keyword
https://read.qxmd.com/read/38701156/impatient-an-integrated-web-application-to-digitize-process-and-explore-multimodal-patient-data
#1
JOURNAL ARTICLE
Corentin Meyer, Norma Beatriz Romero, Teresinha Evangelista, Brunot Cadot, Jocelyn Laporte, Anne Jeannin-Girardon, Pierre Collet, Ali Ayadi, Kirsley Chennen, Olivier Poch
Medical acts, such as imaging, lead to the production of various medical text reports that describe the relevant findings. This induces multimodality in patient data by combining image data with free-text and consequently, multimodal data have become central to drive research and improve diagnoses. However, the exploitation of patient data is problematic as the ecosystem of analysis tools is fragmented according to the type of data (images, text, genetics), the task (processing, exploration) and domain of interest (clinical phenotype, histology)...
April 29, 2024: Journal of Neuromuscular Diseases
https://read.qxmd.com/read/38698877/acid-%C3%AE-glucosidase-gaa-activity-and-glycogen-content-in-muscle-biopsy-specimens-of-patients-with-pompe-disease-a-systematic-review
#2
JOURNAL ARTICLE
Benedikt Schoser, Nina Raben, Fatbardha Varfaj, Mark Walzer, Antonio Toscano
Pompe disease is a rare genetic disorder characterized by a deficiency of acid α-glucosidase (GAA), leading to the accumulation of glycogen in various tissues, especially in skeletal muscles. The disease manifests as a large spectrum of phenotypes from infantile-onset Pompe disease (IOPD) to late-onset Pompe disease (LOPD), depending on the age of symptoms onset. Quantifying GAA activity and glycogen content in skeletal muscle provides important information about the disease severity. However, the distribution of GAA and glycogen levels in skeletal muscles from healthy individuals and those impacted by Pompe disease remains poorly understood, and there is currently no universally accepted standard assay for GAA activity measurement...
June 2024: Molecular Genetics and Metabolism Reports
https://read.qxmd.com/read/38697682/tumour-induced-osteomalacia-the-long-road-to-diagnosis-and-recovery
#3
JOURNAL ARTICLE
Shobitha Vollmer, Karin Olsson
Tumour-induced osteomalacia is caused by tumorous production of fibroblast growth factor 23 (FGF23) leading to urinary phosphate wasting, hypophosphataemia and decreased vitamin D activation. The resulting osteomalacia presents with muscle weakness and bone pain but progresses to multiple pathological fractures. Patients often remain undiagnosed for years with severe physical, psychological and economic ramifications. A young woman presented with multiple spontaneous fractures including bilateral femoral fractures...
May 2, 2024: BMJ Case Reports
https://read.qxmd.com/read/38694826/incidental-finding-of-an-undifferentiated-sarcoma-during-lower-limb-doppler-ultrasound-a-case-report
#4
Christopher Ekene Ilounoh, Rajuno Ernest Eteng, Yuriy Arlachov
INTRODUCTION: Undifferentiated sarcoma is considered a rare and aggressive type of soft tissue sarcoma with the lower extremity reported as the common site for soft tissue sarcomas. CASE PRESENTATION: We present a rare incidental finding of undifferentiated sarcoma during lower limb Doppler ultrasound with a presenting symptom of right thrombotic-like calf pain in a 49-year-old female. DISCUSSION: On ultrasound, the presented undifferentiated sarcoma appeared as a large heterogeneous, oval-shaped, soft tissue mass deeply seated in the right calf with involvement of the soleus muscle...
