Results 161 to 170 of about 40,116 (312)

[Epilepsy in Patients With Moyamoya Angiopathy]. [PDF]

Rev Neurol
Bautista-Lacambra M, Garayoa-Irigoyen V, Tique-Rojas LF, Seral-Moral M, Moles-Herbera J, López-Lafuente A, Barrena-Caballo R, Tejero-Juste C, Palacín-Larroy M, Tejada-Meza H.   +9 more
europepmc   +1 more source

Causal analysis of trade loss from pathogens: A global study of foot and mouth disease impacts on meat exports

American Journal of Agricultural Economics, EarlyView.
Abstract Our general interest is in global trade loss from livestock pathogens, specifically exports. We adopt a causal inference approach that considers animal disease outbreaks over time as non‐staggered binary treatments with the potential for switching in (infection) and out of treatment (recovery) within the sample period. The outcome evolution of
Mohammad Maksudur Rahman, Thomas L. Marsh   +1 more
wiley   +1 more source

Pseudooclusión carotídea: un concepto a tener en cuenta en el ictus agudo

Neurología, 2020
H. Tejada Meza, J. Artal Roy, M. Serrano Ponz, S. Guelbenzu Morte, J. Marta Moreno   +4 more
doaj   +1 more source

Editors' Pick in March 2026. [PDF]

J Korean Neurosurg Soc
Yang HJ.
europepmc   +1 more source

From Multiple Congenital Anomalies to Pituitary Gland Malformation: Wide Spectrum of Clinical Features in a Family With FOXA2 Variant

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT FOXA2 (hepatocyte nuclear factor‐3β, HNF‐3β) encodes a transcriptional activator involved in early embryogenesis, particularly in the patterning and differentiation of midline structures such as the neural tube, foregut, and pituitary gland. Its role in human pathogenesis was first suspected when patients with deletion of chromosome 20p11.2 ...
Christopher Connolly, Hemant A. Parmar, Lauren Hipp, Tomoyasu Higashimoto   +3 more
wiley   +1 more source

Extended CTA scan range for early detection of left atrial and left atrial appendage thrombus and other filling defects in acute ischemic stroke. [PDF]

J Neurol
Marta-Enguita J, Biain S, Ayuso D, Vasquez-Ferreccio S, Del Bosque C, de la Riva P, Diez N, Gonzalez F, de Arce A, Equiza J, Arenaza G, Gomez-Usabiaga V, Martinez-Zabaleta M.   +12 more
europepmc   +1 more source

First Korean Case of 5q35.2q35.3 Microduplication With Reversed Sotos Syndrome Phenotype and Growth Hormone Deficiency: Expanding the Endocrine Spectrum

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Sotos syndrome is an overgrowth disorder caused by nuclear receptor binding SET domain protein 1 (NSD1) haploinsufficiency, whereas reciprocal 5q35.2q35.3 microduplication produces a reversed phenotype with growth retardation, microcephaly, delayed bone age, and neurodevelopmental delay.
Sejin Kim, Jung Sook Ha, Jun Chul Byun
wiley   +1 more source

Remote Language Assessment in School‐Age Children With Phelan–McDermid Syndrome and Genotype–Phenotype Correlation

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT People with Phelan–McDermid syndrome (PMS) have reduced speech and language abilities, yet little research has profiled the communication abilities in this population. The purpose of this study was threefold: identifying the language and communication profiles of school‐aged children with PMS, identifying genetic contributions to language and ...
Sarah Quadri‐Valverde, Jessica Klusek, Linda D. Ward, Diana Ivankovic, Nancy Powers, Vijay Shankar, Rachel A. Lyman, Trudy F. C. Mackay, William Bridges, Katy Phelan, Curtis Rogers, Luigi Boccuto, Sara M. Sarasua   +12 more
wiley   +1 more source

Changes in hemorrhage pattern on consecutive non-contrast CT scans in non-aneurysmal subarachnoid hemorrhage patients. [PDF]

Brain Spine
van den Berg R, Dronkers W, Berkhemer O, Karbe A, Germans M, Vandertop WP, Emmer BJ, Verbaan D.   +7 more
europepmc   +1 more source

Training the ear, or: On learning to hear the alexandrin [PDF]

, 2014
Nowell Smith, David
core