Results 141 to 150 of about 2,286,481 (339)

Visual Recovery Reflects Cortical MeCP2 Sensitivity in Rett Syndrome

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Rett syndrome (RTT) is a devastating neurodevelopmental disorder with developmental regression affecting motor, sensory, and cognitive functions. Sensory disruptions contribute to the complex behavioral and cognitive difficulties and represent an important target for therapeutic interventions.
Alex Joseph Simon, Nathalie Picard, Valeria d'Andrea, Enchi Chang, Joseph Leffler, Eleonora Centofante, Matthew Taylor, Francesca Bardi, Francesca Cavicchiolo, Takao K. Hensch, Stefano Panzeri, Chinfei Chen, Michela Fagiolini   +12 more
wiley   +1 more source

Unraveling the meiotic puzzle: chromosome count, meiotic behaviour, and reproductive challenges in Phlomis cashmeriana Royle ex Benth. from the Kashmir Himalaya

Frontiers in Conservation Science
Meiotic stability is crucial for maintaining reproductive success and genetic diversity in plants, especially in montane regions like the Himalaya, where fluctuating environmental conditions can disrupt normal chromosome behavior.
Roof Ul Qadir, Hanan Javid, Aijaz Hassan Ganie, Bilal A. Wani, Irshad A. Nawchoo, Junaid A. Magray   +5 more
doaj   +1 more source

Characteristics of neurological Wilson’s disease with corpus callosum abnormalities [PDF]

, 2019
Zhihua Zhou, Yunfan Wu, Jin Cao, Jiyuan Hu, Yongzhu Han, Mingfan Hong, Gong-qiang Wang, Shuhu Liu, Wang Xuemin   +8 more
openalex   +1 more source

Skull Abnormalities in Cadavers in the Gross Anatomy Lab [PDF]

, 2020
Jessica De Rose, Brian Yoshio Laing, Maha Ahmad   +2 more
openalex   +1 more source

Abnormal neurobiochemical metabolites in the first- episode schizophrenia and clinical high-risk population. [PDF]

, 2021
Lijun Ouyang, Wenxiao Zheng, Xiaoqian Ma, Yuan Liu, Ying He, Xiaogang Chen   +5 more
openalex   +1 more source

Lesion Location and Functional Connections Reveal Cognitive Impairment Networks in Multiple Sclerosis

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Cognitive impairment, fatigue, and depression are common in multiple sclerosis (MS), potentially due to disruption of regional functional connectivity caused by white matter (WM) lesions. We explored whether WM lesions functionally connected to specific brain regions contribute to these MS‐related manifestations.
Alessandro Franceschini, Paolo Preziosa, Paola Valsasina, Damiano Mistri, Monica Margoni, Federica Esposito, Massimo Filippi, Maria A. Rocca   +7 more
wiley   +1 more source

Interleukin‐6 as a Key Biomarker in Facioscapulohumeral Dystrophy: Evidence From Longitudinal Analyses

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Facioscapulohumeral muscular dystrophy type 1 (FSHD1) is a progressive neuromuscular disorder with no approved treatments. Identifying reliable biomarkers is critical to monitor disease severity, activity, and progression. Interleukin‐6 (IL‐6) has been proposed as a candidate biomarker, but longitudinal validation is limited ...
Jonathan Pini, Emanuela Martinuzzi, Sandra Dhifallah, Abderhmane Slioui, Angela Puma, Luisa Villa, Michele Cavalli, Andra Ezaru, Jérémy Garcia, Manuela Gambella, Federico Torre, Luca Jacopo Pavan, Nicolas Glaichenhaus, Sabrina Sacconi   +13 more
wiley   +1 more source

Nucleosynthesis in the terrestrial and solar atmospheres [PDF]

Variations of Delta D, delta C-13, Delta C-14 and Delta O-18 with time were measured by a lot of experiments. Many abnormalities of isotope abundances in cosmic rays were found by balloons and satellites.
Yu, C., Zhan, S., Zhou, R.
core   +1 more source

Regional Homogeneity Abnormalities in Early-Onset and Adolescent-Onset Conduct Disorder in Boys: A Resting-State fMRI Study [PDF]

, 2019
Wanyi Cao, Chuting Li, Jing Zhang, Daifeng Dong, Xiaoqiang Sun, Shuqiao Yao, Bingsheng Huang, Jun Liu   +7 more
openalex   +1 more source

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