May 2024: Ultrasound: Journal of the British Medical Ultrasound Society
https://read.qxmd.com/read/38692172/elevated-type-i-ifn-signalling-directly-affects-cd8-t-cell-distribution-and-autoantigen-recognition-of-the-skeletal-muscles-in-active-jdm-patients
#5
JOURNAL ARTICLE
Baozhen Huang, Huiyu Li, Qian Jiang, Yucong Li, Zhaowei Jiang, Huijuan Cao, Shaoxi Wang, Xinluan Wang, Jianguo Li, Gang Li
The link between type I IFN and adaptive immunity, especially T-cell immunity, in JDM still remained largely unclear. This study aimed to understand the effect of elevated type I IFN signaling on CD8+ T cell-associated muscle damage in juvenile dermatomyositis (JDM). This study used flow cytometry (FC) and RT‒PCR were used to examine the circulating cell ratio and type I IFN response. And scRNA-seq was used to examine peripheral immunity in 6 active JDM patients, 3 stable JDM patients, 3 juvenile IMNM patients and 3 age-matched healthy children...
April 30, 2024: Journal of Autoimmunity
https://read.qxmd.com/read/38691940/a-novel-deep-intronic-variant-in-lama2-identified-by-rna-sequencing
#6
Djurdja Djordjevic, Issa Alawneh, Kimberly Amburgey, Kyoko E Yuki, Lianna G Kyriakopoulou, Vilma Navickiene, Jim Stavropoulos, Grace Yoon, James J Dowling, Hernan Gonorazky
LAMA2-related muscular dystrophy is caused by pathogenic variants of the alpha2 subunit of Laminin. This common form of muscular dystrophy is characterized by elevated CK >1000IU/L, dystrophic changes on muscle biopsy, complete or partial absence of merosin staining, and both central and peripheral nervous system involvement. Advancements in genomic testing using NGS and wider application of RNA sequencing has expanded our knowledge of novel non-coding pathogenic variants in LAMA2. RNA sequencing is an increasingly utilized technique to directly analyze the transcriptome, through creation of a complementary DNA (cDNA) from the transcript within a tissue sample...
April 5, 2024: Neuromuscular Disorders: NMD
https://read.qxmd.com/read/38690726/a-laing-distal-myopathy-associated-proline-substitution-in-the-%C3%AE-myosin-rod-perturbs-myosin-cross-bridging-activity
#7
JOURNAL ARTICLE
Massimo Buvoli, Genevieve Ck Wilson, Ada Buvoli, Jack F Gugel, Abbi Hau, Carsten G Bönnemann, Carmen Paradas, David M Ryba, Kathleen C Woulfe, Lori A Walker, Tommaso Buvoli, Julien Ochala, Leslie A Leinwand
Proline substitutions within the coiled-coil rod region of the β-myosin gene (MYH7) are the predominant mutations causing Laing distal myopathy (MPD1), an autosomal dominant disorder characterized by progressive weakness of distal/proximal muscles. We report that the MDP1 mutation R1500P, studied in what we believe to be the first mouse model for the disease, adversely affected myosin motor activity despite being in the structural rod domain that directs thick filament assembly. Contractility experiments carried out on isolated mutant muscles, myofibrils, and myofibers identified muscle fatigue and weakness phenotypes, an increased rate of actin-myosin detachment, and a conformational shift of the myosin heads toward the more reactive disordered relaxed (DRX) state, causing hypercontractility and greater ATP consumption...
May 1, 2024: Journal of Clinical Investigation
https://read.qxmd.com/read/38689479/comparison-of-effects-of-sugammadex-and%C3%A2-neostigmine-on-postoperative-neuromuscular-blockade-recovery-in-patients-with-interstitial-lung-diseases-undergoing-transbronchial-cryobiopsy-a-randomized-trial
#8
RANDOMIZED CONTROLLED TRIAL
Liya Lu, Xiaobo Chen, Shiyue Li, Yanyi Cen
BACKGROUND While many studies have been conducted on sugammadex sodium and neostigmine in patients undergoing general anesthesia, few have explored their effects in patients with interstitial lung diseases (ILDs). MATERIAL AND METHODS Sixty-three patients who underwent transbronchial cryobiopsy under general anesthesia were enrolled in a prospective randomized study. The patients were randomly divided into 2 groups: neostigmine combined with atropine group (group C, n=32) and sugammadex group (group S, n=31)...
