Results 61 to 70 of about 1,018,726 (311)

Anomalías congénitas de la columna vertebral: el caso de Fuentenegroso [PDF]

, 2011
X Congreso Nacional de Paleopatología.
Barrio, P., Grueso, I., Martínez Ávila, M., Robledo, B., Trancho, G.J.   +4 more
core  

Brachyury‐Activated Fucoidan Hydrogel Microspheres Rejuvenate Degenerative Intervertebral Discs Microenvironment

Advanced Science, EarlyView.
This study describes the creation of injectable Brachyury (Bry) mRNA‐loaded Fucoidan‐functionalized GelMA hydrogel microspheres (BLNP@GF). These microspheres efficiently suppress inflammation, enhance extracellular matrix (ECM) synthesis in degenerated nucleus pulposus cells, and mitigate intervertebral disc degeneration (IVDD) in rat models.
Yuhao Gong, Wenxiao Shi, Xingzhu Liu, Hang Yu, Yinghui Wu, Yanzhang Xia, Caichun Yue, Chongkai Yang, Cong Shen, Renjun Pei, Tianwen Xin, Hailong Pei, Jun Shen   +12 more
wiley   +1 more source

Factores pronósticos para artrodesis lumbar

Revista Universitas Medica, 2019
El dolor de espalda es uno de los síntomas más frecuentes en las instituciones de salud. La neurocirugía desempeña un papel importante en el diagnóstico y tratamiento del dolor de espalda que a menudo resulta en intervenciones quirúrgicas que incluyen la
Carlos Alberto Lindado Pacheco, Santiago Gutiérrez, Juan Carlos Acevedo González   +2 more
doaj   +1 more source

Tratamiento quirúrgico de la escoliosis en el síndrome de Rett: sistema de instrumentación TRANSPINE [PDF]

, 2010
El Síndrome de Rett es una afectación neurológica que en los estadios últimos presenta deformidades evolutivas que suelen precisar cirugía. Se han revisado en este estudio 11 pacientes con Síndrome de Rett y deformidad en columna que precisaron cirugía ...
Bas Hermida, P., Bas Hermida, Teresa, Bonete Lluch, D., Escribá Roca, Ismael, Pérez Millán, L. A.   +4 more
core  

Worth the Effort: Lessons for Discovery and Care From an Unusual Case of Gorlin Syndrome

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Gorlin‐Goltz Syndrome (GGS) is a rare autosomal dominant genetic disorder encompassing a diverse range of clinical manifestations, including congenital anomalies and predisposition to cancer. Pathogenic variants in PTCH1 and SUFU account for up to 79% and 6% of cases, respectively. Currently, an estimated 15%–27% of individuals with a clinical
V. Taliercio, J. Zhao, S. E. Boyden, R. Mao, P. Bayrak‐Toydemir, A. Pflaum, J. Palumbos, A. Andrews, E. E. Baldwin, C. Welt, Mackenzie Fait, Undiagnosed Diseases Network, L. D. Botto, D. Viskochil   +13 more
wiley   +1 more source

LAMINOPLASTY AND CORPECTOMY IN THE TREATMENT OF CERVICAL SPONDYLOTIC MYELOPATHY

Coluna/Columna
Introduction: Cervical Spondylotic myelopathy (CSM) is a disabling manifestation of extended cervical stenosis characterized by pronounced neurological dysfunction. Decompressive interventions contribute to significant regression of symptoms and, in some
Dreval’ Maxim Dmitrievich, Arestov Sergey Olegovich, Petrosyan David Vazgenovich, Kashcheev Alexey Alexeevich, Vershinin Andrey Vyacheslavovich, Poltorako Ekaterina Nikolaevna, Gushcha Artem Olegovich   +6 more
doaj   +1 more source

Mielopatía compresiva por occipitalización del atlas [PDF]

, 1996
Se presenta un caso clínico de occipitalización del atlas, alteración congénita caracterizada por la existencia de una fusión parcial o total del anillo óseo del atlas con la base del occipucio.
Boronat Pérez, J., Pina Medina, A.
core  

La tumba romana de Orippo, Sevilla [PDF]

, 1992
En este articulo se desarrolla la metodología antropológica sobre dos incineraciones procedentes de una tumba romana de Orippo (Sevilla), excavada en 1988 y datada en el siglo I DC.
Alcázar, José, Mantero, Antonio
core   +1 more source

Survivorship of Individuals With Double Heterozygosity for Achondroplasia and Type 2 Collagenopathy

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Historically, double heterozygosity, or a diagnosis of two separate, dominant genetic conditions, was often thought to be lethal in individuals with autosomal dominant skeletal dysplasias. In previously published studies of individuals with dual dysplasia diagnoses of achondroplasia and type 2 collagenopathy, infants died of respiratory ...
Valerie R. Schwartz, Andrea Schelhaas, Angela L. Duker, Ricki S. Carroll   +3 more
wiley   +1 more source

ASPECTS OF THE USE OF PROPENSITY SCORE MATCHING METHODS IN NEUROSURGERY

Coluna/Columna
Objective Observational studies and register data provide researchers with ample opportunities to obtain answers to questions that randomized controlled trials cannot answer for organizational or ethical reasons. One of the most common tools for solving
ALEKSANDR V. KRUTKO, SHAMIL A. AKHMETYANOV, KIRILLYU ORLOV, VICTOR S. GLADKIKH, ANDREY V. MOSKALEV   +4 more
doaj   +1 more source