Matheus Vernet Machado Bressan Wilke (Matheus V M B Wilke)

Publication Activity (10 Years)

Years Active: 2019-2024
Publications (10 Years): 12

Top Topics

Left Ventricular

Clostridium Difficile

Top Venues

International journal of molecular sciences

Orphanet journal of rare diseases

This page only lists publications with an associated author ORCID identifier.

Publications

Matheus Vernet Machado Bressan Wilke, Myra Wick, Tanya L Schwab, Rodrigo Tzovenos Starosta, Karl J Clark, Heidi M Connolly, Eric W Klee
Nuclear Abnormalities in LMNA p.(Glu2Lys) Variant Segregating with LMNA -Associated Cardiocutaneous Progeria Syndrome. Genes 15 (1) (2024)
Matheus Vernet Machado Bressan Wilke, Gabrielle Dineck Iop, Larissa Faqueti, Layzon Antonio Lemos da Silva, Francyne Kubaski, Fabiano de Oliveira Poswar, Kristiane Michelin-Tirelli, Dévora Randon, Wyllians Vendramini Borelli, Roberto Giugliani, Ida Vanessa D Schwartz
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. International journal of molecular sciences 25 (5) (2024)
Matheus Vernet Machado Bressan Wilke, Myra Wick, Tanya L Schwab, Rodrigo Tzovenos Starosta, Karl J Clark, Heidi M Connolly, Eric W Klee
Nuclear Abnormalities in LMNA p.(Glu2Lys) Variant Segregating with LMNA -Associated Cardiocutaneous Progeria Syndrome. Genes 15 (1) (2024)
Matheus Vernet Machado Bressan Wilke, Gabrielle Dineck Iop, Larissa Faqueti, Layzon Antonio Lemos da Silva, Francyne Kubaski, Fabiano de Oliveira Poswar, Kristiane Michelin-Tirelli, Dévora Randon, Wyllians Vendramini Borelli, Roberto Giugliani, Ida Vanessa D Schwartz
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. International journal of molecular sciences 25 (5) (2024)
Matheus Vernet Machado Bressan Wilke, Gabrielle Dineck Iop, Larissa Faqueti, Layzon Antonio Lemos da Silva, Francyne Kubaski, Fabiano de Oliveira Poswar, Kristiane Michelin-Tirelli, Dévora Randon, Wyllians Vendramini Borelli, Roberto Giugliani, Ida Vanessa D Schwartz
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. International journal of molecular sciences 25 (5) (2024)
Matheus Vernet Machado Bressan Wilke, Gabrielle Dineck Iop, Larissa Faqueti, Layzon Antonio Lemos da Silva, Francyne Kubaski, Fabiano de Oliveira Poswar, Kristiane Michelin-Tirelli, Dévora Randon, Wyllians Vendramini Borelli, Roberto Giugliani, Ida Vanessa D Schwartz
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. International journal of molecular sciences 25 (5) (2024)
Matheus Vernet Machado Bressan Wilke, Myra Wick, Tanya L Schwab, Rodrigo Tzovenos Starosta, Karl J Clark, Heidi M Connolly, Eric W Klee
Nuclear Abnormalities in LMNA p.(Glu2Lys) Variant Segregating with LMNA -Associated Cardiocutaneous Progeria Syndrome. Genes 15 (1) (2024)
Matheus Vernet Machado Bressan Wilke, Myra Wick, Tanya L Schwab, Rodrigo Tzovenos Starosta, Karl J Clark, Heidi M Connolly, Eric W Klee
Nuclear Abnormalities in LMNA p.(Glu2Lys) Variant Segregating with LMNA -Associated Cardiocutaneous Progeria Syndrome. Genes 15 (1) (2024)
Matheus Vernet Machado Bressan Wilke, Bibiana Mello de Oliveira, Rodrigo Tzovenos Starosta, Marwan Shinawi, Liang Lu, Mai He, Yamin Ma, Janis Stoll, Carolina Fischinger Moura de Souza, Ana Cecilia Menezes de Siqueira, Sandra Maria Gonçalves Vieira, Carlos Thadeu Cerski, Lilia Farret Refosco, Ida Vanessa Doederlein Schwartz
A Broad Characterization of Glycogen Storage Disease IV Patients: A Clinical, Genetic, and Histopathological Study. Biomedicines 11 (2) (2023)
Matheus Vernet Machado Bressan Wilke, Fabiano Poswar, Wyllians Vendramini Borelli, Kristiane Michelin Tirelli, Dévora Natalia Randon, Franciele Fátima Lopes, Fernanda Bender Pasetto, Fernanda Medeiros Sebastião, Gabrielle Dineck Iop, Larissa Faqueti, Layzon Antonio da Silva, Francyne Kubaski, Artur Francisco Schumacher Schuh, Roberto Giugliani, Ida Vanessa Döederlein Schwartz
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. Orphanet journal of rare diseases 18 (1) (2023)
Matheus Vernet Machado Bressan Wilke, Bibiana Mello de Oliveira, Rodrigo Tzovenos Starosta, Marwan Shinawi, Liang Lu, Mai He, Yamin Ma, Janis Stoll, Carolina Fischinger Moura de Souza, Ana Cecilia Menezes de Siqueira, Sandra Maria Gonçalves Vieira, Carlos Thadeu Cerski, Lilia Farret Refosco, Ida Vanessa Doederlein Schwartz
A Broad Characterization of Glycogen Storage Disease IV Patients: A Clinical, Genetic, and Histopathological Study. Biomedicines 11 (2) (2023)
Matheus Vernet Machado Bressan Wilke, Alícia D Dornelles, Artur S Schuh, Filippo P Vairo, Suelen P Basgalupp, Marina Siebert, Tatiele Nalin, Otavio B Piltcher, Ida V D Schwartz
Evaluation of the frequency of non-motor symptoms of Parkinson's disease in adult patients with Gaucher disease type 1. Orphanet journal of rare diseases 14 (1) (2019)