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Nature Genetics|February 19, 2013
Somatic mutations in ATP1A1 and ATP2B3 lead to aldosterone-producing adenomas and secondary hypertensionFelix Beuschlein, Sheerazed Boulkroun, Andrea Osswald, et al.
British Journal of Cancer|September 18, 2024
Testing of rapid evaporative mass spectrometry for histological tissue classification and molecular diagnostics in a multi-site studyMartin Kaufmann, Pierre-Maxence Vaysse, Adele Savage, et al.
Neurology(R) Neuroimmunology & Neuroinflammation|July 7, 2025
Comorbidities and Their Influence on Outcomes and Infectious Complications in Autoimmune Encephalitis: A Multicenter Cohort StudyAmelie Bohn, Klemens Angstwurm, Christian G Bien, et al.
European Journal of Medical Genetics|September 30, 2020
Associations between cognitive performance and the rehabilitation, medical care and social support provided to French children with Prader-Willi syndromePierre-Henri Roux-Levy, Marie Bournez, Alice Masurel, et al.
Nature Medicine|November 9, 2019
Loss-of-function mutations in MRAP2 are pathogenic in hyperphagic obesity with hyperglycemia and hypertensionMorgane Baron, Julie Maillet, Marlène Huyvaert, et al.
Emerging Infectious Diseases|June 8, 2021
Delayed Antibody and T-Cell Response to BNT162b2 Vaccination in the Elderly, GermanyTatjana Schwarz, Pinkus Tober-Lau, David Hillus, et al.
Pediatrics|April 1, 2009
Consensus statement on the use of gonadotropin-releasing hormone analogs in childrenJean-Claude Carel, Erica A Eugster, Alan Rogol, et al.
Journal of Neurology|February 22, 2024
Different pain phenotypes are associated with anti-Caspr2 autoantibodiesPatrik Greguletz, Maria Plötz, Carolin Baade-Büttner, et al.
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