Filling landsat ETM+ SLC-off gaps using a segmentation model approachMAXWELL, Susan.Photogrammetric engineering and remote sensing. 2004, Vol 70, Num 10, pp 1109-1111, issn 0099-1112, 3 p.Article

Diverse molecular mechanisms involved in AChR deficiency due to rapsyn mutationsCOSSINS, Judy; BURKE, Georgina; MAXWELL, Susan et al.Brain. 2006, Vol 129, pp 2773-2783, issn 0006-8950, 11 p., 10Article

Identification of ever-cropped land (1984―2010) using Landsat annual maximum NDVI image composites: Southwestern Kansas case studyMAXWELL, Susan K; SYLVESTER, Kenneth M.Remote sensing of environment. 2012, Vol 121, pp 186-195, issn 0034-4257, 10 p.Article

A novel congenital myasthenic syndrome due decreased acetylcholine receptor ion-channel conductanceWEBSTER, Richard; MAXWELL, Susan; SPEARMAN, Hayley et al.Brain. 2012, Vol 135, pp 1070-1080, issn 0006-8950, 11 p., 4Article

Aquaporin-4 Antibodies in Neuromyelitis Optica and Longitudinally Extensive Transverse MyelitisWATERS, Patrick; JARIUS, Sven; MAXWELL, Susan et al.Archives of neurology (Chicago). 2008, Vol 65, Num 7, pp 913-919, issn 0003-9942, 7 p.Article

Clinical features of the DOK7 neuromuscular junction synaptopathyPALACE, Jacqueline; LASHLEY, Daniel; NEWSOM-DAVIS, John et al.Brain. 2007, Vol 130, pp 1507-1515, issn 0006-8950, 9 p., 6Article

A mouse model of AChR deficiency syndrome with a phenotype reflecting the human conditionCOSSINS, Judy; WEBSTER, Richard; MAXWELL, Susan et al.Human molecular genetics (Print). 2004, Vol 13, Num 23, pp 2947-2957, issn 0964-6906, 11 p.Article

Congenital myasthenic syndrome with tubular aggregates caused by GFPT1 mutationsGUERGUELTCHEVA, Velina; MÜLLER, Juliane S; VILCHEZ, Juan J et al.Journal of neurology. 2012, Vol 259, Num 5, pp 838-850, issn 0340-5354, 13 p.Article

Non-radioactive serological diagnosis of myasthenia gravis and clinical features of patients from Tianjin, ChinaLI YANG; MAXWELL, Susan; ISABEL LEITE, M et al.Journal of the neurological sciences. 2011, Vol 301, Num 1-2, pp 71-76, issn 0022-510X, 6 p.Article

N-methyl-D-aspartate antibody encephalitis: temporal progression of clinical and paraclinical observations in a predominantly non-paraneoplastic disorder of both sexesIRANI, Sarosh R; BERA, Katarzyna; LANG, Bethan et al.Brain. 2010, Vol 133, pp 1655-1667, issn 0006-8950, 13 p., 6Article

Mutations in DPAGT1 Cause a Limb-Girdle Congenital Myasthenic Syndrome with Tubular AggregatesBELAYA, Katsiaryna; FINLAYSON, Sarah; PASCUAL PASCUAL, Samuel I et al.American journal of human genetics. 2012, Vol 91, Num 1, pp 193-201, issn 0002-9297, 9 p.Article

Hexosamine Biosynthetic Pathway Mutations Cause Neuromuscular Transmission DefectSENDEREK, Jan; MÜLLER, Juliane S; MUELAS, Nuria et al.American journal of human genetics. 2011, Vol 88, Num 2, pp 162-172, issn 0002-9297, 11 p.Article

Congenital myasthenic syndromes due to mutations in ALG2 and ALG14COSSINS, Judith; BELAYA, Katsiaryna; LAVAL, Steven et al.Brain. 2013, Vol 136, pp 944-956, issn 0006-8950, 13 p., 3Article

The spectrum of mutations that underlie the neuromuscular junction synaptopathy in DOK7 congenital myasthenic syndromeCOSSINS, Judith; WEI WEI LIU; BELAYA, Katsiaryna et al.Human molecular genetics (Print). 2012, Vol 21, Num 17, pp 3765-3775, issn 0964-6906, 11 p.Article

Dok-7 mutations underlie a neuromuscular junction synaptopathyBEESON, David; HIGUCHI, Osamu; MÜLLER, Juliane S et al.Science (Washington, D.C.). 2006, Vol 313, Num 5795, pp 1975-1978, issn 0036-8075, 4 p.Article