Results 141 to 150 of about 1,016,426 (283)

Biomedical Engineering. Three-dimensional Primary Cultures and Characterization of Monolayers with the Rabbit's Tracheal Epithelium.

, 1998
Hiroshi Takano, Mitsuro Kato, Masayuki Itoh   +2 more
openalex   +2 more sources

Expanding Hereditary Spastic Paraplegias Limits: Biallelic SPAST Variants in Cerebral Palsy Mimics

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Hereditary spastic paraplegias (HSP) are rare neurodegenerative disorders marked by spasticity and lower limb weakness. The most common type, SPG4, is usually autosomal dominant and caused by SPAST gene variants, typically presenting as pure HSP.
Gregorio A. Nolasco, Mònica Roldán, Yalda Jamshidi, Ioannis Georvasilis, Rocío Jadraque Rodríguez, Reza Boostani, Ali Shoeibi, Lluís Armengol, Anna Codina, Ehsan Ghayoor Karimiani, Cristina Hernando‐Davalillo, Loreto Martorell, María Luisa Ramírez Almaraz, Jordi Muchart, Carlos Ortez, Andrés Nascimento, Roser Urreizti, Daniel Natera‐de Benito, Mercedes Serrano   +18 more
wiley   +1 more source

Emerging biotechnologies and biomedical engineering technologies for hearing reconstruction. [PDF]

Smart Med, 2023
Hu Y, Fang L, Zhang H, Zheng S, Liao M, Cui Q, Wei H, Wu D, Cheng H, Qi Y, Wang H, Xin T, Wang T, Chai R.   +13 more
europepmc   +1 more source

Biomedical Engineering. Release Property of Swelling Controlled Polymer System.

, 1998
Yoshio Nakano, Yoshimi Seida, Yoji Abe
openalex   +2 more sources

SNUPN‐Related Muscular Dystrophy: Novel Phenotypic, Pathological and Functional Protein Insights

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective SNUPN‐related muscular dystrophy or LGMDR29 is a new entity that covers from a congenital or childhood onset pure muscular dystrophy to more complex phenotypes combining neurodevelopmental features, cataracts, or spinocerebellar ataxia. So far, 12 different variants have been described.
Nuria Muelas, Pablo Iruzubieta, Alberto Damborenea, Laura Pérez‐Fernández, Inmaculada Azorín, Juan Carlos Jiménez García, Ana Töpf, Pilar Martí, Lorena Fores‐Toribio, María Manterola, Rosana Blanco‐Mañez, Oihane Pikatza‐Menoio, Sonia Alonso‐Martín, Volker Straub, Aitziber L. Cortajarena, Adolfo López de Munain, David De Sancho, Lorea Blázquez, Juan J. Vilchez   +18 more
wiley   +1 more source

Exciting Challenge of Biomedical Engineering. Micromachining and Minimally Invasive Therapy.

, 1999
江刺 正喜, 芳賀 洋一
openalex   +2 more sources

CSF Levels of NPTX2 Are Associated With Less Brain Atrophy Over Time in Cognitively Unimpaired Individuals

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Introduction Neuronal pentraxin 2 (NPTX2) is a synaptic protein involved in synaptic plasticity and regulation of neuronal excitability. Lower baseline cerebrospinal fluid (CSF) NPTX2 levels have been shown to be associated with an earlier onset of mild cognitive impairment (MCI), a pre‐dementia syndrome, even after CSF Alzheimer's Disease (AD)
Juan P. Vazquez, Corinne Pettigrew, Yuxin Zhu, Claire Anderson, Guray Erus, Christos Davatzikos, Michael Miller, Abhay Moghekar, Sungtaek Oh, Chan‐Hyun Na, Marilyn Albert, Paul Worley, Anja Soldan   +12 more
wiley   +1 more source

Virtual and augmented reality in biomedical engineering. [PDF]

Biomed Eng Online, 2023
Taghian A, Abo-Zahhad M, Sayed MS, Abd El-Malek AH.   +3 more
europepmc   +1 more source

Engineering of materials for biomedical applications

, 2000
Kay C Dee, David A. Puleo, Rena Bizios
openalex   +1 more source

Introduction to Biomedical Engineering Second edition. Edited by: Enderle J, Blanchard S, Bronzino [PDF]

, 2005
Amit Gefen
openalex   +1 more source