A. Wajner

发表

α-Ketoadipic Acid and α-Aminoadipic Acid Cause Disturbance of Glutamatergic Neurotransmission and Induction of Oxidative Stress In Vitro in Brain of Adolescent Rats

G. Leipnitz, C. Vargas, M. Wajner, 2017, Neurotoxicity Research.

Biochemical characterization of chitotriosidase enzyme: comparison between normal individuals and patients with Gaucher and with Niemann-Pick diseases.

R. Giugliani, R. Pires, J. Coelho, 2004, Clinical biochemistry.

Mevalonolactone disrupts mitochondrial functions and induces permeability transition pore opening in rat brain mitochondria: Implications for the pathogenesis of mevalonic aciduria

C. Vargas, M. Wajner, A. U. Amaral, 2017, Neurochemistry International.

Biochemical properties of beta-glucosidase in leukocytes from patients and obligated heterozygotes for Gaucher disease carriers.

H. Bock, R. Giugliani, R. Pires, 2005, Clinica chimica acta; international journal of clinical chemistry.

Disturbance of bioenergetics and calcium homeostasis provoked by metabolites accumulating in propionic acidemia in heart mitochondria of developing rats.

M. Wajner, A. U. Amaral, S. Wajner, 2020, Biochimica et biophysica acta. Molecular basis of disease.

Application of a comprehensive protocol for the identification of Gaucher disease in Brazil

R. Giugliani, R. Pires, J. Coelho, 2005, American journal of medical genetics. Part A.

Disturbance of mitochondrial functions associated with permeability transition pore opening induced by cis-5-tetradecenoic and myristic acids in liver of adolescent rats.

M. Wajner, A. U. Amaral, S. Wajner, 2019, Mitochondrion.

Metabolite accumulation in VLCAD deficiency markedly disrupts mitochondrial bioenergetics and Ca2+ homeostasis in the heart

M. Wajner, A. U. Amaral, S. Wajner, 2018, The FEBS journal.

mitochondrial permeability transition pore opening in rat brain and liver : possible implications for the pathogenesis of MCAD deficiency

M. Wajner, A. U. Amaral, R. Ribeiro, 2016 .

Comparison between the biochemical properties of plasma chitotriosidase from normal individuals and from patients with Gaucher disease, GM1-gangliosidosis, Krabbe disease and heterozygotes for Gaucher disease.

R. Giugliani, R. Pires, J. Coelho, 2007, Clinical biochemistry.

Biochemical study on β-glucosidase in individuals with Gaucher's disease and normal subjects

R. Giugliani, R. Pires, J. Coelho, 2004 .

Effect of CuCl2, NaCl and EDTA on the enzyme alpha-L-iduronidase in the plasma of normal individuals and heterozygotes for MPS I.

R. Giugliani, R. Pires, J. Coelho, 2002, Clinica chimica acta; international journal of clinical chemistry.

Detection of mucopolysaccharidosis type I heterozygotes based on the biochemical characteristics of leukocyte alpha-L-iduronidase.

R. Giugliani, R. Pires, J. Coelho, 2002, Archives of medical research.

Detection of mucopolysaccharidosis type I heterozygotes on the basis of the biochemical properties of plasma alpha-L-iduronidase.

R. Giugliani, R. Pires, J. Coelho, 2001, Clinica chimica acta; international journal of clinical chemistry.

Mechanistic Bases of Neurotoxicity Provoked by Fatty Acids Accumulating in MCAD and LCHAD Deficiencies

M. Wajner, A. U. Amaral, C. Cecatto, 2017 .

High vulnerability of the heart and liver to 3‐hydroxypalmitic acid–induced disruption of mitochondrial functions in intact cell systems

C. Vargas, M. Wajner, A. U. Amaral, 2018, Journal of cellular biochemistry.

cis-4-Decenoic and decanoic acids impair mitochondrial energy, redox and Ca(2+) homeostasis and induce mitochondrial permeability transition pore opening in rat brain and liver: Possible implications for the pathogenesis of MCAD deficiency.

M. Wajner, A. U. Amaral, R. Ribeiro, 2016, Biochimica et biophysica acta.