May 1, 2024: Medical Science Monitor: International Medical Journal of Experimental and Clinical Research
https://read.qxmd.com/read/38688838/perineal-squamous-cell-carcinoma-arising-in-an-epidermal-cyst
#9
Fuminori Teraishi, Yuki Matsumi, Kota Tachibana, Toshiyuki Watanabe, Toshiyoshi Fujiwara
A 90-year-old Japanese woman who had been aware of a subcutaneous mass on the right perineal region for 5 years was referred to our hospital for further examination and treatment because of the rapid growth of the mass and bleeding that began 3 months earlier. A biopsy of the mass revealed a diagnosis of well-differentiated squamous cell carcinoma. On preoperative examination, the tumor was 90×40 mm in size and was suspected to have partially invaded the levator ani muscle and external sphincter. Since a preoperative cardiac evaluation indicated severe aortic stenosis, we performed transcatheter aortic valve implantation...
April 2024: Acta Medica Okayama
https://read.qxmd.com/read/38687345/merkel-cell-carcinoma-metastases-to-caruncle-with-orbital-extension-report-and-literature-review
#10
JOURNAL ARTICLE
Josefina Herrera, Krishna Tumuluri
Merkel cell carcinoma (MCC) is an uncommon and aggressive skin cancer of neuroendocrine origin. The tumor usually presents with a locoregional spread and most frequently metastasizes to the skin, liver, bone, lung, and brain. Despite the orbit being a relatively common site of metastases, it has rarely been reported in patients with MCC. The authors present a case of biopsy-proven orbital metastatic MCC in an 86-year-old male who presented with a rapidly enlarging right caruncle/subconjunctival mass with orbital extension and a history of forearm MCC excision 3 years prior...
April 29, 2024: Ophthalmic Plastic and Reconstructive Surgery
https://read.qxmd.com/read/38685696/altered-plasma-levels-and-tissue-expression-of-fibroblast-activation-protein-alpha-in-giant-cell-arteritis
#11
JOURNAL ARTICLE
Shuang Xu, William F Jiemy, Annemieke M H Boots, Suzanne Arends, Yannick van Sleen, Pieter H Nienhuis, Kornelis S M van der Geest, Peter Heeringa, Elisabeth Brouwer, Maria Sandovici
OBJECTIVE: Giant cell arteritis (GCA) is characterized by granulomatous inflammation of the medium and large-sized arteries accompanied by remodeling of the vessel wall. Fibroblast activation protein alpha (FAP) is a serine protease which promotes both inflammation and fibrosis. Here we investigated the plasma levels and vascular expression of FAP in GCA. METHODS: Plasma FAP levels were measured with ELISA in treatment-naive GCA (n=60) and polymyalgia rheumatica (PMR, n=63) patients (compared to age- and sex-matched healthy controls (HC), n=42) and during follow-up, including treatment free remission (TFR)...
April 29, 2024: Arthritis Care & Research
https://read.qxmd.com/read/38684305/-clinical-features-and-genetic-analysis-of-a-child-with-central-core-disease-due-to-compound-heterozygous-variants-of-ryr1-gene
#12
JOURNAL ARTICLE
Shanshan Liu, Shuting Mao, Bai Li, Linlin Wei, Yufeng Liu
OBJECTIVE: To explore the clinical features and genetic etiology of a child with Central core disease (CCD). METHODS: A child with CCD who was treated at the Children's Hematology Department of the First Affiliated Hospital of Zhengzhou University in February 2022 was selected as the study subject. Muscle biopsy was performed. Peripheral blood samples were collected from the child and his parents for the extraction of genomic DNA. The child was subjected to whole exome sequencing (WES), and candidate variant was verified by Sanger sequencing...
