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Neurology|January 13, 2010
Correlation of enzyme activity and clinical phenotype in POMT1-associated dystroglycanopathiesM Lommel, S Cirak, T Willer, et al.
Journal of Vector Ecology : Journal of the Society for Vector Ecology|June 6, 2015
Dengue virus detection in Aedes aegypti larvae from southeastern BrazilSamyra Giarola Cecílio, Willer Ferreira Silva Júnior, Antônio Helvécio Tótola, et al.
Wiener Klinische Wochenschrift|May 20, 2026
[Mental and neurocognitive diseases and diabetes mellitus (Update 2026)]Heidemarie Abrahamian, Alexandra Kautzky-Willer, Angelika Rießland-Seifert, et al.
Dental Press Journal of Orthodontics|April 10, 2014
Shear bond resistance and enamel surface comparison after the bonding and debonding of ceramic and metallic bracketsJosé Maurício da Rocha, Marco Abdo Gravina, Marcio José da Silva Campos, et al.
Investigative Ophthalmology & Visual Science|March 11, 2017
Systematic Functional Testing of Rare Variants: Contributions of CFI to Age-Related Macular DegenerationPerciliz L Tan, Melanie E Garrett, Jason R Willer, et al.
European Journal of Nuclear Medicine and Molecular Imaging|May 17, 2023
Excretion of glucose analogue with SGLT2 affinity predicts response effectiveness to sodium glucose transporter 2 inhibitors in patients with type 2 diabetes mellitusBarbara Katharina Geist, Helmut Brath, Lucia Zisser, et al.
The Journal of Clinical Endocrinology and Metabolism|April 29, 2020
The Presence of Active Brown Adipose Tissue Determines Cold-Induced Energy Expenditure and Oxylipin Profiles in HumansOana C Kulterer, Laura Niederstaetter, Carsten T Herz, et al.
Diabetologia|September 25, 2012
A two-step screening algorithm including fasting plasma glucose measurement and a risk estimation model is an accurate strategy for detecting gestational diabetes mellitusC S Göbl, L Bozkurt, P Rivic, et al.
Behavior Research Methods|April 27, 2021
The Croatian psycholinguistic database: Estimates for 6000 nouns, verbs, adjectives and adverbsAnita Peti-Stantić, Maja Anđel, Vedrana Gnjidić, et al.
Neuromuscular Disorders : NMD|April 4, 2009
Further evidence of Fukutin mutations as a cause of childhood onset limb-girdle muscular dystrophy without mental retardationRebecca L Puckett, Steven A Moore, Thomas L Winder, et al.
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