[HTML][HTML] Posterior cortical atrophy

SJ Crutch, M Lehmann, JM Schott… - The Lancet …, 2012 - thelancet.com
Posterior cortical atrophy (PCA) is a neurodegenerative syndrome that is characterised by
progressive decline in visuospatial, visuoperceptual, literacy, and praxic skills. The …

Overtraining in endurance athletes: a brief review.

M Lehmann, C Foster, J Keul - Medicine and science in sports and …, 1993 - europepmc.org
Overtraining is an imbalance between training and recovery, exercise and exercise capacity,
stress and stress tolerance. Stress is the sum of training and nontraining stress factors. …

[PDF][PDF] Online peer-to-peer lending-a literature review

…, M Hilker, F Kock, M Lehmann… - Journal of Internet …, 2011 - researchgate.net
The term online peer-to-peer lending (P2P) describes the loan origination process between
private individuals on online platforms were financial institutions operate only as …

[HTML][HTML] Olfactory transmucosal SARS-CoV-2 invasion as a port of central nervous system entry in individuals with COVID-19

…, J Schneider, S Brünink, S Greuel, M Lehmann… - Nature …, 2021 - nature.com
… Autopsy tissues were fixed with 2.5% glutaraldehyde in 0.1 M sodium cacodylate buffer,
postfixed with 1% osmium tetroxide in 0.05 M sodium cacodylate, dehydrated using a graded …

Genotype-phenotype correlation in the long-QT syndrome: gene-specific triggers for life-threatening arrhythmias

…, W Haverkamp, E Schulze-Bahr, MH Lehmann… - Circulation, 2001 - Am Heart Assoc
Background—The congenital long-QT syndrome (LQTS) is caused by mutations on several
genes, all of which encode cardiac ion channels. The progressive understanding of the …

[HTML][HTML] MiRP1 forms IKr potassium channels with HERG and is associated with cardiac arrhythmia

GW Abbott, F Sesti, I Splawski, ME Buck, MH Lehmann… - Cell, 1999 - cell.com
A novel potassium channel gene has been cloned, characterized, and associated with
cardiac arrhythmia. The gene encodes MinK-related peptide 1 (MiRP1), a small integral …

Spectrum of Mutations in Long-QT Syndrome Genes: KVLQT1, HERG, SCN5A, KCNE1, and KCNE2

I Splawski, J Shen, KW Timothy, MH Lehmann… - Circulation, 2000 - Am Heart Assoc
Background—Long-QT Syndrome (LQTS) is a cardiovascular disorder characterized by
prolongation of the QT interval on ECG and presence of syncope, seizures, and sudden death. …

Fast free-form deformation using graphics processing units

M Modat, GR Ridgway, ZA Taylor, M Lehmann… - Computer methods and …, 2010 - Elsevier
A large number of algorithms have been developed to perform non-rigid registration and it is
a tool commonly used in medical image analysis. The free-form deformation algorithm is a …

Conversion of neuronal growth cone responses from repulsion to attraction by cyclic nucleotides

…, Z He, M Lehmann, L McKerracher, M Tessier-Lavigne… - Science, 1998 - science.org
Nerve growth is regulated by attractive and repulsive factors in the nervous system. Microscopic
gradients of Collapsin-1/Semaphorin III/D (Sema III) and myelin-associated glycoprotein …

Structural basis of cell-cell adhesion by cadherins

…, AM Fannon, PD Kwong, A Thompson, MS Lehmann… - Nature, 1995 - nature.com
Crystal structures of the amino-terminal domain of N-cadherin provide a picture at the atomic
level of a specific adhesive contact between cells. A repeated set of dimer interfaces is …