May 10, 2024: Zhonghua Yi Xue Yi Chuan Xue za Zhi, Zhonghua Yixue Yichuanxue Zazhi, Chinese Journal of Medical Genetics
https://read.qxmd.com/read/38683354/-expert-recommendations-for-magnetic-resonance-imaging-of-muscle-disorders
#13
REVIEW
Rachel Zeng, Sarah Schlaeger, Matthias Türk, Thomas Baum, Marcus Deschauer, Rolf Janka, Dimitrios Karampinos, Jan Kassubek, Sarah Keller-Yamamura, Cornelia Kornblum, Helmar Lehmann, Thorsten Lichtenstein, Armin M Nagel, Jens Reimann, Angela Rosenbohm, Lara Schlaffke, Manuel Schmidt, Christiane Schneider-Gold, Benedikt Schoser, Regina Trollmann, Matthias Vorgerd, Marc-André Weber, Jan S Kirschke, Jens Schmidt
BACKGROUND: Magnetic resonance (MRI) imaging of the skeletal muscles (muscle MRI for short) is increasingly being used in clinical routine for diagnosis and longitudinal assessment of muscle disorders. However, cross-centre standards for measurement protocol and radiological assessment are still lacking. OBJECTIVES: The aim of this expert recommendation is to present standards for the application and interpretation of muscle MRI in hereditary and inflammatory muscle disorders...
April 29, 2024: Der Nervenarzt
https://read.qxmd.com/read/38682238/acute-effects-of-a-ketone-monoester-whey-protein-or-their-co-ingestion-on-mtor-trafficking-and-protein-protein-co-localization-in-human-skeletal-muscle
#14
JOURNAL ARTICLE
Sarkis J Hannaian, Jamie Lov, Zacharie Cheng-Boivin, Sidney Abou Sawan, Nathan Hodson, Benoit J Gentil, José A Morais, Tyler A Churchward-Venne
We recently demonstrated that acute oral ketone monoester intake induces a stimulation of postprandial myofibrillar protein synthesis rates comparable to that elicited following the ingestion of 10 g whey protein or their co-ingestion. The present investigation aimed to determine the acute effects of ingesting a ketone monoester, whey protein, or their co-ingestion on mTOR-related protein-protein co-localization and intracellular trafficking in human skeletal muscle. In a randomized, double-blind, parallel group design, 36 healthy recreationally active young males (age: 24...
April 29, 2024: American Journal of Physiology. Cell Physiology
https://read.qxmd.com/read/38682026/prevalence-and-outcome-of-sarcopenia-in-non-alcoholic-fatty-liver-disease
#15
JOURNAL ARTICLE
Suprabhat Giri, Prajna Anirvan, Sumaswi Angadi, Ankita Singh, Anurag Lavekar
BACKGROUND: Nonalcoholic fatty liver disease (NAFLD) includes a spectrum of conditions, progressing from mild steatosis to advanced fibrosis. Sarcopenia, characterized by decreased muscle strength and mass, shares common pathophysiological traits with NAFLD. An association exists between sarcopenia and increased NAFLD prevalence. However, data on the prevalence of sarcopenia in NAFLD and its impact on the outcomes of NAFLD remain inconsistent. AIM: To analyze the prevalence and outcomes of sarcopenia in patients with NAFLD...
April 22, 2024: World Journal of Gastrointestinal Pathophysiology
https://read.qxmd.com/read/38681027/giant-cell-tumor-of-distal-radius-en-bloc-resection-with-allograft-reconstruction-a-case-report
#16
Parviz Ahangar, Alireza Rahimnia, Mohsen Akbaribazm, Abbas Khalilpour, Mohsen Rahimi, Hosein Pirmohamadi
KEY CLINICAL MESSAGE: Giant cell tumor of bone (GCT) is a rare neoplasm which often presents as a lytic lesion in the epiphyseal region of long bones and which are usually accompanied by pain, swelling, and restricted movement. ABSTRACT: Giant cell tumor of bone (GCT) is a rare neoplasm that affects individuals in their third and fourth decades of life. Clinically, it often presents as a lytic lesion in the epiphyseal region of bones, notably the distal femur and proximal tibia...
