Showing
1 - 5
results of
5
Skip to content
VuFind
Log in
Library Catalogue Plus
Library
Subject guides
Databases
Referencing
Catalogue
Articles Plus
Keyword
Title
Author
Subject
Find
Advanced Search
Search Results - Olivas, Silvia Meavilla
Search Results - Olivas, Silvia Meavilla
Showing
1 - 5
results of
5
Refine Results
Sort
Relevance
Date Descending
Author
Title
1
Loading…
Review and evaluation of the methodological quality of the existing guidelines and recommendations for inherited neurometabolic disorders
by
Cassis, Linda
,
Cortès-Saladelafont, Elisenda
,
Molero-Luis, Marta
,
Yubero, Delia
,
González, Maria Julieta
,
Ormazábal, Aida
,
Fons, Carme
,
Jou, Cristina
,
Sierra, Cristina
,
Castejon Ponce, Esperanza
,
Ramos, Federico
,
Armstrong, Judith
,
O'Callaghan, M Mar
,
Casado, Mercedes
,
Montero, Raquel
,
Meavilla-Olivas, Silvia
,
Artuch, Rafael
,
Barić, Ivo
,
Bartoloni, Franco
,
Bellettato, Cinzia Maria
,
Bonifazi, Fedele
,
Ceci, Adriana
,
Cvitanović-Šojat, Ljerka
,
Dali, Christine I
,
D'Avanzo, Francesca
,
Fumic, Ksenija
,
Giannuzzi, Viviana
,
Lampe, Christina
,
Scarpa, Maurizio
,
Garcia-Cazorla, Ángels
Published in
Orphanet journal of rare diseases
Get full text
Items that this one cites
Items that cite this one
Article
Save to List
Saved in:
2
Loading…
Phenotype, treatment practice and outcome in the cobalamin‐dependent remethylation disorders and MTHFR deficiency: Data from the E‐HOD registry
by
Huemer, Martina
,
Diodato, Daria
,
Martinelli, Diego
,
Olivieri, Giorgia
,
Blom, Henk
,
Gleich, Florian
,
Kölker, Stefan
,
Kožich, Viktor
,
Morris, Andrew A.
,
Seifert, Burkhardt
,
Froese, D. Sean
,
Baumgartner, Matthias R.
,
Dionisi‐Vici, Carlo
,
Martin, Carlos Alcalde
,
Baethmann, Martina
,
Ballhausen, Diana
,
Blasco‐Alonso, Javier
,
Boy, Nikolas
,
Bueno, Maria
,
Burgos Peláez, Rosa
,
Cerone, Roberto
,
Chabrol, Brigitte
,
Chapman, Kimberly A.
,
Couce, Maria Luz
,
Crushell, Ellen
,
Dalmau Serra, Jaime
,
Diogo, Luisa
,
Ficicioglu, Can
,
García Jimenez, Maria Concepcion
,
García Silva, Maria Teresa
,
Gaspar, Ana Maria
,
Gautschi, Matthias
,
González‐Lamuño, Domingo
,
Gouveia, Sofia
,
Grünewald, Stephanie
,
Hendriksz, Chris
,
Janssen, Mirian C. H.
,
Jesina, Pavel
,
Koch, Johannes
,
Konstantopoulou, Vassiliki
,
Lavigne, Christian
,
Lund, Allan M.
,
Martins, Esmeralda G.
,
Meavilla Olivas, Silvia
,
Mention, Karine
,
Mochel, Fanny
,
Mundy, Helen
,
Murphy, Elaine
,
Paquay, Stephanie
,
Pedrón‐Giner, Consuelo
,
Ruiz Gómez, Maria Angeles
,
Santra, Saikat
,
Schiff, Manuel
,
Schwartz, Ida Vanessa
,
Scholl‐Bürgi, Sabine
,
Servais, Aude
,
Skouma, Anastasia
,
Tran, Christel
,
Vives Piñera, Inmaculada
,
Walter, John
,
Weisfeld‐Adams, James
Published in
Journal of inherited metabolic disease
Get full text
Items that this one cites
Items that cite this one
Article
Save to List
Saved in:
3
Loading…
Postauthorization safety study of betaine anhydrous
by
Mütze, Ulrike
,
Gleich, Florian
,
Garbade, Sven F.
,
Plisson, Céline
,
Aldámiz‐Echevarría, Luis
,
Arrieta, Francisco
,
Ballhausen, Diana
,
Zielonka, Matthias
,
Petković Ramadža, Danijela
,
Baumgartner, Matthias R.
,
Cano, Aline
,
García Jiménez, María Concepción
,
Dionisi‐Vici, Carlo
,
Ješina, Pavel
,
Blom, Henk J.
,
Couce, Maria Luz
,
Meavilla Olivas, Silvia
,
Mention, Karine
,
Mochel, Fanny
,
Morris, Andrew A. M.
