Artuch Rafael | Clinical Biochemistry Department Hospital Sant Joan De Deu
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概要
関連著者
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Artuch Rafael
Clinical Biochemistry Department Hospital Sant Joan De Deu
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ARTUCH Rafael
Clinical Biochemistry Department, Hospital Sant Joan de Deu, Barcelona, and Centre for Biomedical Re
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Ormazabal Aida
Clinical Biochemistry Department Hospital Sant Joan De Deu Barcelona And Centre For Biomedical Resea
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Duarte Sofia
Neurology Department Hospital Sant Joan De Deu Barcelona And Centre For Biomedical Research On Rare
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SANMARTI Francesc
Epilepsy Unit, Hospital Sant Joan de Deu, Barcelona, and Centre for Biomedical Research on Rare Dise
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GONZALEZ Veronica
Neurology Department, Hospital Sant Joan de Deu, Barcelona, and Centre for Biomedical Research on Ra
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DUENAS Belen
Neurology Department, Hospital Sant Joan de Deu, Barcelona, and Centre for Biomedical Research on Ra
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ORMAZABAL Aida
Clinical Biochemistry Department, Hospital Sant Joan de Deu, Barcelona, and Centre for Biomedical Re
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CAMPISTOL Jaime
Neurology Department, Hospital Sant Joan de Deu, Barcelona, and Centre for Biomedical Research on Ra
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GARCIA-CAZORLA Angels
Neurology Department, Hospital Sant Joan de Deu, Barcelona, and Centre for Biomedical Research on Ra
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Navarro-sastre Aleix
Institut De Bioquimica Clinica Servei De Bioquimica I Genetica Molecular Hospital Clinic
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Montero Raquel
Clinical Biochemistry Department Hospital Sant Joan De Deu
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Vilaseca Maria
Clinical Biochemistry Department Hospital Sant Joan De Deu
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QUINTANA Ester
Institut de Bioquimica Clinica, Servei de Bioquimica i Genetica Molecular, Hospital Clinic
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CASADO Mercedes
Clinical Biochemistry Department, Hospital Sant Joan de Deu
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BRIONES Paz
Institut de Bioquimica Clinica, Servei de Bioquimica i Genetica Molecular, Hospital Clinic
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Briones Paz
Institut De Bioquimica Clinica Servei De Bioquimica I Genetica Molecular Hospital Clinic
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Garcia-cazorla Angels
Neurology Department Hospital Sant Joan De Deu Barcelona And Centre For Biomedical Research On Rare
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Artuch Rafael
Clinical Biochemistry Department Hospital Sant Joan De Deu Barcelona And Centre For Biomedical Resea
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Duenas Belen
Neurology Department Hospital Sant Joan De Deu Barcelona And Centre For Biomedical Research On Rare
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Campistol Jaime
Neurology Department Hospital Sant Joan De Deu Barcelona And Centre For Biomedical Research On Rare
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Casado Mercedes
Clinical Biochemistry Department Hospital Sant Joan De Deu
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Sanmarti Francesc
Epilepsy Unit Hospital Sant Joan De Deu Barcelona And Centre For Biomedical Research On Rare Disease
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Quintana Ester
Institut De Bioquimica Clinica Servei De Bioquimica I Genetica Molecular Hospital Clinic
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Gonzalez Veronica
Neurology Department Hospital Sant Joan De Deu Barcelona And Centre For Biomedical Research On Rare
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GARCIA-CAZORLA Angels
Department of Pediatric Neurology, Hospital Sant Joan de Deu, Barcelona University, CIBER-ER, Biomedical Network Research Centre on Rare Diseases, Instituto de Salud Carlos III
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FONS Carmen
Department of Pediatric Neurology, Hospital Sant Joan de Deu, Barcelona University, CIBER-ER, Biomedical Network Research Centre on Rare Diseases, Instituto de Salud Carlos III
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RIZZU Patrizia
Clinical Genetics Department, VU Medisch Centrum
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MARTORELL Loreto
Molecular Genetics Department, Hospital Sant Joan de Deu, Barcelona University, CIBER-ER, Biomedical Network Research Centre on Rare Diseases, Instituto de Salud Carlos III
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CAMPISTOL Jaume
Department of Pediatric Neurology, Hospital Sant Joan de Deu, Barcelona University, CIBER-ER, Biomedical Network Research Centre on Rare Diseases, Instituto de Salud Carlos III
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FERNANDEZ-ALVAREZ Emilio
Department of Pediatric Neurology, Hospital Sant Joan de Deu, Barcelona University, CIBER-ER, Biomedical Network Research Centre on Rare Diseases, Instituto de Salud Carlos III
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ARTUCH Rafael
Clinical Biochemistry Department, Hospital Sant Joan de Deu, Barcelona University, CIBER-ER, Biomedical Network Research Centre on Rare Diseases, Instituto de Salud Carlos III
著作論文
- Cerebrospinal fluid pterins and neurotransmitters in early severe epileptic encephalopathies
- Comparison between high performance liquid chromatography and capillary zone electrophoresis for the diagnosis of congenital disorders of glycosylation
- TITF-1 gene mutation in a case of sporadic non-progressive chorea. Response to levodopa treatment