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The long-term safety and efficacy of vestronidase alfa, rhGUS enzyme replacement therapy, in subjects with mucopolysaccharidosis VII

Molecular genetics and metabolism, 2020-03, Vol.129 (3), p.219-227

2020

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Whole sequence of the mitochondrial DNA genome of Kearns Sayre Syndrome patients: Identification of deletions and variants

Gene, 2019-03, Vol.688, p.171-181

2019

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Infantile-onset Pompe disease in seven Mexican children

Gaceta médica de México, 2022, Vol.158 (5), p.265-270

2022

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Primary Immunodeficiency Diseases in Aguascalientes, Mexico: Results from an Educational Program

Journal of clinical immunology, 2016-04, Vol.36 (3), p.173-178

2016

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Myosin 1g as a high-risk biomarker in a pediatric patient with lineage switch from acute lymphoblastic leukemia to myeloid phenotype

Boletin medico del Hospital Infantil de Mexico, 2023-04, Vol.80 (2), p.135-143

2023

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Cystic fibrosis: current concepts

Boletin medico del Hospital Infantil de Mexico, 2021, Vol.78 (6), p.584

2021

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Analysis of the KRT9 Gene in a Mexican Family with Epidermolytic Palmoplantar Keratoderma

Pediatric dermatology, 2013-05, Vol.30 (3), p.354-358

2013

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P019: Mexican Clinical and Molecular Registry of mucopolysaccharidosis type VII

Genetics in Medicine Open, 2023, Vol.1 (1), p.100029, Article 100029

2023

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Hawkinsinuria clinical practice guidelines: a Mexican case report and literature review

Journal of international medical research, 2020-02, Vol.48 (2), p.300060519863543-300060519863543

2020

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Mucopolysaccharidosis type VII (Sly syndrome) - What do we know?

Molecular genetics and metabolism, 2024-03, Vol.141 (3), p.108145-108145, Article 108145

2024

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A Fetus with Hemifacial Microsomia and Sirenomelia. The Same Mesodermal Defect Spectrum?

Fetal and pediatric pathology, 2013-03, Vol.32 (2), p.152-157

2013

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Estudio cromosómico de 303 pérdidas gestacionales en México

Gaceta médica de México, 2024-01, Vol.160 (1), p.81-91

2024

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Enfermedad de Pompe de inicio infantil en siete niños mexicanos

Gaceta médica de México, 2022-10, Vol.158 (5), p.275-280

2022

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P263: Genotype-phenotype associations in CASK disorders: A systematic literature review and report of three cases

Genetics in Medicine Open, 2024, Vol.2, p.101159, Article 101159

2024

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Analysis of the KRT 9 Gene in a Mexican Family with Epidermolytic Palmoplantar Keratoderma

Pediatric dermatology, 2013-05, Vol.30 (3), p.354-358

2013

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Chromosome analysis of 303 pregnancy losses in Mexico

Gaceta médica de México, 2024-06, Vol.160 (1)

2024

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Corrigendum to “The long-term safety and efficacy of vestronidase alfa, rhGUS enzyme replacement therapy, in subjects with mucopolysaccharidosis VII” [Mol Genet Metab 2020 Mar;129(3):219–227]

Molecular genetics and metabolism, 2020-09, Vol.131 (1-2), p.285-285

2020

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Nuevas hipótesis embriológicas, genética y epidemiología de la gastrosquisis

Boletín médico del Hospital Infantil de México (Spanish edition), 2011, Vol.68 (3), p.245-252

2011

Volltextzugriff (PDF)

Chromosome analysis of 303 pregnancy losses in Mexico

Gaceta médica de México, 2024, Vol.160 (1), p.76-85

2024

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Long-term safety and efficacy of vestronidase alfa, rhGUS enzyme replacement therapy, in subjects with mucopolysaccharidosis type VII

Molecular genetics and metabolism, 2020-02, Vol.129 (2), p.S158-S159

2020

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Análisis de la mutación c.187 C>T en el gen ATP6V0A2 mediante PCR-ARMS

TIP. Revista especializada en ciencias químico-biológicas, 2020-10, Vol.23

2020

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Infantile-onset Pompe disease in seven Mexican children

Gaceta médica de México, 2022-12, Vol.158 (5)

2022

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Cystic fibrosis: current concepts

Boletín médico del Hospital Infantil de México (Spanish edition), 2021-12, Vol.78 (6)

2021

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Sustained efficacy and safety of vestronidase alfa (rhGUS) enzyme replacement therapy in patients with MPS VII

Molecular genetics and metabolism, 2018-02, Vol.123 (2), p.S144-S145

2018

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The long-term safety and efficacy of vestronidase alfa, rhGUS enzyme replacement therapy, in subjects with mucopolysaccharidosis VII

Whole sequence of the mitochondrial DNA genome of Kearns Sayre Syndrome patients: Identification of deletions and variants

Infantile-onset Pompe disease in seven Mexican children

Primary Immunodeficiency Diseases in Aguascalientes, Mexico: Results from an Educational Program

Myosin 1g as a high-risk biomarker in a pediatric patient with lineage switch from acute lymphoblastic leukemia to myeloid phenotype

Cystic fibrosis: current concepts

Analysis of the KRT9 Gene in a Mexican Family with Epidermolytic Palmoplantar Keratoderma

P019: Mexican Clinical and Molecular Registry of mucopolysaccharidosis type VII

Hawkinsinuria clinical practice guidelines: a Mexican case report and literature review

Mucopolysaccharidosis type VII (Sly syndrome) - What do we know?

A Fetus with Hemifacial Microsomia and Sirenomelia. The Same Mesodermal Defect Spectrum?

Estudio cromosómico de 303 pérdidas gestacionales en México

Enfermedad de Pompe de inicio infantil en siete niños mexicanos

P263: Genotype-phenotype associations in CASK disorders: A systematic literature review and report of three cases

Analyses of LMNA-negative juvenile progeroid cases confirms biallelic POLR3A mutations in Wiedemann–Rautenstrauch-like syndrome and expands the phenotypic spectrum of PYCR1 mutations

Analysis of the KRT 9 Gene in a Mexican Family with Epidermolytic Palmoplantar Keratoderma

Chromosome analysis of 303 pregnancy losses in Mexico

Corrigendum to “The long-term safety and efficacy of vestronidase alfa, rhGUS enzyme replacement therapy, in subjects with mucopolysaccharidosis VII” [Mol Genet Metab 2020 Mar;129(3):219–227]

Nuevas hipótesis embriológicas, genética y epidemiología de la gastrosquisis

Chromosome analysis of 303 pregnancy losses in Mexico

Long-term safety and efficacy of vestronidase alfa, rhGUS enzyme replacement therapy, in subjects with mucopolysaccharidosis type VII

Análisis de la mutación c.187 C>T en el gen ATP6V0A2 mediante PCR-ARMS

Infantile-onset Pompe disease in seven Mexican children

Cystic fibrosis: current concepts

Sustained efficacy and safety of vestronidase alfa (rhGUS) enzyme replacement therapy in patients with MPS VII

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