: Curēus
https://read.qxmd.com/read/38800176/atypical-guillain-barr%C3%A3-syndrome-in-a-pediatric-patient-with-a-preceding-non-covid-19-coronavirus-infection-a-case-report
#26
Navjot Azad, Ajay Mittal, Michael Marzullo
This study examines a four-year-and-one-month-old male with no significant past medical, family, or surgical history who initially presented to the pediatric clinic with cough, rhinorrhea, conjunctivitis, emesis, leg and arm pain, and increased difficulty ambulating. The patient was transferred to the emergency department and tested positive for a non-COVID-19 coronavirus infection. The patient was stabilized, given intravenous fluids, and discharged only to return to the clinic the next day with the onset of a headache, right eye ptosis, an inability to bear weight, and bilateral upper and lower extremity weakness resulting in an ataxic gait...
April 2024: Curēus
https://read.qxmd.com/read/38797686/-cryopyrin-associated-periodic-fever-syndrome-caps-presenting-as-early-onset-dementia-lacking-typical-recurrent-fever-or-skin-rash-a-case-report
#27
JOURNAL ARTICLE
Tomone Taneda, Mizuki Takahashi, Maiko Umeda, Yoshitaka Umeda, Mutsuo Oyake, Ryuta Nishikomori, Nobuya Fujita
A 54-year-old man with a university degree was admitted to our hospital because of a two-year history of progressive dementia. He had familial sensorineural hearing loss and had been treated for epilepsy since his 30s. On admission, he showed severe dementia and parkinsonism without fever or skin rash. Systemic inflammation was evident, and the CSF cell count and IL-6 level were elevated to 53/μl and 307 ‍pg/ml, respectively. Brain MRI demonstrated diffuse brain atrophy. More detailed anamnesis revealed a history of rheumatoid arthritis in childhood and aseptic meningitis in his 20s...
May 25, 2024: Rinshō Shinkeigaku, Clinical Neurology
https://read.qxmd.com/read/38797685/-juvenile-onset-anti-nuclear-matrix-protein-2-nxp-2-antibody-positive-dermatomyositis-with-joint-contractures-before-manifestation-of-myositis-a-case-report
#28
JOURNAL ARTICLE
Eito Miura, Tomone Taneda, Yoshitaka Umeda, Maiko Umeda, Mutsuo Oyake, Takashi Matsushita, Ichizo Nishino, Nobuya Fujita
A 23-year-old man was admitted to our hospital with a one-year history of muscle weakness and atrophy. He had noticed contractures of the fingers of both hands from the age of 18. Examination revealed a skin rash including heliotrope rash and Gottron's sign, joint contractures in the extremities, dysphagia, extensive muscle weakness and marked muscle atrophy. The serum creatine kinase level was 272 ‍IU/l and muscle biopsy showed typical perifascicular atrophy but little lymphocyte invasion. There was no interstitial pneumonia or malignancy, but muscle tendons showed elevated CT values suggesting calcification or fibrosis...
May 25, 2024: Rinshō Shinkeigaku, Clinical Neurology
https://read.qxmd.com/read/38791946/unsatisfactory-neurological-outcome-in-an-intramedullary-thoracic-intermediate-grade-melanocytoma-systematic-review-and-illustrative-case
#29
REVIEW
Marco Battistelli, Fulvio Grilli, Alessandro Rapisarda, Michele Di Domenico, Nicola Montano, Marco Gessi, Alessandro Olivi, Alessio Albanese, Filippo Maria Polli
BACKGROUND: Intramedullary melanocytomas are exceedingly rare, with only twenty-four cases reported up to now. They present as local invasive tumors despite their benign biological behavior. Attempting a complete safe resection often results in severe post-operative neurological deficits, as in our case presented here. METHODS: A systematic review was conducted across the PubMed and Scopus databases including studies published till February 2024. RESULTS: A total of 19 studies were included, encompassing 24 cases...
May 14, 2024: Cancers
https://read.qxmd.com/read/38790596/lower-urinary-tract-dysfunction-in-pediatric-patients-with-multiple-sclerosis-diagnostic-and-management-concerns
#30
JOURNAL ARTICLE
Maria Laura Sollini, Chiara Pellegrino, Giulia Barone, Maria Luisa Capitanucci, Antonio Maria Zaccara, Leonardo Crescentini, Enrico Castelli, Gessica Della Bella, Federico Scorletti, Laura Papetti, Gabriele Monte, Michela Ada Noris Ferilli, Massimiliano Valeriani, Giovanni Mosiello
BACKGROUND: Multiple sclerosis (MS) is increasing in the pediatric population and, as in adults, symptoms vary among patients. In children the first manifestations can sometimes overlap with acute neurological symptoms. Urological symptoms have not been much studied in childhood. We shared our experience with MS urological manifestation in children. METHODS: This article is a retrospective evaluation of all children with MS, according to the Krupp criteria, who also present with urological symptoms...
