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Biological Psychiatry|April 21, 2019
Genome-wide Burden of Rare Short Deletions Is Enriched in Major Depressive Disorder in Four CohortsXianglong Zhang, Abdel Abdellaoui, James Rucker, et al.
Lung|August 21, 2017
Experience of Lung Transplantation in Patients with Lymphangioleiomyomatosis at a Brazilian Reference CentreBruno Guedes Baldi, Marcos Naoyuki Samano, Silvia Vidal Campos, et al.
Vox Sanguinis|September 14, 2022
Extracorporeal photopheresis in paediatric patients: A retrospective comparison between different 'off-line' protocolsElena Sebastián, Eva María Andrés Esteban, Marta González-Vicent, et al.
American Journal of Human Genetics|March 11, 2000
An unstable trinucleotide-repeat region on chromosome 13 implicated in spinocerebellar ataxia: a common expansion locusJ B Vincent, M L Neves-Pereira, A D Paterson, et al.
Nature Medicine|May 29, 2020
The effect of LRRK2 loss-of-function variants in humansNicola Whiffin, Irina M Armean, Aaron Kleinman, et al.
Magnetic Resonance in Medicine|February 5, 2026
Combined caLculation of Ultra-high field Biases (CLUB) With Sandwich: Fast, Simultaneous Estimation of 3D B0 and Multi-Channel B1 + Maps at 7 TNatalia Pato Montemayor, Jocelyn Phillippe, James L Kent, et al.
Molecular Psychiatry|November 13, 2013
Evidence that duplications of 22q11.2 protect against schizophreniaE Rees, G Kirov, A Sanders, et al.
American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|November 9, 2024
Severe ischemia-reperfusion injury induces epigenetic inactivation of LHX1 in kidney progenitor cells after kidney transplantationJosep M Cruzado, Anna Sola, Miguel L Pato, et al.
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