Results 151 to 160 of about 86,511 (262)

Sex‐specific differences in mortality and neurocardiac interactions in the Kv1.1 knockout mouse model of sudden unexpected death in epilepsy (SUDEP)

The Journal of Physiology, EarlyView.
Abstract figure legend The Kcna1 knockout mouse model of sudden unexpected death in epilepsy (SUDEP) exhibits sex‐specific differences in SUDEP risk. Female mice exhibit a lower SUDEP risk than males, despite similar seizure characteristics and interictal cardiac function across sexes.
Kelsey Paulhus, Praveen Kumar, Kelly Kneale, T. Noah Hutson, Nicole M. Gautier‐Hall, Deng‐Shan Shiau, Megan Watts, Krystle Trosclair, Hemangini A. Dhaibar, Paari Dominic, Leonidas Iasemidis, Edward Glasscock   +11 more
wiley   +1 more source

Ectopic Pregnancy with a Normally Located Levonorgestrel-Releasing Intrauterine System in a Woman with Adenomyosis: Case Report and Literature Review. [PDF]

J Clin Med
Martire FG, Costantini E, Zupi E, Lazzeri L.   +3 more
europepmc   +1 more source

Simulation of dB/dt‐Over‐Electric Field Cardiac Magnetostimulation Safety Ratios in 75 Body Models and 18 Gradient Systems

Magnetic Resonance in Medicine, Volume 95, Issue 3, Page 1753-1761, March 2026.
ABSTRACT Purpose The IEC 60601‐2‐33 standard provides consensus‐based safety provisions for MRI equipment. Protection of patients against cardiac stimulation (CS) is based on limiting the maximum E‐field induced by MRI gradient coils. In practice, this is achieved by imposing a conservative dB/dt threshold on any gradient waveform.
Valerie Klein, Jonathan Edmonson, Mathias Davids, Natalie G. Ferris, Matthias Gebhardt, Dominik Rattenbacher, Johan S. van den Brink, Michael Steckner, Lawrence L. Wald, Bastien Guérin   +9 more
wiley   +1 more source

From Suspicion to Confirmation: An Original Study on a Complete Diagnostic Pathway for Ectopic Pregnancy. [PDF]

J Clin Med
Zorilă MV, Iliescu DG, Zorilă GL, Pirici D, Istrate-Ofiţeru AM, Roşu CG, Busuioc CJ, Mogoantă L, Nimigean VR, Căpitănescu RG, Berbecaru EIA, Drăgușin RC, Comănescu MC, Paitici S.   +13 more
europepmc   +1 more source

Fine mapping and functional analysis of the candidate gene OFP17, regulating both seed and fruit sizes in cotton

The Plant Genome, Volume 19, Issue 1, March 2026.
Abstract Single cotton boll weight (BW) and seed index (SI, 100‐seed weight) are key determinants of lint and seed yield, yet their genetic basis remains poorly understood. Here, a stable interploidy introgression line with small boll from Gossypium arboreum in Gossypium hirsutum, NB298, was employed to map quantitative trait loci (QTLs) of BW and SI ...
Min Xu, Liuchun Feng, Susu Liu, Zhechang Zhang, Chenhui Zhou, Guoli Feng, Ningshan Wang, Nijiang Ai, Baoliang Zhou   +8 more
wiley   +1 more source

Heterotopic Pregnancy: Case Study and Literature Review in the Jordanian Royal Medical Services Context. [PDF]

Cureus
Nawafleh MN, Al-Mousa SM, Al-Smadi AA, Al-Omari EJ, Al-Shorman MA.   +4 more
europepmc   +1 more source

Letters to the Editor [PDF]

, 2000
Catholic Physicians\u27 Guild
core   +1 more source

Cidea Targeting Protects Cochlear Hair Cells and Hearing Function From Drug‐ and Noise‐Induced Damage

Advanced Science, Volume 13, Issue 7, 3 February 2026.
Acquired sensorineural hearing loss is primarily caused by the damage or loss of cochlear hair cells, induced by factors such as noise exposure and ototoxic drugs. The deficiency of apoptosis‐inducing gene Cidea in Cidea KO mice or by delivering CRISPR/SlugCas9‐HF via AAV to edit Cidea effectively alleviated hair cell damage and hearing loss caused by ...
Shasha Zhang, Ruiying Qiang, Yuan Zhang, Jinxian Wan, Chen Tao, Ying Dong, Xujun Tang, Li Xu, Hairong Xiao, Yanqin Lin, Wei Tong, Ying Ma, Yongming Wang, Peng Li, Renjie Chai   +14 more
wiley   +1 more source

Effects of somatostatin on calcitonin and ectopic ACTH release in a patient with medullary thyroid carcinoma [PDF]

, 1977
Landgraf, R., Müller, O. A., Scriba, Peter Christian, Ziegler, R.   +3 more
core   +1 more source

A Novel Missense Variant in LMX1A Leads to Autosomal Dominant Nonsyndromic Hearing Loss

American Journal of Medical Genetics Part A, Volume 200, Issue 2, Page 531-534, February 2026.
ABSTRACT Hereditary nonsyndromic hearing loss (NSHL) is a prevalent entity associated with over 150 known causative genes, including LMX1A, which has fewer than 10 reported pathogenic variants. Here we present a novel missense variant in LMX1A in a family of European descent with hereditary hearing loss. Clinical and family histories were obtained, and
Ryan Chen, Dayna Morel Swols, Guney Bademci, Mustafa Tekin   +3 more
wiley   +1 more source