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Current Opinion in Rheumatology|September 10, 2010
Mitochondrial pathology in immune and inflammatory myopathiesArun S Varadhachary, Conrad C Weihl, Alan PestronkNeuroreport|November 26, 1999
The role of beta-catenin stability in mutant PS1-associated apoptosisC C Weihl, R J Miller, R P RoosPlos One|June 5, 2020
Client processing is altered by novel myopathy-causing mutations in the HSP40 J domainMelanie Y Pullen, Conrad C Weihl, Heather L TrueNature Reviews. Molecular Cell Biology|July 14, 2021
Molecular and cellular basis of genetically inherited skeletal muscle disordersJames J Dowling, Conrad C Weihl, Melissa J SpencerNeuromuscular Disorders : NMD|July 14, 2023
Exploring hand and upper limb function in patients with inclusion body myositis (IBM)Stephanie Hunn, Lindsay Alfano, Michelle Seiffert, et al.Human Molecular Genetics|December 3, 2005
Inclusion body myopathy-associated mutations in p97/VCP impair endoplasmic reticulum-associated degradationConrad C Weihl, Seema Dalal, Alan Pestronk, et al.Plos One|March 30, 2011
A knock-in mouse model for the R120G mutation of αB-crystallin recapitulates human hereditary myopathy and cataractsUsha P Andley, Paul D Hamilton, Nathan Ravi, et al.Neuromuscular Disorders : NMD|June 24, 2018
Homozygous recessive MYH2 mutation mimicking dominant MYH2 associated myopathyAndrew R Findlay, Matthew B Harms, Alan Pestronk, et al.Clinical Endocrinology|February 1, 1979
The relationship between endogenous hyperprolactinaemia and plasma aldosteroneR N Re, I A Kourides, A C Weihl, et al.The Journal of Clinical Endocrinology and Metabolism|June 1, 1977
Thyroid function tests during the early phase of subacute thyroiditisA C Weihl, G H Daniels, E C Ridgway, et al.Pageof 14