M. Lindfors

Diagnostically important muscle pathology in DNAJB6 mutated LGMD1D

H. Haapasalo, B. Udd, J. Palmio, 2016, Acta neuropathologica communications.

Carbonic anhydrase inhibitors: the very weak inhibitors dithiothreitol, beta-mercaptoethanol, tris(carboxyethyl)phosphine and threitol interfere with the binding of sulfonamides to isozymes II and IX.

C. Supuran, A. Scozzafava, M. Kulomaa, 2008, Bioorganic & medicinal chemistry letters.

Biochemical Characterization of CA IX, One of the Most Active Carbonic Anhydrase Isozymes*

A. Scaloni, C. Supuran, A. Scozzafava, 2008, Journal of Biological Chemistry.

Immunolocalization of retinoic acid receptors in rat, mouse and human ovary and uterus

P. Tuohimaa, T. Ylikomi, Y. Zhuang, 1994, The Journal of Steroid Biochemistry and Molecular Biology.

Distinct Muscle Biopsy Findings in Genetically Defined Adult-Onset Motor Neuron Disorders

B. Udd, J. Palmio, O. Raheem, 2016, PloS one.

Late-onset limb-girdle muscular dystrophy caused by GMPPB mutations

B. Udd, G. Solders, J. Palmio, 2015, Neuromuscular Disorders.

Mutations in HSPB8 causing a new phenotype of distal myopathy and motor neuropathy

D. MacArthur, M. Lek, L. Waddell, 2016, Neurology.

Diagnostic anoctamin‐5 protein defect in patients with ANO5‐mutated muscular dystrophy

B. Brais, I. Richard, B. Eymard, 2018, Neuropathology and applied neurobiology.