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Neuromuscular Disorders : NMD|March 17, 2004
Fatal infantile neuromuscular presentation of glycogen storage disease type IVStacey K H Tay, Hasan O Akman, Wendy K Chung, et al.
Neurology|June 1, 1997
Lymphoproliferative disorders and motor neuron disease: an updateP H Gordon, L P Rowland, D S Younger, et al.
The Journal of Pediatrics|October 9, 2018
Factors Associated with Breastfeeding Initiation and Continuation: A Meta-AnalysisSarah S Cohen, Dominik D Alexander, Nancy F Krebs, et al.
Arxiv|January 2, 2026
UNISELF: A Unified Network with Instance Normalization and Self-Ensembled Lesion Fusion for Multiple Sclerosis Lesion SegmentationJinwei Zhang, Lianrui Zuo, Blake E Dewey, et al.
International Journal of Pediatric Otorhinolaryngology|February 2, 2013
Microbial profiling does not differentiate between childhood recurrent acute otitis media and chronic otitis media with effusionKim Stol, Suzanne J C Verhaegh, Kees Graamans, et al.
The Journal of Emergency Medicine|May 7, 2013
Customizing anaphylaxis guidelines for emergency medicineRichard Nowak, Judith Rosen Farrar, Barry E Brenner, et al.
Plos One|May 15, 2013
Comprehensive antigen screening identifies Moraxella catarrhalis proteins that induce protection in a mouse pulmonary clearance modelMargarita Smidt, Patrick Bättig, Suzanne J C Verhaegh, et al.
Annals of Neurology|June 1, 1996
Multiple mitochondrial DNA deletions in sporadic inclusion body myositis: a study of 56 patientsF M Santorelli, M Sciacco, K Tanji, et al.
Human Molecular Genetics|August 15, 2000
Molecular and genetic characterization of sarcospan: insights into sarcoglycan-sarcospan interactionsR H Crosbie, L E Lim, S A Moore, et al.
Plos One|March 20, 2014
Detection and occurrence of plasmid-mediated AmpC in highly resistant gram-negative rodsE Ascelijn Reuland, John P Hays, Denise M C de Jongh, et al.
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