May 2024: Clinical Case Reports
https://read.qxmd.com/read/38679679/presacral-neuroendocrine-neoplasms-a-multi-site-review-of-surgical-outcomes
#17
JOURNAL ARTICLE
Tommaso Violante, Brenda Murphy, Davide Ferrari, Rondell P Graham, Patrick Navin, Amit Merchea, David W Larson, Eric J Dozois, Thorvardur R Halfdanarson, William R Perry
INTRODUCTION: Presacral neuroendocrine neoplasms (PNENs) are rare tumors, with limited data on management and outcomes. METHODS: A retrospective review of institutional medical records was conducted to identify all patients with PNENs between 2008 and 2022. Data collection included demographics, symptoms, imaging, surgical approaches, pathology, complications, and long-term outcomes. RESULTS: Twelve patients were identified; two-thirds were female, averaging 44...
April 28, 2024: Annals of Surgical Oncology
https://read.qxmd.com/read/38678201/an-autosomal-recessive-variant-in-pygm-causes-myophosphorylase-deficiency-in-red-angus-composite-cattle
#18
JOURNAL ARTICLE
Mackenzie C Batt, Leila G Venzor, Keri Gardner, Rachel R Reith, Kelsey A Roberts, Nicolas J Herrera, Anna M Fuller, Gary A Sullivan, J Travis Mulliniks, Matthew L Spangler, Stephanie J Valberg, David J Steffen, Jessica L Petersen
BACKGROUND: Between 2020 and 2022, eight calves in a Nebraska herd (composite Simmental, Red Angus, Gelbvieh) displayed exercise intolerance during forced activity. In some cases, the calves collapsed and did not recover. Available sire pedigrees contained a paternal ancestor within 2-4 generations in all affected calves. Pedigrees of the calves' dams were unavailable, however, the cows were ranch-raised and retained from prior breeding seasons, where bulls used for breeding occasionally had a common ancestor...
April 27, 2024: BMC Genomics
https://read.qxmd.com/read/38674297/uterine-cesarean-scar-tissue-an-immunohistochemical-study
#19
JOURNAL ARTICLE
Maciej Ziętek, Małgorzata Świątkowska-Feund, Sylwester Ciećwież, Tomasz Machałowski, Małgorzata Szczuko
Background and Objectives : Wound healing encompasses a multitude of factors and entails the establishment of interactions among components of the basement membrane. The quantification of particle concentrations can serve as valuable biomarkers for assessing biomechanical muscle properties. The objective of this study was to examine the immunoexpression and immunoconcentration of myometrial collagen type VI, elastin, alpha-smooth muscle actin, and smooth muscle myosin heavy chain, as well as the expression of platelets and clusters of differentiation 31 in the uterine scar following a cesarean section (CS)...
April 18, 2024: Medicina
https://read.qxmd.com/read/38672689/effects-of-adjuvant-exercise-and-nutrition-therapy-on-muscle-fibre-biomechanics-in-gastrointestinal-cancer-patients
#20
JOURNAL ARTICLE
Michael Haug, Raphaela Schwappacher, Charlotte Pollmann, Paul Ritter, Mena Michael, Hans Joachim Hermann, Robert Grützmann, Anke Mittelstädt, Markus Friedrich Neurath, Yurdagül Zopf, Oliver Friedrich
Patients with aggressive cancer, e.g., gastrointestinal cancer, are prone (≥50% chance) to developing cancer cachexia (CC). Little is known about the effects of CC on the biomechanical function of muscle. A promising prevention strategy was found in the form of a multi-modal therapy combining mild resistance exercise (e.g., whole-body electro-myostimulation, WB-EMS) and a protein-rich diet. In a previous study of ours, this was effective in counteracting the loss of muscle mass, yet a systematic and comprehensive assessment of active and passive single muscle fibre functions was so far absent...
April 22, 2024: Cancers
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