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Isolation, Characterization, and Differentiation Potential of Canine Adipose-Derived Stem Cells

Cell Transplantation, 2010-03, Vol.19 (3), p.279-289

2010

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ALS-associated VRK1 R321C mutation causes proteostatic imbalance and mitochondrial defects in iPSC-derived motor neurons

Neurobiology of disease, 2024-08, Vol.198, p.106540, Article 106540

2024

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Facioscapulohumeral Muscular Dystrophy: More Complex than it Appears

Current molecular medicine, 2014-01, Vol.14 (8), p.1052-1068

2014

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Human Adipose-Derived Mesenchymal Stromal Cells Injected Systemically into GRMD Dogs without Immunosuppression are Able to Reach the Host Muscle and Express Human Dystrophin

Cell transplantation, 2012-01, Vol.21 (7), p.1407-1417

2012

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Molecular cloning, localization and circadian expression of chicken melanopsin (Opn4): differential regulation of expression in pineal and retinal cell types

Journal of neurochemistry, 2005-01, Vol.92 (1), p.158-170

2005

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Stem cells for amyotrophic lateral sclerosis modeling and therapy: Myth or fact?

Cytometry. Part A, 2015-03, Vol.87 (3), p.197-211

2015

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A homozygous loss-of-function mutation in inositol monophosphatase 1 (IMPA1) causes severe intellectual disability

Molecular psychiatry, 2016-08, Vol.21 (8), p.1125-1129

2016

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Clinical aspects of hereditary spastic paraplegia 76 and novel CAPN1 mutations

Clinical genetics, 2018-11, Vol.94 (5), p.482-483

2018

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Milder course in Duchenne patients with nonsense mutations and no muscle dystrophin

Neuromuscular disorders : NMD, 2014-11, Vol.24 (11), p.986-989

2014

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African ancestry protects against Alzheimer's disease-related neuropathology

Molecular psychiatry, 2013-01, Vol.18 (1), p.79-85

2013

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Mild course in atypical Duchenne muscular dystrophy patients is not caused by utrophin overexpression

Neuromuscular disorders : NMD, 2015-10, Vol.25, p.S251-S251

2015

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Human Mesenchymal Stromal Cells Transplantation May Enhance or Inhibit 4T1 Murine Breast Adenocarcinoma through Different Approaches

Stem Cells International, 2015-01, Vol.2015 (2015), p.405-415-135

2015

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Nemaline myopathy: Clinical, pathological, muscle imaging and molecular characterization in a cohort of Brazilian patients

Neuromuscular disorders : NMD, 2016-10, Vol.26, p.S132-S132

2016

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Controversial preclinical results in neuromuscular animal models: Are they related to differences in mesenchymal stromal cells (MSCs) secretome?

Neuromuscular disorders : NMD, 2016-10, Vol.26, p.S128-S128

2016

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A normal life without muscle dystrophin

Neuromuscular disorders : NMD, 2015-05, Vol.25 (5), p.371-374

2015

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Long term follow-up of GRMD dogs transplanted with human adipose derived stem cells

Neuromuscular disorders : NMD, 2015-10, Vol.25, p.S290-S290

2015

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Human endometrial-derived mesenchymal stem cells suppress inflammation in the central nervous system of EAE mice

Stem cell reviews, 2012-09, Vol.8 (3), p.940-952

2012

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Nemaline myopathy: Next generation sequencing (NGS) significantly improving the molecular classification of Brazilian families

Neuromuscular disorders : NMD, 2015-10, Vol.25, p.S288-S288

2015

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The p.P56S mutation in the VAPB gene is not due to a single founder: the first European case

Clinical genetics, 2010-03, Vol.77 (3), p.302-303

2010

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What motivates patients' relatives to undergo genetic testing in search of a pathogenic mutation?

Neuromuscular disorders : NMD, 2016-10, Vol.26, p.S208-S208

2016

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Jagged1 as a modifier of the DMD phenotype: What is next?

Neuromuscular disorders : NMD, 2016-10, Vol.26, p.S156-S156

2016

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Discordance Rates Between Preliminary and Final Radiology Reports on Cross-sectional Imaging Studies at a Level 1 Trauma Center

Academic radiology, 2008-10, Vol.15 (10), p.1217-1226

2008

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A.P.14

Neuromuscular disorders : NMD, 2014-10, Vol.24 (9), p.834-835

2014

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P.5.8 Why is LGMD2G rare?

Neuromuscular disorders : NMD, 2013-10, Vol.23 (9), p.766-766

2013

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Neuromuscular patients: Complaints are unrelated to disease

Neuromuscular disorders : NMD, 2015-10, Vol.25, p.S241-S242

2015

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Isolation, Characterization, and Differentiation Potential of Canine Adipose-Derived Stem Cells

ALS-associated VRK1 R321C mutation causes proteostatic imbalance and mitochondrial defects in iPSC-derived motor neurons

Facioscapulohumeral Muscular Dystrophy: More Complex than it Appears

Human Adipose-Derived Mesenchymal Stromal Cells Injected Systemically into GRMD Dogs without Immunosuppression are Able to Reach the Host Muscle and Express Human Dystrophin

Molecular cloning, localization and circadian expression of chicken melanopsin (Opn4): differential regulation of expression in pineal and retinal cell types

Stem cells for amyotrophic lateral sclerosis modeling and therapy: Myth or fact?

A homozygous loss-of-function mutation in inositol monophosphatase 1 (IMPA1) causes severe intellectual disability

Clinical aspects of hereditary spastic paraplegia 76 and novel CAPN1 mutations

Milder course in Duchenne patients with nonsense mutations and no muscle dystrophin

African ancestry protects against Alzheimer's disease-related neuropathology

Mild course in atypical Duchenne muscular dystrophy patients is not caused by utrophin overexpression

Human Mesenchymal Stromal Cells Transplantation May Enhance or Inhibit 4T1 Murine Breast Adenocarcinoma through Different Approaches

Nemaline myopathy: Clinical, pathological, muscle imaging and molecular characterization in a cohort of Brazilian patients

Controversial preclinical results in neuromuscular animal models: Are they related to differences in mesenchymal stromal cells (MSCs) secretome?

A normal life without muscle dystrophin

Long term follow-up of GRMD dogs transplanted with human adipose derived stem cells

Human endometrial-derived mesenchymal stem cells suppress inflammation in the central nervous system of EAE mice

Nemaline myopathy: Next generation sequencing (NGS) significantly improving the molecular classification of Brazilian families

The p.P56S mutation in the VAPB gene is not due to a single founder: the first European case

What motivates patients' relatives to undergo genetic testing in search of a pathogenic mutation?

Jagged1 as a modifier of the DMD phenotype: What is next?

Discordance Rates Between Preliminary and Final Radiology Reports on Cross-sectional Imaging Studies at a Level 1 Trauma Center

A.P.14

P.5.8 Why is LGMD2G rare?

Neuromuscular patients: Complaints are unrelated to disease

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