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Journal of Neuroscience Research|June 26, 2021
The organization of functional neurocognitive networks in focal epilepsy correlates with domain-specific cognitive performanceChristoffer Hatlestad-Hall, Ricardo Bruña, Aksel Erichsen, et al.
Infection & Chemotherapy|July 3, 2021
Nanoemulsions with Chloroaluminium Phthalocyanine and Paromomycin for Combined Photodynamic and Antibiotic Therapy for Cutaneous LeishmaniasisSandra Milena Leal Pinto, Luis Alexandre Muehlmann, Lucía Liliana Mantilla Ojeda, et al.
Clinical Genetics|March 14, 2014
Analysis of current testing practices for biallelic MUTYH mutations in MUTYH-associated polyposisM Landon, S Ceulemans, D S Saraiya, et al.
Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology|June 12, 2014
Improvement of the Rett syndrome phenotype in a MeCP2 mouse model upon treatment with levodopa and a dopa-decarboxylase inhibitorKarolina Szczesna, Olga de la Caridad, Paolo Petazzi, et al.
Frontiers in Medicine|February 27, 2025
Prevalence of gastroparesis symptoms and its associated factors among type 2 diabetes mellitus patients in West Bank in Palestine: a national cross-sectional studyDiya Asad, Qusai Zreqat, Shahd Idais, et al.
BMC Health Services Research|May 2, 2026
Factors associated with healthcare seeking behavior from private clinics among patients in Riyadh, Saudi ArabiaRoa Altaweli, Mamdouh M Shubair, Rawan Ahmed Alshagha, et al.
Frontiers in Medicine|June 26, 2026
Gender differences in symptoms suggestive of diabetic gastroparesis in the West Bank: clinical insights from a cross-sectional studyDiya Asad, Qusai Zreqat, Shahd T Idais, et al.
Blood Advances|March 10, 2020
CLL intraclonal fractions exhibit established and recently acquired patterns of DNA methylationBoris A Bartholdy, Xiahoua Wang, Xiao-Jie Yan, et al.
Rheumatology International|April 25, 2025
Barriers and facilitators associated with diagnostic and treatment delays in lupus in the Global South and North: a systematic review of qualitative and mixed methods studiesAmaranta Manrique de Lara, Tirsa Colmenares-Roa, Laura Athié, et al.
Nature Genetics|October 1, 1993
Evidence for a recessive PMP22 point mutation in Charcot-Marie-Tooth disease type 1AB B Roa, C A Garcia, L Pentao, et al.
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