May 16, 2024: Children
https://read.qxmd.com/read/38790397/fifty-years-of-handedness-research-a-neurological-and-methodological-update
#31
JOURNAL ARTICLE
Anna Rita Giovagnoli, Alessandra Parisi
Handedness, a complex human aspect that reflects the functional lateralization of the hemispheres, also interacts with the immune system. This study aimed to expand the knowledge of the lateralization of hand, foot, and eye activities in patients with immune-mediated (IM) or other (noIM) neurological diseases and to clarify the properties of the Edinburgh Handedness Inventory (EHI) in an Italian population. Three hundred thirty-four patients with IM or noIM diseases affecting the brain or spine and peripheral nervous system were interviewed about stressful events preceding the disease, subjective handedness, and familiarity for left-handedness or ambidexterity...
April 24, 2024: Brain Sciences
https://read.qxmd.com/read/38788763/outcome-trajectories-after-intracerebral-hemorrhage
#32
JOURNAL ARTICLE
Lourdes Carhuapoma, Santosh Murthy, Vishank A Shah
Spontaneous intracerebral hemorrhage (ICH) is the most morbid of all stroke types with a high early mortality and significant early disability burden. Traditionally, outcome assessments after ICH have mirrored those of acute ischemic stroke, with 3 months post-ICH being considered a standard time point in most clinical trials, observational studies, and clinical practice. At this time point, the majority of ICH survivors remain with moderate to severe functional disability. However, emerging data suggest that recovery after ICH occurs over a more protracted course and requires longer periods of follow-up, with more than 40% of ICH survivors with initial severe disability improving to partial or complete functional independence over 1 year...
May 24, 2024: Seminars in Neurology
https://read.qxmd.com/read/38788281/optic-nerve-edema-in-pediatric-middle-cranial-fossa-arachnoid-cysts-report-of-51-patients-from-a-single-institution
#33
JOURNAL ARTICLE
Joanna E Papadakis, Anna L Slingerland, Shivani D Rangwala, Mark R Proctor, Ankoor S Shah, Alfred P See
BACKGROUND: Middle fossa arachnoid cysts (MFACs) are rare, congenital lesions that may rupture and cause symptoms of elevated intracranial pressure. We sought to describe the presence of and factors associated with optic nerve edema in MFACs, focusing on the utility of ophthalmologic evaluations for guiding cyst management. METHODS: We reviewed clinical and radiographic information for all patients with MFACs with ophthalmologic evaluations at our institution. Headache, cranial nerve palsy, emesis, altered mental status, fatigue, and seizures were considered MFAC-related symptoms...
April 13, 2024: Pediatric Neurology
https://read.qxmd.com/read/38788051/drop-foot-with-posterior-tibialis-weakness-treated-with-peroneus-longus-transfer-in-a-child-a-case-report
#34
JOURNAL ARTICLE
Robert M Kay, Alison Hanson
CASE: An 8-year-old girl with a history of acute flaccid paralysis presented with chronic valgus drop foot causing tripping and falling. Traditionally surgical correction of this deformity is accomplished by transferring the posterior tibialis tendon to enhance dorsiflexion. The authors describe a new technique which transfers the peroneus longus tendon to the dorsum of the foot in a patient with weakness of the posterior tibialis muscle. The patient's drop foot and gait were improved at the 22-month follow-up...
April 1, 2024: JBJS Case Connector
https://read.qxmd.com/read/38785164/heterogeneity-of-comprehensive-clinical-phenotype-and-longitudinal-adaptive-function-and-correlation-with-computational-predictions-of-severity-of-missense-genotypes-in-kif1a-associated-neurological-disorder
#35
JOURNAL ARTICLE
Khemika K Sudnawa, Wenxing Li, Sean Calamia, Cara H Kanner, Jennifer M Bain, Aliaa H Abdelhakim, Alexa Geltzeiler, Caroline M Mebane, Frank A Provenzano, Tristan T Sands, Robert J Fee, Jacqueline Montes, Yufeng Shen, Wendy K Chung
PURPOSE: Pathogenic variants in Kinesin Family Member 1A (KIF1A) are associated with KIF1A-associated neurological disorder (KAND). We report the clinical phenotypes and correlate genotypes of individuals with KAND. METHODS: Medical history and adaptive function were assessed longitudinally. In-person evaluations included neurological, motor, ophthalmologic and cognitive assessments. RESULTS: We collected online data on 177 individuals. Fifty-seven individuals were also assessed in-person...
