Results 171 to 180 of about 382,892 (381)

Electrode construction Patent [PDF]

, 1970
Electrode attached to helmets for detecting low level signals from skin of living ...
Westbrook, R. M., Zuccaro, J. J.
core   +1 more source

Artificial Intelligence Software Changes Rare Disease Testing Strategy in Real Time: An International Case Series Using Face2Gene

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Genetic disorders commonly share features such as developmental delays, cognitive impairment, and behavioral challenges, yet many conditions also present unique dysmorphic features that distinguish them. Performing a thorough medical and family history and a detailed physical exam with attention to dysmorphic features is often the first step ...
Natasha L. Rudy, Adriana Gomes, Tinatin Tkemaladze, Omar Abdul‐Rahman, Drew Cratsenberg, Giulia Pascolini, Giovanni Di Zenzo, Daniele Castiglia, Emily Black, Camerun Washington, Lauren Chad, Cynthia Curry, Miguel Del Campo, Nicole Fleischer, Lynne M. Bird, Anna C. E. Hurst   +15 more
wiley   +1 more source

Hydrogel and scalp/skin conductivities impact dose from tumor treating fields

Frontiers in Bioengineering and Biotechnology
PurposeTumor Treating Fields (TTFields) are delivered by transducer arrays applied to scalp or body surface for treatment of multiple malignancies. Dermatologic complications are thought to be related to hydrogel situated between the electrodes and scalp
Edwin Lok, Edwin Lok, Olivia Liang, Olivia Liang, Monika Haack, Eric T. Wong, Eric T. Wong, Eric T. Wong   +7 more
doaj   +1 more source

A CASE OF MULTIPLE BENIGN BASAL-CELL EPITHELIOMA OF THE SCALP, WITH SOME REMARKS ON THE TUMOURS OF THE SCALP COMMONLY CALLED "ENDOTHELIOMA CAPITIS" AND "SARCOMA CAPITIS." [PDF]

, 1918
H. G. Adamson
openalex   +1 more source

Genotype–Phenotype Correlations, Mortality, and Clinical Insights in Keratitis–Ichthyosis–Deafness Syndrome: A Comprehensive Review and Case Report

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Keratosis–ichthyosis–deafness (KID) syndrome is a rare autosomal dominant ectodermal disease caused by mutations in the GJB2 gene, which encodes the gap junction protein Connexin 26 (Cx26) located on Chr. 13q12.11. This study presents the first mortality analysis associated with KID syndrome, focusing on a case report of a Latin American ...
Leslie Patrón‐Romero, Marco Antonio Hernández Lepe, José de Jesús Manríquez Torres, Diego Daniel Aguirre‐Gómez, Natsuo Hayashi‐Mercado, Genaro Rodríguez Uribe, Tadeo Cerón, María Ruiz‐Gamboa, Jesús Alonso Gándara‐Mireles, Ismael Lares‐Asseff, Verónica Loera‐Castañeda, Jorge Alvelais‐Palacios, Lucrecia Arzamendi‐Cepeda, Lidia Magdalena Castañeda‐González, Adolfo García‐Barrón, Francisco Yamal Quiroz Herrera, Francisco González‐Salazar, Horacio Almanza‐Reyes   +17 more
wiley   +1 more source

Glioblastoma multiforme recurrence on skin and subcutaneous tissue: a case report

Exploration of Neuroscience
Glioblastoma multiforme (GBM) is the most common malignant primary central nervous system (CNS) tumor. It presents an aggressive pattern, with a tendency for intracranial progression despite optimal treatment.
Maria Ciscar-Fabuel, Alexandre De Vilalta-Bufurull, Gemma Blanch-Pujol, Marina Romero-Quintela, Gerard Plans-Ahicart, Andreu Gabarros-Canals   +5 more
doaj   +1 more source

Note on the Scalp of a Negro [PDF]

, 1873
Charles Stewart
openalex   +1 more source

Optimising the number of channels in EEG-augmented image search [PDF]

, 2011
Recent proof-of-concept research has appeared showing the applicability of Brain Computer Interface (BCI) technology in combination with the human visual system, to classify images.
Healy, Graham, Smeaton, Alan F.
core  

Poland Anomaly and Atretic Cephalocele in the Same Child: Coincidence or Association?

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Poland Anomaly is a rare congenital disorder typically characterized by hypoplasia or agenesis of pectoral muscle with or without ipsilateral limb hypoplasia. The association of central nervous system malformation with Poland Anomaly has been rarely reported and includes craniofacial dysplasia, microcephaly, and Dandy‐Walker malformation ...
Alessandra Greta Grassi, Silvia Pontesilli, Laura Demelas, Francesca Vigliani, Massimo Agosti, Angelo Selicorni   +5 more
wiley   +1 more source

An Extensive Bruise on the Hemiface: CARE Clinical Case

Journal of International Advanced Otology
Cutaneous angiosarcomas of the scalp are rare and aggressive tumors with non-specific appearances. They rarely affect the retroauricular region, and diagnoses are often difficult and delayed.
Mathilda Rausch, Raphaële Quatre
doaj   +1 more source