,
Mundy, Helen
,
Redonnet‐Vernhet, Isabelle
,
Santra, Saikat
,
Schiff, Manuel
,
Servais, Aude
,
Vitoria, Isidro
,
Huemer, Martina
,
Kožich, Viktor
,
Kölker, Stefan
Published in
Journal of inherited metabolic disease
Get full text
Items that this one cites
Items that cite this one
Article
Save to List
Saved in:
4
Loading…
Erratum to: Review and evaluation of the methodological quality of the existing guidelines and recommendations for inherited neurometabolic disorders
by
Cassis, Linda
,
Cortès-Saladelafont, Elisenda
,
Molero-Luis, Marta
,
Yubero, Delia
,
González, Maria Julieta
,
Ormazábal, Aida
,
Fons, Carme
,
Jou, Cristina
,
Sierra, Cristina
,
Ponce, Esperanza Castejon
,
Ramos, Federico
,
Armstrong, Judith
,
O'Callaghan, M Mar
,
Casado, Mercedes
,
Montero, Raquel
,
Meavilla-Olivas, Silvia
,
Artuch, Rafael
,
Barić, Ivo
,
Bartoloni, Franco
,
Bellettato, Cinzia Maria
,
Bonifazi, Fedele
,
Ceci, Adriana
,
Cvitanović-Šojat, Ljerka
,
Dali, Christine I
,
D'Avanzo, Francesca
,
Fumic, Ksenija
,
Giannuzzi, Viviana
,
Lampe, Christina
,
Scarpa, Maurizio
,
Garcia-Cazorla, Ángels
Published in
Orphanet journal of rare diseases
Get full text
Items that this one cites
Article
Save to List
Saved in:
5
Loading…
Cystathionine β‐synthase deficiency in the E‐HOD registry‐part I: pyridoxine responsiveness as a determinant of biochemical and clinical phenotype at diagnosis
by
Kožich, Viktor
,
Sokolová, Jitka
,
Morris, Andrew A. M.
,
Pavlíková, Markéta
,
Gleich, Florian
,
Kölker, Stefan
,
Krijt, Jakub
,
Dionisi‐Vici, Carlo
,
Baumgartner, Matthias R.
,
Blom, Henk J.
,
Huemer, Martina
,
Aldámiz‐Echevarría, Luis
,
Arantes, Rodrigo Rezende
,
Arrieta, Francisco
,
Blasco‐Alonso, Javier
,
Brouwers, Martijn
,
Brunner‐Krainz, Michaela
,
Bueno, María
,
Peláez, Rosa Burgos
,
Cano, Aline
,
Couce, María‐Luz
,
Crushell, Ellen
,
Ficicioglu, Can
,
Forny, Patrick
,
García Jiménez, María Concepción
,
Gaspar, Ana
,
González‐Lamuño Leguina, Domingo
,
Chapman, Kimberly A.
,
Chien, Yin‐Hsiu
,
Janssen, Mirian C.H.
,
Ješina, Pavel
,
Lachmann, Robin
,
Lavigne, Christian
,
Lund, Allan M.
,
Lüsebrink, Natalia
,
Maillot, Francois
,
Martins, Ana Maria
,
Olivas, Silvia Meavilla
,
Mention, Karine
,
Mochel, Fanny
,
Monavari, Ahmad
,
Moreira, Sónia
,
Moreno, Carolina Araujo
,
Muačević‐Katanec, Diana
,
Mundy, Helen
,
Murphy, Elaine
,
Olivieri, Giorgia
,
Paquay, Stéphanie
,
Pedrón‐Giner, Consuelo
,
Quintana, Luís Peña
,
Porras‐Hurtado, Gloria L.
,
Fraile, Pilar Quijada
,
Redonnet‐Vernhet, Isabelle
,
Rennings, Alexander J.M.
,
Pons, Mònica Ruiz
,
Santra, Saikat
,
Servais, Aude
,
Schiaffino, Maria Cristina
,
Schiff, Manuel
,
Schwahn, Bernd C.
,
Schwartz, Ida V.D.
,
Sremba, Leighann J.
,
Stainforth, Collette
,
Stepien, Karolina M.
,
Sykut‐Cegielska, Jolanta
,
Terry, Allyson
,
Tran, Christel
,
Miñana, Isidro Vitoria
,
Vives‐Piñera, Inmaculada
,
Williams, Monique
,
Zeman, Jiří
,
Zielonka, Matthias
Published in
Journal of inherited metabolic disease
Get full text
Items that this one cites
Items that cite this one
Article
Save to List
Saved in:
Search Tools:
RSS Feed
Email Search
Save Search
Back
Refine Results
Page will reload when a filter is selected or excluded.
Limit To
Peer Reviewed
5 results
5
Full Text
5 results
5
Format
Articles
5 results
5
Journal Title
Journal Of Inherited Metabolic Disease
3 results
3
Orphanet Journal Of Rare Diseases
2 results
2
Subjects
Genetics & Heredity
4 results
4
Life Sciences & Biomedicine
4 results
4
Medicine, Research & Experimental
4 results
4
Research & Experimental Medicine
4 results
4
Science & Technology
4 results
4
Endocrinology & Metabolism
3 results
3
Homocysteine
3 results
3
Cognitive Ability
2 results
2
Diagnosis
2 results
2
Homocystinuria
2 results
2
Humans
2 results
2
Methylation
2 results
2
Methylenetetrahydrofolate Reductase
2 results
2
Patients
2 results
2
Phenotypes
2 results
2
Rare Diseases
2 results
2
Thromboembolism
2 results
2
Vitamin B12
2 results
2
Adolescent
1 results
1
Adult
1 results
1
Year of Publication
From:
To:
Source
Springerlink Contemporary
5 results
5
Science Citation Index Expanded (Web Of Science)
4 results
4
Wiley Journal Backfiles
3 results
3
Wiley Online Library (Online Service)
3 results
3
Wiley-Blackwell Read & Publish Collection
3 results
3
Springerlink 过刊(Nstl购买)
3 results
3
Wiley Open Access Journals
2 results
2
Doaj Directory Of Open Access Journals
2 results
2
Road: Directory Of Open Access Scholarly Resources
2 results
2
Ezb Electronic Journals Library
2 results
2
Publicly Available Content Database
2 results
2
Pubmed Central
2 results
2
Ingentaconnect Journals
1 results
1