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The Lancet. Haematology|November 18, 2017
Response comparison of multiple myeloma and monoclonal gammopathy of undetermined significance to the same anti-myeloma therapy: a retrospective cohort studyJohn P Campbell, Jennifer L J Heaney, Sankalp Pandya, et al.
American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|January 3, 2013
Precision diagnostics in transplantation: from bench to bedsideM Mengel, P Campbell, H Gebel, et al.
Developmental Cell|November 27, 2012
An HMGA2-IGF2BP2 axis regulates myoblast proliferation and myogenesisZhizhong Li, Jason A Gilbert, Yunyu Zhang, et al.
European Journal of Human Genetics : EJHG|January 21, 2011
Congenital muscular dystrophy type 1D (MDC1D) due to a large intragenic insertion/deletion, involving intron 10 of the LARGE geneNigel F Clarke, Svetlana Maugenre, Aurélie Vandebrouck, et al.
International Forum of Allergy & Rhinology|October 14, 2017
A validated model for the 22-item Sino-Nasal Outcome Test subdomain structure in chronic rhinosinusitisAllen L Feng, Nicholas C Wesely, Lloyd P Hoehle, et al.
Nature|July 26, 2002
Post-translational disruption of dystroglycan-ligand interactions in congenital muscular dystrophiesDaniel E Michele, Rita Barresi, Motoi Kanagawa, et al.
BMC Research Notes|December 15, 2011
Variable disease severity in Saudi Arabian and Sudanese families with c.3924 + 2 T > C mutation of LAMA2Claudia Di Blasi, Emanuela Bellafiore, Mustafa Am Salih, et al.
The British Journal of Ophthalmology|August 25, 2020
Automated detection of early-stage ROP using a deep convolutional neural networkYo-Ping Huang, Haobijam Basanta, Eugene Yu-Chuan Kang, et al.
The Lancet. Child & Adolescent Health|March 12, 2021
Factors linked to severe outcomes in multisystem inflammatory syndrome in children (MIS-C) in the USA: a retrospective surveillance studyJoseph Y Abrams, Matthew E Oster, Shana E Godfred-Cato, et al.
Neuromuscular Disorders : NMD|October 16, 2021
Muscular dystrophy-dystroglycanopathy in a family of Labrador retrievers with a LARGE1 mutationG Diane Shelton, Katie M Minor, Ling T Guo, et al.
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