Matheus Vernet Machado Bressan Wilke

7PUBLICATIONS
11CO-AUTHORS
Medical virologyPharmaceutical delivery technologiesGene expression (incl. microarray and other genome-wide approaches)Cell and nuclear divisionNeurology and neuromuscular diseases
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Publications (7)

|Jul 01, 2026
A Second Report of a Missense Variant in AMMECR1 Causing Midface Hypoplasia, Hearing Impairment, Elliptocytosis, and Nephrocalcinosis: Case Report and Literature Review.

|Aug 13, 2025
Functional Characterization of Two Novel Biallelic PIGV Variants in a Patient With Myoclonic Seizures and Elevated Alkaline Phosphatase: A Case Report.

Matheus Vernet Machado Bressan Wilke, Deepak Panwar, Johannes M Verheijen

|Mar 13, 2024
A Brazilian Rare-Disease Center's Experience with Glucosylsphingosine (lyso-Gb1) in Patients with Gaucher Disease: Exploring a Novel Correlation with IgG Levels in Plasma and a Biomarker Measurement in CSF.

Matheus Vernet Machado Bressan Wilke, Gabrielle Dineck Iop, Larissa Faqueti

|Jan 23, 2024
Nuclear Abnormalities in LMNA p.(Glu2Lys) Variant Segregating with LMNA-Associated Cardiocutaneous Progeria Syndrome.

Matheus V M B Wilke, Myra Wick, Tanya L Schwab

|Oct 02, 2023
Follow-up of pre-motor symptoms of Parkinson's disease in adult patients with Gaucher disease type 1 and analysis of their lysosomal enzyme profiles in the CSF.

Matheus Vernet Machado Bressan Wilke, Fabiano Poswar, Wyllians Vendramini Borelli

|Feb 25, 2023
A Broad Characterization of Glycogen Storage Disease IV Patients: A Clinical, Genetic, and Histopathological Study.

Matheus Vernet Machado Bressan Wilke, Bibiana Mello de Oliveira, Rodrigo Tzovenos Starosta

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Frequent Collaborators

2 joint publications

Rodrigo Tzovenos Starosta

1 joint publications

Bibiana Mello de Oliveira

1 joint publications

Ida Vanessa Doederlein Schwartz

1 joint publications

Gabrielle Dineck Iop