Results 31 to 40 of about 7,576 (238)

Characterizing Cutaneous α‐Synuclein Deposition and Seeding Activity in Parkinson's Disease Subtypes

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Cutaneous phosphorylated α‐synuclein (p‐syn) and α‐synuclein seeding activity are promising biomarkers for Parkinson's disease (PD), but their clinical value remains uncertain due to disease heterogeneity. This study evaluates these two biomarkers in PD patients to inform phenotype‐specific diagnosis and disease severity assessment ...
Yuting Jin, Tianyuan Yang, Minglei Liu, Haiyang Luo, Jing Yuan, Ke Zhang, Xinsheng Han, Jing Yang, Yuming Xu   +8 more
wiley   +1 more source

Two-level total disc replacement with Mobi-C(r) over 3-years

Coluna/Columna, 2014
Objective: To evaluate the safety and effectiveness of two-level total disc replacement (TDR) using a Mobi-C(r) Cervical Artificial Disc at the 36 month follow-up.
Reginald Davis, Pierce Dalton Nunley, Kee Kim, Michael Hisey, Hyun Bae, Gregory Hoffman, Steven Gaede   +6 more
doaj   +1 more source

Intelligent Orthopedics: Machine Learning in Diagnosis of Bone Disease, Implants, and Bone Health Monitoring

Advanced Healthcare Materials, EarlyView.
Efficient recovery from traumatic or degenerative diseases is a great challenge, even after all the advancements in bone and cartilage regeneration. Machine learning (ML) algorithms have presented opportunities to enhance these aspects by accurately analyzing imaging data.
Maryam Kamaei, Hesam Mohammadi, Shamim Golafshan, Mojtaba Alehosseini, Mahsa Mohammadzadeh, Atefeh Golshirazi, Nasim Golafshan, Tatiane Eufrásio‐da‐Silva, Alireza Dolatshahi‐Pirouz, Gorka Orive   +9 more
wiley   +1 more source

Restos de un dinosaurio (Ornithopoda: Styracosterna) cf. Magnamanus soriaensis del Cretácico Inferior de Soria, España

Estudios Geologicos
La especie Magnamanus soriaensis (Ornithopoda: Styracosterna) se describió en el año 2016 a partir de un esqueleto parcial descubierto en el año 2000 en el yacimiento de “Zorralbo I” en la localidad de Golmayo (Soria, España), perteneciente ...
Carolina Fuentes-Vidarte, Manuel Meijide-Fuentes, Federico Meijide-Fuentes, Manuel Meijide-Calvo   +3 more
doaj   +1 more source

Mielopatía estenótica vertebral cervical (MEVC) en un caballo criollo colombiano.

Revista Colombiana de Ciencia Animal Recia, 2014
Se expone el caso de un caballo criollo Colombiano, de trocha fina, color moro, macho entero y 17 años de edad, el cual fue diagnosticado con Mielopatía Estenótica Vertebral Cervical (MEVC), procedente del municipio de Chimá (Córdoba, Colombia).
JOSE CARDONA A., M MARTINEZ, O.J PEREZ
doaj   +1 more source

Deubiquitination of Vangl by USP6 and USP32 Regulates Planar Cell Polarity Signaling

Advanced Science, EarlyView.
Compartment‐specific deubiquitination controls Vangl dosage and planar cell polarity signaling. USP6 and USP32 regulate distinct subcellular pools of Vangl by removing distinct ubiquitin modifications from Vangl proteins. This regulatory mechanism safeguards PCP‐dependent embryonic morphogenesis, while aberrant USP32‐dependent stabilization of VANGL ...
Fangzi Zha, Di Feng, Ziru Xue, Zhiying Liu, Xiaochen Lin, Zhe Wang, Ling Xu, Jasper Fuk Woo Chan, Martin Cheung, Michael Shing Yan Huen, Yusong Guo, Kui Ming Chan, Yun Liu, Bo Gao   +13 more
wiley   +1 more source

Indicadores de maduración esquelética y dental en pacientes de ortodoncia con menarquía

Revista Cubana de Estomatología, 2012
El propósito del presente trabajo fue determinar según la menarquía: la edad ósea, los estadios de maduración esquelética, los estadios de maduración de las vértebras cervicales y los estadios de calcificación del canino y el segundo premolar ...
Gladia Toledo Mayarí
doaj  

Spinal Involvement in Charge Syndrome: Implications for Management

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT CHARGE syndrome (OMIM #214800) is an autosomal dominant disorder caused by mutations in the CHD7 gene in most cases. Although originally defined by the CHARGE acronym (coloboma, heart defects, choanal atresia, growth restriction, genital hypoplasia, and ear anomalies), the recognized phenotype has expanded considerably to include highly ...
Adriana Gomes, Álvaro Martín‐Rodríguez, Miguel del Campo Casanelles, Marilyn C. Jones, Daniela Carvalho, Lynne M. Bird   +5 more
wiley   +1 more source

Relación entre la calcificación del canino mandibular permanente y la maduración ósea de las vértebras cervicales [PDF]

, 2016
Compara la maduración ósea de las vértebras cervicales y la calcificación del canino mandibular izquierdo, para lo cual se evaluaron 150 radiografías panorámicas y 150 radiografías cefalométricas de pacientes entre los 6 y 19 años; 96 de sexo femenino y
Poma Salazar, Giuliana Gina María
core  

A Rare Form of Microcephalic Primordial Dwarfism due to NSMCE2 Deficiency (Seckel Syndrome Type 10): A Report of Macular Involvement

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Biallelic variants in NSMCE2 (MMS21), which encodes the SUMO E3 ligase subunit of the SMC5/6 chromatin‐maintenance complex, have recently been implicated in microcephalic primordial dwarfism (MPD), corresponding to Seckel syndrome type 10 (OMIM #617246).
Cristina Peduto, Céline Huber, Clément Paya, Isabelle Audo, Nathalie Boddaert, Valérie Cormier‐Daire   +5 more
wiley   +1 more source