Genetics And Genomic Of Neuromuscular Diseases. Carmen Espinós Lab.
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- Annual Conference of the Society of Neurology
- 15th Scientific Conference on Wilson's Disease
- European Society Human Genetics 2024
- International Meeting on Wilson's Disease
- Defense of the dissertation by Isabel Hinarejos
- VIII Conference of Female Researchers in Rare Diseases
- International Wilson Meeting in Valencia
- New grants awarded
- Neurons from fibroblasts
- International Conference on Human Genetics
- VII Conference of Female Researchers in Rare Diseases
- New project on Wilson disease in collaboration with the FPAA
- International Meeting on Hereditary Metabolic Diseases
- XIII Scientific and Coexistence Conference on Wilson disease
- Dr. Candela Machuca
- Wilson Aarhus
- VI Female Researchers Conference on Rare Diseases
- February, 11th: International Day of Women and Girls in Science
- Inaugural International Scientific Conference on INAD
- III Interdisciplinary Congress on Human Genetics
- XII Scientific Meeting on Wilson's disease
- Referent Awards ANASBABI
- European Meeting of Human Genetics
- CIPF Seminars: Wilson’s disease & NBIA-PLAN
- A new project
- Dr. Sánchez-Monteagudo
- XXVI Conference - ALEH, 2021
- International Rare Diseases Day 2021
- Rare Disease Day 2020
- V Female Researchers Conference on Rare Diseases
- Annual Conference of the Spanish Society of Neurology - 2019
- New York Stem Cell Foundation Conference
- Latest findings on Wilson's disease research
- Dr. Paula Sancho
- European Human Genetics Conference - 2019
- III National Congress of Young Researchers in Biomedicine
- Spanish Conference on Human Genetics
- IV Female Researchers Conference on Rare Diseases
- International Day of Women and Girls in Science
- Seminar by Prof. José A. Sánchez-Alcázar at the CIPF
- Conference on Movement Disorders
- 15th International Congress on Neuromuscular Diseases
- III National Meeting of Women Researchers on Rare Diseases
- II Meeting of the Consortium on Rare Diseases – Comunitat Valenciana
- X Scientific meeting for patients with Wilson disease
- Science Week in Quart
- Funds obtained for the project on ataxias and paraplegias
- Master Students and Graduate Students
- 2017 Peripheral Nerve Society Annual Meeting
- European Human Genetics Conference 2017
- Research on Ataxias and Paraplegias
- Spanish Meeting on Human Genetics
- II National Meeting of Women Researchers on Rare Diseases
- BIOGRAU2 – Speech Series - Universitat de València
- 11 February: International Day of Women and Girls in Science
- Conbiopreval Conference at CIPF
- Annual Meeting of the Spanish Society of Neurology
- Genetics and Genomics Departaments at the CIPF with the Neuromuscular Disorders
- Seminar by Petra Lassuthova at the CIPF
- 6th International Charcot-Marie-Tooth and Related Neuropathy Consortium (CMTR) Meeting
- 2nd National Conference on Rare Diseases
- Indacea: a crowdfunding platform
- Rare Diseases Subject at the Faculty of Medicine
- Defense of the doctoral thesis by Eduardo Calpena
- Seminar by Roman Chrast at CIPF
- Female Researchers Conference on Rare Diseases
- World Rare Disease Day at FISABIO
- I Conference on Traslational Research on Rare Diseases in Valencia
- CIB-2016 Medical Research Meeting
- Research on the Wilson Disease
- New article about a new tool for molecular diagnosis of Charcot-Marie-Tooth and Hereditary Motor Neuropathy
- II Biomedicine Conference for Predocs
- Neurodegeneration with Brain Iron Accumulation Disorders
- European Society of Human Genetics. Glasgow, 6-9 June 2015
- They study the characterization of a new gene involved in hereditary neuropathy clinical form of recurrent
- JPH 1 gene characterized as the modifier CMT clinical expression caused by mutations in the gene GDAP1
- TREAT-CMT researchers describe the relationship between the NRG1 / ErbB route myelination and neuropathy Charcot-Marie-Tooth (CMT)
- Teresa Sevilla and Carmen Espinós presented the TREAT-CMT project at the Symposium on Neuromuscular Diseases
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