May 20, 2024: Genetics in Medicine: Official Journal of the American College of Medical Genetics
https://read.qxmd.com/read/38785158/myoclonus-an-update
#36
JOURNAL ARTICLE
Betsy Thomas, Steven J Frucht
PURPOSE OF REVIEW: Myoclonus, a common hyperkinetic movement disorder, can be disabling for patients. It is important to identify and classify myoclonus correctly to ensure appropriate workup and treatment. While the clinical history, examination, and process of classifying myoclonus remain largely unchanged, new causes and triggers for myoclonus are being elucidated, and new genetic causes have been found. Treatment can be challenging, though preliminary data about new options has been promising...
May 27, 2024: Current Opinion in Neurology
https://read.qxmd.com/read/38784900/a-case-report-gliosarcoma-associated-with-a-germline-heterozygous-mutation-in-msh2
#37
Yuhan Wang, Zhiyuan Zhang
Gliosarcoma is a rare subtype of glioblastoma (GBM) with a shorter medical history and a worse prognosis compared to other Grade 4 gliomas. Most gliosarcomas are sporadic, but it is undeniable that a small percentage are linked to germline mutations and several inherited cancer susceptibility syndromes, including Lynch Syndrome (LS). The authors present a case of a primary mismatch repair-deficient gliosarcoma in LS. A 54-year-old Chinese male patient was admitted to the hospital with a history of facial asymmetry for over 1 month and right temporo-occipital pain for 5 days...
2024: Frontiers in Neurology
https://read.qxmd.com/read/38784872/bilateral-knee-arthrodesis-and-total-hip-arthroplasty-for-knee-and-hip-dysplasia-secondary-to-spina-bifida-a-case-report
#38
Colin Neitzke, Charles Gusho, Austin Yu, Joel Williams
INTRODUCTION: Spina bifida is a rare neurological condition that, if uncorrected, may cause chronic valgus knee stress difficulty with independent ambulation and significant pain. Current literature lacks comprehensive guidance on surgically correcting progressive hip and knee deformities in spina bifida patients, which include osteotomy and primary. When these options are contraindicated, alternative approaches such as arthrodesis may be indicated, although they remain understudied in this population...
May 2024: Journal of Orthopaedic Case Reports
https://read.qxmd.com/read/38784860/bing-neel-syndrome-presenting-as-isolated-cranial-nerve-palsies-a-case-report
#39
Dipti Baskar, Davuluri Durga Srinivas Anudeep, Seena Vengalil, Preetham Patavaradhan, Karthik Kulanthaivelu, Ravindu Tiwari, Bevinahalli Nanjegowda Nandeesh, Keerti Sitani, Pritam Raja, Ravindranadh C Mundlamuri, Ravi Yadav, Atchayaram Nalini
BACKGROUND AND AIMS: Waldenstroms macroglobulinemia (WM) is a low-grade B cell neoplasm. Bing Neel syndrome is a rare manifestation of WM characterized by infiltrative involvement of the central nervous system. CASE REPORT: 64-year-old man, presented with 4 years history of slowly progressive diplopia and ptosis of eyes. Examination showed left oculomotor (internal and external ophthalmoplegia), with trochlear, abducens, and right partial oculomotor and abducens nerve involvement...
June 2024: ENeurologicalSci
https://read.qxmd.com/read/38782432/hemichorea-hemiballismus-due-to-diabetic-striatopathy-a-serious-complication-of-uncontrolled-diabetes
#40
JOURNAL ARTICLE
Brian Middleton, Zhanna Albany, Aaron Kamer, Areeba Kara
We report the case of a man in his mid-80s with diabetes mellitus who presented to the emergency department with a 1-day history of right-sided choreiform movements and falls. Laboratory tests revealed blood glucose of 597 mg/dL. Non-contrast CT imaging of his head demonstrated a faint hyperdensity involving the left lentiform nucleus and brain MRI showed a hyperintensity in the left basal ganglia on T1-weighted images. These lesions are typical of diabetic striatopathy. Symptoms of hemichorea/hemiballismus did not resolve with glycaemic control and several pharmacological agents were tried with eventual improvement with risperidone...
May 22, 2024: BMJ Case Reports
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