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Pharmaceutics
|
August 28, 2025
Bioactive Chalcone-Loaded Mesoporous Silica KIT-6 Nanocarrier: A Promising Strategy for Inflammation and Pain Management in Zebrafish
Maria Kueirislene Amâncio Ferreira, Francisco Rogenio Silva Mendes, Emmanuel Silva Marinho, et al.
Frontiers in Genetics
|
April 12, 2024
Comparison of ddRADseq and EUChip60K SNP genotyping systems for population genetics and genomic selection in <i>Eucalyptus dunnii</i> (Maiden)
Natalia Cristina Aguirre, Pamela Victoria Villalba, Martín Nahuel García, et al.
The Journal of Pediatrics
|
September 22, 2009
Guidelines to diagnosis and monitoring of Fabry disease and review of treatment experiences
Ana Maria Martins, Vânia D'Almeida, Sandra Obikawa Kyosen, et al.
The Journal of Pediatrics
|
September 22, 2009
Guidelines for the management of mucopolysaccharidosis type I
Ana Maria Martins, Ana Paula Dualibi, Denise Norato, et al.
Blood Cells, Molecules & Diseases
|
April 28, 2019
Addendum to Letter to the Editor: Safety, efficacy, and authorization of eliglustat as a first-line therapy in Gaucher disease type 1
Pramod K Mistry, Manisha Balwani, Hagit N Baris, et al.
Blood Cells, Molecules & Diseases
|
April 23, 2018
Safety, efficacy, and authorization of eliglustat as a first-line therapy in Gaucher disease type 1
Pramod K Mistry, Manisha Balwani, Hagit N Baris, et al.
Arquivos Brasileiros De Cardiologia
|
March 9, 2022
Clinical, Laboratory, and Imaging Profile in Patients with Systemic Amyloidosis in a Brazilian Cardiology Referral Center
Fábio Fernandes, Aristóteles Comte de Alencar Neto, Bruno Vaz Kerges Bueno, et al.
Endocrine Oncology (Bristol, England)
|
January 17, 2025
NET Models Meeting 2024 white paper: the current state of neuroendocrine tumour research models and our future aspirations
Po Hien Ear, Ilaria Marinoni, Talya Dayton, et al.
Molecular Genetics and Metabolism
|
March 29, 2013
Enzyme replacement therapy with galsulfase in 34 children younger than five years of age with MPS VI
Dafne D G Horovitz, Tatiana S P C Magalhães, Angelina Acosta, et al.
Genetics and Molecular Biology
|
June 4, 2011
Mucopolysaccharidosis I, II, and VI: Brief review and guidelines for treatment
Roberto Giugliani, Andressa Federhen, Maria Verônica Muñoz Rojas, et al.
Page
of 32
Search research articles
Search
Showing results (301-310 of 313) with videos related to
Sort By:
Page
of 32
Pharmaceutics
|
August 28, 2025
Bioactive Chalcone-Loaded Mesoporous Silica KIT-6 Nanocarrier: A Promising Strategy for Inflammation and Pain Management in Zebrafish
Maria Kueirislene Amâncio Ferreira, Francisco Rogenio Silva Mendes, Emmanuel Silva Marinho, et al.
Frontiers in Genetics
|
April 12, 2024
Comparison of ddRADseq and EUChip60K SNP genotyping systems for population genetics and genomic selection in <i>Eucalyptus dunnii</i> (Maiden)
Natalia Cristina Aguirre, Pamela Victoria Villalba, Martín Nahuel García, et al.
The Journal of Pediatrics
|
September 22, 2009
Guidelines to diagnosis and monitoring of Fabry disease and review of treatment experiences
Ana Maria Martins, Vânia D'Almeida, Sandra Obikawa Kyosen, et al.
The Journal of Pediatrics
|
September 22, 2009
Guidelines for the management of mucopolysaccharidosis type I
Ana Maria Martins, Ana Paula Dualibi, Denise Norato, et al.
Blood Cells, Molecules & Diseases
|
April 28, 2019
Addendum to Letter to the Editor: Safety, efficacy, and authorization of eliglustat as a first-line therapy in Gaucher disease type 1
Pramod K Mistry, Manisha Balwani, Hagit N Baris, et al.
Blood Cells, Molecules & Diseases
|
April 23, 2018
Safety, efficacy, and authorization of eliglustat as a first-line therapy in Gaucher disease type 1
Pramod K Mistry, Manisha Balwani, Hagit N Baris, et al.
Arquivos Brasileiros De Cardiologia
|
March 9, 2022
Clinical, Laboratory, and Imaging Profile in Patients with Systemic Amyloidosis in a Brazilian Cardiology Referral Center
Fábio Fernandes, Aristóteles Comte de Alencar Neto, Bruno Vaz Kerges Bueno, et al.
Endocrine Oncology (Bristol, England)
|
January 17, 2025
NET Models Meeting 2024 white paper: the current state of neuroendocrine tumour research models and our future aspirations
Po Hien Ear, Ilaria Marinoni, Talya Dayton, et al.
Molecular Genetics and Metabolism
|
March 29, 2013
Enzyme replacement therapy with galsulfase in 34 children younger than five years of age with MPS VI
Dafne D G Horovitz, Tatiana S P C Magalhães, Angelina Acosta, et al.
Genetics and Molecular Biology
|
June 4, 2011
Mucopolysaccharidosis I, II, and VI: Brief review and guidelines for treatment
Roberto Giugliani, Andressa Federhen, Maria Verônica Muñoz Rojas, et al.
Page
of 32