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Journal of Immunology (Baltimore, Md. : 1950)|January 22, 2024
A Noncanonical CD56dimCD16dim/- NK Cell Subset Indicative of Prior Cytotoxic Activity Is Elevated in Patients with Autoantibody-Mediated Neurologic DiseasesSoumya S Yandamuri, Beata Filipek, Nikhil Lele, et al.
Neurology(R) Neuroimmunology & Neuroinflammation|April 27, 2022
Heterogeneity of Acetylcholine Receptor Autoantibody-Mediated Complement Activity in Patients With Myasthenia GravisAbeer H Obaid, Chryssa Zografou, Douangsone D Vadysirisack, et al.
Neuromuscular Disorders : NMD|February 13, 2001
Mild phenotype of nemaline myopathy with sleep hypoventilation due to a mutation in the skeletal muscle alpha-actin (ACTA1) geneH Jungbluth, C A Sewry, S C Brown, et al.
Cancer|July 15, 2005
Pediatric aggressive fibromatosis: a retrospective analysis of 13 patients and review of literatureSaskia Buitendijk, Cees P van de Ven, Ton G Dumans, et al.
British Journal of Cancer|October 14, 2005
Array comparative genomic hybridisation (aCGH) analysis of premenopausal breast cancers from a nuclear fallout area and matched cases from Western New YorkG Varma, R Varma, H Huang, et al.
Muscle & Nerve|January 6, 2015
Demographic and clinical features of inclusion body myositis in North AmericaA David Paltiel, Einar Ingvarsson, Donald K K Lee, et al.
G3 (Bethesda, Md.)|July 20, 2017
Gene Expression Networks in the Murine Pulmonary Myocardium Provide Insight into the Pathobiology of Atrial FibrillationJordan K Boutilier, Rhonda L Taylor, Tracy Mann, et al.
Genes, Chromosomes & Cancer|July 19, 2006
20q11.1 amplification in giant-cell tumor of bone: Array CGH, FISH, and association with outcomeLaura T Smith, Joel Mayerson, Norma J Nowak, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|July 17, 1999
Novel mutation in the myelin protein zero gene in a family with intermediate hereditary motor and sensory neuropathyF L Mastaglia, K J Nowak, R Stell, et al.
European Journal of Pediatrics|October 20, 2009
Microcephaly, sensorineural deafness and Currarino triad with duplication-deletion of distal 7qPiero Pavone, Martino Ruggieri, Ilaria Lombardo, et al.
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