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Strahlentherapie Und Onkologie : Organ Der Deutschen Rontgengesellschaft ... [Et Al]|May 25, 2019
Radiogenomics in head and neck cancer: correlation of radiomic heterogeneity and somatic mutations in TP53, FAT1 and KMT2DKerstin Zwirner, Franz J Hilke, German Demidov, et al.
Critical Care (London, England)|September 8, 2017
Weekends affect mortality risk and chance of discharge in critically ill patients: a retrospective study in the Austrian registry for intensive carePaul Zajic, Peter Bauer, Andrew Rhodes, et al.
Philosophical Transactions. Series A, Mathematical, Physical, and Engineering Sciences|April 11, 2019
Assessing the scales in numerical weather and climate predictions: will exascale be the rescue?Philipp Neumann, Peter Düben, Panagiotis Adamidis, et al.
Annals of Neurology|July 3, 2003
Do CTG expansions at the SCA8 locus cause ataxia?Ludger Schöls, Ingrid Bauer, Christine Zühlke, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|December 1, 2022
How relevant are cerebral white matter lesions in the D313Y variant of the α-galactosidase A gene? Neurological, cardiological, laboratory, and MRI data of 21 patients within a follow-up of 3 yearsDaniel Strunk, Jana Becker, Roland Veltkamp, et al.
Life (Basel, Switzerland)|December 23, 2023
Basic ctDNA Panel Promises Affordable Clinical Validity in Colon Cancer Patients but Not in Pancreas Cancer PatientsMandy Radefeldt, Silke Stellmacher-Kaiser, Susann Krake, et al.
The Journal of Allergy and Clinical Immunology|March 19, 2003
The effect of hydrolyzed cow's milk formula for allergy prevention in the first year of life: the German Infant Nutritional Intervention Study, a randomized double-blind trialAndrea von Berg, Sibylle Koletzko, Armin Grübl, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 27, 2016
Individual changes in preclinical spinocerebellar ataxia identified via increased motor complexityWinfried Ilg, Zofia Fleszar, Cornelia Schatton, et al.
Orphanet Journal of Rare Diseases|January 23, 2019
Recommendations for patient screening in ultra-rare inherited metabolic diseases: what have we learned from Niemann-Pick disease type C?María-Jesús Sobrido, Peter Bauer, Tom de Koning, et al.
Neurology|November 8, 2013
De novo mutations in hereditary diffuse leukoencephalopathy with axonal spheroids (HDLS)Kathrin N Karle, Saskia Biskup, Rebecca Schüle, et al.
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