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Frontiers in Rehabilitation Sciences|October 13, 2022
Reduction in school individualized education program (IEP) services during the COVID-19 pandemicBelinda Chen, Patrick Rasmussen, Mallory Legg, et al.
American Journal of Human Genetics|April 6, 2010
Mutations in the gene encoding the RER protein FKBP65 cause autosomal-recessive osteogenesis imperfectaYasemin Alanay, Hrispima Avaygan, Natalia Camacho, et al.
Pneumologie (Stuttgart, Germany)|January 18, 2013
[German guideline for diagnosis and management of idiopathic pulmonary fibrosis]J Behr, A Günther, W Ammenwerth, et al.
Biochemical and Biophysical Research Communications|September 24, 2004
4-Epidoxycycline: an alternative to doxycycline to control gene expression in conditional mouse modelsK Eger, M Hermes, K Uhlemann, et al.
Cell Reports|September 22, 2021
CCR2 deficiency alters activation of microglia subsets in traumatic brain injuryKerri Somebang, Joshua Rudolph, Isabella Imhof, et al.
Nature Genetics|October 5, 2010
Mutations in GRIN2A and GRIN2B encoding regulatory subunits of NMDA receptors cause variable neurodevelopmental phenotypesSabine Endele, Georg Rosenberger, Kirsten Geider, et al.
Europace : European Pacing, Arrhythmias, and Cardiac Electrophysiology : Journal of the Working Groups on Cardiac Pacing, Arrhythmias, and Cardiac Cellular Electrophysiology of the European Society of Cardiology|October 11, 2017
Sex differences in outcomes of primary prevention implantable cardioverter-defibrillator therapy: combined registry data from eleven European countriesChristian Sticherling, Barbora Arendacka, Jesper Hastrup Svendsen, et al.
Nature Communications|November 5, 2025
Shifting dominant periods in extreme climate impacts under global warmingKarim Zantout, Juraj Balkovic, Maik Billing, et al.
The New England Journal of Medicine|February 28, 2014
Constitutive activation of PKA catalytic subunit in adrenal Cushing's syndromeFelix Beuschlein, Martin Fassnacht, Guillaume Assié, et al.
American Journal of Medical Genetics. Part A|September 11, 2010
Phenotypic features of carbohydrate sulfotransferase 3 (CHST3) deficiency in 24 patients: congenital dislocations and vertebral changes as principal diagnostic featuresSheila Unger, Ekkehart Lausch, Antonio Rossi, et al.
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