Latest Research Publications - Life Science Network

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Created 29 Jul 2026

Temporal changes in hyaluronan concentrations in preterm human milk.

by Joan Lien, Lise DeShea, Jeffrey Eckert, Addison Franca, Adam Wilson, Kathryn Burge, William H Beasley, Misty Good, Hala Chaaban — Journal of perinatology : official journal of the California Perinatal Association. Jul 28, 2026.
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Created 29 Jul 2026

Sustainable dietary recommendations for the Spanish population.

by Esther Lopez-Garcia, Irene Bretón-Lesmes, Araceli Díaz-Perales, M Victoria Moreno-Arribas, María P Portillo, Ana Rivas, Ujué Fresán, Lydia Parro-Magán, Cristina Recuero-Carretero, María Ángeles Carlos-Chillerón — European journal of clinical nutrition. Jul 28, 2026.
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Created 29 Jul 2026

Key Points of Endoscopic Minimally Invasive Surgery for Gynecomastia Based on Refined Anatomy: A Case Series.

by Weifang Zhang, Yueyao Sun, Mengyang An, Xin Chen, Yifang Wang, Jianping Feng, Ji Feng, Fangjian Shang, Bo Liu — Aesthetic plastic surgery. Jul 28, 2026.
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Created 29 Jul 2026

Comparative Clinical Efficacy of Septoaponeurotic Junctional Thickening Versus Bridge Technique in Double-Eyelid Blepharoplasty.

by Tianshi Li, Wentao Fang, Huaxin Hu, Jian Hao — Aesthetic plastic surgery. Jul 28, 2026.
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Created 29 Jul 2026

Comparable lung injury with and without distal perfusion during aortic arch procedure in piglets.

by Sabine Meier, Maja-Theresa Dieterlen, Christian Mühlfeld, Janine Schob, Kristin Klaeske, Susann Oßmann, Enrika Schütze, Mia Bovet, Michael A Borger, Martin Kostelka, Marcel Vollroth — Pediatric research. Jul 28, 2026.
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Created 29 Jul 2026

A call to educate: counteracting enacted stigma in children with long COVID.

by Alexandra B Yonts — Pediatric research. Jul 28, 2026.
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Created 29 Jul 2026

Consensus recommendations for next-generation sequencing-based genetic testing in Rare Neurological diseases.

by Aleš Maver, Katja Lohmann, Lena-Marie Urbanczyk, Astri Arnesen, Ivo Barić, Peter Bauer, Kailash P Bhatia, Sylvia Boesch, Fran Borovečki, Norbert Brüggemann, Zih-Hua Fang, Heinz Gabriel, Tobias B Haack, Henry Houlden, Milena Janković, Erik-Jan Kamsteeg, Michelangelo Mancuso, Deborah Mascalzoni, Maria Judit Molnar, Alexander Münchau, Kornelia Neveling, Ivana Novaković, Borut Peterlin, Ludger Schols, Nika Schuermans, Katie Shiels, Marc Sturm, Rachel Taylor, Marina A J Tijssen, Lisenka E L M Vissers, Victoria Williams, Holm Graessner, European Reference Network for Rare Neurological Disorders (ERN-RND) — European journal of human genetics : EJHG. Jul 28, 2026.
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Created 29 Jul 2026

Tofersen treatment in respiratory onset amyotrophic lateral sclerosis and a variant of uncertain significance in SOD1; a case report.

by Sean W Willemse, Koen C Demaegd, Wouter Koole, Ruben P A van Eijk, Wouter van Rheenen, Jan H Veldink, Leonard H van den Berg, Michael A van Es — European journal of human genetics : EJHG. Jul 28, 2026.
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Created 29 Jul 2026

Lived experiences in rare genetic diseases: a narrative synthesis of 317 qualitative studies (2004-2024).

by Marianne Gush, Shahida Moosa — European journal of human genetics : EJHG. Jul 29, 2026.
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Created 29 Jul 2026

Global economic burden of depression in 154 countries from 2025 to 2050.

by Zhong Cao, Yuheng Luo, Lirui Jiao, Wenjin Chen, Klaus Prettner, Michael Kuhn, David E Bloom, Dean T Jamison, Till Winfried Bärnighausen, Simiao Chen — Nature medicine. Jul 28, 2026.
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