Results 31 to 40 of about 2,008 (151)

Homonymous hemiatrophy of ganglion cell layer from retrochiasmal lesions in the visual pathway. [PDF]

, 2020
OBJECTIVE To determine the temporal evolution, morphology, and frequency of macular ganglion cell atrophy in patients with retrochiasmal lesions of the visual pathway. METHODS In a consecutive retrospective case series, we identified 47 patients
Mühlemann, Fabian, Wagner, Franca, Sheldon, Claire A, Brügger, Dominik, Grabe, Hilary, Fok, Anthony, Abegg, Mathias, Grabe H, Wagner F, Mühlemann F, Fok A, Sheldon CA, Brügger D, Abegg M   +13 more
core   +2 more sources

Dyke-Davidoff-Masson Syndrome (DDMS) in Adult: A Rare Case in Rural Area

Aksona, 2023
Highlight: • Dyke-Davidoff-Masson syndrome (DDMS) is an uncommon neurological disease defined as cerebral hemiatrophy with a contralateral motor deficit, facial asymmetry, and seizures.
Indra Pramanasari
doaj   +1 more source

Dyke-Davidoff-Masson syndrome: An endocrine perspective [PDF]

Romanian Medical Journal, 2020
Dyke-Davidoff-Masson syndrome (DDMS) represents a severe disease that is caused by brain anomalies of different mechanisms early in life during fetal period or within first years after birth.
Cristina Dumitrescu, Anda Dumitrascu, Corina Chirita, Eugenia Petrova, Nicoleta Dumitru, Adina Ghemigian, Mara Carsote, Dana Terzea, Ana Valea   +8 more
doaj   +1 more source

Marked hemiatrophy in carriers of Duchenne muscular dystrophy

, 2010
OBJECTIVE: To describe the clinical and molecular genetic findings in 2 carriers of Duchenne muscular dystrophy (DMD) who exhibited marked hemiatrophy. Duchenne muscular dystrophy is an X-linked disorder in which affected male patients harbor mutations ...
Holton, Janice L., Yau, Shu C., Yousry, Tarek, Dunand, Murielle, Farmer, Simon, Abbs, Stephen, Thonney, Francine, Rajakulendran, Sanjeev, McCauley, Joanna, Hanna, Michael G., Kuntzer, Thierry, Storey, Helen, Lobrinus, Johannes Alexander, Ashton, Emma J., Leturcq, France, Shu C. Yau, Murielle Dunand, France Leturcq, Michael G. Hanna, Tarek Yousry, Janice L. Holton, Helen Storey, Francine Thonney, Sanjeev Rajakulendran, Simon Farmer, Thierry Kuntzer, Johannes A. Lobrinus, Joanna McCauley, Stephen Abbs, Emma J. Ashton   +29 more
core   +2 more sources

Computed Tomographical Characterisation of Dyke-Davidoff-Masson Syndrome: A Case Series [PDF]

Journal of Clinical and Diagnostic Research
Dyke-Davidoff-Masson Syndrome (DDMS) is a rare neurological disorder that primarily manifests through various neurological symptoms, with a significant focus on contralateral hemiparesis and convulsive disorders that often show resistance to standard ...
Krishna Madhukarrao Maske, Kalyani Santosh Jethlia, Anil Gopal Tapdiya, Ameet Chandrakant Panchmahalkar, T Rajalakshmi   +4 more
doaj   +1 more source

Progressive Facial Hemiatrophy Revisited

, 2011
ObjectiveTo report a case of progressive facial hemiatrophy with unusual features of contralateral brain atrophy and transcranial Doppler ultrasound evidence of autonomic dysfunction.DesignCase report.SettingA teaching hospital.PatientA 63-year-old man ...
Hong-Liang Zhang, Zhen-Ni Guo, Yi Yang, Hong-Wei Zhou, Wen-Jing Lan, Jiang Wu   +5 more
core   +1 more source

Dyke-Davidoff-Masson Syndrome

Journal of Nobel Medical College, 2012
Dyke-Davidoff-Masson Syndrome (DDMS) is characterized by seizures, facial asymmetry, contralateral hemiplegia and mental retardation. The characteristic radiologic features are cerebral hemiatrophy with homolateral hypertrophy of the skull and sinuses ...
Naba Raj Koirala, Roshana Khadka, Manoj Bhattarai, Dibya Tulachan, Ajay Kumar Das, Jwalanta Poudel   +5 more
doaj   +1 more source

Progressive facial hemiatrophy with associated osseous lesions [PDF]

, 2007
Progressive facial hemiatrophy (PFH) is a rare condition characterized by the slow, progressive appearance of a unilateral facial atrophy that affects the skin, subcutaneous tissue, muscle and bone.
Pérez Oliva,Narciso, López Escobar,María, Junquera Gutiérrez,Luis, Gallego López,Lorena, Gómez Diez,Santiago   +4 more
core   +3 more sources

Unilateral cerebral atrophy: Severe neuroimaging feature of incontinentia pigmenti without acute encephalopathic state

Journal of Pediatric Neurosciences, 2018
Incontinentia pigmenti (IP) is a rare X-linked multisystem disease caused because of mutation in the IKBKG (inhibitor of kappa-B kinase gamma, previously NEMO) gene.
Debopam Samanta
doaj   +1 more source

Characterizing Metabolic and Compositional Heterogeneity of Calf Muscle Using CEST MRI at 3 T

NMR in Biomedicine, Volume 39, Issue 8, August 2026.
This study used 3 T CEST MRI to characterize metabolic and compositional heterogeneity in eight healthy calf muscles, focusing on amide, PCr, rNOE, and MT contrasts. Distinct signatures emerged between deep stabilizer and superficial powerhouse muscles. Significant correlations with age, fat content, BMI, and strength (e.g., rNOE vs. strength) revealed
Huabin Zhang, Kangli Pi, Ziyan Wang, Fan Huang, Juan Wei, Patrick Liebig, Lin Chen, Yang Zhou, Yi Zhang, Varut Vardhanabhuti, Jianpan Huang   +10 more
wiley   +1 more source