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Developmental Medicine and Child Neurology|July 14, 2022
Niemann-Pick type C disease as proof-of-concept for intelligent biomarker panel selection in neurometabolic disordersApostolos Papandreou, Ivan Doykov, Justyna Spiewak, et al.Surgical Endoscopy|June 1, 2012
Does fellow participation in laparoscopic Roux-en-Y gastric bypass affect perioperative outcomes?Neil H Bhayani, Aditya Gupta, Ashwin A Kurian, et al.Molecular Autism|December 12, 2025
Atypical GNAO1 variants in severe childhood speech disorders: clinical, genetic, and molecular insightsYonika A Larasati, Moritz Thiel, Ainara Salazar-Villacorta, et al.Journal of Inherited Metabolic Disease|July 20, 2023
Fetal gene therapySimon N Waddington, William H Peranteau, Ahad A Rahim, et al.Tremor and Other Hyperkinetic Movements (New York, N.Y.)|April 22, 2017
TBC1D24 Mutations in a Sibship with Multifocal PolymyoclonusAdeline Ngoh, Jose Bras, Rita Guerreiro, et al.Archives of Environmental Contamination and Toxicology|August 15, 2001
Chemical contamination and toxicity of sediment from a coastal area receiving industrial effluents in KuwaitM U Beg, S Al-Muzaini, T Saeed, et al.Nucleosides, Nucleotides & Nucleic Acids|December 2, 2004
Adenylosuccinate lyase deficiency--first British caseA M Marinaki, M Champion, M A Kurian, et al.Epigenomics|May 4, 2022
Comparison of methylation episignatures in KMT2B- and KMT2D-related human disordersSunwoo Lee, Eguzkine Ochoa, Katy Barwick, et al.Developmental Medicine and Child Neurology|March 31, 2018
Phenotypes, genotypes, and the management of paroxysmal movement disordersLaura Silveira-Moriyama, Stjepana Kovac, Manju A Kurian, et al.American Journal of Medical Genetics. Part A|September 15, 2015
Familial recurrences of FOXG1-related disorder: Evidence for mosaicismKelly Q McMahon, Apostolos Papandreou, Mandy Ma, et al.Pageof 33